CombiUgiResults

Experiment Number (Comp'd ID/Lib Rank)

hyperlink

Rajarshi prediction precipiate

Precipitate

Ugi product

Aldehyde

SMILES aldehyde

Amine

SMILES amine

Acid

SMILES acid

Isocyanide

SMILES isonitrile

Yield %

Researcher

Solvent

Solvent amount (mL)

Aldehyde amount (mmol)

Amine amount (mmol)

Acid amount (mmol)

Isocyanide amount (mmol)

Ald density

Mol Wt of the ald

Amine density

Mol Wt of the amine

Acid density

Mol Wt of the acid

isocyanide density

Mol Wt of the isocyanide

Ald vol mL

Amine vol mL

Acid vol mL

isocyanide vol mL

max conc of ugi product possible (M)

Ugi Product SMILES

ChemSpider link

Comment

logP (ACD)


.	UCExp241-12	http://usefulchem.wikispaces.com/Exp241	No	No	veratraldehyde	COC1=C(OC)C=C(C=O)C=C1	Methylamine	NC	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	1-pentylisocyanide	[C-]#[N+]CCCCC	Khalid	methanol	0.13324	0.1	0.1	0.1	0.1	1.114	166.17	0.785	31.06	1.406	180.15	0.772	97.16	0.014916517055655	0.003956687898089	0.012812944523471	0.012585492227979	0.56334333365063	COc1ccc(cc1OC)C(C(=O)NCCCCC)N(C)C(=O)Cc2ccc3OCOc3c2
.	UCExp241-13	http://usefulchem.wikispaces.com/Exp241	No	No	veratraldehyde	COC1=C(OC)C=C(C=O)C=C1	Methylamine	NC	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	1-pentylisocyanide	[C-]#[N+]CCCCC	Khalid	methanol	0.13324	0.1	0.1	0.1	0.1	1.114	166.17	0.785	31.06	1.406	180.15	0.772	97.16	0.014916517055655	0.003956687898089	0.012812944523471	0.012585492227979	0.56334333365063	COc1ccc(cc1OC)C(C(=O)NCCCCC)N(C)C(=O)Cc2ccc3OCOc3c2
.	Exp242-9	http://usefulchem.wikispaces.com/Exp242	No	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	5-Methylfurfurylamine	NCc1oc(cc1)C	phenylacetic acid	O=C(O)Cc1ccccc1	1,1,3,3-Tetramethylbutyl isocyanide	[C-]#[N+]C(C)(C)CC(C)(C)C	Marshall	benzene	0.2286	0.1	0.1	0.1	0.1	1.217	206.24	0.997	111.14	1.164	136.15	0.794	139.24	0.016946589975349	0.011147442326981	0.011696735395189	0.017536523929471	0.34973926214241	CC(C)(C)CC(C)(C)NC(=O)C(N(Cc1ccc(C)o1)C(=O)Cc2ccccc2)C=5C=C3C=CC=CC3C4C=CC=CC4=5
.	Exp242-4	http://usefulchem.wikispaces.com/Exp242	Yes	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	furfurylamine	o1c(ccc1)CN	phenylacetic acid	O=C(O)Cc1ccccc1	1,1,3,3-Tetramethylbutyl isocyanide	[C-]#[N+]C(C)(C)CC(C)(C)C	Marshall	benzene	0.19461385052278	0.1	0.1	0.1	0.1	1.217	206.24	1.099	97.12	1.164	136.15	0.794	139.24	0.016946589975349	0.008837124658781	0.011696735395189	0.017536523929471	0.40059155437906	CC(C)(C)CC(C)(C)NC(=O)C(N(Cc1ccco1)C(=O)Cc2ccccc2)C=5C=C3C=CC=CC3C4C=CC=CC4=5
.	UCExp241-10	http://usefulchem.wikispaces.com/Exp241	No	No	veratraldehyde	COC1=C(OC)C=C(C=O)C=C1	Methylamine	NC	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	1,1,3,3-Tetramethylbutyl isocyanide	[C-]#[N+]C(C)(C)CC(C)(C)C	Khalid	methanol	0.13324	0.1	0.1	0.1	0.1	1.114	166.17	0.785	31.06	1.406	180.15	0.794	139.24	0.014916517055655	0.003956687898089	0.012812944523471	0.017536523929471	0.54805729924341	c1cc2OCOc2cc1CC(=O)N(C)C(c1ccc(OC)c(OC)c1)C(=O)NC(C)(C)CC(C)(C)C
.	UCExp241-11	http://usefulchem.wikispaces.com/Exp241	No	No	veratraldehyde	COC1=C(OC)C=C(C=O)C=C1	Methylamine	NC	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	1,1,3,3-Tetramethylbutyl isocyanide	[C-]#[N+]C(C)(C)CC(C)(C)C	Khalid	methanol	0.13324	0.1	0.1	0.1	0.1	1.114	166.17	0.785	31.06	1.406	180.15	0.794	139.24	0.014916517055655	0.003956687898089	0.012812944523471	0.017536523929471	0.54805729924341	c1cc2OCOc2cc1CC(=O)N(C)C(c1ccc(OC)c(OC)c1)C(=O)NC(C)(C)CC(C)(C)C
.	UCExp245-35	http://usefulchem.wikispaces.com/Exp245	No	No	piperonal	O=Cc1ccc2OCOc2c1	furfurylamine	o1c(ccc1)CN	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	1,1,3,3-Tetramethylbutyl isocyanide	[C-]#[N+]C(C)(C)CC(C)(C)C	Khalid	methanol	0.15296	0.1	0.1	0.1	0.1	1.337	150.13	1.099	97.12	1.406	180.15	0.794	139.24	0.011228870605834	0.008837124658781	0.012812944523471	0.017536523929471	0.49170139884169	c1cc2OCOc2cc1CC(=O)N(Cc1ccco1)C(c1cc(OC)c(OC)cc1)C(=O)NC(C)(C)CC(C)(C)C
.	UCExp245-36	http://usefulchem.wikispaces.com/Exp245	No	No	piperonal	O=Cc1ccc2OCOc2c1	furfurylamine	o1c(ccc1)CN	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	1,1,3,3-Tetramethylbutyl isocyanide	[C-]#[N+]C(C)(C)CC(C)(C)C	Khalid	methanol	0.09596	0.1	0.1	0.1	0.1	1.337	150.13	1.099	97.12	1.406	180.15	0.794	139.24	0.011228870605834	0.008837124658781	0.012812944523471	0.017536523929471	0.68317460768533	c1cc2OCOc2cc1CC(=O)N(Cc1ccco1)C(c1cc(OC)c(OC)cc1)C(=O)NC(C)(C)CC(C)(C)C
.	UCExp245-09	http://usefulchem.wikispaces.com/Exp245	No	No	piperonal	O=Cc1ccc2OCOc2c1	furfurylamine	o1c(ccc1)CN	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	1,1,3,3-Tetramethylbutyl isocyanide	[C-]#[N+]C(C)(C)CC(C)(C)C	Khalid	methanol	0.15296	0.1	0.1	0.1	0.1	1.337	150.13	1.099	97.12	1.406	180.15	0.794	139.24	0.011228870605834	0.008837124658781	0.012812944523471	0.017536523929471	0.49170139884169	c1cc2OCOc2cc1CC(=O)N(Cc1ccco1)C(c1ccc2OCOc2c1)C(=O)NC(C)(C)CC(C)(C)C
.	UCExp245-10	http://usefulchem.wikispaces.com/Exp245	No	No	piperonal	O=Cc1ccc2OCOc2c1	furfurylamine	o1c(ccc1)CN	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	1,1,3,3-Tetramethylbutyl isocyanide	[C-]#[N+]C(C)(C)CC(C)(C)C	Khalid	methanol	0.09596	0.1	0.1	0.1	0.1	1.337	150.13	1.099	97.12	1.406	180.15	0.794	139.24	0.011228870605834	0.008837124658781	0.012812944523471	0.017536523929471	0.68317460768533	c1cc2OCOc2cc1CC(=O)N(Cc1ccco1)C(c1ccc2OCOc2c1)C(=O)NC(C)(C)CC(C)(C)C
.	UCExp245-15	http://usefulchem.wikispaces.com/Exp245	No	No	piperonal	O=Cc1ccc2OCOc2c1	5-Methylfurfurylamine	NCc1oc(cc1)C	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	1,1,3,3-Tetramethylbutyl isocyanide	[C-]#[N+]C(C)(C)CC(C)(C)C	Khalid	methanol	0.15296	0.1	0.1	0.1	0.1	1.337	150.13	0.997	111.14	1.406	180.15	0.794	139.24	0.011228870605834	0.011147442326981	0.012812944523471	0.017536523929471	0.48617847731756	c1cc2OCOc2cc1CC(=O)N(Cc1oc(cc1)C)C(c1ccc2OCOc2c1)C(=O)NC(C)(C)CC(C)(C)C
.	UCExp245-16	http://usefulchem.wikispaces.com/Exp245	No	No	piperonal	O=Cc1ccc2OCOc2c1	5-Methylfurfurylamine	NCc1oc(cc1)C	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	1,1,3,3-Tetramethylbutyl isocyanide	[C-]#[N+]C(C)(C)CC(C)(C)C	Khalid	methanol	0.09596	0.1	0.1	0.1	0.1	1.337	150.13	0.997	111.14	1.406	180.15	0.794	139.24	0.011228870605834	0.011147442326981	0.012812944523471	0.017536523929471	0.67255926604411	c1cc2OCOc2cc1CC(=O)N(Cc1oc(cc1)C)C(c1ccc2OCOc2c1)C(=O)NC(C)(C)CC(C)(C)C
.	UCExp245-25	http://usefulchem.wikispaces.com/Exp245	No	No	piperonal	O=Cc1ccc2OCOc2c1	furfurylamine	o1c(ccc1)CN	cbz-proline	O=C(O)[C@H]2N(C(=O)OCc1ccccc1)CCC2	1,1,3,3-Tetramethylbutyl isocyanide	[C-]#[N+]C(C)(C)CC(C)(C)C	Khalid	methanol	0.13973	0.1	0.1	0.1	0.1	1.337	150.13	1.099	97.12	1.309	249.262	0.794	139.24	0.011228870605834	0.008837124658781	0.019042169595111	0.017536523929471	0.50923059696022	c1ccccc1COC(=O)N1CCCC1C(=O)N(Cc1ccco1)C(c1ccc2OCOc2c1)C(=O)NC(C)(C)CC(C)(C)C
.	UCExp245-26	http://usefulchem.wikispaces.com/Exp245	No	No	piperonal	O=Cc1ccc2OCOc2c1	furfurylamine	o1c(ccc1)CN	cbz-proline	O=C(O)[C@H]2N(C(=O)OCc1ccccc1)CCC2	1,1,3,3-Tetramethylbutyl isocyanide	[C-]#[N+]C(C)(C)CC(C)(C)C	Khalid	methanol	0.03973	0.1	0.1	0.1	0.1	1.337	150.13	1.099	97.12	1.309	249.262	0.794	139.24	0.011228870605834	0.008837124658781	0.019042169595111	0.017536523929471	1.03761683961163	c1ccccc1COC(=O)N1CCCC1C(=O)N(Cc1ccco1)C(c1ccc2OCOc2c1)C(=O)NC(C)(C)CC(C)(C)C
.	UCExp245-29	http://usefulchem.wikispaces.com/Exp245	No	No	piperonal	O=Cc1ccc2OCOc2c1	5-Methylfurfurylamine	NCc1oc(cc1)C	cbz-proline	O=C(O)[C@H]2N(C(=O)OCc1ccccc1)CCC2	1,1,3,3-Tetramethylbutyl isocyanide	[C-]#[N+]C(C)(C)CC(C)(C)C	Khalid	methanol	0.13973	0.1	0.1	0.1	0.1	1.337	150.13	0.997	111.14	1.309	249.262	0.794	139.24	0.011228870605834	0.011147442326981	0.019042169595111	0.017536523929471	0.50330924201592	c1ccccc1COC(=O)N1CCCC1C(=O)N(Cc1oc(cc1)C)C(c1ccc2OCOc2c1)C(=O)NC(C)(C)CC(C)(C)C
.	UCExp245-30	http://usefulchem.wikispaces.com/Exp245	No	No	piperonal	O=Cc1ccc2OCOc2c1	5-Methylfurfurylamine	NCc1oc(cc1)C	cbz-proline	O=C(O)[C@H]2N(C(=O)OCc1ccccc1)CCC2	1,1,3,3-Tetramethylbutyl isocyanide	[C-]#[N+]C(C)(C)CC(C)(C)C	Khalid	methanol	0.03973	0.1	0.1	0.1	0.1	1.337	150.13	0.997	111.14	1.309	249.262	0.794	139.24	0.011228870605834	0.011147442326981	0.019042169595111	0.017536523929471	1.01332516042517	c1ccccc1COC(=O)N1CCCC1C(=O)N(Cc1oc(cc1)C)C(c1ccc2OCOc2c1)C(=O)NC(C)(C)CC(C)(C)C
.	EXP232-25	http://usefulchem.wikispaces.com/Exp232	No	No	diphenylacetaldehyde	O=CC(c1ccccc1)c2ccccc2	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	1,1,3,3-Tetramethylbutyl isocyanide	[C-]#[N+]C(C)(C)CC(C)(C)C	Khalid	methanol	0.031	0.1	0.1	0.1	0.1	1.106	196.24	1.099	97.12	1.159	175.18	0.794	139.24	0.01774321880651	0.017856232939036	0.015114754098361	0.017536523929471	1.00754926667374	CC(C)(C)CC(C)(C)NC(=O)C(C(c1ccccc1)c2ccccc2)N(Cc3ccco3)C(=O)CNC(=O)OC(C)(C)C	Need Link
.	EXP232-75	http://usefulchem.wikispaces.com/Exp232	No	No	2-ethylbutyraldehyde	O=CC(CC)CC	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	1,1,3,3-Tetramethylbutyl isocyanide	[C-]#[N+]C(C)(C)CC(C)(C)C	Khalid	methanol	0.0364	0.1	0.1	0.1	0.1	0.814	100.16	1.099	97.12	1.159	175.18	0.794	139.24	0.012304668304668	0.009113739763421	0.015114754098361	0.017536523929471	1.10534262154921	CC(C)(C)CC(C)(C)NC(=O)C(C(CC)CC)N(Cc1ccco1)C(=O)CNC(=O)OC(C)(C)C	Need Link
.	EXP232-30	http://usefulchem.wikispaces.com/Exp232	No	No	cyclohexancarboxaldehyde	O=CC1CCCCC1	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	1,1,3,3-Tetramethylbutyl isocyanide	[C-]#[N+]C(C)(C)CC(C)(C)C	Khalid	methanol	0.0366	0.1	0.1	0.1	0.1	0.926	112.17	1.099	97.12	1.159	175.18	0.794	139.24	0.012113390928726	0.010206551410373	0.015114754098361	0.017536523929471	1.09204616471523	CC(C)(C)CC(C)(C)NC(=O)C(C1CCCCC1)N(Cc2ccco2)C(=O)CNC(=O)OC(C)(C)C	Need Link
.	EXP232-55	http://usefulchem.wikispaces.com/Exp232	No	No	hexanaldehyde	O=CCCCCC	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	1,1,3,3-Tetramethylbutyl isocyanide	[C-]#[N+]C(C)(C)CC(C)(C)C	Khalid	methanol	0.0364	0.1	0.1	0.1	0.1	0.815	100.16	1.099	97.12	1.159	175.18	0.794	139.24	0.012289570552147	0.009113739763421	0.015114754098361	0.017536523929471	1.10552711400733	CC(C)(C)CC(C)(C)NC(=O)C(CCCCC)N(Cc1ccco1)C(=O)CNC(=O)OC(C)(C)C	Need Link


.	EXP232-60	http://usefulchem.wikispaces.com/Exp232	No	No	trans-2-hexenal	O=C/C=C/CCC	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	1,1,3,3-Tetramethylbutyl isocyanide	[C-]#[N+]C(C)(C)CC(C)(C)C		Khalid	methanol	0.0371	0.1	0.1	0.1	0.1	0.846	98.14	1.099	97.12	1.159	175.18	0.794	139.24	0.011600472813239	0.008837124658781	0.015114754098361	0.017536523929471	1.10878419811504	CC(C)(C)OC(=O)NCC(=O)N(CC(=O)NC(C)(C)CC(C)(C)C)C(\C=C\CCC)c1ccco1	Need Link
.	EXP232-65	http://usefulchem.wikispaces.com/Exp232	No	No	2-phenylpropionaldehyde	O=CC(c1ccccc1)C	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	1,1,3,3-Tetramethylbutyl isocyanide	[C-]#[N+]C(C)(C)CC(C)(C)C		Khalid	methanol	0.0353	0.1	0.1	0.1	0.1	1.002	134.18	1.099	97.12	1.159	175.18	0.794	139.24	0.01339121756487	0.012209281164695	0.015114754098361	0.017536523929471	1.06892678542413	CC(C)(C)OC(=O)NCC(=O)N(CC(=O)NC(C)(C)CC(C)(C)C)C(c1ccco1)C(C)c2ccccc2	Need Link
.	EXP232-20	http://usefulchem.wikispaces.com/Exp232	No	No	crotonaldehyde	O=C/C=C/C	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	1,1,3,3-Tetramethylbutyl isocyanide	[C-]#[N+]C(C)(C)CC(C)(C)C		Khalid	methanol	0.0404	0.1	0.1	0.1	0.1	0.853	0.853	1.099	97.12	1.159	175.18	0.794	139.24	0.0001	0.000077616014559	0.015114754098361	0.017536523929471	1.36558118632944	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(\C=C\C)C(=O)NC(C)(C)CC(C)(C)C	Need Link
.	EXP232-10	http://usefulchem.wikispaces.com/Exp232	No	No	4-methylbenzaldehyde	Cc1ccc(C=O)cc1	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	1,1,3,3-Tetramethylbutyl isocyanide	[C-]#[N+]C(C)(C)CC(C)(C)C		Khalid	methanol	0.037	0.1	0.1	0.1	0.1	1.019	120.15	1.099	97.12	1.159	175.18	0.794	139.24	0.011790971540726	0.010932666060055	0.015114754098361	0.017536523929471	1.08254496709955	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(=O)NC(C)(C)CC(C)(C)C)c2ccc(C)cc2	Need Link
.	EXP232-50	http://usefulchem.wikispaces.com/Exp232	No	No	p-anisaldehyde	COc1ccc(C=O)cc1	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	1,1,3,3-Tetramethylbutyl isocyanide	[C-]#[N+]C(C)(C)CC(C)(C)C		Khalid	methanol	0.0366	0.1	0.1	0.1	0.1	1.119	136.15	1.099	97.12	1.159	175.18	0.794	139.24	0.012167113494191	0.012388535031847	0.015114754098361	0.017536523929471	1.06601936204118	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(=O)NC(C)(C)CC(C)(C)C)c2ccc(OC)cc2	Need Link
.	EXP232-70	http://usefulchem.wikispaces.com/Exp232	No	No	m-anisaldehyde	COc1cc(C=O)ccc1	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	1,1,3,3-Tetramethylbutyl isocyanide	[C-]#[N+]C(C)(C)CC(C)(C)C		Khalid	methanol	0.0365	0.1	0.1	0.1	0.1	1.117	136.15	1.099	97.12	1.159	175.18	0.794	139.24	0.012188898836168	0.012388535031847	0.015114754098361	0.017536523929471	1.0669089329972	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(=O)NC(C)(C)CC(C)(C)C)c2cccc(OC)c2	Need Link
.	EXP232-05	http://usefulchem.wikispaces.com/Exp232	No	No	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	1,1,3,3-Tetramethylbutyl isocyanide	[C-]#[N+]C(C)(C)CC(C)(C)C		Khalid	methanol	0.0386	0.1	0.1	0.1	0.1	1.045	106.12	1.099	97.12	1.159	175.18	0.794	139.24	0.010155023923445	0.009656050955414	0.015114754098361	0.017536523929471	1.09814865098497	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(=O)NC(C)(C)CC(C)(C)C)c2ccccc2	Need Link
.	EXP232-45	http://usefulchem.wikispaces.com/Exp232	Yes	Pending	o-tolualdehyde	O=Cc1ccccc1C	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	1,1,3,3-Tetramethylbutyl isocyanide	[C-]#[N+]C(C)(C)CC(C)(C)C		Khalid	methanol	0.0372	0.1	0.1	0.1	0.1	1.039	120.15	1.099	97.12	1.159	175.18	0.794	139.24	0.011564003849856	0.010932666060055	0.015114754098361	0.017536523929471	1.08286109473073	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(=O)NC(C)(C)CC(C)(C)C)c2ccccc2C	Need Link
.	EXP232-40	http://usefulchem.wikispaces.com/Exp232	No	No	2-hydroxybenzaldehyde	O=Cc1ccccc1O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	1,1,3,3-Tetramethylbutyl isocyanide	[C-]#[N+]C(C)(C)CC(C)(C)C		Khalid	methanol	0.0381	0.1	0.1	0.1	0.1	1.146	122.12	1.099	97.12	1.159	175.18	0.794	139.24	0.010656195462478	0.011111919927207	0.015114754098361	0.017536523929471	1.08085447068082	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(=O)NC(C)(C)CC(C)(C)C)c2ccccc2O	Need Link
.	EXP232-35	http://usefulchem.wikispaces.com/Exp232	No	No	2-furaldehyde	O=Cc1ccco1	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	1,1,3,3-Tetramethylbutyl isocyanide	[C-]#[N+]C(C)(C)CC(C)(C)C		Khalid	methanol	0.0404	0.1	0.1	0.1	0.1	1.16	96.08	1.099	97.12	1.159	175.18	0.794	139.24	0.00828275862069	0.008742493175614	0.015114754098361	0.017536523929471	1.11016710118872	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(=O)NC(C)(C)CC(C)(C)C)c2ccco2	Need Link
.	EXP232-15	http://usefulchem.wikispaces.com/Exp232	No	No	4-(trifluoromethyl)benzaldehyde	FC(F)(F)c1ccc(C=O)cc1	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	1,1,3,3-Tetramethylbutyl isocyanide	[C-]#[N+]C(C)(C)CC(C)(C)C		Khalid	methanol	0.0351	0.1	0.1	0.1	0.1	1.275	174.12	1.099	97.12	1.159	175.18	0.794	139.24	0.013656470588235	0.015843494085532	0.015114754098361	0.017536523929471	1.02826449536316	FC(F)(F)c1ccc(cc1)C(C(=O)NC(C)(C)CC(C)(C)C)N(Cc2ccco2)C(=O)CNC(=O)OC(C)(C)C	Need Link
.	UCExp240-10	http://usefulchem.wikispaces.com/Exp240	No	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	5-Methylfurfurylamine	NCc1oc(cc1)C	phenylacetic acid	O=C(O)Cc1ccccc1	1,1,3,3-Tetramethylbutyl isocyanide	[C-]#[N+]C(C)(C)CC(C)(C)C		Khalid	THF	0.03431	1	1	1	1	1.217	206.24	0.997	111.14	1.164	136.15	0.794	139.24	0.16946589975349	0.11147442326981	0.11696735395189	0.17536523929471	1.64586589455023	CC(C)(C)CC(C)(C)NC(=O)C(N(Cc1ccc(C)o1)C(=O)Cc2ccccc2)c4cc5ccccc5c3ccccc34
.	UCExp240-04	http://usefulchem.wikispaces.com/Exp240	No	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	furfurylamine	o1c(ccc1)CN	phenylacetic acid	O=C(O)Cc1ccccc1	1,1,3,3-Tetramethylbutyl isocyanide	[C-]#[N+]C(C)(C)CC(C)(C)C		Khalid	THF	0.03661	1	1	1	1	1.217	206.24	1.099	97.12	1.164	136.15	0.794	139.24	0.16946589975349	0.18766151046406	0.11696735395189	0.17536523929471	1.45757720779328	CC(C)(C)CC(C)(C)NC(=O)C(N(Cc1ccco1)C(=O)Cc2ccccc2)c4cc5ccccc5c3ccccc34
.	EXP225-8	http://usefulchem.wikispaces.com/Exp225	No	No	piperonal	O=Cc1ccc2OCOc2c1	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	2-chloro-6-methylphenyl isocyanide	[C-]#[N+]c1c(C)cccc1Cl		Khalid	methanol	0.099957747498545	1	1	1	0.5	1.337	150.13	1.099	97.12	1.159	175.18	1	151.59	0.11228870605834	0.13660600545951	0.15114754098361	0.075795	0.868364608932	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(=O)Nc2c(C)cccc2Cl)c3ccc4OCOc4c3	Need Link	0.5 mmol of isocyanide was added to 500uL of a 2M solution of aldehyde, amine and acid
.	EXP226-8	http://usefulchem.wikispaces.com/Exp226	No	No	Benzaldehyde	c1ccccc1C=O	5-Methylfurfurylamine	NCc1oc(cc1)C	1-Pyrenebutyric acid	O=C(O)CCCc4ccc2ccc1cccc3c1c2c4cc3	2-chloro-6-methylphenyl isocyanide	[C-]#[N+]c1c(C)cccc1Cl		David	THF	0.39112269239863	0.25	0.25	0.25	0.5	1.045	106.12	0.997	111.14	1.296	288.34	1	151.59	0.025387559808612	0.027868605817452	0.055621141975309	0.075795	0.434182304466	Cc7cccc(Cl)c7NC(=O)C(N(Cc1ccc(C)o1)C(=O)CCCc5ccc4ccc3cccc2ccc5c4c23)c6ccccc6	Need Link	0.5 mmol of isocyanide was added to 500uL of a 0.5M solution of aldehyde, amine and acid
.	EXP227-8	http://usefulchem.wikispaces.com/Exp227	No	No	piperonal	O=Cc1ccc2OCOc2c1	furfurylamine	o1c(ccc1)CN	1-Pyrenebutyric acid	O=C(O)CCCc4ccc2ccc1cccc3c1c2c4cc3	2-chloro-6-methylphenyl isocyanide	[C-]#[N+]c1c(C)cccc1Cl		Khalid	THF	0.38215518014523	0.25	0.25	0.25	0.5	1.337	150.13	1.099	97.12	1.296	288.34	1	151.59	0.028072176514585	0.034151501364877	0.055621141975309	0.075795	0.434182304466	Cc8cccc(Cl)c8NC(=O)C(N(Cc1ccco1)C(=O)CCCc5ccc4ccc3cccc2ccc5c4c23)c6ccc7OCOc7c6	Need Link	0.5 mmol of isocyanide was added to 500uL of a 0.5M solution of aldehyde, amine and acid
.	EXP225-7	http://usefulchem.wikispaces.com/Exp225	No	No	piperonal	O=Cc1ccc2OCOc2c1	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	2-Morpholinoethyl isocyanide	[C-]#[N+]CCN1CCOCC1		Khalid	methanol	0.099957747498545	1	1	1	0.5	1.337	150.13	1.099	97.12	1.159	175.18	1.017	140.18	0.11228870605834	0.13660600545951	0.15114754098361	0.068918387413963	0.87886067854612	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(c2ccc3OCOc3c2)C(=O)NCCN4CCOCC4	Need Link	0.5 mmol of isocyanide was added to 500uL of a 2M solution of aldehyde, amine and acid
.	EXP226-7	http://usefulchem.wikispaces.com/Exp226	No	No	Benzaldehyde	c1ccccc1C=O	5-Methylfurfurylamine	NCc1oc(cc1)C	1-Pyrenebutyric acid	O=C(O)CCCc4ccc2ccc1cccc3c1c2c4cc3	2-Morpholinoethyl isocyanide	[C-]#[N+]CCN1CCOCC1		David	THF	0.68224538479725	0.5	0.5	0.5	0.5	1.045	106.12	0.997	111.14	1.296	288.34	1.017	140.18	0.050775119617225	0.055737211634905	0.11124228395062	0.068918387413963	0.51603933467967	Cc1ccc(o1)CN(C(=O)CCCc5ccc4ccc3cccc2ccc5c4c23)C(c6ccccc6)C(=O)NCCN7CCOCC7	Need Link	0.5 mmol of isocyanide was added to 900uL of a 0.55M solution of aldehyde, amine and acid
.	EXP227-7	http://usefulchem.wikispaces.com/Exp227	No	No	piperonal	O=Cc1ccc2OCOc2c1	furfurylamine	o1c(ccc1)CN	1-Pyrenebutyric acid	O=C(O)CCCc4ccc2ccc1cccc3c1c2c4cc3	2-Morpholinoethyl isocyanide	[C-]#[N+]CCN1CCOCC1		Khalid	THF	0.38215518014523	0.25	0.25	0.25	0.5	1.337	150.13	1.099	97.12	1.296	288.34	1.017	140.18	0.028072176514585	0.034151501364877	0.055621141975309	0.068918387413963	0.43943033927306	O=C(CCCc4ccc3ccc2cccc1ccc4c3c12)N(Cc5ccco5)C(c6ccc7OCOc7c6)C(=O)NCCN8CCOCC8	Need Link	0.5 mmol of isocyanide was added to 500uL of a 0.5M solution of aldehyde, amine and acid
.	EXP064C	http://usefulchem.wikispaces.com/Exp064	Yes	Yes	veratraldehyde	COC1=C(OC)C=C(C=O)C=C1	5-Methylfurfurylamine	NCc1oc(cc1)C	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	benzyl isocyanide	[C-]#[N+]Cc1ccccc1	43.8	Khalid	methanol	4	2	2.2	2	2	1.114	166.17	0.997	111.14	1.159	175.18	0.962	117.15	0.29833034111311	0.24524373119358	0.30229508196721	0.24355509355509	0.39297175920305	COC1=CC=C(C(C(NCC2=CC=CC=C2)=O)N(C(CNC(OC(C)(C)C)=O)=O)CC3=CC=C(C)O3)C=C1OC	http://www.chemspider.com/Chemical-Structure.10481870.html	Solution was made up to 4 mL - methanol amount probably closer to 3 mL	4.63


.	EXP109C	http://usefulchem.wikispaces.com/Exp109	Yes	Pending	Benzaldehyde	c1ccccc1C=O	5-(trifluoromethyl)-2-furylmethylamine	FC(F)(F)c1ccc(CN)o1	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	benzyl isocyanide	[C-]#[N+]Cc1ccccc1	31.16	Khalid	methanol	4	1.04	1.01	1	1	1.045	106.12	1.313	165.11	1.159	175.18	0.962	117.15	0.10561224880383	0.12700769230769	0.15114754098361	0.12177754677755	0.22194873064008	FC(F)(F)C(O2)=CC=C2CN(C(CNC(OC(C)(C)C)=O)=O)C(C(NCC3=CC=CC=C3)=O)C1=CC=CC=C1	http://www.chemspider.com/RecordView.aspx?id=21105565	Imine was preformed	5
.	EXP108C	http://usefulchem.wikispaces.com/Exp108	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	benzyl isocyanide	[C-]#[N+]Cc1ccccc1	20.4	Khalid	methanol	4	2.09	2.66	1.99	1.97	1.045	106.12	1.099	97.12	1.159	175.18	0.962	117.15	0.21224	0.25685095541401	0.30078360655738	0.23990176715177	0.39323112861304	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NCc3ccccc3	http://www.chemspider.com/Chemical-Structure.21106009.html	Imine was preformed	4.43
.	EXP131-4	http://usefulchem.wikispaces.com/Exp131	No	No	o-Vanillin	Oc1c(cccc1OC)C=O	1-heptylamine	NCCCCCCC	Boc-Trp-OH	OC(C(CC1=CNC2=CC=CC=C21)NC(OC(C)(C)C)=O)=O	benzyl isocyanide	[C-]#[N+]Cc1ccccc1	0	Rikesh	methanol	0.5	0.5	0.5	0.5	0.5	1.231	152.15	0.777	115.22	1.262	304.34	0.962	117.15	0.061799350121852	0.074144144144144	0.12057844690967	0.060888773388773	0.61168760219448	O=C(N(C(C1=CC=CC(OC)=C1O)C(NCC2=CC=CC=C2)=O)CCCCCCC)C(NC(OC(C)(C)C)=O)CC3=CNC4=CC=CC=C43	http://www.chemspider.com/Search.aspx?rid=769044cc-beec-4d0c-9de5-3e47087af759	Protocol from Explan005 followed	7.66
.	EXP131-5	http://usefulchem.wikispaces.com/Exp131	No	No	o-Vanillin	Oc1c(cccc1OC)C=O	1-octylamine	NCCCCCCCC	Boc-Trp-OH	OC(C(CC1=CNC2=CC=CC=C21)NC(OC(C)(C)C)=O)=O	benzyl isocyanide	[C-]#[N+]Cc1ccccc1	0	Rikesh	methanol	0.5	0.5	0.5	0.5	0.5	1.231	152.15	0.782	129.24	1.262	304.34	0.962	117.15	0.061799350121852	0.082634271099744	0.12057844690967	0.060888773388773	0.60539955266273	O=C(N(C(C1=CC=CC(OC)=C1O)C(NCC2=CC=CC=C2)=O)CCCCCCCC)C(NC(OC(C)(C)C)=O)CC3=CNC4=CC=CC=C43	http://www.chemspider.com/Search.aspx?rid=92f9b316-05cd-40d6-a62f-c48da1af6042	Protocol from Explan005 followed	8.19
.	EXP130-4	http://usefulchem.wikispaces.com/Exp130	Yes	Not Determined	2-Naphthaldehyde	O=Cc2ccc1c(cccc1)c2	furfurylamine	o1c(ccc1)CN	formic acid	O=CO	benzyl isocyanide	[C-]#[N+]Cc1ccccc1	0	Rikesh	methanol	0.5	0.53	0.53	0.53	0.53	1.155	156.18	1.099	97.12	1.22	46.02	0.962	117.15	0.071667012987013	0.075318835304823	0.019992295081967	0.0645420997921	0.72451856931019	O=CN(Cc1ccco1)C(c2ccc3ccccc3c2)C(NCc4ccccc4)=O	http://www.chemspider.com/Search.aspx?rid=f4cf25b3-591d-464d-a70a-b50ae00e531b	Protocol from Explan005 followed	3.86
.	UCExp241-14	http://usefulchem.wikispaces.com/Exp241	No	No	veratraldehyde	COC1=C(OC)C=C(C=O)C=C1	Methylamine	NC	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	benzylisocyanide	[C-]#[N+]Cc1ccccc1		Khalid	methanol	0.13324	0.1	0.1	0.1	0.1	1.114	166.17	0.785	31.06	1.406	180.15	0.962	117.15	0.014916517055655	0.003956687898089	0.012812944523471	0.012177754677755	0.56464029111689	c1cc2OCOc2cc1CC(=O)N(C)C(c1ccc(OC)c(OC)c1)C(=O)NCc1ccccc1
.	UCExp241-15	http://usefulchem.wikispaces.com/Exp241	No	No	veratraldehyde	COC1=C(OC)C=C(C=O)C=C1	Methylamine	NC	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	benzylisocyanide	[C-]#[N+]Cc1ccccc1		Khalid	methanol	0.13324	0.1	0.1	0.1	0.1	1.114	166.17	0.785	31.06	1.406	180.15	0.962	117.15	0.014916517055655	0.003956687898089	0.012812944523471	0.012177754677755	0.56464029111689	c1cc2OCOc2cc1CC(=O)N(C)C(c1ccc(OC)c(OC)c1)C(=O)NCc1ccccc1
.	UCExp241-16	http://usefulchem.wikispaces.com/Exp241	No	No	veratraldehyde	COC1=C(OC)C=C(C=O)C=C1	Methylamine	NC	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	benzylisocyanide	[C-]#[N+]Cc1ccccc1		Khalid	methanol	0.13324	0.1	0.1	0.1	0.1	1.114	166.17	0.785	31.06	1.406	180.15	0.962	117.15	0.014916517055655	0.003956687898089	0.012812944523471	0.012177754677755	0.56464029111689	c1cc2OCOc2cc1CC(=O)N(C)C(c1ccc(OC)c(OC)c1)C(=O)NCc1ccccc1
.	EXP225-5	http://usefulchem.wikispaces.com/Exp225	Yes	Pending	piperonal	O=Cc1ccc2OCOc2c1	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	benzylisocyanide	[C-]#[N+]Cc1ccccc1		Khalid	methanol	0.099957747498545	1	1	1	0.5	1.337	150.13	1.099	97.12	1.159	175.18	0.962	117.15	0.11228870605834	0.13660600545951	0.15114754098361	0.060888773388773	0.89144233887782	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(=O)NCc2ccccc2)c3ccc4OCOc4c3	Need Link	0.5 mmol of isocyanide was added to 500uL of a 2M solution of aldehyde, amine and acid
.	UCExp241-03	http://usefulchem.wikispaces.com/Exp241	No	No	2-furaldehyde	O=Cc1ccco1	Methylamine	NC	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	benzylisocyanide	[C-]#[N+]Cc1ccccc1		Khalid	methanol	0.15824	0.1	0.1	0.1	0.1	1.16	96.08	0.785	31.06	1.406	180.15	0.962	117.15	0.00828275862069	0.003956687898089	0.012812944523471	0.012177754677755	0.51158707449496	CN(C(C(=O)Nc1ccccc1)c2ccco2)C(=O)Cc3ccc4OCOc4c3
.	UCExp241-01	http://usefulchem.wikispaces.com/Exp241	No	No	p-anisaldehyde	COc1ccc(C=O)cc1	Methylamine	NC	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	benzylisocyanide	[C-]#[N+]Cc1ccccc1		Khalid	methanol	0.15824	0.1	0.1	0.1	0.1	1.119	136.15	0.785	31.06	1.406	180.15	0.962	117.15	0.012167113494191	0.003956687898089	0.012812944523471	0.012177754677755	0.50161897374921	COc1ccc(cc1)C(C(=O)Nc2ccccc2)N(C)C(=O)Cc3ccc4OCOc4c3
.	UCExp241-02	http://usefulchem.wikispaces.com/Exp241	No	No	m-anisaldehyde	COc1cc(C=O)ccc1	Methylamine	NC	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	benzylisocyanide	[C-]#[N+]Cc1ccccc1		Khalid	methanol	0.15824	0.1	0.1	0.1	0.1	1.117	136.15	0.785	31.06	1.406	180.15	0.962	117.15	0.012188898836168	0.003956687898089	0.012812944523471	0.012177754677755	0.50156416311396	COc1cccc(c1)C(C(=O)Nc2ccccc2)N(C)C(=O)Cc3ccc4OCOc4c3
.	UCExp240-11	http://usefulchem.wikispaces.com/Exp240	No	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	5-Methylfurfurylamine	NCc1oc(cc1)C	phenylacetic acid	O=C(O)Cc1ccccc1	benzylisocyanide	[C-]#[N+]Cc1ccccc1		Khalid	THF	0.03971	1	1	1	1	1.217	206.24	0.997	111.14	1.164	136.15	0.962	117.15	0.16946589975349	0.11147442326981	0.11696735395189	0.12177754677755	1.7876448663459	O=C(Cc1ccccc1)N(Cc2ccc(C)o2)C(C(=O)NCc3ccccc3)c5cc6ccccc6c4ccccc45
.	UCExp240-05	http://usefulchem.wikispaces.com/Exp240	No	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	furfurylamine	o1c(ccc1)CN	phenylacetic acid	O=C(O)Cc1ccccc1	benzylisocyanide	[C-]#[N+]Cc1ccccc1		Khalid	THF	0.04201	1	1	1	1	1.217	206.24	1.099	97.12	1.164	136.15	0.962	117.15	0.16946589975349	0.18766151046406	0.11696735395189	0.12177754677755	1.56768730350183	O=C(Cc1ccccc1)N(Cc2ccco2)C(C(=O)NCc3ccccc3)c5cc6ccccc6c4ccccc45
.	EXP226-5	http://usefulchem.wikispaces.com/Exp226	No	No	Benzaldehyde	c1ccccc1C=O	5-Methylfurfurylamine	NCc1oc(cc1)C	1-Pyrenebutyric acid	O=C(O)CCCc4ccc2ccc1cccc3c1c2c4cc3	benzylisocyanide	[C-]#[N+]Cc1ccccc1		David	THF	0.68224538479725	0.5	0.5	0.5	0.5	1.045	106.12	0.997	111.14	1.296	288.34	0.962	117.15	0.050775119617225	0.055737211634905	0.11124228395062	0.060888773388773	0.52035158891143	O=C(CCCc4ccc3ccc2cccc1ccc4c3c12)N(Cc5ccc(C)o5)C(C(=O)NCc6ccccc6)c7ccccc7	Need Link	0.5 mmol of isocyanide was added to 900uL of a 0.55M solution of aldehyde, amine and acid
.	EXP227-5	http://usefulchem.wikispaces.com/Exp227	No	No	piperonal	O=Cc1ccc2OCOc2c1	furfurylamine	o1c(ccc1)CN	1-Pyrenebutyric acid	O=C(O)CCCc4ccc2ccc1cccc3c1c2c4cc3	benzylisocyanide	[C-]#[N+]Cc1ccccc1		Khalid	THF	0.38215518014523	0.25	0.25	0.25	0.5	1.337	150.13	1.099	97.12	1.296	288.34	0.962	117.15	0.028072176514585	0.034151501364877	0.055621141975309	0.060888773388773	0.44572116943891	O=C(CCCc4ccc3ccc2cccc1ccc4c3c12)N(Cc5ccco5)C(C(=O)NCc6ccccc6)c7ccc8OCOc8c7	Need Link	0.5 mmol of isocyanide was added to 500uL of a 0.5M solution of aldehyde, amine and acid
.	EXP215G	http://usefulchem.wikispaces.com/Exp215	No	No	5-Bromo-2-thiophenecarboxaldehyde	O=CC1=CC=C(Br)S1	3-Chloroaniline	NC1=CC(Cl)=CC=C1	chloroacetic acid	ClCC(=O)O	benzylisocyanide	[C-]#[N+]Cc1ccccc1		Khalid	THF + methanol	3	1	1	1	1	1.607	191.05	1.206	127.57	1.12	94.5	0.962	117.15	0.11888612321095	0.10577943615257	0.084375	0.12177754677755	0.29147566821162	Brc1ccc(s1)C(N(C(=O)CCl)c2cccc(Cl)c2)C(=O)NCc3ccccc3	Need Link
.	Exp242-8	http://usefulchem.wikispaces.com/Exp242	No	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	5-Methylfurfurylamine	NCc1oc(cc1)C	phenylacetic acid	O=C(O)Cc1ccccc1	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1		Marshall	benzene	0.19456325408425	0.1	0.1	0.1	0.1	1.217	206.24	0.997	111.14	1.164	136.15	0.878	109.17	0.016946589975349	0.011147442326981	0.011696735395189	0.012433940774488	0.4052061492959	O=C(Cc1ccccc1)N(Cc2ccc(C)o2)C(C(=O)NC3CCCCC3)C=6C=C4C=CC=CC4C5C=CC=CC5=6
.	Exp242-3	http://usefulchem.wikispaces.com/Exp242	Yes	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	furfurylamine	o1c(ccc1)CN	phenylacetic acid	O=C(O)Cc1ccccc1	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1		Marshall	benzene	-0.087840559363523	0.1	0.1	0.1	0.1	1.217	206.24	1.099	97.12	1.164	136.15	0.878	109.17	0.016946589975349	0.008837124658781	0.011696735395189	0.012433940774488	-2.63670188151345	O=C(Cc1ccccc1)N(Cc2ccco2)C(C(=O)NC3CCCCC3)C=6C=C4C=CC=CC4C5C=CC=CC5=6
.	UCExp241-08	http://usefulchem.wikispaces.com/Exp241	YES	YES	veratraldehyde	COC1=C(OC)C=C(C=O)C=C1	Methylamine	NC	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1		Khalid	methanol	0.14824	0.1	0.1	0.1	0.1	1.114	166.17	0.785	31.06	1.406	180.15	0.878	109.17	0.014916517055655	0.003956687898089	0.012812944523471	0.012433940774488	0.51985835455343	c1cc(OC)c(OC)cc1C(C(=O)NC2CCCCC2)N(C)C(=O)Cc3ccc4OCOc4c3


.	UCExp241-09	http://usefulchem.wikispaces.com/Exp241	YES	YES	veratraldehyde	COC1=C(OC)C=C(C=O)C=C1	Methylamine	NC	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	Khalid	methanol	0.13324	0.1	0.1	0.1	0.1	1.114	166.17	0.785	31.06	1.406	180.15	0.878	109.17	0.014916517055655	0.003956687898089	0.012812944523471	0.012433940774488	0.56382470181473	c1cc(OC)c(OC)cc1C(C(=O)NC2CCCCC2)N(C)C(=O)Cc3ccc4OCOc4c3
.	UCExp245-07	http://usefulchem.wikispaces.com/Exp245	No	No	piperonal	O=Cc1ccc2OCOc2c1	furfurylamine	o1c(ccc1)CN	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	Khalid	methanol	0.15296	0.1	0.1	0.1	0.1	1.337	150.13	1.099	97.12	1.406	180.15	0.878	109.17	0.011228870605834	0.008837124658781	0.012812944523471	0.012433940774488	0.50435541016131	c1cc2OCOc2cc1CC(=O)N(Cc1ccco1)C(c1ccc2OCOc2c1)C(=O)NC1CCCCC1
.	UCExp245-08	http://usefulchem.wikispaces.com/Exp245	No	No	piperonal	O=Cc1ccc2OCOc2c1	furfurylamine	o1c(ccc1)CN	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	Khalid	methanol	0.09596	0.1	0.1	0.1	0.1	1.337	150.13	1.099	97.12	1.406	180.15	0.878	109.17	0.011228870605834	0.008837124658781	0.012812944523471	0.012433940774488	0.70784993978875	c1cc2OCOc2cc1CC(=O)N(Cc1ccco1)C(c1ccc2OCOc2c1)C(=O)NC1CCCCC1
.	UCExp245-13	http://usefulchem.wikispaces.com/Exp245	No	No	piperonal	O=Cc1ccc2OCOc2c1	5-Methylfurfurylamine	NCc1oc(cc1)C	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	Khalid	methanol	0.15296	0.1	0.1	0.1	0.1	1.337	150.13	0.997	111.14	1.406	180.15	0.878	109.17	0.011228870605834	0.011147442326981	0.012812944523471	0.012433940774488	0.49854624356397	c1cc2OCOc2cc1CC(=O)N(Cc1oc(cc1)C)C(c1ccc2OCOc2c1)C(=O)NC1CCCCC1
.	UCExp245-14	http://usefulchem.wikispaces.com/Exp245	No	No	piperonal	O=Cc1ccc2OCOc2c1	5-Methylfurfurylamine	NCc1oc(cc1)C	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	Khalid	methanol	0.09596	0.1	0.1	0.1	0.1	1.337	150.13	0.997	111.14	1.406	180.15	0.878	109.17	0.011228870605834	0.011147442326981	0.012812944523471	0.012433940774488	0.6964603187016	c1cc2OCOc2cc1CC(=O)N(Cc1oc(cc1)C)C(c1ccc2OCOc2c1)C(=O)NC1CCCCC1
.	EXP234-2	http://usefulchem.wikispaces.com/Exp234	Yes	Pending	3,5-Bis(trifluoromethyl)benzaldehyde	O=CC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1	Benzylamine	NCc1ccccc1	Phenylpropynoic acid	O=C(O)C#CC1=CC=CC=C1	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	David	methanol	0.04821	0.1	0.1	0.1	0.1	1.469	242.12	0.981	107.15	1.24	146.14	0.878	109.17	0.016481960517359	0.01092252803262	0.011785483870968	0.012433940774488	1.00166363111743	c1ccc(cc1)CN(C(c2cc(cc(c2)C(F)(F)F)C(F)(F)F)C(=O)NC3CCCCC3)C(=O)C#Cc4ccccc4	Need Link
.	EXP234-4	http://usefulchem.wikispaces.com/Exp234	Yes	Pending	3,5-Bis(trifluoromethyl)benzaldehyde	O=CC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1	Benzylamine	NCc1ccccc1	Phenylpropynoic acid	O=C(O)C#CC1=CC=CC=C1	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	David	methanol	0.04821	0.1	0.1	0.1	0.1	1.469	242.12	0.981	107.15	1.24	146.14	0.878	109.17	0.016481960517359	0.01092252803262	0.011785483870968	0.012433940774488	1.00166363111743	c1ccc(cc1)CN(C(c2cc(cc(c2)C(F)(F)F)C(F)(F)F)C(=O)NC3CCCCC3)C(=O)C#Cc4ccccc4	Need Link
.	UCExp245-23	http://usefulchem.wikispaces.com/Exp245	No	No	piperonal	O=Cc1ccc2OCOc2c1	furfurylamine	o1c(ccc1)CN	cbz-proline	O=C(O)[C@H]2N(C(=O)OCc1ccccc1)CCC2	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	Khalid	methanol	0.14973	0.1	0.1	0.1	0.1	1.337	150.13	1.099	97.12	1.309	249.262	0.878	109.17	0.011228870605834	0.008837124658781	0.019042169595111	0.012433940774488	0.49683983622518	c1ccccc1COC(=O)N1CCCC1C(=O)N(Cc1ccco1)C(c1ccc2OCOc2c1)C(=O)NC1CCCCC1
.	UCExp245-24	http://usefulchem.wikispaces.com/Exp245	No	No	piperonal	O=Cc1ccc2OCOc2c1	furfurylamine	o1c(ccc1)CN	cbz-proline	O=C(O)[C@H]2N(C(=O)OCc1ccccc1)CCC2	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	Khalid	methanol	0.03973	0.1	0.1	0.1	0.1	1.337	150.13	1.099	97.12	1.309	249.262	0.878	109.17	0.011228870605834	0.008837124658781	0.019042169595111	0.012433940774488	1.09562499194185	c1ccccc1COC(=O)N1CCCC1C(=O)N(Cc1ccco1)C(c1ccc2OCOc2c1)C(=O)NC1CCCCC1
.	UCExp245-31	http://usefulchem.wikispaces.com/Exp245	No	No	piperonal	O=Cc1ccc2OCOc2c1	5-Methylfurfurylamine	NCc1oc(cc1)C	cbz-proline	O=C(O)[C@H]2N(C(=O)OCc1ccccc1)CCC2	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	Khalid	methanol	0.14473	0.1	0.1	0.1	0.1	1.337	150.13	0.997	111.14	1.309	249.2625	0.878	109.17	0.011228870605834	0.011147442326981	0.019042207792208	0.012433940774488	0.50356914324101	c1ccccc1COC(=O)N1CCCC1C(=O)N(Cc1oc(cc1)C)C(c1ccc2OCOc2c1)C(=O)NC1CCCCC1
.	UCExp245-32	http://usefulchem.wikispaces.com/Exp245	No	No	piperonal	O=Cc1ccc2OCOc2c1	5-Methylfurfurylamine	NCc1oc(cc1)C	cbz-proline	O=C(O)[C@H]2N(C(=O)OCc1ccccc1)CCC2	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	Khalid	methanol	0.04596	0.1	0.1	0.1	0.1	1.337	150.13	0.997	111.14	1.309	249.262	0.878	109.17	0.011228870605834	0.011147442326981	0.019042169595111	0.012433940774488	1.00187929208991	c1ccccc1COC(=O)N1CCCC1C(=O)N(Cc1oc(cc1)C)C(c1ccc2OCOc2c1)C(=O)NC1CCCCC1
.	EXP233-12	http://usefulchem.wikispaces.com/Exp233	No	No	3,5-dimethoxybenzaldehyde	COC1=C(OC)C=C(C=O)C=C1	Benzylamine	NCc1ccccc1	Boc-Pro-OH	O=C(OC(C)(C)C)N1[C@H](C(=O)O)CCC1	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	David	methanol	0.42	1	1	1	1	1.114	166.17	0.981	107.15	1.201	215.24	0.878	109.17	0.14916517055655	0.1092252803262	0.17921731890092	0.12433940774487	1.01838471853129	CC(C)(C)OC(=O)N4CCC[C@H]4C(=O)N(Cc1ccccc1)C(c2cc(OC)cc(OC)c2)C(=O)NC3CCCCC3	Need Link
.	EXP233-6	http://usefulchem.wikispaces.com/Exp233	No	No	3,5-dimethoxybenzaldehyde	COC1=C(OC)C=C(C=O)C=C1	Benzylamine	NCc1ccccc1	Boc-Pro-OH	O=C(OC(C)(C)C)N1[C@H](C(=O)O)CCC1	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	David	methanol	0.529	1	1	1	1	1.114	166.17	0.981	107.15	1.201	215.24	0.878	109.17	0.14916517055655	0.1092252803262	0.17921731890092	0.12433940774487	0.916634664444	CC(C)(C)OC(=O)N4CCC[C@H]4C(=O)N(Cc1ccccc1)C(c2cc(OC)cc(OC)c2)C(=O)NC3CCCCC3	Need Link
.	EXP232-59	http://usefulchem.wikispaces.com/Exp232	No	No	trans-2-hexenal	O=C/C=C/CCC	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	Khalid	methanol	0.0422	0.1	0.1	0.1	0.1	0.846	98.14	1.099	97.12	1.159	175.18	0.878	109.17	0.011600472813239	0.008837124658781	0.015114754098361	0.012433940774488	1.10881595639396	CC(C)(C)OC(=O)NCC(=O)N(CC(=O)NC1CCCCC1)C(\C=C\CCC)c2ccco2	Need Link
.	EXP232-64	http://usefulchem.wikispaces.com/Exp232	No	No	2-phenylpropionaldehyde	O=CC(c1ccccc1)C	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	Khalid	methanol	0.0404	0.1	0.1	0.1	0.1	1.002	134.18	1.099	97.12	1.159	175.18	0.878	109.17	0.01339121756487	0.012209281164695	0.015114754098361	0.012433940774488	1.0689563014835	CC(C)(C)OC(=O)NCC(=O)N(CC(=O)NC1CCCCC1)C(c2ccco2)C(C)c3ccccc3	Need Link
.	EXP232-19	http://usefulchem.wikispaces.com/Exp232	No	No	crotonaldehyde	O=C/C=C/C	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	Khalid	methanol	0.0455	0.1	0.1	0.1	0.1	0.853	0.853	1.099	97.12	1.159	175.18	0.878	109.17	0.0001	0.000077616014559	0.015114754098361	0.012433940774488	1.36562935901223	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(\C=C\C)C(=O)NC2CCCCC2	Need Link
.	EXP232-09	http://usefulchem.wikispaces.com/Exp232	Yes	Pending	4-methylbenzaldehyde	Cc1ccc(C=O)cc1	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	Khalid	methanol	0.0421	0.1	0.1	0.1	0.1	1.019	120.15	1.099	97.12	1.159	175.18	0.878	109.17	0.011790971540726	0.010932666060055	0.015114754098361	0.012433940774488	1.08257524003249	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(=O)NC2CCCCC2)c3ccc(C)cc3	Need Link
.	EXP232-49	http://usefulchem.wikispaces.com/Exp232	Yes	Pending	p-anisaldehyde	COc1ccc(C=O)cc1	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	Khalid	methanol	0.0417	0.1	0.1	0.1	0.1	1.119	136.15	1.099	97.12	1.159	175.18	0.878	109.17	0.012167113494191	0.012388535031847	0.015114754098361	0.012433940774488	1.06604871775252	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(=O)NC2CCCCC2)c3ccc(OC)cc3	Need Link
.	EXP225-4	http://usefulchem.wikispaces.com/Exp225	Yes	Pending	piperonal	O=Cc1ccc2OCOc2c1	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	Khalid	methanol	0.099957747498545	1	1	1	0.5	1.337	150.13	1.099	97.12	1.159	175.18	0.878	109.17	0.11228870605834	0.13660600545951	0.15114754098361	0.062169703872437	0.88941114499022	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(=O)NC2CCCCC2)c3ccc4OCOc4c3	Need Link	0.5 mmol of isocyanide was added to 500uL of a 2M solution of aldehyde, amine and acid
.	EXP232-69	http://usefulchem.wikispaces.com/Exp232	No	No	m-anisaldehyde	COc1cc(C=O)ccc1	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	Khalid	methanol	0.0416	0.1	0.1	0.1	0.1	1.117	136.15	1.099	97.12	1.159	175.18	0.878	109.17	0.012188898836168	0.012388535031847	0.015114754098361	0.012433940774488	1.06693833772312	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(=O)NC2CCCCC2)c3cccc(OC)c3	Need Link


.	EXP232-04	http://usefulchem.wikispaces.com/Exp232	Yes	Pending	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1		Khalid	methanol	0.0437	0.1	0.1	0.1	0.1	1.045	106.12	1.099	97.12	1.159	175.18	0.878	109.17	0.010155023923445	0.009656050955414	0.015114754098361	0.012433940774488	1.09817980292142	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(=O)NC2CCCCC2)c3ccccc3	Need Link
.	EXP232-44	http://usefulchem.wikispaces.com/Exp232	Yes	Pending	o-tolualdehyde	O=Cc1ccccc1C	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1		Khalid	methanol	0.0423	0.1	0.1	0.1	0.1	1.039	120.15	1.099	97.12	1.159	175.18	0.878	109.17	0.011564003849856	0.010932666060055	0.015114754098361	0.012433940774488	1.08289138534727	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(=O)NC2CCCCC2)c3ccccc3C	Need Link
.	EXP232-39	http://usefulchem.wikispaces.com/Exp232	No	No	2-hydroxybenzaldehyde	O=Cc1ccccc1O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1		Khalid	methanol	0.0432	0.1	0.1	0.1	0.1	1.146	122.12	1.099	97.12	1.159	175.18	0.878	109.17	0.010656195462478	0.011111919927207	0.015114754098361	0.012433940774488	1.08088464913816	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(=O)NC2CCCCC2)c3ccccc3O	Need Link
.	EXP232-34	http://usefulchem.wikispaces.com/Exp232	No	No	2-furaldehyde	O=Cc1ccco1	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1		Khalid	methanol	0.0455	0.1	0.1	0.1	0.1	1.16	96.08	1.099	97.12	1.159	175.18	0.878	109.17	0.00828275862069	0.008742493175614	0.015114754098361	0.012433940774488	1.1101989387376	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(=O)NC2CCCCC2)c3ccco3	Need Link
.	EXP232-24	http://usefulchem.wikispaces.com/Exp232	Yes	Pending	diphenylacetaldehyde	O=CC(c1ccccc1)c2ccccc2	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1		Khalid	methanol	0.0361	0.1	0.1	0.1	0.1	1.106	196.24	1.099	97.12	1.159	175.18	0.878	109.17	0.01774321880651	0.017856232939036	0.015114754098361	0.012433940774488	1.00757549039679	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(c2ccccc2)c3ccccc3)C(=O)NC4CCCCC4	Need Link
.	EXP232-74	http://usefulchem.wikispaces.com/Exp232	No	No	2-ethylbutyraldehyde	O=CC(CC)CC	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1		Khalid	methanol	0.0415	0.1	0.1	0.1	0.1	0.814	100.16	1.099	97.12	1.159	175.18	0.878	109.17	0.012304668304668	0.009113739763421	0.015114754098361	0.012433940774488	1.10537418298103	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(CC)CC)C(=O)NC2CCCCC2	Need Link
.	EXP232-29	http://usefulchem.wikispaces.com/Exp232	No	No	cyclohexancarboxaldehyde	O=CC1CCCCC1	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1		Khalid	methanol	0.0417	0.1	0.1	0.1	0.1	0.926	112.17	1.099	97.12	1.159	175.18	0.878	109.17	0.012113390928726	0.010206551410373	0.015114754098361	0.012433940774488	1.092076971382	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C2CCCCC2)C(=O)NC3CCCCC3	Need Link
.	EXP232-54	http://usefulchem.wikispaces.com/Exp232	No	No	hexanaldehyde	O=CCCCCC	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1		Khalid	methanol	0.0415	0.1	0.1	0.1	0.1	0.815	100.16	1.099	97.12	1.159	175.18	0.878	109.17	0.012289570552147	0.009113739763421	0.015114754098361	0.012433940774488	1.105558685976	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(CCCCC)C(=O)NC2CCCCC2	Need Link
.	EXP232-14	http://usefulchem.wikispaces.com/Exp232	Yes	Pending	4-(trifluoromethyl)benzaldehyde	FC(F)(F)c1ccc(C=O)cc1	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1		Khalid	methanol	0.0402	0.1	0.1	0.1	0.1	1.275	174.12	1.099	97.12	1.159	175.18	0.878	109.17	0.013656470588235	0.015843494085532	0.015114754098361	0.012433940774488	1.02829180850627	FC(F)(F)c1ccc(cc1)C(C(=O)NC2CCCCC2)N(Cc3ccco3)C(=O)CNC(=O)OC(C)(C)C	Need Link
.	UCExp235-2	http://usefulchem.wikispaces.com/Exp235	Yes	No	4-(trifluoromethyl)benzaldehyde	FC(F)(F)c1ccc(C=O)cc1	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	67.7	Khalid	methanol	1.71805361813537	4	4	4	4	1.275	174.12	1.099	97.12	1.159	175.18	0.878	109.17	0.54625882352941	0.63373976342129	0.60459016393443	0.4973576309795	1	FC(F)(F)c1ccc(cc1)C(C(=O)NC2CCCCC2)N(Cc3ccco3)C(=O)CNC(=O)OC(C)(C)C	Need Link
.	EXP233-2	http://usefulchem.wikispaces.com/Exp233	No	No	3,5-dimethoxybenzaldehyde	COC1=C(OC)C=C(C=O)C=C1	Benzylamine	NCc1ccccc1	1-aminocyclohexane-1-carboxylic acid	O=C(O)C1(N)CCCCC1	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1		David	methanol	0.58	1	1	1	1	1.114	166.17	0.981	107.15	1.148	143.18	0.878	109.17	0.14916517055655	0.1092252803262	0.1247212543554	0.12433940774487	0.91958156836758	O=C(C1CCCCC1N)N(Cc2ccccc2)C(c3cc(OC)cc(OC)c3)C(=O)NC4CCCCC4	Need Link
.	EXP233-8	http://usefulchem.wikispaces.com/Exp233	No	No	3,5-dimethoxybenzaldehyde	COC1=C(OC)C=C(C=O)C=C1	Benzylamine	NCc1ccccc1	1-aminocyclohexane-1-carboxylic acid	O=C(O)C1(N)CCCCC1	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1		David	methanol	0.475	1	1	1	1	1.114	166.17	0.981	107.15	1.148	143.18	0.878	109.17	0.14916517055655	0.1092252803262	0.1247212543554	0.12433940774487	1.01786235140361	O=C(C1CCCCC1N)N(Cc2ccccc2)C(c3cc(OC)cc(OC)c3)C(=O)NC4CCCCC4	Need Link
.	EXP234-12	http://usefulchem.wikispaces.com/Exp234	No	No	3,5-dimethoxybenzaldehyde	COC1=C(OC)C=C(C=O)C=C1	glycine methyl ester hydrochloride	Cl.O=C(OC)CN	Boc-L-Threonine	CC(C)(C)OC(=O)N[C@@H](C(=O)O)C(C)O	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1		David	methanol	0.5437	1	1	1	1	1.114	166.17	1.045	125.55	1.108	205.25	0.878	109.17	0.14916517055655	0.12014354066986	0.18524368231047	0.12433940774487	0.89079574504127	O=C(NC1CCCCC1)C(c2cc(OC)cc(OC)c2)N(CC(=O)OC)C(=O)[C@H](NC(=O)OC(C)(C)C)C(C)O	Need Link
.	EXP234-10	http://usefulchem.wikispaces.com/Exp234	Reactants insoluble	No	3,5-dimethoxybenzaldehyde	COC1=C(OC)C=C(C=O)C=C1	Benzylamine	NCc1ccccc1	Boc-L-Serine	O=C(OC(C)(C)C)N[C@H](C(=O)O)CO	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1		David	methanol	0.5432	1	1	1	1	1.114	166.17	0.981	107.15	1.24	205.21	0.878	109.17	0.14916517055655	0.1092252803262	0.16549193548387	0.12433940774487	0.91623605593663	O=C(NC1CCCCC1)C(c2cc(OC)cc(OC)c2)N(Cc3ccccc3)C(=O)[C@H](CO)NC(=O)OC(C)(C)C	Need Link
.	EXP233-10	http://usefulchem.wikispaces.com/Exp233	Yes	Pending	3,5-dimethoxybenzaldehyde	COC1=C(OC)C=C(C=O)C=C1	Benzylamine	NCc1ccccc1	Phenylpropynoic acid	O=C(O)C#CC1=CC=CC=C1	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1		David	methanol	0.482	1	1	1	1	1.114	166.17	0.981	107.15	1.24	146.14	0.878	109.17	0.14916517055655	0.1092252803262	0.11785483870968	0.12433940774487	1.01772397098173	O=C(NC1CCCCC1)C(c2cc(OC)cc(OC)c2)N(Cc3ccccc3)C(=O)C#Cc4ccccc4	Need Link
.	EXP233-4	http://usefulchem.wikispaces.com/Exp233	Yes	Pending	3,5-dimethoxybenzaldehyde	COC1=C(OC)C=C(C=O)C=C1	Benzylamine	NCc1ccccc1	Phenylpropynoic acid	O=C(O)C#CC1=CC=CC=C1	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1		David	methanol	0.59	1	1	1	1	1.114	166.17	0.981	107.15	1.24	146.14	0.878	109.17	0.14916517055655	0.1092252803262	0.11785483870968	0.12433940774487	0.91693932845521	O=C(NC1CCCCC1)C(c2cc(OC)cc(OC)c2)N(Cc3ccccc3)C(=O)C#Cc4ccccc4	Need Link
.	EXP234-8	http://usefulchem.wikispaces.com/Exp234	Reactants insoluble	No	3,5-dimethoxybenzaldehyde	COC1=C(OC)C=C(C=O)C=C1	Benzylamine	NCc1ccccc1	Boc-diglycine	O=C(OC(C)(C)C)NCC(=O)NCC(=O)O	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1		David	methanol	0.5187	1	1	1	1	1.114	166.17	0.981	107.15	1.222	232.23	0.878	109.17	0.14916517055655	0.1092252803262	0.19004091653028	0.12433940774487	0.91619493875622	O=C(NC1CCCCC1)C(c2cc(OC)cc(OC)c2)N(Cc3ccccc3)C(=O)CNC(=O)CNC(=O)OC(C)(C)C	Need Link
.	EXP234-6	http://usefulchem.wikispaces.com/Exp234	Reactants insoluble	No	3,5-dimethoxybenzaldehyde	COC1=C(OC)C=C(C=O)C=C1	Benzylamine	NCc1ccccc1	Fmoc-Diglycine	O=C(O)CNC(=O)CNC(=O)OCC3c1ccccc1c2c3cccc2	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1		David	methanol	0.4437	1	1	1	1	1.114	166.17	0.981	107.15	1.338	354.35	0.878	109.17	0.14916517055655	0.1092252803262	0.2648355754858	0.12433940774487	0.91636733716617	O=C(NC1CCCCC1)C(c2cc(OC)cc(OC)c2)N(Cc3ccccc3)C(=O)CNC(=O)CNC(=O)OCC6c4ccccc4c5ccccc56	Need Link
.	UCExp238-06	http://usefulchem.wikispaces.com/Exp238	No	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	cyclohexylamine	NC1CCCCC1	crotonic acid	O=C(O)C=CC	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1		Khalid	THF	0.049775110683349	0.99883829296	0.999	0.999	0.999	1.217	206.24	0.867	99.17	1.039	86.09	0.878	109.17	0.16926903002471	0.1142685467128	0.082775659287777	0.12421506833713	1.84866181694482	C\C=C\C(=O)N(C(C(=O)NC1CCCCC1)c3cc4ccccc4c2ccccc23)C5CCCCC5
.	UCExp238-07	http://usefulchem.wikispaces.com/Exp238	No	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	furfurylamine	o1c(ccc1)CN	crotonic acid	O=C(O)C=CC	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1		Khalid	THF	0.049775110683349	0.996237124659	0.996	0.996	0.996	1.217	206.24	1.099	97.12	1.039	86.09	0.878	109.17	0.16882822069817	0.1869108644222	0.08252708373436	0.1238420501139	1.62776129326239	C\C=C\C(=O)N(Cc1ccco1)C(C(=O)NC2CCCCC2)c4cc5ccccc5c3ccccc34


.	UCExp238-30	http://usefulchem.wikispaces.com/Exp238	Yes but solvent evaporated	Awaiting Characterization	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	cyclohexylamine	NC1CCCCC1	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	Khalid	THF	0.042945245901639	0.99883829296	0.999	0.999	0.999	1.217	206.24	0.867	99.17	1.159	175.18	0.878	109.17	0.16926903002471	0.2376398615917	0.15099639344262	0.12421506833713	1.37758334408272	CC(C)(C)OC(=O)NCC(=O)N(C(C(=O)NC1CCCCC1)c3cc4ccccc4c2ccccc23)C5CCCCC5
.	UCExp238-31	http://usefulchem.wikispaces.com/Exp238	Yes but solvent evaporated	Awaiting Characterization	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	Khalid	THF	0.042945245901639	0.996237124659	0.996	0.996	0.996	1.217	206.24	1.099	97.12	1.159	175.18	0.878	109.17	0.16882822069817	0.1869108644222	0.15054295081967	0.1238420501139	1.47978811797316	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(=O)NC2CCCCC2)c4cc5ccccc5c3ccccc34
.	UCExp240-09	http://usefulchem.wikispaces.com/Exp240	Yes	Yes	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	5-Methylfurfurylamine	NCc1oc(cc1)C	phenylacetic acid	O=C(O)Cc1ccccc1	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	Khalid	THF	0.03941	1	1	1	1	1.217	206.24	0.997	111.14	1.164	136.15	0.878	109.17	0.16946589975349	0.11147442326981	0.11696735395189	0.12433940774487	1.78044580439755	O=C(Cc1ccccc1)N(Cc2ccc(C)o2)C(C(=O)NC3CCCCC3)c5cc6ccccc6c4ccccc45
.	UCExp240-03	http://usefulchem.wikispaces.com/Exp240	No	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	furfurylamine	o1c(ccc1)CN	phenylacetic acid	O=C(O)Cc1ccccc1	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	Khalid	THF	0.04171	1	1	1	1	1.217	206.24	1.099	97.12	1.164	136.15	0.878	109.17	0.16946589975349	0.18766151046406	0.11696735395189	0.12433940774487	1.56214809706	O=C(Cc1ccccc1)N(Cc2ccco2)C(C(=O)NC3CCCCC3)c5cc6ccccc6c4ccccc45
.	EXP226-4	http://usefulchem.wikispaces.com/Exp226	No	No	Benzaldehyde	c1ccccc1C=O	5-Methylfurfurylamine	NCc1oc(cc1)C	1-Pyrenebutyric acid	O=C(O)CCCc4ccc2ccc1cccc3c1c2c4cc3	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	David	THF	0.68224538479725	0.5	0.5	0.5	0.5	1.045	106.12	0.997	111.14	1.296	288.34	0.878	109.17	0.050775119617225	0.055737211634905	0.11124228395062	0.062169703872437	0.51965884810928	O=C(CCCc4ccc3ccc2cccc1ccc4c3c12)N(Cc5ccc(C)o5)C(C(=O)NC6CCCCC6)c7ccccc7	Need Link	0.5 mmol of isocyanide was added to 900uL of a 0.55M solution of aldehyde, amine and acid
.	EXP227-4	http://usefulchem.wikispaces.com/Exp227	No	No	piperonal	O=Cc1ccc2OCOc2c1	furfurylamine	o1c(ccc1)CN	1-Pyrenebutyric acid	O=C(O)CCCc4ccc2ccc1cccc3c1c2c4cc3	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	Khalid	THF	0.38215518014523	0.25	0.25	0.25	0.5	1.337	150.13	1.099	97.12	1.296	288.34	0.878	109.17	0.028072176514585	0.034151501364877	0.055621141975309	0.062169703872437	0.44470557249511	O=C(CCCc4ccc3ccc2cccc1ccc4c3c12)N(Cc5ccco5)C(C(=O)NC6CCCCC6)c7ccc8OCOc8c7	Need Link	0.5 mmol of isocyanide was added to 500uL of a 0.5M solution of aldehyde, amine and acid
.	UCExp238-12	http://usefulchem.wikispaces.com/Exp238	Yes but solvent evaporated	Awaiting Characterization	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	t-butylamine	NC(C)(C)C	crotonic acid	O=C(O)C=CC	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	Khalid	THF	0.049775110683349	0.99790862069	0.998	0.998	0.998	1.217	206.24	0.696	73.14	1.039	86.09	0.878	109.17	0.169111482277	0.10487603448276	0.082692800769971	0.12409072892938	1.88090820611117	O=C(NC1CCCCC1)C(c3cc4ccccc4c2ccccc23)N(C(=O)\C=C\C)C(C)(C)C
.	UCExp238-36	http://usefulchem.wikispaces.com/Exp238	Yes but solvent evaporated	Awaiting Characterization	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	t-butylamine	NC(C)(C)C	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	Khalid	THF	0.042945245901639	0.99790862069	0.998	0.998	0.998	1.217	206.24	0.696	73.14	1.159	175.18	0.878	109.17	0.169111482277	0.10487603448276	0.15084524590164	0.12409072892938	1.6860302926589	O=C(NC1CCCCC1)C(c3cc4ccccc4c2ccccc23)N(C(=O)CNC(=O)OC(C)(C)C)C(C)(C)C
.	UCExp238-10	http://usefulchem.wikispaces.com/Exp238	No	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	Methylamine	NC	crotonic acid	O=C(O)C=CC	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	Khalid	THF	0.09581842278526	0.72780203784571	0.728	0.728	0.728	1.217	206.24	0.785	31.06	1.039	86.09	0.878	109.17	0.12333762718595	0.028804687898089	0.060321000962464	0.090519088838269	1.82497624716039	O=C(NC1CCCCC1)C(c3cc4ccccc4c2ccccc23)N(C)C(=O)\C=C\C
.	UCExp238-34	http://usefulchem.wikispaces.com/Exp238	Yes	Awaiting Characterization	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	Methylamine	NC	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	Khalid	THF	0.08898855800355	0.72780203784571	0.728	0.728	0.728	1.217	206.24	0.785	31.06	1.159	175.18	0.878	109.17	0.12333762718595	0.028804687898089	0.11003540983607	0.090519088838269	1.64778388503663	O=C(NC1CCCCC1)C(c3cc4ccccc4c2ccccc23)N(C)C(=O)CNC(=O)OC(C)(C)C
.	UCExp238-02	http://usefulchem.wikispaces.com/Exp238	No	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	3-Chloroaniline	NC1=CC(Cl)=CC=C1	crotonic acid	O=C(O)C=CC	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	Khalid	THF	0.049775110683349	0.99797794362	0.998	0.998	0.998	1.217	206.24	1.206	127.57	1.039	86.09	0.878	109.17	0.1691232301497	0.10556787728027	0.082692800769971	0.12409072892938	1.87854760915934	O=C(NC1CCCCC1)C(c3cc4ccccc4c2ccccc23)N(c5cccc(Cl)c5)C(=O)\C=C\C
.	UCExp238-26	http://usefulchem.wikispaces.com/Exp238	No	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	3-Chloroaniline	NC1=CC(Cl)=CC=C1	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	Khalid	THF	0.042945245901639	0.99797794362	0.998	0.998	0.998	1.217	206.24	1.206	127.57	1.159	175.18	0.878	109.17	0.1691232301497	0.10556787728027	0.15084524590164	0.12409072892938	1.68414537127374	O=C(NC1CCCCC1)C(c3cc4ccccc4c2ccccc23)N(c5cccc(Cl)c5)C(=O)CNC(=O)OC(C)(C)C
.	UCExp238-03	http://usefulchem.wikispaces.com/Exp238	No	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	Aniline	Nc1ccccc1	crotonic acid	O=C(O)C=CC	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	Khalid	THF	0.049775110683349	0.996512524462	0.997	0.997	0.997	1.217	206.24	1.022	93.13	1.039	86.09	0.878	109.17	0.16887489157358	0.09085186888454	0.082609942252166	0.12396638952164	1.93093317801993	O=C(NC1CCCCC1)C(c3cc4ccccc4c2ccccc23)N(c5ccccc5)C(=O)\C=C\C
.	UCExp238-27	http://usefulchem.wikispaces.com/Exp238	Yes	Awaiting Characterization	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	Aniline	Nc1ccccc1	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	Khalid	THF	0.042945245901639	0.996512524462	0.997	0.997	0.997	1.217	206.24	1.022	93.13	1.159	175.18	0.878	109.17	0.16887489157358	0.09085186888454	0.15069409836066	0.12396638952164	1.72606346325659	O=C(NC1CCCCC1)C(c3cc4ccccc4c2ccccc23)N(c5ccccc5)C(=O)CNC(=O)OC(C)(C)C
.	UCExp238-01	http://usefulchem.wikispaces.com/Exp238	No	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	2-Chloroaniline	NC1=C(Cl)C=CC=C1	crotonic acid	O=C(O)C=CC	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	Khalid	THF	0.049775110683349	0.99791690025	0.998	0.998	0.998	1.217	206.24	1.213	127.57	1.039	86.09	0.878	109.17	0.16911288538008	0.10495866446826	0.082692800769971	0.12409072892938	1.88062593991398	O=C(NC1CCCCC1)C(c3cc4ccccc4c2ccccc23)N(c5ccccc5Cl)C(=O)\C=C\C
.	UCExp238-25	http://usefulchem.wikispaces.com/Exp238	Yes	Awaiting Characterization	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	2-Chloroaniline	NC1=C(Cl)C=CC=C1	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	Khalid	THF	0.042945245901639	0.99791690025	0.998	0.998	0.998	1.217	206.24	1.213	127.57	1.159	175.18	0.878	109.17	0.16911288538008	0.10495866446826	0.15084524590164	0.12409072892938	1.68580493215791	O=C(NC1CCCCC1)C(c3cc4ccccc4c2ccccc23)N(c5ccccc5Cl)C(=O)CNC(=O)OC(C)(C)C
.	UCExp238-04	http://usefulchem.wikispaces.com/Exp238	No	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	Benzylamine	NCc1ccccc1	crotonic acid	O=C(O)C=CC	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	Khalid	THF	0.049775110683349	0.99832252803	0.998	0.998	0.998	1.217	206.24	0.981	107.15	1.039	86.09	0.878	109.17	0.16918162545678	0.10900682976555	0.082692800769971	0.12409072892938	1.86630279659737	O=C(NC1CCCCC1)C(c3cc4ccccc4c2ccccc23)N(Cc5ccccc5)C(=O)\C=C\C
.	UCExp238-28	http://usefulchem.wikispaces.com/Exp238	Yes	Awaiting Characterization	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	Benzylamine	NCc1ccccc1	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	Khalid	THF	0.042945245901639	0.99832252803	0.998	0.998	0.998	1.217	206.24	0.981	107.15	1.159	175.18	0.878	109.17	0.16918162545678	0.10900682976555	0.15084524590164	0.12409072892938	1.6743009085323	O=C(NC1CCCCC1)C(c3cc4ccccc4c2ccccc23)N(Cc5ccccc5)C(=O)CNC(=O)OC(C)(C)C
.	UCExp238-11	http://usefulchem.wikispaces.com/Exp238	No	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	1-propylamine	NCCC	crotonic acid	O=C(O)C=CC	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	Khalid	THF	0.049775110683349	0.995621140473	0.996	0.996	0.996	1.217	206.24	0.719	59.11	1.039	86.09	0.878	109.17	0.16872383238386	0.081882559109875	0.08252708373436	0.1238420501139	1.96471611418604	O=C(NC1CCCCC1)C(c3cc4ccccc4c2ccccc23)N(CCC)C(=O)\C=C\C
.	UCExp238-35	http://usefulchem.wikispaces.com/Exp238	Yes	Awaiting Characterization	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	1-propylamine	NCCC	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1	Khalid	THF	0.042945245901639	0.995621140473	0.996	0.996	0.996	1.217	206.24	0.719	59.11	1.159	175.18	0.878	109.17	0.16872383238386	0.081882559109875	0.15054295081967	0.1238420501139	1.7530496771655	O=C(NC1CCCCC1)C(c3cc4ccccc4c2ccccc23)N(CCC)C(=O)CNC(=O)OC(C)(C)C


.	UCExp238-05	http://usefulchem.wikispaces.com/Exp238	No	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	butylamine	NCCCC	crotonic acid	O=C(O)C=CC	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1		Khalid	THF	0.049775110683349	0.997283783784	0.997	0.997	0.997	1.217	206.24	0.74	73.14	1.039	86.09	0.878	109.17	0.16900559372852	0.098541324324324	0.082609942252166	0.12396638952164	1.9030408856967	O=C(NC1CCCCC1)C(c3cc4ccccc4c2ccccc23)N(CCCC)C(=O)\C=C\C
.	UCExp238-29	http://usefulchem.wikispaces.com/Exp238	Yes	Awaiting Characterization	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	butylamine	NCCCC	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1		Khalid	THF	0.042945245901639	0.997283783784	0.997	0.997	0.997	1.217	206.24	0.74	73.14	1.159	175.18	0.878	109.17	0.16900559372852	0.098541324324324	0.15069409836066	0.12396638952164	1.70382890151901	O=C(NC1CCCCC1)C(c3cc4ccccc4c2ccccc23)N(CCCC)C(=O)CNC(=O)OC(C)(C)C
.	UCExp238-09	http://usefulchem.wikispaces.com/Exp238	No	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	1-hexylamine	NCCCCCC	crotonic acid	O=C(O)C=CC	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1		Khalid	THF	0.049775110683349	1.00061018277	1.001	1.001	1.001	1.217	206.24	0.774	101.19	1.039	86.09	0.878	109.17	0.16956930492562	0.13086717054264	0.082941376323388	0.12446374715262	1.79444081479951	O=C(NC1CCCCC1)C(c3cc4ccccc4c2ccccc23)N(CCCCCC)C(=O)\C=C\C
.	UCExp238-33	http://usefulchem.wikispaces.com/Exp238	Yes	Awaiting Characterization	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	1-hexylamine	NCCCCCC	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1		Khalid	THF	0.042945245901639	1.00061018277	1.001	1.001	1.001	1.217	206.24	0.774	101.19	1.159	175.18	0.878	109.17	0.16956930492562	0.13086717054264	0.15129868852459	0.12446374715262	1.61611826806575	O=C(NC1CCCCC1)C(c3cc4ccccc4c2ccccc23)N(CCCCCC)C(=O)CNC(=O)OC(C)(C)C
.	UCExp238-08	http://usefulchem.wikispaces.com/Exp238	No	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	1-heptylamine	NCCCCCCC	crotonic acid	O=C(O)C=CC	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1		Khalid	THF	0.049775110683349	1.00222882883	1.002	1.002	1.002	1.217	206.24	0.777	115.22	1.039	86.09	0.878	109.17	0.16984361023656	0.14858486486486	0.083024234841194	0.12458808656036	1.74013949162358	O=C(NC1CCCCC1)C(c3cc4ccccc4c2ccccc23)N(CCCCCCC)C(=O)\C=C\C
.	UCExp238-32	http://usefulchem.wikispaces.com/Exp238	Yes	Awaiting Characterization	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	1-heptylamine	NCCCCCCC	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	cyclohexylisocyanide	[C-]#[N+]C1CCCCC1		Khalid	THF	0.042945245901639	1.00222882883	1.002	1.002	1.002	1.217	206.24	0.777	115.22	1.159	175.18	0.878	109.17	0.16984361023656	0.14858486486486	0.15144983606557	0.12458808656036	1.57198257988396	O=C(NC1CCCCC1)C(c3cc4ccccc4c2ccccc23)N(CCCCCCC)C(=O)CNC(=O)OC(C)(C)C
.	UCExp236-20	http://usefulchem.wikispaces.com/Exp236	No	No	4-(trifluoromethyl)benzaldehyde	FC(F)(F)c1ccc(C=O)cc1	t-butylamine	NC(C)(C)C	methacrylic acid	O=C(O)\C(=C)C	n-butyl isocyanide	[C-]#[N+]CCCC	0	Khalid	methanol	0.1155	0.1	0.1	0.1	0.1	1.275	174.12	0.696	73.14	1.015	86.09	0.795	83.13	0.013656470588235	0.010508620689655	0.008481773399015	0.010456603773585	0.6305032353767	C(=O)(C(=C)C)N(C(C)(C)C)C(c1ccc(C(F)(F)F)cc1)C(=O)NCCCC	Need Link
.	UCExp236-10	http://usefulchem.wikispaces.com/Exp236	No	No	4-(trifluoromethyl)benzaldehyde	FC(F)(F)c1ccc(C=O)cc1	Methylamine	NC	methacrylic acid	O=C(O)\C(=C)C	n-butyl isocyanide	[C-]#[N+]CCCC	0	Khalid	methanol	0.076	0.1	0.1	0.1	0.1	1.275	174.12	0.785	31.06	1.015	86.09	0.795	83.13	0.013656470588235	0.003956687898089	0.008481773399015	0.010456603773585	0.88848188000775	C(=O)(C(=C)C)N(C)C(c1ccc(C(F)(F)F)cc1)C(=O)NCCCC	Need Link
.	UCExp236-23	http://usefulchem.wikispaces.com/Exp236	No	No	4-(trifluoromethyl)benzaldehyde	FC(F)(F)c1ccc(C=O)cc1	3-Chloroaniline	NC1=CC(Cl)=CC=C1	methacrylic acid	O=C(O)\C(=C)C	n-butyl isocyanide	[C-]#[N+]CCCC	0	Khalid	methanol	0.1154	0.1	0.1	0.1	0.1	1.275	174.12	1.206	127.57	1.015	86.09	0.795	83.13	0.013656470588235	0.010577943615257	0.008481773399015	0.010456603773585	0.63062521087131	C(=O)(C(=C)C)N(c1cccc(Cl)c1)C(c1ccc(C(F)(F)F)cc1)C(=O)NCCCC	Need Link
.	UCExp236-24	http://usefulchem.wikispaces.com/Exp236	No	No	4-(trifluoromethyl)benzaldehyde	FC(F)(F)c1ccc(C=O)cc1	Benzylamine	NCc1ccccc1	methacrylic acid	O=C(O)\C(=C)C	n-butyl isocyanide	[C-]#[N+]CCCC	0	Khalid	methanol	0.1151	0.1	0.1	0.1	0.1	1.275	174.12	0.981	107.15	1.015	86.09	0.795	83.13	0.013656470588235	0.01092252803262	0.008481773399015	0.010456603773585	0.63044795376148	C(=O)(C(=C)C)N(Cc1ccccc1)C(c1ccc(C(F)(F)F)cc1)C(=O)NCCCC	Need Link
.	UCExp236-01	http://usefulchem.wikispaces.com/Exp236	No	No	4-(trifluoromethyl)benzaldehyde	FC(F)(F)c1ccc(C=O)cc1	t-butylamine	NC(C)(C)C	3,3'-dichloropivalic acid	ClCC(C(=O)O)(C)CCl	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.1155	0.1	0.1	0.1	0.1	1.275	174.12	0.696	73.14	1.33	171.022	0.795	83.13	0.013656470588235	0.010508620689655	0.012858796992481	0.010456603773585	0.61357036505344	C(=O)(C(CCl)(C)CCl)N(C(C)(C)C)C(c1ccc(C(F)(F)F)cc1)C(=O)NCCCC	Need Link
.	UCExp236-02	http://usefulchem.wikispaces.com/Exp236	No	No	4-(trifluoromethyl)benzaldehyde	FC(F)(F)c1ccc(C=O)cc1	3-Chloroaniline	NC1=CC(Cl)=CC=C1	3,3'-dichloropivalic acid	ClCC(C(=O)O)(C)CCl	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.1154	0.1	0.1	0.1	0.1	1.275	174.12	1.206	127.57	1.33	171.022	0.795	83.13	0.013656470588235	0.010577943615257	0.012858796992481	0.010456603773585	0.61368587634593	C(=O)(C(CCl)(C)CCl)N(c1cccc(Cl)c1)C(c1ccc(C(F)(F)F)cc1)C(=O)NCCCC	Need Link
.	UCExp236-17	http://usefulchem.wikispaces.com/Exp236	No	No	4-(trifluoromethyl)benzaldehyde	FC(F)(F)c1ccc(C=O)cc1	Aniline	Nc1ccccc1	3,3'-dichloropivalic acid	ClCC(C(=O)O)(C)CCl	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.1169	0.1	0.1	0.1	0.1	1.275	174.12	1.022	93.13	1.33	171.022	0.795	83.13	0.013656470588235	0.00911252446184	0.012858796992481	0.010456603773585	0.61355566892924	C(=O)(C(CCl)(C)CCl)N(c1ccccc1)C(c1ccc(C(F)(F)F)cc1)C(=O)NCCCC	Need Link
.	UCExp236-03	http://usefulchem.wikispaces.com/Exp236	No	No	4-(trifluoromethyl)benzaldehyde	FC(F)(F)c1ccc(C=O)cc1	Benzylamine	NCc1ccccc1	3,3'-dichloropivalic acid	ClCC(C(=O)O)(C)CCl	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.1151	0.1	0.1	0.1	0.1	1.275	174.12	0.981	107.15	1.33	171.022	0.795	83.13	0.013656470588235	0.01092252803262	0.012858796992481	0.010456603773585	0.61351801274237	C(=O)(C(CCl)(C)CCl)N(Cc1ccccc1)C(c1ccc(C(F)(F)F)cc1)C(=O)NCCCC	Need Link
.	UCExp236-13	http://usefulchem.wikispaces.com/Exp236	No	No	4-(trifluoromethyl)benzaldehyde	FC(F)(F)c1ccc(C=O)cc1	1-propylamine	NCCC	3,3'-dichloropivalic acid	ClCC(C(=O)O)(C)CCl	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.1178	0.1	0.1	0.1	0.1	1.275	174.12	0.719	59.11	1.33	171.022	0.795	83.13	0.013656470588235	0.008221140472879	0.012858796992481	0.010456603773585	0.61352323562208	C(=O)(C(CCl)(C)CCl)N(CCC)C(c1ccc(C(F)(F)F)cc1)C(=O)NCCCC	Need Link
.	UCExp236-19	http://usefulchem.wikispaces.com/Exp236	No	No	4-(trifluoromethyl)benzaldehyde	FC(F)(F)c1ccc(C=O)cc1	Methylamine	NC	formic acid	O=CO	n-butyl isocyanide	[C-]#[N+]CCCC	0	Khalid	methanol	0.076	0.1	0.1	0.1	0.1	1.275	174.12	0.785	31.06	1.22	46.02	0.795	83.13	0.013656470588235	0.003956687898089	0.003772131147541	0.010456603773585	0.92728342242822	C(=O)N(C)C(c1ccc(C(F)(F)F)cc1)C(=O)NCCCC	Need Link
.	EXP180	http://usefulchem.wikispaces.com/Exp180	no and aldehyde alone not solube	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	1-heptylamine	NCCCCCCC	acetic acid	O=C(O)C	n-butyl isocyanide	[C-]#[N+]CCCC	0	Shannon	methanol	1	0.5	0.5	0.5	0.5	1.217	206.24	0.777	115.22	1.049	60.05	0.795	83.13	0.084732949876746	0.074144144144144	0.028622497616778	0.052283018867924	0.40329651001968	CC(=O)N(CCCCCCC)C(C(=O)NCCCC)c2cc3ccccc3c1ccccc12	http://www.chemspider.com/Chemical-Structure.21105834.html	Protocol from Explan005 followed	7.16
.	EXP232-62	http://usefulchem.wikispaces.com/Exp232	No	No	2-phenylpropionaldehyde	O=CC(c1ccccc1)C	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.0424	0.1	0.1	0.1	0.1	1.002	134.18	1.099	97.12	1.159	175.18	0.795	83.13	0.01339121756487	0.012209281164695	0.015114754098361	0.010456603773585	1.0686974014619	CC(C)(C)OC(=O)NCC(=O)N(CC(=O)NCCCC)C(c1ccco1)C(C)c2ccccc2	Need Link
.	EXP232-57	http://usefulchem.wikispaces.com/Exp232	No	No	trans-2-hexenal	O=C/C=C/CCC	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.0442	0.1	0.1	0.1	0.1	0.846	98.14	1.099	97.12	1.159	175.18	0.795	83.13	0.011600472813239	0.008837124658781	0.015114754098361	0.010456603773585	1.10853739097966	CC(C)(C)OC(=O)NCC(=O)N(CC(=O)NCCCCC)C(\C=C\CCC)c1ccco1	Need Link
.	EXP232-17	http://usefulchem.wikispaces.com/Exp232	No	No	crotonaldehyde	O=C/C=C/C	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.0475	0.1	0.1	0.1	0.1	0.853	0.853	1.099	97.12	1.159	175.18	0.795	83.13	0.0001	0.000077616014559	0.015114754098361	0.010456603773585	1.36520683764042	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(\C=C\C)C(=O)NCCCC	Need Link


.	EXP232-07	http://usefulchem.wikispaces.com/Exp232		No	No	4-methylbenzaldehyde	Cc1ccc(C=O)cc1	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.0441	0.1	0.1	0.1	0.1	1.019	120.15	1.099	97.12	1.159	175.18	0.795	83.13	0.011790971540726	0.010932666060055	0.015114754098361	0.010456603773585	1.08230970182274	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(=O)NCCCC)c2ccc(C)cc2	Need Link
.	EXP232-47	http://usefulchem.wikispaces.com/Exp232		No	No	p-anisaldehyde	COc1ccc(C=O)cc1	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.0437	0.1	0.1	0.1	0.1	1.119	136.15	1.099	97.12	1.159	175.18	0.795	83.13	0.012167113494191	0.012388535031847	0.015114754098361	0.010456603773585	1.06579122407287	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(=O)NCCCC)c2ccc(OC)cc2	Need Link
.	EXP225-2	http://usefulchem.wikispaces.com/Exp225		Yes	Pending	piperonal	O=Cc1ccc2OCOc2c1	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.099957747498545	1	1	1	0.5	1.337	150.13	1.099	97.12	1.159	175.18	0.795	83.13	0.11228870605834	0.13660600545951	0.15114754098361	0.052283018867924	0.90533292337126	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(=O)NCCCC)c2ccc3OCOc3c2	Need Link	0.5 mmol of isocyanide was added to 500uL of a 2M solution of aldehyde, amine and acid
.	EXP232-67	http://usefulchem.wikispaces.com/Exp232		No	No	m-anisaldehyde	COc1cc(C=O)ccc1	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.0435	0.1	0.1	0.1	0.1	1.117	136.15	1.099	97.12	1.159	175.18	0.795	83.13	0.012188898836168	0.012388535031847	0.015114754098361	0.010456603773585	1.06781943623656	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(=O)NCCCC)c2cccc(OC)c2	Need Link
.	EXP232-02	http://usefulchem.wikispaces.com/Exp232		No	No	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.0457	0.1	0.1	0.1	0.1	1.045	106.12	1.099	97.12	1.159	175.18	0.795	83.13	0.010155023923445	0.009656050955414	0.015114754098361	0.010456603773585	1.09790655541221	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(=O)NCCCC)c2ccccc2	Need Link
.	EXP232-42	http://usefulchem.wikispaces.com/Exp232		No	No	o-tolualdehyde	O=Cc1ccccc1C	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.0443	0.1	0.1	0.1	0.1	1.039	120.15	1.099	97.12	1.159	175.18	0.795	83.13	0.011564003849856	0.010932666060055	0.015114754098361	0.010456603773585	1.08262569204323	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(=O)NCCCC)c2ccccc2C	Need Link
.	EXP232-37	http://usefulchem.wikispaces.com/Exp232		No	No	2-hydroxybenzaldehyde	O=Cc1ccccc1O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.0452	0.1	0.1	0.1	0.1	1.146	122.12	1.099	97.12	1.159	175.18	0.795	83.13	0.010656195462478	0.011111919927207	0.015114754098361	0.010456603773585	1.08061993952869	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(=O)NCCCC)c2ccccc2O	Need Link
.	EXP232-32	http://usefulchem.wikispaces.com/Exp232		No	No	2-furaldehyde	O=Cc1ccco1	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.0475	0.1	0.1	0.1	0.1	1.16	96.08	1.099	97.12	1.159	175.18	0.795	83.13	0.00828275862069	0.008742493175614	0.015114754098361	0.010456603773585	1.10991967809018	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(=O)NCCCC)c2ccco2	Need Link
.	EXP232-22	http://usefulchem.wikispaces.com/Exp232		No	No	diphenylacetaldehyde	O=CC(c1ccccc1)c2ccccc2	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.0381	0.1	0.1	0.1	0.1	1.106	196.24	1.099	97.12	1.159	175.18	0.795	83.13	0.01774321880651	0.017856232939036	0.015114754098361	0.010456603773585	1.0073454662586	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(c2ccccc2)c3ccccc3)C(=O)NCCCC	Need Link
.	EXP232-72	http://usefulchem.wikispaces.com/Exp232		No	No	2-ethylbutyraldehyde	O=CC(CC)CC	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.0435	0.1	0.1	0.1	0.1	0.814	100.16	1.099	97.12	1.159	175.18	0.795	83.13	0.012304668304668	0.009113739763421	0.015114754098361	0.010456603773585	1.10509734400537	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(CC)CC)C(=O)NCCCC	Need Link
.	EXP232-27	http://usefulchem.wikispaces.com/Exp232		No	No	cyclohexancarboxaldehyde	O=CC1CCCCC1	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.0437	0.1	0.1	0.1	0.1	0.926	112.17	1.099	97.12	1.159	175.18	0.795	83.13	0.012113390928726	0.010206551410373	0.015114754098361	0.010456603773585	1.09180675205593	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C2CCCCC2)C(=O)NCCCC	Need Link
.	EXP232-52	http://usefulchem.wikispaces.com/Exp232		No	No	hexanaldehyde	O=CCCCCC	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.0435	0.1	0.1	0.1	0.1	0.815	100.16	1.099	97.12	1.159	175.18	0.795	83.13	0.012289570552147	0.009113739763421	0.015114754098361	0.010456603773585	1.10528175458731	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(CCCCC)C(=O)NCCCC	Need Link
.	EXP228-3	http://usefulchem.wikispaces.com/Exp228		No	No	2,4-dimethylbenzaldehyde	O=CC1=CC=C(C)C=C1C	octadecylamine	NCCCCCCCCCCCCCCCCCC	Boc-Trp-OH	OC(C(CC1=CNC2=CC=CC=C21)NC(OC(C)(C)C)=O)=O	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.1	0.1	0.1	0.1	0.1	0.962	134.18	0.818	269.51	1.262	304.34	0.795	83.13	0.013948024948025	0.032947432762836	0.024115689381933	0.010456603773585	0.55106210069046	Cc1ccc(cc1)S(=O)(=O)CNC(=O)C(c3ccc(OC)c2ccc(OC)cc23)N(CCCCCCCCCCCCCCCCCC)C(=O)C(NC(=O)OC(C)(C)C)Cc5cnc4ccccc45	Need Link	Protocol from Explan005 followed
.	EXP228-6	http://usefulchem.wikispaces.com/Exp228		No	No	4-(trifluoromethyl)benzaldehyde	FC(F)(F)c1ccc(C=O)cc1	5-Methylfurfurylamine	NCc1oc(cc1)C	Boc-Trp-OH	OC(C(CC1=CNC2=CC=CC=C21)NC(OC(C)(C)C)=O)=O	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.1	0.1	0.1	0.1	0.1	1.275	174.12	0.997	111.14	1.262	304.34	0.795	83.13	0.013656470588235	0.011147442326981	0.024115689381933	0.010456603773585	0.62744623219113	Cc1ccc(cc1)S(=O)(=O)CNC(=O)C(N(Cc2ccc(C)o2)C(=O)C(Cc4cnc3ccccc34)NC(=O)OC(C)(C)C)c5ccc(cc5)N(C)C	Need Link	Protocol from Explan005 followed
.	EXP173G/V2B19	http://usefulchem.wikispaces.com/Exp173	YES	Yes	Yes	3,5-dimethoxybenzaldehyde	O=CC1=CC(OC)=CC(OC)=C1	Benzylamine	NCc1ccccc1	Phenylpropynoic acid	O=C(O)C#CC1=CC=CC=C1	n-butyl isocyanide	[C-]#[N+]CCCC	0	Khalid	methanol	4	1	1	1	1	1.114	166.17	0.981	107.15	1.24	146.14	0.795	83.13	0.14916517055655	0.1092252803262	0.11785483870968	0.10456603773585	0.22317386896008	CCCCNC(=O)C(c1cc(cc(c1)OC)OC)N(Cc2ccccc2)C(=O)C#Cc3ccccc3	http://www.chemspider.com/Search.aspx?rid=e9291700-32f9-4da2-8eb4-aead1298bb1f	Protocol from Explan005 followed	6.39
.	EXP181-103V2	http://usefulchem.wikispaces.com/Exp181		no and aldehyde alone not solube	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	Methylamine	NC	mandelic acid	O=C(O)[C@@H](O)c1ccccc1	n-butyl isocyanide	[C-]#[N+]CCCC	0	Khalid	methanol	2	0.5	0.5	0.5	0.5	1.217	206.24	0.785	31.06	1.321	152.15	0.795	83.13	0.084732949876746	0.019783439490446	0.057588947766843	0.052283018867924	0.22579598499278	CCCCNC(=O)C(c1cc2ccccc2c3c1cccc3)N(C)C(=O)C(c4ccccc4)O	http://www.chemspider.com/Chemical-Structure.21108640.html	Protocol from Explan005 followed	5.63
.	EXP174C/V2B34	http://usefulchem.wikispaces.com/Exp174		Yes but the aldehyde alone is not soluble in methanol	pending	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	Methylamine	NC	5-nitrosalicylic acid	O=C(O)c1cc(ccc1O)[N+]([O-])=O	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	2	0.5	0.5	0.5	0.5	1.217	206.24	0.785	31.06	1.631	183.12	0.795	83.13	0.084732949876746	0.019783439490446	0.056137339055794	0.052283018867924	0.22594409922114	CCCCNC(=O)C(c1cc2ccccc2c3c1cccc3)N(C)C(=O)c4cc(ccc4O)[N+](=O)[O-]	http://www.chemspider.com/Search.aspx?rid=95858b98-67c3-44ea-aafd-45e887561396	Protocol from Explan005 followed	5.12
.	EXP181-114V2	http://usefulchem.wikispaces.com/Exp181		Reactants Insoluble	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	5-Methylfurfurylamine	NCc1oc(cc1)C	2,4,6-trihydroxybenzoic acid.H2O	O=C(O)c1c(O)cc(O)cc1O	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	2	0.5	0.5	0.5	0.5	1.217	206.24	0.997	111.14	1.749	188.13	0.795	83.13	0.084732949876746	0.055737211634905	0.053782161234991	0.052283018867924	0.22256493843567	CCCCNC(=O)C(c1cc2ccccc2c3c1cccc3)N(Cc4ccc(o4)C)C(=O)c5c(cc(cc5O)O)O	http://www.chemspider.com/Chemical-Structure.21108651.html	Protocol from Explan005 followed	6.36
.	EXP181-055V2	http://usefulchem.wikispaces.com/Exp181		no and aldehyde alone not solube	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	5-Methylfurfurylamine	NCc1oc(cc1)C	2,6-dihydroxybenzoic aicd	O=C(O)c1c(O)cccc1O	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	2	0.5	0.5	0.5	0.5	1.217	206.24	0.997	111.14	1.559	154.12	0.795	83.13	0.084732949876746	0.055737211634905	0.049429121231559	0.052283018867924	0.22299703268584	CCCCNC(=O)C(c1cc2ccccc2c3c1cccc3)N(Cc4ccc(o4)C)C(=O)c5c(cccc5O)O	http://www.chemspider.com/Chemical-Structure.21108593.html	Protocol from Explan005 followed	6.7
.	EXP159C-V1B18	http://usefulchem.wikispaces.com/Exp159		Yes but the aldehyde alone is not soluble in methanol	Not Determined	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	Benzylamine	NCc1ccccc1	4-chlorophenylacetic acid	O=C(O)CC1=CC=C(Cl)C=C1	n-butyl isocyanide	[C-]#[N+]CCCC	0	Emily	methanol	0.5	0.5	0.5	0.5	0.5	1.217	206.24	0.981	107.15	1.324	170.59	0.795	83.13	0.084732949876746	0.054612640163099	0.064422205438066	0.052283018867924	0.66133121016822	CCCCNC(=O)C(c1cc2ccccc2c3c1cccc3)N(Cc4ccccc4)C(=O)Cc5ccc(cc5)Cl	http://www.chemspider.com/Search.aspx?rid=084ee4ca-35ec-4a6c-b6e0-bbe3d4f18d6c	Protocol from Explan005 followed	8.33


.	EXP181-075V2	http://usefulchem.wikispaces.com/Exp181	no and aldehyde alone not solube	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	furfurylamine	o1c(ccc1)CN	mandelic acid	O=C(O)[C@@H](O)c1ccccc1	n-butyl isocyanide	[C-]#[N+]CCCC	0	Khalid	methanol	2	0.5	0.5	0.5	0.5	1.217	206.24	1.099	97.12	1.321	152.15	0.795	83.13	0.084732949876746	0.093830755232029	0.057588947766843	0.052283018867924	0.21848986457157	CCCCNC(=O)C(c1cc2ccccc2c3c1cccc3)N(Cc4ccco4)C(=O)C(Cc5ccccc5)O	http://www.chemspider.com/Chemical-Structure.21108612.html	Protocol from Explan005 followed	7.01
.	EXP181-056V2	http://usefulchem.wikispaces.com/Exp181	Reactants Insoluble	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	furfurylamine	o1c(ccc1)CN	2,4,6-trihydroxybenzoic acid.H2O	O=C(O)c1c(O)cc(O)cc1O	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	2	0.5	0.5	0.5	0.5	1.217	206.24	1.099	97.12	1.749	188.13	0.795	83.13	0.084732949876746	0.093830755232029	0.053782161234991	0.052283018867924	0.21885392557035	CCCCNC(=O)C(c1cc2ccccc2c3c1cccc3)N(Cc4ccco4)C(=O)c5c(cc(cc5O)O)O	http://www.chemspider.com/Chemical-Structure.21108594.html	Protocol from Explan005 followed	5.9
.	EXP160C-V1B19	http://usefulchem.wikispaces.com/Exp160	No	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	furfurylamine	o1c(ccc1)CN	3,4-dihydroxyphenylacetic acid	O=C(O)Cc1cc(O)c(O)cc1	n-butyl isocyanide	[C-]#[N+]CCCC	0	Emily	methanol	1	0.5	0.5	0.5	0.5	1.217	206.24	1.099	97.12	1.478	168.15	0.795	83.13	0.084732949876746	0.093830755232029	0.056884303112314	0.052283018867924	0.38827984220453	CCCCNC(=O)C(c1cc2ccccc2c3c1cccc3)N(Cc4ccco4)C(=O)Cc5ccc(c(c5)O)O	http://www.chemspider.com/Search.aspx?rid=e5af2e41-d54e-43ad-8bc0-92875dfffbcd	Protocol from Explan005 followed	5.56
.	EXP181-119V2	http://usefulchem.wikispaces.com/Exp181	No	No	3,4-dihydroxybenzaldehyde	O=Cc1cc(O)c(O)cc1	Methylamine	NC	diphenylacetic acid	O=C(O)C(C1=CC=CC=C1)C2=CC=CC=C2	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	2	0.5	0.5	0.5	0.5	1.409	138.12	0.785	31.06	1.174	212.24	0.795	83.13	0.049013484740951	0.019783439490446	0.090391822827939	0.052283018867924	0.22609377506131	CCCCNC(=O)C(c1ccc(c(c1)O)O)N(C)C(=O)C(c2ccccc2)c3ccccc3	http://www.chemspider.com/Chemical-Structure.21108656.html	Protocol from Explan005 followed	3.8
.	EXP181-088V2	http://usefulchem.wikispaces.com/Exp181	No	No	3,4-dihydroxybenzaldehyde	O=Cc1cc(O)c(O)cc1	5-Methylfurfurylamine	o1c(ccc1CN)C	diphenylacetic acid	O=C(O)C(C1=CC=CC=C1)C2=CC=CC=C2	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	2	0.5	0.5	0.5	0.5	1.409	138.12	0.997	111.14	1.174	212.24	0.795	83.13	0.049013484740951	0.055737211634905	0.090391822827939	0.052283018867924	0.22247678133488	CCCCNC(=O)C(c1ccc(c(c1)O)O)N(Cc2ccc(o2)C)C(=O)C(c3ccccc3)c4ccccc4	http://www.chemspider.com/Chemical-Structure.21108625.html	Protocol from Explan005 followed	5.38
.	EXP181-076V2	http://usefulchem.wikispaces.com/Exp181	No	No	3,4-dihydroxybenzaldehyde	O=Cc1cc(O)c(O)cc1	1-propylamine	NCCC	diphenylacetic acid	O=C(O)C(C1=CC=CC=C1)C2=CC=CC=C2	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	2	0.5	0.5	0.5	0.5	1.409	138.12	0.719	59.11	1.174	212.24	0.795	83.13	0.049013484740951	0.041105702364395	0.090391822827939	0.052283018867924	0.22393467267935	CCCCNC(=O)C(c1ccc(c(c1)O)O)N(CCC)C(=O)C(c2ccccc2)c3ccccc3	http://www.chemspider.com/Chemical-Structure.21108613.html	Protocol from Explan005 followed	4.86
.	EXP174S/V2B52	http://usefulchem.wikispaces.com/Exp174	No	No	4,7-dimethoxy-1-naphthaldehyde	O=Cc1c2c(c(OC)cc1)ccc(OC)c2	Methylamine	NC	2-hydroxy-5-nitrobenzoicacid	O=C(O)c1cc(ccc1O)[N+]([O-])=O	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	2	0.5	0.5	0.5	0.5	1.18	216.23	0.785	31.06	1.631	183.12	0.795	83.13	0.091622881355932	0.019783439490446	0.056137339055794	0.052283018867924	0.22524281052295	CCCCNC(=O)C(c1ccc(c2c1cc(cc2)OC)OC)N(C)C(=O)c3cc(ccc3O)[N+](=O)[O-]	http://www.chemspider.com/Search.aspx?rid=37fae936-d220-4c1c-bac9-b83c3b28d499	Protocol from Explan005 followed	4.03
.	EXP174N/V2B46	http://usefulchem.wikispaces.com/Exp174	No	No	3-hydroxybenzaldehyde	O=CC1=CC(O)=CC=C1	Methylamine	NC	Boc-Trp-OH	OC(C(CC1=CNC2=CC=CC=C21)NC(OC(C)(C)C)=O)=O	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	2	0.5	0.5	0.5	0.5	1.226	122.12	0.785	31.06	1.262	304.34	0.795	83.13	0.049804241435563	0.019783439490446	0.12057844690967	0.052283018867924	0.22297049667102	CCCCNC(=O)C(c1cccc(c1)O)N(C)C(=O)C(Cc2c[nH]c3c2cccc3)NC(=O)OC(C)(C)C	http://www.chemspider.com/Search.aspx?rid=a3cda2d6-50e1-434e-b2b4-f1cadc9b8346	Protocol from Explan005 followed	4.45
.	EXP181-077V2	http://usefulchem.wikispaces.com/Exp181	Reactants Insoluble	No	3-methoxybenzaldehyde	O=CC1=CC(OC)=CC=C1	5-Methylfurfurylamine	o1c(ccc1CN)C	2,4,6-trihydroxybenzoic acid.H2O	O=C(O)c1c(O)cc(O)cc1O	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	2	0.5	0.5	0.5	0.5	1.117	136.15	0.997	111.14	1.749	188.13	0.795	83.13	0.060944494180842	0.055737211634905	0.053782161234991	0.052283018867924	0.22494689033986	CCCCNC(=O)C(c1cccc(c1)OC)N(Cc2ccc(o2)C)C(=O)c3c(cc(cc3O)O)O	Need Link	Protocol from Explan005 followed
.	EXP181-084V2	http://usefulchem.wikispaces.com/Exp181	No	No	3-methoxybenzaldehyde	O=CC1=CC(OC)=CC=C1	Benzylamine	NCc1ccccc1	mandelic acid	O=C(O)[C@@H](O)c1ccccc1	n-butyl isocyanide	[C-]#[N+]CCCC	0	Khalid	methanol	2	0.5	0.5	0.5	0.5	1.117	136.15	0.981	107.15	1.321	152.15	0.795	83.13	0.060944494180842	0.054612640163099	0.057588947766843	0.052283018867924	0.22467577141869	CCCCNC(=O)C(c1cccc(c1)OC)N(Cc2ccccc2)C(=O)C(c3ccccc3)O	Need Link	Protocol from Explan005 followed
.	EXP228-4	http://usefulchem.wikispaces.com/Exp228	No	No	Benzaldehyde	c1ccccc1C=O	1-hexylamine	NCCCCCC	Boc-Trp-OH	OC(C(CC1=CNC2=CC=CC=C21)NC(OC(C)(C)C)=O)=O	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.1	0.1	0.1	0.1	0.1	1.045	106.12	0.774	101.19	1.262	304.34	0.795	83.13	0.010155023923445	0.013073643410853	0.024115689381933	0.010456603773585	0.633709704235	CCCCNC(=O)C(c1ccccc1)N(CCCCCC)C(=O)C(NC(=O)OC(C)(C)C)Cc3cnc2ccccc23	Need Link	Protocol from Explan005 followed
.	EXP229-2	http://usefulchem.wikispaces.com/Exp229	No	No	Benzaldehyde	c1ccccc1C=O	1-hexylamine	NCCCCCC	Boc-Trp-OH	OC(C(CC1=CNC2=CC=CC=C21)NC(OC(C)(C)C)=O)=O	n-butyl isocyanide	[C-]#[N+]CCCC		David	methanol	0.092199039510184	0.1	0.1	0.1	0.1	1.045	106.12	0.774	101.19	1.262	304.34	0.795	83.13	0.010155023923445	0.013073643410853	0.024115689381933	0.010456603773585	0.66666666666667	CCCCNC(=O)C(c1ccccc1)N(CCCCCC)C(=O)C(NC(=O)OC(C)(C)C)Cc3cnc2ccccc23	Need Link	Protocol from Explan005 followed
.	EXP174E/V2B36	http://usefulchem.wikispaces.com/Exp174	No	No	2-hydroxybenzaldehyde	O=Cc1ccccc1O	Methylamine	NC	Boc-Trp-OH	OC(C(CC1=CNC2=CC=CC=C21)NC(OC(C)(C)C)=O)=O	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	2	0.5	0.5	0.5	0.5	1.146	122.12	0.785	31.06	1.262	304.34	0.795	83.13	0.053280977312391	0.019783439490446	0.12057844690967	0.052283018867924	0.22262533411189	CCCCNC(=O)C(c1ccccc1O)N(C)C(=O)C(Cc2c[nH]c3c2cccc3)NC(=O)OC(C)(C)C	http://www.chemspider.com/Search.aspx?rid=2f7ce97e-5398-4c2e-a04e-811f90c96480	Protocol from Explan005 followed	4.45
.	EXP173D/V2B16	http://usefulchem.wikispaces.com/Exp173	Reactants Insoluble	No	2-hydroxybenzaldehyde	O=Cc1ccccc1O	Methylamine	NC	1-Pyrenebutyric acid	O=C(O)CCCc4ccc2ccc1cccc3c1c2c4cc3	n-butyl isocyanide	[C-]#[N+]CCCC	0	Khalid	methanol	4	1	1	1	1	1.146	122.12	0.785	31.06	1.296	288.34	0.795	83.13	0.10656195462478	0.039566878980892	0.22248456790123	0.10456603773585	0.2235546357088	CCCCNC(C(N(C(CCCC1=CC=C2C=CC3=C(C2=C1C=C4)C4=CC=C3)=O)C)C5=C(O)C=CC=C5)=O	http://www.chemspider.com/Search.aspx?rid=496fd6c5-1e89-43fa-af54-cd7e654d3dfd	Protocol from Explan005 followed	6.35
.	EXP181-070V2	http://usefulchem.wikispaces.com/Exp181	Reactants Insoluble	No	2-methylbenzaldehyde	CC1=CC=CC=C1C=O	3-Chloroaniline	NC1=CC(Cl)=CC=C1	1-Pyrenebutyric acid	O=C(O)CCCc4ccc2ccc1cccc3c1c2c4cc3	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	2	0.5	0.5	0.5	0.5	1.039	120.15	1.206	127.57	1.296	288.34	0.795	83.13	0.057820019249278	0.052889718076285	0.11124228395062	0.052283018867924	0.21985414487692	CCCCNC(C(N(C(CCCC1=CC=C2C=CC3=C(C2=C1C=C4)C4=CC=C3)=O)c5cc(Cl)ccc5)c6c(C)cccc6)=O	Need Link	Protocol from Explan005 followed
.	EXP181-083V2	http://usefulchem.wikispaces.com/Exp181	Reactants Insoluble	No	Benzaldehyde	c1ccccc1C=O	Aniline	Nc1ccccc1	1-Pyrenebutyric acid	O=C(O)CCCc4ccc2ccc1cccc3c1c2c4cc3	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	2	0.5	0.5	0.5	0.5	1.045	106.12	1.022	93.13	1.296	288.34	0.795	83.13	0.050775119617225	0.045562622309198	0.11124228395062	0.052283018867924	0.22125234587233	CCCCNC(C(N(C(CCCC1=CC=C2C=CC3=C(C2=C1C=C4)C4=CC=C3)=O)c5ccccc5)c6ccccc6)=O	Need Link	Protocol from Explan005 followed
.	EXP175C	http://usefulchem.wikispaces.com/Exp175	Yes but the aldehyde alone is not soluble in methanol	Yes	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	Benzylamine	NCc1ccccc1	4-chlorophenylacetic acid	O=C(O)CC1=CC=C(Cl)C=C1	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid/ Emily	methanol	1	0.5	0.5	0.5	0.5	1.217	206.24	0.981	107.15	1.324	170.59	0.795	83.13	0.084732949876746	0.054612640163099	0.064422205438066	0.052283018867924	0.39807306702031	Clc5ccc(CC(=O)N(Cc1ccccc1)C(c3cc4ccccc4c2ccccc23)C(=O)NCCCC)cc5	http://www.chemspider.com/Chemical-Structure.21106077.html	Protocol from Explan005 followed	8.33
.	EXP232-12	http://usefulchem.wikispaces.com/Exp232	Yes	Pending	4-(trifluoromethyl)benzaldehyde	FC(F)(F)c1ccc(C=O)cc1	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.0422	0.1	0.1	0.1	0.1	1.275	174.12	1.099	97.12	1.159	175.18	0.795	83.13	0.013656470588235	0.015843494085532	0.015114754098361	0.010456603773585	1.02805222940199	FC(F)(F)c1ccc(cc1)C(C(=O)NCCCC)N(Cc2ccco2)C(=O)CNC(=O)OC(C)(C)C	Need Link
.	EXP164	http://usefulchem.wikispaces.com/Exp164	Reactants Insoluble	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	Aniline	Nc1ccccc1	phenylacetic acid	O=C(Oc1ccccc1)C	n-butyl isocyanide	[C-]#[N+]CCCC	0	Emily/Shannon	methanol	1.5	0.5	0.5	0.5	0.5	1.217	206.24	1.022	93.13	1.164	136.15	0.795	83.13	0.084732949876746	0.045562622309198	0.058483676975945	0.052283018867924	0.28718099816487	O=C(Cc1ccccc1)N(c2ccccc2)C(c4cc5ccccc5c3ccccc34)C(=O)NCCCC	http://www.chemspider.com/Chemical-Structure.21106183.html	Protocol from Explan005 followed	7.11
.	EXP178	http://usefulchem.wikispaces.com/Exp178	Yes but the aldehyde alone is not soluble in methanol	Not determined	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	furfurylamine	o1c(ccc1)CN	phenylacetic acid	O=C(O)Cc1ccccc1	n-butyl isocyanide	[C-]#[N+]CCCC	Waiting Isolation	Shannon	methanol	1	0.5	0.5	0.5	0.5	1.217	206.24	1.099	97.12	1.164	136.15	0.795	83.13	0.084732949876746	0.093830755232029	0.058483676975945	0.052283018867924	0.38779819325641	O=C(Cc1ccccc1)N(Cc2ccco2)C(c4cc5ccccc5c3ccccc34)C(=O)NCCCC	http://www.chemspider.com/Chemical-Structure.21105594.html	Protocol from Explan005 followed	6.9


.	UCExp237-01	http://usefulchem.wikispaces.com/Exp237	Yes	Awaiting Characterization	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	furfurylamine	o1c(ccc1)CN	phenylacetic acid	O=C(O)Cc1ccccc1	n-butyl isocyanide	[C-]#[N+]CCCC	Waiting Characterization	Khalid	methanol	2.825	4	4	4	4	1.217	206.24	1.099	97.12	1.164	136.15	0.795	83.13	0.67786359901397	0.75064604185623	0.46786941580756	0.4182641509434	0.77826413982759	O=C(Cc1ccccc1)N(Cc2ccco2)C(c4cc5ccccc5c3ccccc34)C(=O)NCCCC	http://www.chemspider.com/Chemical-Structure.21105594.html		6.9
.	EXP177	http://usefulchem.wikispaces.com/Exp177	Reactants Insoluble	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	1-propylamine	NCCC	phenylacetic acid	O=C(O)Cc1ccccc1	n-butyl isocyanide	[C-]#[N+]CCCC	0	Shannon	methanol	2	0.5	0.5	0.5	0.5	1.217	206.24	0.719	59.11	1.164	136.15	0.795	83.13	0.084732949876746	0.041105702364395	0.058483676975945	0.052283018867924	0.22355307360241	O=C(Cc1ccccc1)N(CCC)C(c3cc4ccccc4c2ccccc23)C(=O)NCCCC	http://www.chemspider.com/Chemical-Structure.21105831.html	Protocol from Explan005 followed	6.87
.	EXP131-1	http://usefulchem.wikispaces.com/Exp131	No	No	3,5-dimethoxybenzaldehyde	COC1=C(OC)C=C(C=O)C=C1	furfurylamine	o1c(ccc1)CN	Boc-Trp-OH	OC(C(CC1=CNC2=CC=CC=C21)NC(OC(C)(C)C)=O)=O	n-butyl isocyanide	[C-]#[N+]CCCC	0	Rikesh	methanol	0.5	0.5	0.5	0.5	0.5	1.114	166.17	1.099	97.12	1.262	304.34	0.795	83.13	0.074582585278276	0.075600545950864	0.12057844690967	0.052283018867924	0.60750049489227	O=C(N(C(C1=CC=C(OC)C(OC)=C1)C(NCCCC)=O)CC2=CC=CO2)C(NC(OC(C)(C)C)=O)CC3=CNC4=CC=CC=C43	http://www.chemspider.com/Search.aspx?rid=7280ee7c-14de-4478-baca-3611b8de0311	Protocol from Explan005 followed	6.07
.	EXP134-1	http://usefulchem.wikispaces.com/Exp134	No	No	o-Vanillin	Oc1c(cccc1OC)C=O	1-propylamine	NCCC	Boc-Trp-OH	OC(C(CC1=CNC2=CC=CC=C21)NC(OC(C)(C)C)=O)=O	n-butyl isocyanide	[C-]#[N+]CCCC	0	Rikesh	methanol	0.5	0.5	0.5	0.5	0.5	1.231	152.15	0.719	59.11	1.262	304.34	0.795	83.13	0.061799350121852	0.041105702364395	0.12057844690967	0.052283018867924	0.64452382028422	O=C(N(C(C1=CC=CC(OC)=C1O)C(NCCCC)=O)CCC)C(NC(OC(C)(C)C)=O)CC2=CNC3=CC=CC=C32	http://www.chemspider.com/Search.aspx?rid=87833cd4-7a3b-47f9-944a-b56b6ba2d55d	Protocol from Explan005 followed	5.21
.	EXP131-6	http://usefulchem.wikispaces.com/Exp131	No	No	o-Vanillin	Oc1c(cccc1OC)C=O	1-hexylamine	NCCCCCC	Boc-Trp-OH	OC(C(CC1=CNC2=CC=CC=C21)NC(OC(C)(C)C)=O)=O	n-butyl isocyanide	[C-]#[N+]CCCC	0	Rikesh	methanol	0.5	0.5	0.5	0.5	0.5	1.231	152.15	0.774	101.19	1.262	304.34	0.795	83.13	0.061799350121852	0.065368217054264	0.12057844690967	0.052283018867924	0.62497731882804	O=C(N(C(C1=CC=CC(OC)=C1O)C(NCCCC)=O)CCCCCC)C(NC(OC(C)(C)C)=O)CC2=CNC3=CC=CC=C32	http://www.chemspider.com/Search.aspx?rid=4fdfb83f-c3fb-48c0-80f2-2977c9d22be4	Protocol from Explan005 followed	6.81
.	EXP131-8	http://usefulchem.wikispaces.com/Exp131	No	No	o-Vanillin	Oc1c(cccc1OC)C=O	1-heptylamine	NCCCCCCC	Boc-Trp-OH	OC(C(CC1=CNC2=CC=CC=C21)NC(OC(C)(C)C)=O)=O	n-butyl isocyanide	[C-]#[N+]CCCC	0	Rikesh	methanol	0.5	0.5	0.5	0.5	0.5	1.231	152.15	0.777	115.22	1.262	304.34	0.795	83.13	0.061799350121852	0.074144144144144	0.12057844690967	0.052283018867924	0.61819601102972	O=C(N(C(C1=CC=CC(OC)=C1O)C(NCCCC)=O)CCCCCCC)C(NC(OC(C)(C)C)=O)CC2=CNC3=CC=CC=C32	http://www.chemspider.com/Search.aspx?rid=e48d700d-f24b-4323-94eb-9b196412c353	Protocol from Explan005 followed	7.34
.	EXP134-3	http://usefulchem.wikispaces.com/Exp134	No	No	o-Vanillin	Oc1c(cccc1OC)C=O	1-octylamine	NCCCCCCCC	Boc-Trp-OH	OC(C(CC1=CNC2=CC=CC=C21)NC(OC(C)(C)C)=O)=O	n-butyl isocyanide	[C-]#[N+]CCCC	0	Rikesh	methanol	0.5	0.5	0.5	0.5	0.5	1.231	152.15	0.782	129.24	1.262	304.34	0.795	83.13	0.061799350121852	0.082634271099744	0.12057844690967	0.052283018867924	0.61177414125395	O=C(N(C(C1=CC=CC(OC)=C1O)C(NCCCC)=O)CCCCCCCC)C(NC(OC(C)(C)C)=O)CC2=CNC3=CC=CC=C32	http://www.chemspider.com/Search.aspx?rid=c9b4dce6-9e8b-48c5-a609-c244bc04c333	Protocol from Explan005 followed	7.87
.	EXP182	http://usefulchem.wikispaces.com/Exp182	Reactants Insoluble	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	1-heptylamine	NCCCCCCC	furoic acid	OC(=O)c1ccco1	n-butyl isocyanide	[C-]#[N+]CCCC	0	Emily	methanol	1	0.5	0.5	0.5	0.5	1.217	206.24	0.777	115.22	1.22	112.08	0.795	83.13	0.084732949876746	0.074144144144144	0.045934426229508	0.052283018867924	0.39774255987993	O=C(N(CCCCCCC)C(c2cc3ccccc3c1ccccc12)C(=O)NCCCC)c4ccco4	Need Link
.	EXP130-1	http://usefulchem.wikispaces.com/Exp130	No	No	2-Naphthaldehyde	O=Cc2ccc1c(cccc1)c2	5-Methylfurfurylamine	NCc1oc(cc1)C	formic acid	O=CO	n-butyl isocyanide	[C-]#[N+]CCCC	0	Rikesh	methanol	0.5	0.53	0.53	0.53	0.53	1.155	156.18	0.997	111.14	1.22	46.02	0.795	83.13	0.071667012987013	0.059081444332999	0.019992295081967	0.05542	0.75053732198685	O=CN(Cc1ccc(C)o1)C(c2ccc3ccccc3c2)C(NCCCC)=O	http://www.chemspider.com/Search.aspx?rid=fa5a57c9-b418-4317-9145-1c5f8fcc3ecc	Protocol from Explan005 followed	4
.	EXP130-5	http://usefulchem.wikispaces.com/Exp130	No	No	2-Naphthaldehyde	O=Cc2ccc1c(cccc1)c2	furfurylamine	o1c(ccc1)CN	formic acid	O=CO	n-butyl isocyanide	[C-]#[N+]CCCC	0	Rikesh	methanol	0.5	0.53	0.53	0.53	0.53	1.155	156.18	1.099	97.12	1.22	46.02	0.795	83.13	0.071667012987013	0.075318835304823	0.019992295081967	0.05542	0.73366744483139	O=CN(Cc1ccco1)C(c2ccc3ccccc3c2)C(NCCCC)=O	http://www.chemspider.com/Search.aspx?rid=07011c39-1082-4141-af1f-1a734566d96b	Protocol from Explan005 followed	3.54
.	EXP228-2	http://usefulchem.wikispaces.com/Exp228	No	No	3-hydroxybenzaldehyde	O=CC1=CC(O)=CC=C1	octadecylamine	NCCCCCCCCCCCCCCCCCC	Boc-Trp-OH	OC(C(CC1=CNC2=CC=CC=C21)NC(OC(C)(C)C)=O)=O	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.3	0.1	0.1	0.1	0.1	1.226	122.12	0.818	269.51	1.262	304.34	0.795	83.13	0.009960848287113	0.032947432762836	0.024115689381933	0.010456603773585	0.2649142944918	Oc1cccc(c1)C(C(=O)NCCCC)N(CCCCCCCCCCCCCCCCCC)C(=O)C(NC(=O)OC(C)(C)C)Cc3cnc2ccccc23	Need Link	Protocol from Explan005 followed
.	EXP167A-V1B12	http://usefulchem.wikispaces.com/Exp167	Reactants Insoluble	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	1-propylamine	NCCC	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	n-butyl isocyanide	[C-]#[N+]CCCC	0	Tim	methanol	1	0.5	0.5	0.5	0.5	1.217	206.24	0.719	59.11	1.406	180.15	0.795	83.13	0.084732949876746	0.041105702364395	0.064064722617354	0.052283018867924	0.40251608174523	CCCCNC(=O)C(c2cc3ccccc3c1ccccc12)N(CCC)C(=O)Cc4ccc5OCOc5c4	http://www.chemspider.com/Search.aspx?rid=cd8abe97-97a1-4577-a10c-1be0708035db	Protocol from Explan005 followed	6.73
.	UCExp240-07	http://usefulchem.wikispaces.com/Exp240	Yes	Yes	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	5-Methylfurfurylamine	NCc1oc(cc1)C	phenylacetic acid	O=C(O)Cc1ccccc1	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	THF	0.04131	1	1	1	1	1.217	206.24	0.997	111.14	1.164	136.15	0.795	83.13	0.16946589975349	0.11147442326981	0.11696735395189	0.10456603773585	1.8389664363733	CCCCNC(=O)C(N(Cc1ccc(C)o1)C(=O)Cc2ccccc2)c4cc5ccccc5c3ccccc34
.	EXP226-2	http://usefulchem.wikispaces.com/Exp226	No	No	Benzaldehyde	c1ccccc1C=O	5-Methylfurfurylamine	NCc1oc(cc1)C	1-Pyrenebutyric acid	O=C(O)CCCc4ccc2ccc1cccc3c1c2c4cc3	n-butyl isocyanide	[C-]#[N+]CCCC		David	THF	0.68224538479725	0.5	0.5	0.5	0.5	1.045	106.12	0.997	111.14	1.296	288.34	0.795	83.13	0.050775119617225	0.055737211634905	0.11124228395062	0.052283018867924	0.525053991401	CCCCNC(=O)C(N(Cc1ccc(C)o1)C(=O)CCCc5ccc4ccc3cccc2ccc5c4c23)c6ccccc6	Need Link	0.5 mmol of isocyanide was added to 900uL of a 0.55M solution of aldehyde, amine and acid
.	UCExp240-01	http://usefulchem.wikispaces.com/Exp240	Yes but after 48h	Awaiting Characterization	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	furfurylamine	o1c(ccc1)CN	phenylacetic acid	O=C(O)Cc1ccccc1	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	THF	0.04361	1	1	1	1	1.217	206.24	1.099	97.12	1.164	136.15	0.795	83.13	0.16946589975349	0.18766151046406	0.11696735395189	0.10456603773585	1.60701739007867	CCCCNC(=O)C(N(Cc1ccco1)C(=O)Cc2ccccc2)c4cc5ccccc5c3ccccc34
.	EXP227-2	http://usefulchem.wikispaces.com/Exp227	No	No	piperonal	O=Cc1ccc2OCOc2c1	furfurylamine	o1c(ccc1)CN	1-Pyrenebutyric acid	O=C(O)CCCc4ccc2ccc1cccc3c1c2c4cc3	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	THF	0.02590523583056	0.25	0.25	0.25	0.5	1.337	150.13	1.099	97.12	1.296	288.34	0.795	83.13	0.028072176514585	0.034151501364877	0.055621141975309	0.052283018867924	1.27529500095702	CCCCNC(=O)C(N(Cc1ccco1)C(=O)CCCc5ccc4ccc3cccc2ccc5c4c23)c6ccc7OCOc7c6	Need Link	0.5 mmol of isocyanide was added to 500uL of a 0.5M solution of aldehyde, amine and acid
.	EXP231-7	http://usefulchem.wikispaces.com/Exp231	Yes	Pending	2-furaldehyde	O=Cc1ccco1	furfurylamine	o1c(ccc1)CN	1-Pyrenebutyric acid	O=C(O)CCCc4ccc2ccc1cccc3c1c2c4cc3	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	THF	1.00269687639988	1	1	1	1	1.16	96.08	1.099	97.12	1.296	288.34	0.795	83.13	0.082827586206897	0.087424931756142	0.22248456790123	0.10456603773585	0.66666666666667	CCCCNC(=O)C(N(Cc1ccco1)C(=O)CCCc5ccc4ccc3cccc2ccc5c4c23)c6ccco6	Need Link	Protocol from Explan005 followed
.	EXP215F	http://usefulchem.wikispaces.com/Exp215	Yes but not at room temperature	Yes	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	Benzylamine	NCc1ccccc1	4-chlorophenylacetic acid	O=C(O)CC1=CC=C(Cl)C=C1	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	THF	2	2	2	2	2	1.217	206.24	0.981	107.15	1.324	170.59	0.795	83.13	0.33893179950698	0.2184505606524	0.25768882175227	0.2091320754717	0.66133121016822	Clc5ccc(CC(=O)N(Cc1ccccc1)C(c3cc4ccccc4c2ccccc23)C(=O)NCCCC)cc5	http://www.chemspider.com/Chemical-Structure.21106077.html		8.33
.	EXP217-1	http://usefulchem.wikispaces.com/Exp217	No	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	Benzylamine	NCc1ccccc1	4-chlorophenylacetic acid	O=C(O)CC1=CC=C(Cl)C=C1	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	THF	0.41849288180884	0.2	0.2	0.2	0.2	1.217	206.24	0.981	107.15	1.324	170.59	0.795	83.13	0.033893179950698	0.02184505606524	0.025768882175227	0.02091320754717	0.38394111936947	Clc5ccc(CC(=O)N(Cc1ccccc1)C(c3cc4ccccc4c2ccccc23)C(=O)NCCCC)cc5	http://www.chemspider.com/Chemical-Structure.21106077.html		8.33
.	EXP231-4	http://usefulchem.wikispaces.com/Exp231	Yes	Pending	4-(trifluoromethyl)benzaldehyde	FC(F)(F)c1ccc(C=O)cc1	5-Methylfurfurylamine	NCc1oc(cc1)C	2-methoxyacetic acid	O=C(O)COC	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	THF	0.14133140387304	2	2	2	2	1.275	174.12	0.997	111.14	1.174	90.08	0.795	83.13	0.27312941176471	0.22294884653962	0.15345826235094	0.2091320754717	2	FC(F)(F)c1ccc(cc1)C(C(=O)NCCCC)N(Cc2ccc(C)o2)C(=O)COC	Need Link	Protocol from Explan005 followed


.	EXP217-5	http://usefulchem.wikispaces.com/Exp217	Yes	Pending	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	n-butyl isocyanide	[C-]#[N+]CCCC		Khalid	THF	0.39834500975977	0.2	0.2	0.2	0.2	1.217	206.24	1.099	97.12	1.159	175.18	0.795	83.13	0.033893179950698	0.037532302092812	0.030229508196721	0.02091320754717	0.38394111936947	O=C(Cc1ccccc1)N(Cc2ccco2)C(c4cc5ccccc5c3ccccc34)C(=O)NCCCC	http://www.chemspider.com/Chemical-Structure.21105594.html	6.9
.	UCExp237-02	http://usefulchem.wikispaces.com/Exp237	No	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	furfurylamine	o1c(ccc1)CN	phenylacetic acid	O=C(O)Cc1ccccc1	n-butyl isocyanide	[C-]#[N+]CCCC	0	Khalid	THF	0.1523	0.2	0.2	0.2	0.2	1.217	206.24	1.099	97.12	1.164	136.15	0.795	83.13	0.033893179950698	0.037532302092812	0.023393470790378	0.02091320754717	0.74617911416176	O=C(Cc1ccccc1)N(Cc2ccco2)C(c4cc5ccccc5c3ccccc34)C(=O)NCCCC	http://www.chemspider.com/Chemical-Structure.21105594.html	6.9
.	Exp242-6	http://usefulchem.wikispaces.com/Exp242	No	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	5-Methylfurfurylamine	NCc1oc(cc1)C	phenylacetic acid	O=C(O)Cc1ccccc1	n-butylisocyanide	[C-]#[N+]CCCC		Marshall	benzene	-0.59347118191165	0.1	0.1	0.1	0.1	1.217	206.24	0.997	111.14	1.164	136.15	0.795	83.13	0.016946589975349	0.011147442326981	0.011696735395189	0.010456603773585	-0.18408618708908	CCCCNC(=O)C(N(Cc1ccc(C)o1)C(=O)Cc2ccccc2)C=5C=C3C=CC=CC3C4C=CC=CC4=5
.	Exp242-1	http://usefulchem.wikispaces.com/Exp242	No	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	furfurylamine	o1c(ccc1)CN	phenylacetic acid	O=C(O)Cc1ccccc1	n-butylisocyanide	[C-]#[N+]CCCC		Marshall	benzene	0.18181954997068	0.1	0.1	0.1	0.1	1.217	206.24	1.099	97.12	1.164	136.15	0.795	83.13	0.016946589975349	0.008837124658781	0.011696735395189	0.010456603773585	0.43524320240451	CCCCNC(=O)C(N(Cc1ccco1)C(=O)Cc2ccccc2)C=5C=C3C=CC=CC3C4C=CC=CC4=5
.	UCExp241-26	http://usefulchem.wikispaces.com/Exp241	No	No	2,4-dimethylbenzaldehyde	O=CC1=CC=C(C)C=C1C	Methylamine	NC	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	n-butylisocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.13324	0.1	0.1	0.1	0.1	0.962	134.18	0.785	31.06	1.406	180.15	0.795	83.13	0.013948024948025	0.003956687898089	0.012812944523471	0.010456603773585	0.57334761128228	C(=O)(Cc1ccc2OCOc2c1)N(C)C(c1ccc(cc1C)C)C(=O)NCCCC
.	UCExp241-23	http://usefulchem.wikispaces.com/Exp241	No	No	5-bromo--thiophenecarboxaldehyde		Methylamine	NC	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	n-butylisocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.13324	0.1	0.1	0.1	0.1	1.18	216.23	0.785	31.06	1.406	180.15	0.795	83.13	0.018324576271186	0.003956687898089	0.012812944523471	0.010456603773585	0.55931285629585	C(=O)(Cc1ccc2OCOc2c1)N(C)C(c1sc(Br)cc1)C(=O)NCCCC
.	UCExp241-32	http://usefulchem.wikispaces.com/Exp241	No	No	4-(trifluoromethyl)benzaldehyde	FC(F)(F)c1ccc(C=O)cc1	Aniline	Nc1ccccc1	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	n-butylisocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.08719	0.1	0.1	0.1	0.1	1.275	174.12	1.022	93.13	1.406	180.15	0.795	83.13	0.013656470588235	0.00911252446184	0.012812944523471	0.010456603773585	0.75058990729522	C(=O)(Cc1ccc2OCOc2c1)N(c1ccccc1)C(c1ccc(C(F)(F)F)cc1)C(=O)NCCCC
.	UCExp241-31	http://usefulchem.wikispaces.com/Exp241	No	No	4-(trifluoromethyl)benzaldehyde	FC(F)(F)c1ccc(C=O)cc1	2-Chloroaniline	NC1=C(Cl)C=CC=C1	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	n-butylisocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.08719	0.1	0.1	0.1	0.1	1.275	174.12	1.213	127.57	1.406	180.15	0.795	83.13	0.013656470588235	0.010516900247321	0.012812944523471	0.010456603773585	0.74276039355205	C(=O)(Cc1ccc2OCOc2c1)N(c1ccccc1Cl)C(c1ccc(C(F)(F)F)cc1)C(=O)NCCCC
.	UCExp241-29	http://usefulchem.wikispaces.com/Exp241	No	No	4-(trifluoromethyl)benzaldehyde	FC(F)(F)c1ccc(C=O)cc1	1-hexylamine	NCCCCCC	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	n-butylisocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.08719	0.1	0.1	0.1	0.1	1.275	174.12	0.774	101.19	1.406	180.15	0.795	83.13	0.013656470588235	0.013073643410853	0.012812944523471	0.010456603773585	0.72891789604479	C(=O)(Cc1ccc2OCOc2c1)N(CCCCCC)C(c1ccc(C(F)(F)F)cc1)C(=O)NCCCC
.	UCExp241-44	http://usefulchem.wikispaces.com/Exp241	No	No	4-(trifluoromethyl)benzaldehyde	FC(F)(F)c1ccc(C=O)cc1	1-heptylamine	NCCCCCCC	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	n-butylisocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.08719	0.1	0.1	0.1	0.1	1.275	174.12	0.777	115.22	1.406	180.15	0.795	83.13	0.013656470588235	0.014828828828829	0.012812944523471	0.010456603773585	0.71971002628144	C(=O)(Cc1ccc2OCOc2c1)N(CCCCCCC)C(c1ccc(C(F)(F)F)cc1)C(=O)NCCCC
.	UCExp241-04	http://usefulchem.wikispaces.com/Exp241	No	No	veratraldehyde	COC1=C(OC)C=C(C=O)C=C1	Methylamine	NC	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	n-butylisocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.14824	0.1	0.1	0.1	0.1	1.114	166.17	0.785	31.06	1.406	180.15	0.795	83.13	0.014916517055655	0.003956687898089	0.012812944523471	0.010456603773585	0.52525766274777	c1cc2OCOc2cc1CC(=O)N(C)C(c1ccc(OC)c(OC)c1)C(=O)NCCCC
.	UCExp241-05	http://usefulchem.wikispaces.com/Exp241	No	No	veratraldehyde	COC1=C(OC)C=C(C=O)C=C1	Methylamine	NC	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	n-butylisocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.14824	0.1	0.1	0.1	0.1	1.114	166.17	0.785	31.06	1.406	180.15	0.795	83.13	0.014916517055655	0.003956687898089	0.012812944523471	0.010456603773585	0.52525766274777	c1cc2OCOc2cc1CC(=O)N(C)C(c1ccc(OC)c(OC)c1)C(=O)NCCCC
.	UCExp245-37	http://usefulchem.wikispaces.com/Exp245	No	No	piperonal	O=Cc1ccc2OCOc2c1	furfurylamine	o1c(ccc1)CN	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	n-butylisocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.15296	0.1	0.1	0.1	0.1	1.337	150.13	1.099	97.12	1.406	180.15	0.795	83.13	0.011228870605834	0.008837124658781	0.012812944523471	0.010456603773585	0.50943591579084	c1cc2OCOc2cc1CC(=O)N(Cc1ccco1)C(c1cc(OC)c(OC)cc1)C(=O)NCCCC
.	UCExp245-38	http://usefulchem.wikispaces.com/Exp245	No	No	piperonal	O=Cc1ccc2OCOc2c1	furfurylamine	o1c(ccc1)CN	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	n-butylisocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.09596	0.1	0.1	0.1	0.1	1.337	150.13	1.099	97.12	1.406	180.15	0.795	83.13	0.011228870605834	0.008837124658781	0.012812944523471	0.010456603773585	0.7178980564854	c1cc2OCOc2cc1CC(=O)N(Cc1ccco1)C(c1cc(OC)c(OC)cc1)C(=O)NCCCC
.	UCExp245-01	http://usefulchem.wikispaces.com/Exp245	No	No	piperonal	O=Cc1ccc2OCOc2c1	furfurylamine	o1c(ccc1)CN	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	n-butylisocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.15296	0.1	0.1	0.1	0.1	1.337	150.13	1.099	97.12	1.406	180.15	0.795	83.13	0.011228870605834	0.008837124658781	0.012812944523471	0.010456603773585	0.50943591579084	c1cc2OCOc2cc1CC(=O)N(Cc1ccco1)C(c1ccc2OCOc2c1)C(=O)NCCCC
.	UCExp245-02	http://usefulchem.wikispaces.com/Exp245	No	No	piperonal	O=Cc1ccc2OCOc2c1	furfurylamine	o1c(ccc1)CN	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	n-butylisocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.09596	0.1	0.1	0.1	0.1	1.337	150.13	1.099	97.12	1.406	180.15	0.795	83.13	0.011228870605834	0.008837124658781	0.012812944523471	0.010456603773585	0.7178980564854	c1cc2OCOc2cc1CC(=O)N(Cc1ccco1)C(c1ccc2OCOc2c1)C(=O)NCCCC
.	UCExp245-39	http://usefulchem.wikispaces.com/Exp245	No	No	piperonal	O=Cc1ccc2OCOc2c1	5-Methylfurfurylamine	NCc1oc(cc1)C	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	n-butylisocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.15296	0.1	0.1	0.1	0.1	1.337	150.13	0.997	111.14	1.406	180.15	0.795	83.13	0.011228870605834	0.011147442326981	0.012812944523471	0.010456603773585	0.50350981275552	c1cc2OCOc2cc1CC(=O)N(Cc1oc(cc1)C)C(c1cc(OC)c(OC)cc1)C(=O)NCCCC
.	UCExp245-40	http://usefulchem.wikispaces.com/Exp245	No	No	piperonal	O=Cc1ccc2OCOc2c1	5-Methylfurfurylamine	NCc1oc(cc1)C	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	n-butylisocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.09596	0.1	0.1	0.1	0.1	1.337	150.13	0.997	111.14	1.406	180.15	0.795	83.13	0.011228870605834	0.011147442326981	0.012812944523471	0.010456603773585	0.70618545822527	c1cc2OCOc2cc1CC(=O)N(Cc1oc(cc1)C)C(c1cc(OC)c(OC)cc1)C(=O)NCCCC
.	UCExp245-03	http://usefulchem.wikispaces.com/Exp245	No	No	piperonal	O=Cc1ccc2OCOc2c1	5-Methylfurfurylamine	NCc1oc(cc1)C	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	n-butylisocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.15296	0.1	0.1	0.1	0.1	1.337	150.13	0.997	111.14	1.406	180.15	0.795	83.13	0.011228870605834	0.011147442326981	0.012812944523471	0.010456603773585	0.50350981275552	c1cc2OCOc2cc1CC(=O)N(Cc1oc(cc1)C)C(c1ccc2OCOc2c1)C(=O)NCCCC
.	UCExp245-04	http://usefulchem.wikispaces.com/Exp245	No	No	piperonal	O=Cc1ccc2OCOc2c1	5-Methylfurfurylamine	NCc1oc(cc1)C	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	n-butylisocyanide	[C-]#[N+]CCCC		Khalid	methanol	0.09596	0.1	0.1	0.1	0.1	1.337	150.13	0.997	111.14	1.406	180.15	0.795	83.13	0.011228870605834	0.011147442326981	0.012812944523471	0.010456603773585	0.70618545822527	c1cc2OCOc2cc1CC(=O)N(Cc1oc(cc1)C)C(c1ccc2OCOc2c1)C(=O)NCCCC


.	UCExp245-17	http://usefulchem.wikispaces.com/Exp245	No	No	piperonal	O=Cc1ccc2OCOc2c1	furfurylamine	o1c(ccc1)CN	cbz-proline	O=C(O)[C@H]2N(C(=O)OCc1ccccc1)CCC2	n-butylisocyanide	[C-]#[N+]CCCC	Khalid	methanol	0.14973	0.1	0.1	0.1	0.1	1.337	150.13	1.099	97.12	1.309	249.262	0.795	83.13	0.011228870605834	0.008837124658781	0.019042169595111	0.010456603773585	0.50176931730704	c1ccccc1COC(=O)N1CCCC1C(=O)N(Cc1ccco1)C(c1ccc2OCOc2c1)C(=O)NCCCC
.	UCExp245-18	http://usefulchem.wikispaces.com/Exp245	No	No	piperonal	O=Cc1ccc2OCOc2c1	furfurylamine	o1c(ccc1)CN	cbz-proline	O=C(O)[C@H]2N(C(=O)OCc1ccccc1)CCC2	n-butylisocyanide	[C-]#[N+]CCCC	Khalid	methanol	0.03973	0.1	0.1	0.1	0.1	1.337	150.13	1.099	97.12	1.309	249.262	0.795	83.13	0.011228870605834	0.008837124658781	0.019042169595111	0.010456603773585	1.11988643378036	c1ccccc1COC(=O)N1CCCC1C(=O)N(Cc1ccco1)C(c1ccc2OCOc2c1)C(=O)NCCCC
.	UCExp245-19	http://usefulchem.wikispaces.com/Exp245	No	No	piperonal	O=Cc1ccc2OCOc2c1	5-Methylfurfurylamine	NCc1oc(cc1)C	cbz-proline	O=C(O)[C@H]2N(C(=O)OCc1ccccc1)CCC2	n-butylisocyanide	[C-]#[N+]CCCC	Khalid	methanol	0.14973	0.1	0.1	0.1	0.1	1.337	150.13	0.997	111.14	1.309	249.2625	0.795	83.13	0.011228870605834	0.011147442326981	0.019042207792208	0.010456603773585	0.49601913765188	c1ccccc1COC(=O)N1CCCC1C(=O)N(Cc1oc(cc1)C)C(c1ccc2OCOc2c1)C(=O)NCCCC
.	UCExp245-20	http://usefulchem.wikispaces.com/Exp245	No	No	piperonal	O=Cc1ccc2OCOc2c1	5-Methylfurfurylamine	NCc1oc(cc1)C	cbz-proline	O=C(O)[C@H]2N(C(=O)OCc1ccccc1)CCC2	n-butylisocyanide	[C-]#[N+]CCCC	Khalid	methanol	0.03973	0.1	0.1	0.1	0.1	1.337	150.13	0.997	111.14	1.309	249.262	0.795	83.13	0.011228870605834	0.011147442326981	0.019042169595111	0.010456603773585	1.09164244080136	c1ccccc1COC(=O)N1CCCC1C(=O)N(Cc1oc(cc1)C)C(c1ccc2OCOc2c1)C(=O)NCCCC
.	Exp242-10	http://usefulchem.wikispaces.com/Exp242	No	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	5-Methylfurfurylamine	NCc1oc(cc1)C	phenylacetic acid	O=C(O)Cc1ccccc1	n-pentyl isocyanide	[C-]#[N+]CCCCC	Marshall	benzene	0.19082106021191	0.1	0.1	0.1	0.1	1.217	206.24	0.997	111.14	1.164	136.15	0.772	97.16	0.016946589975349	0.011147442326981	0.011696735395189	0.012585492227979	0.41118874148571	CCCCCNC(=O)C(N(Cc1ccc(C)o1)C(=O)Cc2ccccc2)C=5C=C3C=CC=CC3C4C=CC=CC4=5
.	Exp242-5	http://usefulchem.wikispaces.com/Exp242	No	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	furfurylamine	o1c(ccc1)CN	phenylacetic acid	O=C(O)Cc1ccccc1	n-pentyl isocyanide	[C-]#[N+]CCCCC	Marshall	benzene	0.18229183514027	0.1	0.1	0.1	0.1	1.217	206.24	1.099	97.12	1.164	136.15	0.772	97.16	0.016946589975349	0.008837124658781	0.011696735395189	0.012585492227979	0.43037078904786	CCCCCNC(=O)C(N(Cc1ccco1)C(=O)Cc2ccccc2)C=5C=C3C=CC=CC3C4C=CC=CC4=5
.	EXP232-58	http://usefulchem.wikispaces.com/Exp232	No	No	trans-2-hexenal	O=C/C=C/CCC	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	n-pentyl isocyanide	[C-]#[N+]CCCCC	Khalid	methanol	0.042	0.1	0.1	0.1	0.1	0.846	98.14	1.099	97.12	1.159	175.18	0.772	97.16	0.011600472813239	0.008837124658781	0.015114754098361	0.012585492227979	1.10941193827204	CC(C)(C)OC(=O)NCC(=O)N(CC(=O)NCCCCC)C(\C=C\CCC)c1ccco1	Need Link
.	EXP232-63	http://usefulchem.wikispaces.com/Exp232	No	No	2-phenylpropionaldehyde	O=CC(c1ccccc1)C	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	n-pentyl isocyanide	[C-]#[N+]CCCCC	Khalid	methanol	0.0402	0.1	0.1	0.1	0.1	1.002	134.18	1.099	97.12	1.159	175.18	0.772	97.16	0.01339121756487	0.012209281164695	0.015114754098361	0.012585492227979	1.06951019417234	CC(C)(C)OC(=O)NCC(=O)N(CC(=O)NCCCCC)C(c1ccco1)C(C)c2ccccc2	Need Link
.	EXP232-18	http://usefulchem.wikispaces.com/Exp232	No	No	crotonaldehyde	O=C/C=C/C	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	n-pentyl isocyanide	[C-]#[N+]CCCCC	Khalid	methanol	0.0453	0.1	0.1	0.1	0.1	0.853	0.853	1.099	97.12	1.159	175.18	0.772	97.16	0.0001	0.000077616014559	0.015114754098361	0.012585492227979	1.36653349525504	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(\C=C\C)C(=O)NCCCCC	Need Link
.	EXP232-08	http://usefulchem.wikispaces.com/Exp232	No	No	4-methylbenzaldehyde	Cc1ccc(C=O)cc1	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	n-pentyl isocyanide	[C-]#[N+]CCCCC	Khalid	methanol	0.0419	0.1	0.1	0.1	0.1	1.019	120.15	1.099	97.12	1.159	175.18	0.772	97.16	0.011790971540726	0.010932666060055	0.015114754098361	0.012585492227979	1.08314334001523	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(=O)NCCCCC)c2ccc(C)cc2	Need Link
.	EXP232-48	http://usefulchem.wikispaces.com/Exp232	No	No	p-anisaldehyde	COc1ccc(C=O)cc1	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	n-pentyl isocyanide	[C-]#[N+]CCCCC	Khalid	methanol	0.0415	0.1	0.1	0.1	0.1	1.119	136.15	1.099	97.12	1.159	175.18	0.772	97.16	0.012167113494191	0.012388535031847	0.015114754098361	0.012585492227979	1.06659960056328	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(=O)NCCCCC)c2ccc(OC)cc2	Need Link
.	EXP225-3	http://usefulchem.wikispaces.com/Exp225	Yes	Pending	piperonal	O=Cc1ccc2OCOc2c1	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	n-pentyl isocyanide	[C-]#[N+]CCCCC	Khalid	methanol	0.099957747498545	1	1	1	0.5	1.337	150.13	1.099	97.12	1.159	175.18	0.772	97.16	0.11228870605834	0.13660600545951	0.15114754098361	0.062927461139896	0.88821390768098	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(=O)NCCCCC)c2ccc3OCOc3c2	Need Link	0.5 mmol of isocyanide was added to 500uL of a 2M solution of aldehyde, amine and acid
.	EXP232-68	http://usefulchem.wikispaces.com/Exp232	Yes	Pending	m-anisaldehyde	COc1cc(C=O)ccc1	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	n-pentyl isocyanide	[C-]#[N+]CCCCC	Khalid	methanol	0.0414	0.1	0.1	0.1	0.1	1.117	136.15	1.099	97.12	1.159	175.18	0.772	97.16	0.012188898836168	0.012388535031847	0.015114754098361	0.012585492227979	1.06749014058127	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(=O)NCCCCC)c2cccc(OC)c2	Need Link
.	EXP232-03	http://usefulchem.wikispaces.com/Exp232	No	No	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	n-pentyl isocyanide	[C-]#[N+]CCCCC	Khalid	methanol	0.0435	0.1	0.1	0.1	0.1	1.045	106.12	1.099	97.12	1.159	175.18	0.772	97.16	0.010155023923445	0.009656050955414	0.015114754098361	0.012585492227979	1.09876440288714	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(=O)NCCCCC)c2ccccc2	Need Link
.	EXP232-43	http://usefulchem.wikispaces.com/Exp232	No	No	o-tolualdehyde	O=Cc1ccccc1C	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	n-pentyl isocyanide	[C-]#[N+]CCCCC	Khalid	methanol	0.0421	0.1	0.1	0.1	0.1	1.039	120.15	1.099	97.12	1.159	175.18	0.772	97.16	0.011564003849856	0.010932666060055	0.015114754098361	0.012585492227979	1.08345981727095	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(=O)NCCCCC)c2ccccc2C	Need Link
.	EXP232-38	http://usefulchem.wikispaces.com/Exp232	No	No	2-hydroxybenzaldehyde	O=Cc1ccccc1O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	n-pentyl isocyanide	[C-]#[N+]CCCCC	Khalid	methanol	0.043	0.1	0.1	0.1	0.1	1.146	122.12	1.099	97.12	1.159	175.18	0.772	97.16	0.010656195462478	0.011111919927207	0.015114754098361	0.012585492227979	1.08145097570892	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(=O)NCCCCC)c2ccccc2O	Need Link
.	EXP232-33	http://usefulchem.wikispaces.com/Exp232	No	No	2-furaldehyde	O=Cc1ccco1	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	n-pentyl isocyanide	[C-]#[N+]CCCCC	Khalid	methanol	0.0453	0.1	0.1	0.1	0.1	1.16	96.08	1.099	97.12	1.159	175.18	0.772	97.16	0.00828275862069	0.008742493175614	0.015114754098361	0.012585492227979	1.11079640863267	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(=O)NCCCCC)c2ccco2	Need Link
.	EXP232-23	http://usefulchem.wikispaces.com/Exp232	No	No	diphenylacetaldehyde	O=CC(c1ccccc1)c2ccccc2	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	n-pentyl isocyanide	[C-]#[N+]CCCCC	Khalid	methanol	0.0359	0.1	0.1	0.1	0.1	1.106	196.24	1.099	97.12	1.159	175.18	0.772	97.16	0.01774321880651	0.017856232939036	0.015114754098361	0.012585492227979	1.00806758431396	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(c2ccccc2)c3ccccc3)C(=O)NCCCCC	Need Link
.	EXP232-73	http://usefulchem.wikispaces.com/Exp232	No	No	2-ethylbutyraldehyde	O=CC(CC)CC	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	n-pentyl isocyanide	[C-]#[N+]CCCCC	Khalid	methanol	0.0413	0.1	0.1	0.1	0.1	0.814	100.16	1.099	97.12	1.159	175.18	0.772	97.16	0.012304668304668	0.009113739763421	0.015114754098361	0.012585492227979	1.10596646974831	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C(CC)CC)C(=O)NCCCCC	Need Link
.	EXP232-28	http://usefulchem.wikispaces.com/Exp232	No	No	cyclohexancarboxaldehyde	O=CC1CCCCC1	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	n-pentyl isocyanide	[C-]#[N+]CCCCC	Khalid	methanol	0.0415	0.1	0.1	0.1	0.1	0.926	112.17	1.099	97.12	1.159	175.18	0.772	97.16	0.012113390928726	0.010206551410373	0.015114754098361	0.012585492227979	1.09265509018518	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(C2CCCCC2)C(=O)NCCCCC	Need Link


.	EXP232-53	http://usefulchem.wikispaces.com/Exp232	No	No	hexanaldehyde	O=CCCCCC	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	n-pentyl isocyanide	[C-]#[N+]CCCCC		Khalid	methanol	0.0413	0.1	0.1	0.1	0.1	0.815	100.16	1.099	97.12	1.159	175.18	0.772	97.16	0.012289570552147	0.009113739763421	0.015114754098361	0.012585492227979	1.10615117053529	CC(C)(C)OC(=O)NCC(=O)N(Cc1ccco1)C(CCCCC)C(=O)NCCCCC	Need Link
.	EXP130-2	http://usefulchem.wikispaces.com/Exp130	No	No	2-Naphthaldehyde	O=Cc2ccc1c(cccc1)c2	1-hexylamine	NCCCCCC	formic acid	O=CO	n-pentyl isocyanide	[C-]#[N+]CCCCC	0	Rikesh	methanol	0.5	0.53	0.53	0.53	0.53	1.155	156.18	0.774	101.19	1.22	46.02	0.772	97.16	0.071667012987013	0.069290310077519	0.019992295081967	0.06670310880829	0.72836942729266	CCCCCNC(C(c1cc2ccccc2cc1)N(CCCCCC)C=O)=O	http://www.chemspider.com/Search.aspx?rid=2a9a33a2-e65d-4161-b53e-1e64792a7151	Protocol from Explan005 followed	5.67
.	EXP232-13	http://usefulchem.wikispaces.com/Exp232	Yes	Pending	4-(trifluoromethyl)benzaldehyde	FC(F)(F)c1ccc(C=O)cc1	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	n-pentyl isocyanide	[C-]#[N+]CCCCC		Khalid	methanol	0.04	0.1	0.1	0.1	0.1	1.275	174.12	1.099	97.12	1.159	175.18	0.772	97.16	0.013656470588235	0.015843494085532	0.015114754098361	0.012585492227979	1.02880435105115	FC(F)(F)c1ccc(cc1)C(C(=O)NCCCCC)N(Cc2ccco2)C(=O)CNC(=O)OC(C)(C)C	Need Link
.	EXP131-3	http://usefulchem.wikispaces.com/Exp131	No	No	veratraldehyde	COC1=C(OC)C=C(C=O)C=C1	5-Methylfurfurylamine	NCc1oc(cc1)C	Boc-Trp-OH	OC(C(CC1=CNC2=CC=CC=C21)NC(OC(C)(C)C)=O)=O	n-pentyl isocyanide	[C-]#[N+]CCCCC	0	Rikesh	methanol	0.5	0.5	0.5	0.5	0.5	1.114	166.17	0.997	111.14	1.262	304.34	0.772	97.16	0.074582585278276	0.055737211634905	0.12057844690967	0.062927461139896	0.61438216678458	O=C(N(C(C1=CC=C(OC)C(OC)=C1)C(NCCCCC)=O)CC2=CC=C(C)O2)C(NC(OC(C)(C)C)=O)CC3=CNC4=CC=CC=C43	http://www.chemspider.com/Search.aspx?rid=fadab1dd-49fa-4a82-9a75-95c345803177	Protocol from Explan005 followed	7.07
.	EXP131-2	http://usefulchem.wikispaces.com/Exp131	No	No	veratraldehyde	COC1=C(OC)C=C(C=O)C=C1	furfurylamine	o1c(ccc1)CN	Boc-Trp-OH	OC(C(CC1=CNC2=CC=CC=C21)NC(OC(C)(C)C)=O)=O	n-pentyl isocyanide	[C-]#[N+]CCCCC	0	Rikesh	methanol	0.5	0.5	0.5	0.5	0.5	1.114	166.17	1.099	97.12	1.262	304.34	0.772	97.16	0.074582585278276	0.044185623293904	0.12057844690967	0.062927461139896	0.62322838247035	O=C(N(C(C1=CC=C(OC)C(OC)=C1)C(NCCCCC)=O)CC2=CC=CO2)C(NC(OC(C)(C)C)=O)CC3=CNC4=CC=CC=C43	http://www.chemspider.com/Search.aspx?rid=990b96be-6a78-4add-a027-61b74f5de822	Protocol from Explan005 followed	6.61
.	EXP134-2	http://usefulchem.wikispaces.com/Exp134	No	No	o-Vanillin	Oc1c(cccc1OC)C=O	1-propylamine	NCCC	Boc-Trp-OH	OC(C(CC1=CNC2=CC=CC=C21)NC(OC(C)(C)C)=O)=O	n-pentyl isocyanide	[C-]#[N+]CCCCC	0	Rikesh	methanol	0.5	0.5	0.5	0.5	0.5	1.231	152.15	0.719	59.11	1.262	304.34	0.772	97.16	0.061799350121852	0.041105702364395	0.12057844690967	0.062927461139896	0.63579988719808	O=C(N(C(C1=CC=CC(OC)=C1O)C(NCCCCC)=O)CCC)C(NC(OC(C)(C)C)=O)CC2=CNC3=CC=CC=C32	http://www.chemspider.com/Search.aspx?rid=9c13dea8-6c84-44ce-bab0-1d4cfac221f4	Protocol from Explan005 followed	5.74
.	EXP131-7	http://usefulchem.wikispaces.com/Exp131	No	No	o-Vanillin	Oc1c(cccc1OC)C=O	1-hexylamine	NCCCCCC	Boc-Trp-OH	OC(C(CC1=CNC2=CC=CC=C21)NC(OC(C)(C)C)=O)=O	n-pentyl isocyanide	[C-]#[N+]CCCCC	0	Rikesh	methanol	0.5	0.5	0.5	0.5	0.5	1.231	152.15	0.774	101.19	1.262	304.34	0.772	97.16	0.061799350121852	0.065368217054264	0.12057844690967	0.062927461139896	0.61677113570394	O=C(N(C(C1=CC=CC(OC)=C1O)C(NCCCCC)=O)CCCCCC)C(NC(OC(C)(C)C)=O)CC2=CNC3=CC=CC=C32	http://www.chemspider.com/Search.aspx?rid=d79e6652-177b-418b-8621-890761e238f4	Protocol from Explan005 followed	7.34
.	EXP131-9	http://usefulchem.wikispaces.com/Exp131	No	No	o-Vanillin	Oc1c(cccc1OC)C=O	1-heptylamine	NCCCCCCC	Boc-Trp-OH	OC(C(CC1=CNC2=CC=CC=C21)NC(OC(C)(C)C)=O)=O	n-pentyl isocyanide	[C-]#[N+]CCCCC	0	Rikesh	methanol	0.5	0.5	0.5	0.5	0.5	1.231	152.15	0.777	115.22	1.262	304.34	0.772	97.16	0.061799350121852	0.074144144144144	0.12057844690967	0.062927461139896	0.61016579984942	O=C(N(C(C1=CC=CC(OC)=C1O)C(NCCCCC)=O)CCCCCCC)C(NC(OC(C)(C)C)=O)CC2=CNC3=CC=CC=C32	http://www.chemspider.com/Search.aspx?rid=f4ca043b-c944-464e-8152-474634edaa01	Protocol from Explan005 followed	7.87
.	EXP134-4	http://usefulchem.wikispaces.com/Exp134	No	No	o-Vanillin	Oc1c(cccc1OC)C=O	1-octylamine	NCCCCCCCC	Boc-Trp-OH	OC(C(CC1=CNC2=CC=CC=C21)NC(OC(C)(C)C)=O)=O	n-pentyl isocyanide	[C-]#[N+]CCCCC	0	Rikesh	methanol	0.5	0.5	0.5	0.5	0.5	1.231	152.15	0.782	129.24	1.262	304.34	0.772	97.16	0.061799350121852	0.082634271099744	0.12057844690967	0.062927461139896	0.60390883913968	O=C(N(C(C1=CC=CC(OC)=C1O)C(NCCCCC)=O)CCCCCCCC)C(NC(OC(C)(C)C)=O)CC2=CNC3=CC=CC=C32	http://www.chemspider.com/Search.aspx?rid=29ec72e8-5452-4943-8af5-166b2ce1dffd	Protocol from Explan005 followed	8.4
.	UCExp240-12	http://usefulchem.wikispaces.com/Exp240	Yes but 48h	Awaiting Characterization	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	5-Methylfurfurylamine	NCc1oc(cc1)C	phenylacetic acid	O=C(O)Cc1ccccc1	n-pentyl isocyanide	[C-]#[N+]CCCCC		Khalid	THF	0.03921	1	1	1	1	1.217	206.24	0.997	111.14	1.164	136.15	0.772	97.16	0.16946589975349	0.11147442326981	0.11696735395189	0.12585492227979	1.77628538462327	CCCCCNC(=O)C(N(Cc1ccc(C)o1)C(=O)Cc2ccccc2)c4cc5ccccc5c3ccccc34
.	EXP226-3	http://usefulchem.wikispaces.com/Exp226	No	No	Benzaldehyde	c1ccccc1C=O	5-Methylfurfurylamine	NCc1oc(cc1)C	1-Pyrenebutyric acid	O=C(O)CCCc4ccc2ccc1cccc3c1c2c4cc3	n-pentyl isocyanide	[C-]#[N+]CCCCC		David	THF	0.68224538479725	0.5	0.5	0.5	0.5	1.045	106.12	0.997	111.14	1.296	288.34	0.772	97.16	0.050775119617225	0.055737211634905	0.11124228395062	0.062927461139896	0.51924991256154	CCCCCNC(=O)C(N(Cc1ccc(C)o1)C(=O)CCCc5ccc4ccc3cccc2ccc5c4c23)c6ccccc6	Need Link	0.5 mmol of isocyanide was added to 900uL of a 0.55M solution of aldehyde, amine and acid
.	UCExp240-06	http://usefulchem.wikispaces.com/Exp240	Yes	Yes	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	furfurylamine	o1c(ccc1)CN	phenylacetic acid	O=C(O)Cc1ccccc1	n-pentyl isocyanide	[C-]#[N+]CCCCC		Khalid	THF	0.04151	1	1	1	1	1.217	206.24	1.099	97.12	1.164	136.15	0.772	97.16	0.16946589975349	0.18766151046406	0.11696735395189	0.12585492227979	1.55894442180061	CCCCCNC(=O)C(N(Cc1ccco1)C(=O)Cc2ccccc2)c4cc5ccccc5c3ccccc34
.	EXP227-3	http://usefulchem.wikispaces.com/Exp227	No	No	piperonal	O=Cc1ccc2OCOc2c1	furfurylamine	o1c(ccc1)CN	1-Pyrenebutyric acid	O=C(O)CCCc4ccc2ccc1cccc3c1c2c4cc3	n-pentyl isocyanide	[C-]#[N+]CCCCC		Khalid	THF	0.38215518014523	0.25	0.25	0.25	0.5	1.337	150.13	1.099	97.12	1.296	288.34	0.772	97.16	0.028072176514585	0.034151501364877	0.055621141975309	0.062927461139896	0.44410695384049	CCCCCNC(=O)C(N(Cc1ccco1)C(=O)CCCc5ccc4ccc3cccc2ccc5c4c23)c6ccc7OCOc7c6	Need Link	0.5 mmol of isocyanide was added to 500uL of a 0.5M solution of aldehyde, amine and acid
.	EXP184-2/49	http://usefulchem.wikispaces.com/Exp184	Reactants insoluble	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	cyclohexylamine	NC1CCCCC1	mandelic acid	O=C(O)[C@@H](O)c1ccccc1	t-butyl isocyanide	CC(C)(C)[N+]#[C-]		Emily	acetonitrile	1	0.5	0.5	0.5	0.5	1.217	206.24	0.867	99.17	1.321	152.15	0.735	83.13	0.084732949876746	0.057191464821223	0.057588947766843	0.056551020408163	0.39806876687034	CC(C)(C)NC(=O)C(C(NC1CCCCC1)C(=O)C(O)c2ccccc2)c4cc5ccccc5c3ccccc34	Need Link	Protocol from Explan005 followed
.	EXP201-31	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	39.23	Khalid	acetonitrile	0.6	0.2	0.2	0.2	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.02031004784689	0.019312101910828	0.030229508196721	0.022620408163265	0.28882031461758	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-32	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	40.58	Khalid	acetonitrile	0.6	0.2	0.24	0.2	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.02031004784689	0.023174522292994	0.030229508196721	0.022620408163265	0.28721828930993	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-33	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	43.85	Khalid	acetonitrile	0.6	0.24	0.2	0.2	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.024372057416268	0.019312101910828	0.030229508196721	0.022620408163265	0.28713598800276	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-34	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	35.4	Khalid	acetonitrile	0.6	0.2	0.2	0.24	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.02031004784689	0.019312101910828	0.036275409836066	0.022620408163265	0.28632048026224	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-35	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	41.37	Khalid	acetonitrile	0.6	0.2	0.2	0.2	0.24	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.02031004784689	0.019312101910828	0.030229508196721	0.027144489795918	0.286945631831	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-36	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	39.23	Khalid	acetonitrile	0.6	0.24	0.24	0.2	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.024372057416268	0.023174522292994	0.030229508196721	0.022620408163265	0.28555254219922	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74


.	EXP201-37	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	0.68	Khalid	acetonitrile	2.6	0.2	0.2	0.2	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.02031004784689	0.019312101910828	0.030229508196721	0.022620408163265	0.074281179187267	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-38	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	1.8	Khalid	acetonitrile	2.6	0.2	0.24	0.2	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.02031004784689	0.023174522292994	0.030229508196721	0.022620408163265	0.074174773568105	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-39	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	1.01	Khalid	acetonitrile	2.6	0.24	0.2	0.2	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13			0.030229508196721	0.022620408163265	0.001982713712159	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74	Max Conc Correct?
.	EXP201-40	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	0.9	Khalid	acetonitrile	2.6	0.2	0.2	0.24	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.02031004784689	0.019312101910828	0.036275409836066	0.022620408163265	0.07411475572506	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-41	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	1.01	Khalid	acetonitrile	2.6	0.2	0.2	0.2	0.24	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.02031004784689	0.019312101910828	0.030229508196721	0.027144489795918	0.074156576073283	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-42	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	0.45	Khalid	acetonitrile	2.6	0.24	0.24	0.2	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.024372057416268	0.023174522292994	0.030229508196721	0.022620408163265	0.074063197864137	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP184-3/49	http://usefulchem.wikispaces.com/Exp184	Reactants insoluble	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	cyclohexylamine	NC1CCCCC1	mandelic acid	O=C(O)[C@@H](O)c1ccccc1	t-butyl isocyanide	CC(C)(C)[N+]#[C-]		Emily	dichloromethane	1	0.5	0.5	0.5	0.5	1.217	206.24	0.867	99.17	1.321	152.15	0.735	83.13	0.084732949876746	0.057191464821223	0.057588947766843	0.056551020408163	0.39806876687034	CC(C)(C)NC(=O)C(C(NC1CCCCC1)C(=O)C(O)c2ccccc2)c4cc5ccccc5c3ccccc34	Need Link	Protocol from Explan005 followed
.	EXP222-1	http://usefulchem.wikispaces.com/Exp222	Yes	YES	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]		Khalid	DMSO	0.3253708551139	0.5	0.5	0.5	0.5	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.050775119617225	0.04828025477707	0.075573770491803	0.056551020408163	0.89839023138132	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html		3.74
.	EXP222-3	http://usefulchem.wikispaces.com/Exp222	No	No	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]		Khalid	DMSO	0.41268542755695	0.25	0.25	0.25	0.25	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.025387559808612	0.024140127388535	0.037786885245902	0.028275510204082	0.47323791311738	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html		3.74
.	EXP184-1/49	http://usefulchem.wikispaces.com/Exp184	Reactants insoluble	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	cyclohexylamine	NC1CCCCC1	mandelic acid	O=C(O)[C@@H](O)c1ccccc1	t-butyl isocyanide	CC(C)(C)[N+]#[C-]		Emily	ethanol	1	0.5	0.5	0.5	0.5	1.217	206.24	0.867	99.17	1.321	152.15	0.735	83.13	0.084732949876746	0.057191464821223	0.057588947766843	0.056551020408163	0.39806876687034	CC(C)(C)NC(=O)C(C(NC1CCCCC1)C(=O)C(O)c2ccccc2)c4cc5ccccc5c3ccccc34	Need Link	Protocol from Explan005 followed
.	EXP201-19	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	51.52	Khalid	ethanol	0.6	0.2	0.2	0.2	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.02031004784689	0.019312101910828	0.030229508196721	0.022620408163265	0.28882031461758	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-20	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	46.78	Khalid	ethanol	0.6	0.2	0.24	0.2	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.02031004784689	0.023174522292994	0.030229508196721	0.022620408163265	0.28721828930993	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-21	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	51.29	Khalid	ethanol	0.6	0.24	0.2	0.2	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.024372057416268	0.019312101910828	0.030229508196721	0.022620408163265	0.28713598800276	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-22	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	54.11	Khalid	ethanol	0.6	0.2	0.2	0.24	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.02031004784689	0.019312101910828	0.036275409836066	0.022620408163265	0.28632048026224	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-23	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	55.91	Khalid	ethanol	0.6	0.2	0.2	0.2	0.24	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.02031004784689	0.019312101910828	0.030229508196721	0.027144489795918	0.286945631831	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-24	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	58.28	Khalid	ethanol	0.6	0.24	0.24	0.2	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.024372057416268	0.023174522292994	0.030229508196721	0.022620408163265	0.28555254219922	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-25	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	1.24	Khalid	ethanol	2.6	0.2	0.2	0.2	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.02031004784689	0.019312101910828	0.030229508196721	0.022620408163265	0.074281179187267	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-26	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	2.25	Khalid	ethanol	2.6	0.2	0.24	0.2	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.02031004784689	0.023174522292994	0.030229508196721	0.022620408163265	0.074174773568105	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-27	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	7.78	Khalid	ethanol	2.6	0.24	0.2	0.2	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.024372057416268	0.019312101910828	0.030229508196721	0.022620408163265	0.074169283378716	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-28	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	1.13	Khalid	ethanol	2.6	0.2	0.2	0.24	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.02031004784689	0.019312101910828	0.036275409836066	0.022620408163265	0.07411475572506	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74


.	EXP201-29	http://usefulchem.wikispaces.com/Exp201		Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	0.79	Khalid	ethanol	2.6	0.2	0.2	0.2	0.24	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.02031004784689	0.019312101910828	0.030229508196721	0.027144489795918	0.074156576073283	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-30	http://usefulchem.wikispaces.com/Exp201		Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	0.23	Khalid	ethanol	2.6	0.24	0.24	0.2	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.024372057416268	0.023174522292994	0.030229508196721	0.022620408163265	0.074063197864137	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	UCExp236-27	http://usefulchem.wikispaces.com/Exp236		No	No	2,4-dimethylbenzaldehyde	O=CC1=CC=C(C)C=C1C	t-butylamine	NC(C)(C)C	3,3'-dichloropivalic acid	ClCC(C(=O)O)(C)CCl	t-butyl isocyanide	CC(C)(C)[N+]#[C-]		Khalid	methanol	0.1143	0.1	0.1	0.1	0.1	0.962	134.18	0.696	73.14	1.33	171.022	0.795	83.13	0.013948024948025	0.010508620689655	0.012858796992481	0.010456603773585	0.61700954741378	C(=O)(C(CCl)(C)CCl)N(C(C)(C)C)C(c1ccc(cc1C)C)C(=O)NC(C)(C)C	Need Link
.	EXP232-71	http://usefulchem.wikispaces.com/Exp232		No	No	2-ethylbutyraldehyde	O=CC(CC)CC	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]		Khalid	methanol	0.0426	0.1	0.1	0.1	0.1	0.814	100.16	1.099	97.12	1.159	175.18	0.735	83.13	0.012304668304668	0.009113739763421	0.015114754098361	0.011310204081633	1.10566428637456	CC(C)(C)NC(=O)C(C(CC)CC)N(Cc1ccco1)C(=O)CNC(=O)OC(C)(C)C	Need Link
.	EXP181-065V2	http://usefulchem.wikispaces.com/Exp181		No	No	3,5-dimethoxybenzaldehyde	O=CC1=CC(OC)=CC(OC)=C1	Benzylamine	NCc1ccccc1	D-(−)-Quinic acid	O=C(O)C1(O)C[C@@H](O)C(O)[C@H](O)C1	t-butyl isocyanide	CC(C)(C)[N+]#[C-]		Khalid	methanol	2	0.5	0.5	0.5	0.5	1.114	166.17	0.981	107.15	1.828	192.17	0.735	83.13	0.074582585278276	0.054612640163099	0.052562910284464	0.056551020408163	0.22338290429174	CC(C)(C)NC(=O)C(c1cc(cc(c1)OC)OC)N(Cc2ccccc2)C(=O)C3(CC(C(C(C3)O)O)O)O	http://www.chemspider.com/Chemical-Structure.21108602.html	Protocol from Explan005 followed	1.79
.	EXP181-111V2	http://usefulchem.wikispaces.com/Exp181		Reactants Insoluble	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	Methylamine	NC	2,4,6-trihydroxybenzoic acid.H2O	O=C(O)c1c(O)cc(O)cc1O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]		Khalid	methanol	2	0.5	0.5	0.5	0.5	1.217	206.24	0.785	31.06	1.749	188.13	0.735	83.13	0.084732949876746	0.019783439490446	0.053782161234991	0.056551020408163	0.22574896577374	CC(C)(C)NC(=O)C(c1cc2ccccc2c3c1cccc3)N(C)C(=O)c4c(cc(cc4O)O)O	http://www.chemspider.com/Chemical-Structure.21108648.html	Protocol from Explan005 followed	4.48
.	EXP181-079V2	http://usefulchem.wikispaces.com/Exp181		Reactants Insoluble	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	furfurylamine	o1c(ccc1)CN	2,4,6-trihydroxybenzoic acid.H2O	O=C(O)c1c(O)cc(O)cc1O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]		Khalid	methanol	2	0.5	0.5	0.5	0.5	1.217	206.24	1.099	97.12	1.749	188.13	0.735	83.13	0.084732949876746	0.093830755232029	0.053782161234991	0.056551020408163	0.21844583864568	CC(C)(C)NC(=O)C(c1cc2ccccc2c3c1cccc3)N(Cc4ccco4)C(=O)c5c(cc(cc5O)O)O	http://www.chemspider.com/Chemical-Structure.21108616.html	Protocol from Explan005 followed	5.54
.	EXP173F/V2B18	http://usefulchem.wikispaces.com/Exp173		no and aldehyde alone not solube	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	furfurylamine	o1c(ccc1)CN	2,3-dihydroxybenzoic acid	O=C(O)c1cccc(O)c1O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	0	Khalid	methanol	4	1	1	1	1	1.217	206.24	1.099	97.12	1.559	154.12	0.735	83.13	0.16946589975349	0.18766151046406	0.098858242463117	0.11310204081633	0.21886207205505	CC(C)(C)NC(=O)C(c1cc2ccccc2c3c1cccc3)N(Cc4ccco4)C(=O)c5cccc(c5O)O	http://www.chemspider.com/Search.aspx?rid=c3149f26-a585-45a3-b0e3-c4899e85749d	Protocol from Explan005 followed	5.64
.	EXP181-074V2	http://usefulchem.wikispaces.com/Exp181		No	No	3,4-dihydroxybenzaldehyde	O=Cc1cc(O)c(O)cc1	Aniline	Nc1ccccc1	3,4-dihydroxyphenylacetic acid	O=C(O)Cc1cc(O)c(O)cc1	t-butyl isocyanide	CC(C)(C)[N+]#[C-]		Khalid	methanol	2	0.5	0.5	0.5	0.5	1.409	138.12	1.022	93.13	1.478	168.15	0.735	83.13	0.049013484740951	0.045562622309198	0.056884303112314	0.056551020408163	0.22644810306565	CC(C)(C)NC(=O)C(c1ccc(c(c1)O)O)N(c2ccccc2)C(=O)Cc3ccc(c(c3)O)O	http://www.chemspider.com/Chemical-Structure.21108611.html	Protocol from Explan005 followed	1.61
.	EXP181-115V2	http://usefulchem.wikispaces.com/Exp181		Reactants Insoluble	No	2-Naphthaldehyde	O=Cc2ccc1c(cccc1)c2	3-Chloroaniline	NC1=CC(Cl)=CC=C1	3,4-dihydroxyphenylacetic acid	O=C(O)Cc1cc(O)c(O)cc1	t-butyl isocyanide	CC(C)(C)[N+]#[C-]		Khalid	methanol	2	0.5	0.5	0.5	0.5	1.155	156.18	1.206	127.57	1.478	168.15	0.735	83.13	0.06761038961039	0.052889718076285	0.056884303112314	0.056551020408163	0.22382025595512	CC(C)(C)NC(=O)C(c1ccc2ccccc2c1)N(c3cccc(c3)Cl)C(=O)Cc4ccc(c(c4)O)O	http://www.chemspider.com/Chemical-Structure.21108652.html	Protocol from Explan005 followed	4.9
.	EXP181-081V2	http://usefulchem.wikispaces.com/Exp181		Reactants Insoluble	No	2-Naphthaldehyde	O=Cc2ccc1c(cccc1)c2	2-Chloroaniline	NC1=C(Cl)C=CC=C1	3,4-dihydroxyphenylacetic acid	O=C(O)Cc1cc(O)c(O)cc1	t-butyl isocyanide	CC(C)(C)[N+]#[C-]		Khalid	methanol	2	0.5	0.5	0.5	0.5	1.155	156.18	1.213	127.57	1.478	168.15	0.735	83.13	0.06761038961039	0.052584501236604	0.056884303112314	0.056551020408163	0.2238508401184	CC(C)(C)NC(=O)C(c1ccc2ccccc2c1)N(c3ccccc3Cl)C(=O)Cc4ccc(c(c4)O)O	Need Link	Protocol from Explan005 followed	4.89
.	EXP181-073V2	http://usefulchem.wikispaces.com/Exp181		No	No	Benzaldehyde	c1ccccc1C=O	Methylamine	NC	Boc-Trp-OH	OC(C(CC1=CNC2=CC=CC=C21)NC(OC(C)(C)C)=O)=O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]		Khalid	methanol	2	0.5	0.5	0.5	0.5	1.045	106.12	0.785	31.06	1.262	304.34	0.735	83.13	0.050775119617225	0.019783439490446	0.12057844690967	0.056551020408163	0.22245080016516	CC(C)(C)NC(=O)C(c1ccccc1)N(C)C(=O)C(Cc2c[nH]c3c2cccc3)NC(=O)OC(C)(C)C	Need Link	Protocol from Explan005 followed
.	EXP150D-V1B155	http://usefulchem.wikispaces.com/Exp150		Yes but the aldehyde alone is not soluble in methanol	Yes	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	Benzylamine	NCc1ccccc1	crotonic acid	O=C(O)C=CC	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	59	Khalid/Emily	methanol	1	0.5	0.5	0.5	0.5	1.217	206.24	0.981	107.15	1.039	86.09	0.735	83.13	0.084732949876746	0.054612640163099	0.041429258902791	0.056551020408163	0.40409726522758	CC(C)(C)NC(=O)C(N(Cc1ccccc1)C(=O)\C=C\C)c3cc4ccccc4c2ccccc23	http://www.chemspider.com/Search.aspx?q=UC-150D	Protocol from Explan005 followed	6.18
.	EXP173E/V2B17	http://usefulchem.wikispaces.com/Exp173		No	No	3,4-dihydroxybenzaldehyde	O=Cc1cc(O)c(O)cc1	Methylamine	NC	Boc-Trp-OH	OC(C(CC1=CNC2=CC=CC=C21)NC(OC(C)(C)C)=O)=O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	0	Khalid	methanol	4	1	1	1	1	1.409	138.12	0.785	31.06	1.262	304.34	0.735	83.13	0.098026969481902	0.039566878980892	0.24115689381933	0.11310204081633	0.22262528366083	CC(C)(NC(C(C1=CC(O)=C(C=C1)O)N(C)C(C(CC2=CNC3=C2C=CC=C3)NC(OC(C)(C)C)=O)=O)=O)C	http://www.chemspider.com/Search.aspx?rid=80addae4-1180-466f-9cd6-c371891206d2	Protocol from Explan005 followed	3.48
.	EXP147-3V2B6	http://usefulchem.wikispaces.com/Exp+147	YES	No	No	2-Naphthaldehyde	O=Cc2ccc1c(cccc1)c2	Methylamine	NC	1-Pyrenebutyric acid	O=C(O)CCCc4ccc2ccc1cccc3c1c2c4cc3	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	0	Mitesh	methanol	0.25	0.25	0.25	0.25	0.25	1.155	156.18	0.785	31.06	1.296	288.34	0.735	83.13	0.033805194805195	0.009891719745223	0.055621141975309	0.028275510204082	0.66208755134563	CC(C)(NC(C(N(C(CCCC1=CC=C2C=CC3=C(C2=C1C=C4)C4=CC=C3)=O)C)c(cc5)cc6c5cccc6)=O)C	http://www.chemspider.com/Chemical-Structure.21105841.html	Protocol from Explan005 followed	7.95
.	EXP173J/V2B22	http://usefulchem.wikispaces.com/Exp173		Reactants Insoluble	No	3,4-dihydroxybenzaldehyde	O=Cc1cc(O)c(O)cc1	Methylamine	NC	1-Pyrenebutyric acid	O=C(O)CCCc4ccc2ccc1cccc3c1c2c4cc3	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	0	Khalid	methanol	4	1	1	1	1	1.409	138.12	0.785	31.06	1.296	288.34	0.735	83.13	0.098026969481902	0.039566878980892	0.22248456790123	0.11310204081633	0.22355458483567	CC(C)(NC(C(N(C(CCCC1=CC=C2C=CC3=C(C2=C1C=C4)C4=CC=C3)=O)C)C5=CC(O)=C(O)C=C5)=O)C	http://www.chemspider.com/Search.aspx?rid=7b443241-bfbf-479a-bf8f-308f68bb1610	Protocol from Explan005 followed	5.38
.	EXP173P/V2B28	http://usefulchem.wikispaces.com/Exp173		Reactants Insoluble	No	3-methoxybenzaldehyde	O=CC1=CC(OC)=CC=C1	Methylamine	NC	1-Pyrenebutyric acid	O=C(O)CCCc4ccc2ccc1cccc3c1c2c4cc3	t-butyl isocyanide	CC(C)(C)[N+]#[C-]		Khalid	methanol	4	1	1	1	1	1.117	136.15	0.785	31.06	1.296	288.34	0.735	83.13	0.12188898836168	0.039566878980892	0.22248456790123	0.11310204081633	0.22236836883874	CC(C)(NC(C(N(C(CCCC1=CC=C2C=CC3=C(C2=C1C=C4)C4=CC=C3)=O)C)C5=CC(OC)=CC=C5)=O)C	http://www.chemspider.com/Search.aspx?rid=bd4742a4-c05a-43f6-bc41-b66614941a0d	Protocol from Explan005 followed	6.64
.	EXP173C/V2B15	http://usefulchem.wikispaces.com/Exp173		Reactants Insoluble	No	4-(trifluoromethyl)benzaldehyde	FC(F)(F)c1ccc(C=O)cc1	Methylamine	NC	1-Pyrenebutyric acid	O=C(O)CCCc4ccc2ccc1cccc3c1c2c4cc3	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	0	Khalid	methanol	4	1	1	1	1	1.275	174.12	0.785	31.06	1.296	288.34	0.735	83.13	0.13656470588235	0.039566878980892	0.22248456790123	0.11310204081633	0.22164504897996	CC(C)(NC(C(N(C(CCCC1=CC=C2C=CC3=C(C2=C1C=C4)C4=CC=C3)=O)C)C5=CC=C(C(F)(F)F)C=C5)=O)C	http://www.chemspider.com/Search.aspx?rid=1e1db62e-2428-40e7-8f55-545e66d903c7	Protocol from Explan005 followed	7.29
.	EXP171KV2B11	http://usefulchem.wikispaces.com/Exp171		Yes	Yes	4-(Dimethylamino)benzaldehyde	O=Cc1ccc(N(C)C)cc1	Methylamine	NC	1-Pyrenebutyric acid	O=C(O)CCCc4ccc2ccc1cccc3c1c2c4cc3	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	0	Khalid	methanol	4	1	1	1	1	1.072	149.19	0.785	31.06	1.296	288.34	0.735	83.13	0.1391697761194	0.039566878980892	0.22248456790123	0.11310204081633	0.22151714477671	CC(C)(NC(C(N(C(CCCC1=CC=C2C=CC3=C(C2=C1C=C4)C4=CC=C3)=O)C)C5=CC=C(N(C)C)C=C5)=O)C	http://www.chemspider.com/Search.aspx?rid=9b9e8e2e-10d4-43dd-8852-cf96e5d3540d	Protocol from Explan005 followed	6.83
.	EXP171FV2B6	http://usefulchem.wikispaces.com/Exp171	YES	Yes but reactants initially insoluble	Yes	2-Naphthaldehyde	O=Cc2ccc1c(cccc1)c2	Methylamine	NC	1-Pyrenebutyric acid	O=C(O)CCCc4ccc2ccc1cccc3c1c2c4cc3	t-butyl isocyanide	CC(C)(C)[N+]#[C-]		Khalid	methanol	4	1	1	1	1	1.155	156.18	0.785	31.06	1.296	288.34	0.735	83.13	0.13522077922078	0.039566878980892	0.22248456790123	0.11310204081633	0.22171109110265	CC(C)(NC(C(N(C(CCCC1=CC=C2C=CC3=C(C2=C1C=C4)C4=CC=C3)=O)C)C5=CC=C6C=CC=CC6=C5)=O)C	http://www.chemspider.com/Chemical-Structure.21105841.html	Protocol from Explan005 followed	7.95


.	EXP171LV2B-12	http://usefulchem.wikispaces.com/Exp171		Reactants Insoluble	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	Methylamine	NC	1-Pyrenebutyric acid	O=C(O)CCCc4ccc2ccc1cccc3c1c2c4cc3	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	0	Khalid	methanol	4	1	1	1	1	1.217	206.24	0.785	31.06	1.296	288.34	0.735	83.13	0.16946589975349	0.039566878980892	0.22248456790123	0.11310204081633	0.22004042907555	CC(C)(NC(C(N(C(CCCC1=CC=C2C=CC3=C(C2=C1C=C4)C4=CC=C3)=O)C)C5=CC6=C(C7=C5C=CC=C7)C=CC=C6)=O)C	http://www.chemspider.com/Search.aspx?rid=a5c2b73a-4d3c-4615-b97d-213d7fe2f223	Protocol from Explan005 followed	9.18
.	EXP171D/V2B4	http://usefulchem.wikispaces.com/Exp171		Yes	No	2-hydroxy-3-methoxybenzaldehyde	Oc1c(cccc1OC)C=O	Benzylamine	NCc1ccccc1	1-Pyrenebutyric acid	O=C(O)CCCc4ccc2ccc1cccc3c1c2c4cc3	t-butyl isocyanide	CC(C)(C)[N+]#[C-]		Khalid	methanol	4	1	1	1	1	1.231	152.15	0.981	107.15	1.296	288.34	0.735	83.13	0.1235987002437	0.1092252803262	0.22248456790123	0.11310204081633	0.21889451056455	CC(C)(NC(C(N(C(CCCC1=CC=C2C=CC3=C(C2=C1C=C4)C4=CC=C3)=O)CC5=CC=CC=C5)C6=C(O)C(OC)=CC=C6)=O)C	http://www.chemspider.com/Search.aspx?rid=f3956de5-56ed-4d2d-b803-89469711b930	Protocol from Explan005 followed	7.59
.	EXP052E	http://usefulchem.wikispaces.com/Exp052		Yes	Yes	Piperonal	O=Cc1ccc2OCOc2c1	5-Methylfurfurylamine	NCc1oc(cc1)C	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	32	Alicia	methanol	4	1	1	1	1	1.337	150.13	0.997	111.14	1.159	175.18	0.735	83.13	0.11228870605834	0.11147442326981	0.15114754098361	0.11310204081633	0.22281576821752	CC(C)(NC(C(N(C(CNC(OC(C)(C)C)=O)=O)Cc1oc(C)cc1)c2cc3c(OCO3)cc2)=O)C	http://www.chemspider.com/Chemical-Structure.10481872.html	1M solutions of the starting materials was made	4.06
.	EXP173B/V2B14	http://usefulchem.wikispaces.com/Exp173	YES	Yes but reactants initially insoluble	Yes	4-methylbenzaldehyde	Cc1ccc(C=O)cc1	Methylamine	NC	1-Pyrenebutyric acid	O=C(O)CCCc4ccc2ccc1cccc3c1c2c4cc3	t-butyl isocyanide	CC(C)(C)[N+]#[C-]		Khalid	methanol	4	1	1	1	1	1.019	120.15	0.785	31.06	1.296	288.34	0.735	83.13	0.11790971540726	0.039566878980892	0.22248456790123	0.11310204081633	0.22256530896533	CC1=CC=C(C(N(C(CCCC2=CC=C3C=CC4=C(C3=C2C=C5)C5=CC=C4)=O)C)C(NC(C)(C)C)=O)C=C1	http://chemspider.com/Search.aspx?rid=964c68c4-4f65-4a67-9e9a-a573adc54223	Protocol from Explan005 followed	7.18
.	EXP171B/V2B2	http://usefulchem.wikispaces.com/Exp171		No	No	2-hydroxy-3-methoxybenzaldehyde	Oc1c(cccc1OC)C=O	5-Methylfurfurylamine	o1c(ccc1CN)C	1-Pyrenebutyric acid	O=C(O)CCCc4ccc2ccc1cccc3c1c2c4cc3	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	0	Khalid	methanol	4	1	1	1	1	1.231	152.15	0.997	111.14	1.296	288.34	0.735	83.13	0.1235987002437	0.11147442326981	0.22248456790123	0.11310204081633	0.21878679634545	CC1=CC=C(CN(C(CCCC2=CC=C3C=CC4=C(C3=C2C=C5)C5=CC=C4)=O)C(C(NC(C)(C)C)=O)C6=C(O)C(OC)=CC=C6)O1	http://www.chemspider.com/Search.aspx?rid=f9e6c6c5-0f9c-48bb-9c71-1fdee2a72cff	Protocol from Explan005 followed	7.21
.	EXP181-087V2	http://usefulchem.wikispaces.com/Exp181		Reactants Insoluble	No	2,4-dimethylbenzaldehyde	O=CC1=CC=C(C)C=C1C	Methylamine	NC	1-Pyrenebutyric acid	O=C(O)CCCc4ccc2ccc1cccc3c1c2c4cc3	t-butyl isocyanide	CC(C)(C)[N+]#[C-]		Khalid	methanol	2	0.5	0.5	0.5	0.5	0.962	134.18	0.785	31.06	1.296	288.34	0.735	83.13	0.069740124740125	0.019783439490446	0.11124228395062	0.056551020408163	0.22150191094459	Cc1cc(C)c(C(N(C(CCCC2=CC=C3C=CC4=C(C3=C2C=C5)C5=CC=C4)=O)C)C(NC(C)(C)C)=O)cc1	http://www.chemspider.com/Chemical-Structure.21106206.html	Protocol from Explan005 followed	7.64
.	EXP174O/V2B47	http://usefulchem.wikispaces.com/Exp174		No	No	3,5-dimethoxybenzaldehyde	O=CC1=CC(OC)=CC(OC)=C1	5-Methylfurfurylamine	o1c(ccc1CN)C	D-(−)-Quinic acid	O=C(O)C1(O)C[C@@H](O)C(O)[C@H](O)C1	t-butyl isocyanide	CC(C)(C)[N+]#[C-]		Khalid	methanol	2	0.5	0.5	0.5	0.5	1.114	166.17	0.997	111.14	1.828	192.17	0.735	83.13	0.074582585278276	0.055737211634905	0.052562910284464	0.056551020408163	0.22327072859377	Cc1ccc(o1)CN(C(c2cc(cc(c2)OC)OC)C(=O)NC(C)(C)C)C(=O)C3(CC(C(C(C3)O)O)O)O	http://www.chemspider.com/Search.aspx?rid=a9df0810-4973-49de-931f-c402f4ea77ee	Protocol from Explan005 followed	1.41
.	EXP155B-V1B159	http://usefulchem.wikispaces.com/Exp155		No	No	Benzaldehyde	O=Cc1ccccc1	5-Methylfurfurylamine	o1c(ccc1CN)C	3-(4-methoxyphenyl)propionic acid	O=C(O)CCc1ccc(OC)cc1	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	0	Emily	methanol	0.5	0.5	0.5	0.5	0.5	1.045	106.12	0.997	111.14	1.144	180.2	0.735	83.13	0.050775119617225	0.055737211634905	0.078758741258741	0.056551020408163	0.67401605421662	Cc1ccc(o1)CN(C(c2ccccc2)C(=O)NC(C)(C)C)C(=O)CCc3ccc(cc3)OC	http://www.chemspider.com/Search.aspx?rid=56b47e4d-b976-483b-90bc-ee78d6c5c2c9	Protocol from Explan005 followed	4.8
.	EXP181-078V2	http://usefulchem.wikispaces.com/Exp181		Reactants Insoluble	No	2-hydroxybenzaldehyde	O=Cc1ccccc1O	1-hexylamine	NCCCCCC	1-Pyrenebutyric acid	O=C(O)CCCc4ccc2ccc1cccc3c1c2c4cc3	t-butyl isocyanide	CC(C)(C)[N+]#[C-]		Khalid	methanol	2	0.5	0.5	0.5	0.5	1.146	122.12	0.774	101.19	1.296	288.34	0.735	83.13	0.053280977312391	0.065368217054264	0.11124228395062	0.056551020408163	0.21868032993558	CCCCCCN(C(CCCC1=CC=C2C=CC3=C(C2=C1C=C4)C4=CC=C3)=O)C(C(NC(C)(C)C)=O)c5c(O)cccc5	http://www.chemspider.com/Chemical-Structure.21108615.html	Protocol from Explan005 followed	8.64
.	EXP156B-V1B155	http://usefulchem.wikispaces.com/Exp156		Yes but reactants initially insoluble	Not Determined	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	Benzylamine	NCc1ccccc1	crotonic acid	O=C(O)C=CC	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	Waiting Isolation	Emily	methanol	0.5	0.5	0.5	0.5	0.5	1.217	206.24	0.981	107.15	1.039	86.09	0.735	83.13	0.084732949876746	0.054612640163099	0.041429258902791	0.056551020408163	0.67812621363772	CCCCNC(=O)C(c1cc2ccccc2c3c1cccc3)N(Cc4ccccc4)C(=O)C=CC	http://www.chemspider.com/Search.aspx?rid=0a7c56c0-e39b-46e1-8c55-0243c4aaf28d	Protocol from Explan005 followed	6.55
.	EXP179	http://usefulchem.wikispaces.com/Exp179		Reactants Insoluble	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	Aniline	Nc1ccccc1	4-chlorophenylacetic acid	Clc1ccc(cc1)CC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	0	Shannon	methanol	1.5	0.5	0.5	0.5	0.5	1.217	206.24	1.022	93.13	1.324	170.59	0.735	83.13	0.084732949876746	0.045562622309198	0.064422205438066	0.056551020408163	0.28550728509628	Clc5ccc(CC(=O)N(c1ccccc1)C(c3cc4ccccc4c2ccccc23)C(=O)NC(C)(C)C)cc5	http://www.chemspider.com/Chemical-Structure.21105833.html	Protocol from Explan005 followed	7.34
.	EXP148A-V1B153	http://usefulchem.wikispaces.com/Exp148		Yes but the aldehyde alone is not soluble in methanol	Yes	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	1-heptylamine	NCCCCCCC	crotonic acid	O=C(O)C=CC	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	50.1	Khalid/Emily	methanol	1	0.5	0.5	0.5	0.5	1.217	206.24	0.777	115.22	1.039	86.09	0.735	83.13	0.084732949876746	0.074144144144144	0.041429258902791	0.056551020408163	0.39781761288835	O=C(/C=C/C)N(CCCCCCC)C(C(NC(C)(C)C)=O)C1=CC2=CC=CC=C2C3=C1C=CC=C3	http://www.chemspider.com/Chemical-Structure.21106058.html	Protocol from Explan005 followed	7.47
.	EXP162	http://usefulchem.wikispaces.com/Exp162		Reactants Insoluble	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	cyclohexylamine	NC1CCCCC1	phenylacetic acid	O=C(O)Cc1ccccc1	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	0	Shannon	methanol	1.5	0.5	0.5	0.5	0.5	1.217	206.24	0.867	99.17	1.164	136.15	0.735	83.13	0.084732949876746	0.057191464821223	0.058483676975945	0.056551020408163	0.28458260443379	O=C(Cc1ccccc1)N(C(c3cc4ccccc4c2ccccc23)C(=O)NC(C)(C)C)C5CCCCC5	http://www.chemspider.com/Chemical-Structure.21105590.html	Protocol from Explan005 followed	7.5
.	EXP086B	http://usefulchem.wikispaces.com/Exp086		Yes	Yes	Benzaldehyde	c1ccccc1C=O	5-Methylfurfurylamine	NCc1oc(cc1)C	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	38	Khalid	methanol	4	2	2.2	2	2	1.045	106.12	0.997	111.14	1.159	175.18	0.735	83.13	0.2031004784689	0.24524373119358	0.30229508196721	0.22620408163265	0.40186114972893	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccc(C)o1)C(c2ccccc2)C(=O)NC(C)(C)C	http://chemspider.com/Search.aspx?rid=a8fc6c3d-770e-47ad-8b6f-3861b3a61358	Solution was made up to 4 mL - methanol amount probably closer to 3 mL	4.2
.	EXP104C	http://usefulchem.wikispaces.com/Exp104		Yes	Yes	veratraldehyde	COC1=C(OC)C=C(C=O)C=C1	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	12	Khalid	methanol	4	2	2.2	2	2	1.114	166.17	1.099	97.12	1.159	175.18	0.735	83.13	0.29833034111311	0.19441674249318	0.30229508196721	0.22620408163265	0.39830749211171	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccc(OC)c(OC)c2)C(=O)NC(C)(C)C	http://www.chemspider.com/Search.aspx?rid=434f464b-e9b9-425e-80f0-1b10e7a1f73b	Imine was preformed	3.48
.	EXP201-01	http://usefulchem.wikispaces.com/Exp201		Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	50.73	Khalid	methanol	0.1	0.2	0.2	0.2	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.02031004784689	0.019312101910828	0.030229508196721	0.022620408163265	1.03911182559703	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-02	http://usefulchem.wikispaces.com/Exp201		Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	59.07	Khalid	methanol	0.1	0.2	0.24	0.2	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.02031004784689	0.023174522292994	0.030229508196721	0.022620408163265	1.01866973839123	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-03	http://usefulchem.wikispaces.com/Exp201		Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	61.55	Khalid	methanol	0.1	0.24	0.2	0.2	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.024372057416268	0.019312101910828	0.030229508196721	0.022620408163265	1.01763523348712	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-04	http://usefulchem.wikispaces.com/Exp201		Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	60.31	Khalid	methanol	0.1	0.2	0.2	0.24	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.02031004784689	0.019312101910828	0.036275409836066	0.022620408163265	1.00746548163723	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-05	http://usefulchem.wikispaces.com/Exp201		Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	60.2	Khalid	methanol	0.1	0.2	0.2	0.2	0.24	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.02031004784689	0.019312101910828	0.030229508196721	0.027144489795918	1.01524827913614	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74


.	EXP201-06	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	69.22	Khalid	methanol	0.1	0.24	0.24	0.2	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.024372057416268	0.023174522292994	0.030229508196721	0.022620408163265	0.9980214421059	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-07	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	52.42	Khalid	methanol	0.6	0.2	0.2	0.2	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.02031004784689	0.019312101910828	0.030229508196721	0.022620408163265	0.28882031461758	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-08	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	44.64	Khalid	methanol	0.6	0.2	0.24	0.2	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.02031004784689	0.023174522292994	0.030229508196721	0.022620408163265	0.28721828930993	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-09	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	50.28	Khalid	methanol	0.6	0.24	0.2	0.2	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.024372057416268	0.019312101910828	0.030229508196721	0.022620408163265	0.28713598800276	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-10	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	54.79	Khalid	methanol	0.6	0.2	0.2	0.24	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.02031004784689	0.019312101910828	0.036275409836066	0.022620408163265	0.28632048026224	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-11	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	53.43	Khalid	methanol	0.6	0.2	0.2	0.2	0.24	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.02031004784689	0.019312101910828	0.030229508196721	0.027144489795918	0.286945631831	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-12	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	54.67	Khalid	methanol	0.6	0.24	0.24	0.2	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.024372057416268	0.023174522292994	0.030229508196721	0.022620408163265	0.28555254219922	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-13	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	0.34	Khalid	methanol	2.6	0.2	0.2	0.2	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.02031004784689	0.019312101910828	0.030229508196721	0.022620408163265	0.074281179187267	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-14	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	1.35	Khalid	methanol	2.6	0.2	0.24	0.2	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.02031004784689	0.023174522292994	0.030229508196721	0.022620408163265	0.074174773568105	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-15	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	10.37	Khalid	methanol	2.6	0.24	0.2	0.2	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.024372057416268	0.019312101910828	0.030229508196721	0.022620408163265	0.074169283378716	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-16	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	16.35	Khalid	methanol	2.6	0.2	0.2	0.24	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.02031004784689	0.019312101910828	0.036275409836066	0.022620408163265	0.07411475572506	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-17	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	8.68	Khalid	methanol	2.6	0.2	0.2	0.2	0.24	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.02031004784689	0.019312101910828	0.030229508196721	0.027144489795918	0.074156576073283	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-18	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	5.64	Khalid	methanol	2.6	0.24	0.24	0.2	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.024372057416268	0.023174522292994	0.030229508196721	0.022620408163265	0.074063197864137	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP099C	http://usefulchem.wikispaces.com/Exp099	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	47.2	Khalid	methanol	4	2	2.2	2	2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.2031004784689	0.21243312101911	0.30229508196721	0.22620408163265	0.40452806359456	O=C(CNC(OC(C)(C)C)=O)N(CC1=CC=CO1)C(C2=CC=CC=C2)C(NC(C)(C)C)=O	http://www.chemspider.com/Chemical-Structure.21106059.html	Solution was made up to 4 mL - methanol amount probably closer to 3 mL	3.74
.	EXP183-049V1	http://usefulchem.wikispaces.com/Exp183	Reactants Insoluble	No	phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	cyclohexylamine	NC1CCCCC1	mandelic acid	O=C(O)[C@@H](O)c1ccccc1	t-butyl isocyanide	CC(C)(C)[N+]#[C-]		Emily	methanol	1	0.5	0.5	0.5	0.5	1.217	206.24	0.867	99.17	1.321	152.15	0.735	83.13	0.084732949876746	0.057191464821223	0.057588947766843	0.056551020408163	0.39806876687034	O=C(N(C1CCCCC1)C(c3cc4ccccc4c2ccccc23)C(=O)NC(C)(C)C)c5ccco5	Need Link
.	EXP163A-V1B14	http://usefulchem.wikispaces.com/Exp163	no and aldehyde alone not solube	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	furfurylamine	o1c(ccc1)CN	mandelic acid	O=C(C(O)c1ccccc1)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	0	Tim	methanol	1	0.5	0.5	0.5	0.5	1.217	206.24	1.099	97.12	1.321	152.15	0.735	83.13	0.084732949876746	0.093830755232029	0.057588947766843	0.056551020408163	0.38678624524202	O=C(N(Cc1ccco1)C(c3cc4ccccc4c2ccccc23)C(=O)NC(C)(C)C)C(O)c5ccccc5	http://www.chemspider.com/Search.aspx?rid=472e901f-5aa1-4255-9af6-334fae0c316e	Protocol from Explan005 followed	6.49
.	EXP231-3	http://usefulchem.wikispaces.com/Exp231	No	No	2-Naphthaldehyde	O=Cc2ccc1c(cccc1)c2	Methylamine	NC	1-Pyrenebutyric acid	O=C(O)CCCc4ccc2ccc1cccc3c1c2c4cc3	t-butyl isocyanide	CC(C)(C)[N+]#[C-]		Khalid	THF	0.82262573308077	1	1	1	1	1.155	156.18	0.785	31.06	1.296	288.34	0.735	83.13	0.13522077922078	0.039566878980892	0.22248456790123	0.11310204081633	0.75018754688672	CC(C)(C)NC(=O)C(N(C)C(=O)CCCc4ccc3ccc2cccc1ccc4c3c12)c5ccc6ccccc6c5	Need Link	Protocol from Explan005 followed
.	EXP222-5	http://usefulchem.wikispaces.com/Exp222	No	No	4-(Dimethylamino)benzaldehyde	O=Cc1ccc(N(C)C)cc1	Methylamine	NC	1-Pyrenebutyric acid	O=C(O)CCCc4ccc2ccc1cccc3c1c2c4cc3	t-butyl isocyanide	CC(C)(C)[N+]#[C-]		Khalid	THF	0.29938938849924	0.5	0.5	0.5	0.5	1.072	149.19	0.785	31.06	1.296	288.34	0.735	83.13	0.069584888059702	0.019783439490446	0.11124228395062	0.056551020408163	0.89839023138132	CC(C)(NC(C(N(C(CCCC1=CC=C2C=CC3=C(C2=C1C=C4)C4=CC=C3)=O)C)C5=CC=C(N(C)C)C=C5)=O)C	http://www.chemspider.com/Search.aspx?rid=9b9e8e2e-10d4-43dd-8852-cf96e5d3540d		6.83
.	EXP201-43	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	6.54	Khalid	THF	0.6	0.2	0.2	0.2	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.02031004784689	0.019312101910828	0.030229508196721	0.022620408163265	0.28882031461758	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-44	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	7.89	Khalid	THF	0.6	0.2	0.24	0.2	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.02031004784689	0.023174522292994	0.030229508196721	0.022620408163265	0.28721828930993	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74


.	EXP201-45	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	10.03	Khalid	THF	0.6	0.24	0.2	0.2	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.024372057416268	0.019312101910828	0.030229508196721	0.022620408163265	0.28713598800276	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-46	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	9.92	Khalid	THF	0.6	0.2	0.2	0.24	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.02031004784689	0.019312101910828	0.036275409836066	0.022620408163265	0.28632048026224	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-47	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	7.44	Khalid	THF	0.6	0.2	0.2	0.2	0.24	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.02031004784689	0.019312101910828	0.030229508196721	0.027144489795918	0.286945631831	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP201-48	http://usefulchem.wikispaces.com/Exp201	Yes	Yes	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]	12.06	Khalid	THF	0.6	0.24	0.24	0.2	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.024372057416268	0.023174522292994	0.030229508196721	0.022620408163265	0.28555254219922	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html	Automated liquid handling	3.74
.	EXP222-2	http://usefulchem.wikispaces.com/Exp222	Yes	YES	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]		Khalid	THF	0.3253708551139	0.5	0.5	0.5	0.5	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.050775119617225	0.04828025477707	0.075573770491803	0.056551020408163	0.89839023138132	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html		3.74
.	EXP222-4	http://usefulchem.wikispaces.com/Exp222	Yes	YES	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butyl isocyanide	CC(C)(C)[N+]#[C-]		Khalid	THF	0.41268542755695	0.25	0.25	0.25	0.25	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.025387559808612	0.024140127388535	0.037786885245902	0.028275510204082	0.47323791311738	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html		3.74
.	Exp242-7	http://usefulchem.wikispaces.com/Exp242	No	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	5-Methylfurfurylamine	NCc1oc(cc1)C	phenylacetic acid	O=C(O)Cc1ccccc1	t-butylisocyanide	CC(C)(C)[N+]#[C-]		Marshall	benzene	0.14848633247618	0.1	0.1	0.1	0.1	1.217	206.24	0.997	111.14	1.164	136.15	0.735	83.13	0.016946589975349	0.011147442326981	0.011696735395189	0.011310204081633	0.50103387273606	CC(C)(C)NC(=O)C(N(Cc1ccc(C)o1)C(=O)Cc2ccccc2)C=5C=C3C=CC=CC3C4C=CC=CC4=5
.	Exp242-2	http://usefulchem.wikispaces.com/Exp242	No	No	Phenanthrene-9-carboxaldehyde	O=Cc2cc3c(c1c2cccc1)cccc3	furfurylamine	o1c(ccc1)CN	phenylacetic acid	O=C(O)Cc1ccccc1	t-butylisocyanide	CC(C)(C)[N+]#[C-]		Marshall	benzene	0.18030923230248	0.1	0.1	0.1	0.1	1.217	206.24	1.099	97.12	1.164	136.15	0.735	83.13	0.016946589975349	0.008837124658781	0.011696735395189	0.011310204081633	0.43649083186161	CC(C)(C)NC(=O)C(N(Cc1ccco1)C(=O)Cc2ccccc2)C=5C=C3C=CC=CC3C4C=CC=CC4=5
.	EXP217-4	http://usefulchem.wikispaces.com/Exp217	Yes	Pending	Benzaldehyde	c1ccccc1C=O	furfurylamine	o1c(ccc1)CN	Boc-Gly-OH	O=C(OC(C)(C)C)NCC(=O)O	t-butylisocyanide	CC(C)(C)[N+]#[C-]		Khalid	DMSO	0.43014834204556	0.2	0.2	0.2	0.2	1.045	106.12	1.099	97.12	1.159	175.18	0.735	83.13	0.02031004784689	0.019312101910828	0.030229508196721	0.022620408163265	0.38268693085081	O=C(CNC(=O)OC(C)(C)C)N(Cc1ccco1)C(c2ccccc2)C(=O)NC(C)(C)C	http://www.chemspider.com/Chemical-Structure.21106059.html		3.74
.	UCExp236-12	http://usefulchem.wikispaces.com/Exp236	No	No	4-(trifluoromethyl)benzaldehyde	FC(F)(F)c1ccc(C=O)cc1	Aniline	Nc1ccccc1	methacrylic acid	O=C(O)\C(=C)C	t-butylisocyanide	CC(C)(C)[N+]#[C-]		Khalid	methanol	0.1146	0.1	0.1	0.1	0.1	1.275	174.12	1.022	93.13	1.015	86.09	0.735	83.13	0.013656470588235	0.00911252446184	0.008481773399015	0.011310204081633	0.63629028498441	C(=O)(C(=C)C)N(c1ccccc1)C(c1ccc(C(F)(F)F)cc1)C(=O)NC(C)(C)C	Need Link
.	UCExp236-04	http://usefulchem.wikispaces.com/Exp236	No	No	4-(trifluoromethyl)benzaldehyde	FC(F)(F)c1ccc(C=O)cc1	butylamine	NCCCC	methacrylic acid	O=C(O)\C(=C)C	t-butylisocyanide	CC(C)(C)[N+]#[C-]		Khalid	methanol	0.0751	0.1	0.1	0.1	0.1	1.275	174.12	0.74	73.14	1.015	86.09	0.735	83.13	0.013656470588235	0.009883783783784	0.008481773399015	0.011310204081633	0.84436473446184	C(=O)(C(=C)C)N(CCC)C(c1ccc(C(F)(F)F)cc1)C(=O)NC(C)(C)C	Need Link
.	UCExp236-28	http://usefulchem.wikispaces.com/Exp236	No	No	4-(trifluoromethyl)benzaldehyde	FC(F)(F)c1ccc(C=O)cc1	2-Chloroaniline	NC1=C(Cl)C=CC=C1	methacrylic acid	O=C(O)\C(=C)C	t-butylisocyanide	CC(C)(C)[N+]#[C-]		Khalid	methanol	0.1146	0.1	0.1	0.1	0.1	1.275	174.12	1.213	127.57	1.015	86.09	0.735	83.13	0.013656470588235	0.010516900247321	0.008481773399015	0.011310204081633	0.63065481242841	C(=O)(C(=C)C)N(CCCCCC)C(c1ccc(C(F)(F)F)cc1)C(=O)NC(C)(C)C	Need Link
.	UCExp236-22	http://usefulchem.wikispaces.com/Exp236	No	No	5-Bromo-2-thiophenecarboxaldehyde	O=CC1=CC=C(Br)S1	t-butylamine	NC(C)(C)C	3,3'-dichloropivalic acid	ClCC(C(=O)O)(C)CCl	t-butylisocyanide	CC(C)(C)[N+]#[C-]		Khalid	methanol	0.1163	0.1	0.1	0.1	0.1	1.607	191.05	0.696	73.14	1.33	171.022	0.735	83.13	0.011888612321095	0.010508620689655	0.012858796992481	0.011310204081633	0.6140008121505	C(=O)(C(CCl)(C)CCl)N(C(C)(C)C)C(c1sc(Br)cc1)C(=O)NC(C)(C)C	Need Link
.	UCExp236-18	http://usefulchem.wikispaces.com/Exp236	No	No	4-(trifluoromethyl)benzaldehyde	FC(F)(F)c1ccc(C=O)cc1	Methylamine	NC	3,3'-dichloropivalic acid	ClCC(C(=O)O)(C)CCl	t-butylisocyanide	CC(C)(C)[N+]#[C-]		Khalid	methanol	0.0748	0.1	0.1	0.1	0.1	1.275	174.12	0.785	31.06	1.33	171.022	0.735	83.13	0.013656470588235	0.003956687898089	0.012858796992481	0.011310204081633	0.85776417572843	C(=O)(C(CCl)(C)CCl)N(C)C(c1ccc(cc1C)C)C(=O)NC(C)(C)C	Need Link
.	UCExp236-14	http://usefulchem.wikispaces.com/Exp236	No	No	5-Bromo-2-thiophenecarboxaldehyde	O=CC1=CC=C(Br)S1	Methylamine	NC	3,3'-dichloropivalic acid	ClCC(C(=O)O)(C)CCl	t-butylisocyanide	CC(C)(C)[N+]#[C-]		Khalid	methanol	0.0768	0.1	0.1	0.1	0.1	1.607	191.05	0.785	31.06	1.33	171.022	0.735	83.13	0.011888612321095	0.003956687898089	0.012858796992481	0.011310204081633	0.85605956542016	C(=O)(C(CCl)(C)CCl)N(C)C(c1sc(Br)cc1)C(=O)NC(C)(C)C	Need Link
.	UCExp236-25	http://usefulchem.wikispaces.com/Exp236	No	No	5-Bromo-2-thiophenecarboxaldehyde	O=CC1=CC=C(Br)S1	3-Chloroaniline	NC1=CC(Cl)=CC=C1	3,3'-dichloropivalic acid	ClCC(C(=O)O)(C)CCl	t-butylisocyanide	CC(C)(C)[N+]#[C-]		Khalid	methanol	0.1159	0.1	0.1	0.1	0.1	1.607	191.05	1.206	127.57	1.33	171.022	0.735	83.13	0.011888612321095	0.010577943615257	0.012858796992481	0.011310204081633	0.61524999107463	C(=O)(C(CCl)(C)CCl)N(c1cccc(Cl)c1)C(c1sc(Br)cc1)C(=O)NC(C)(C)C	Need Link
.	UCExp236-29	http://usefulchem.wikispaces.com/Exp236	No	No	4-(trifluoromethyl)benzaldehyde	FC(F)(F)c1ccc(C=O)cc1	cyclohexylamine	NC1CCCCC1	3,3'-dichloropivalic acid	ClCC(C(=O)O)(C)CCl	t-butylisocyanide	CC(C)(C)[N+]#[C-]		Khalid	methanol	0.1137	0.1	0.1	0.1	0.1	1.275	174.12	0.867	99.17	1.33	171.022	0.735	83.13	0.013656470588235	0.011438292964244	0.012858796992481	0.011310204081633	0.61363334499012	C(=O)(C(CCl)(C)CCl)N(C1CCCCC1)C(c1ccc(C(F)(F)F)cc1)C(=O)NC(C)(C)C	Need Link
.	UCExp236-09	http://usefulchem.wikispaces.com/Exp236	No	No	4-(trifluoromethyl)benzaldehyde	FC(F)(F)c1ccc(C=O)cc1	2-Chloroaniline	NC1=C(Cl)C=CC=C1	3,3'-dichloropivalic acid	ClCC(C(=O)O)(C)CCl	t-butylisocyanide	CC(C)(C)[N+]#[C-]		Khalid	methanol	0.1146	0.1	0.1	0.1	0.1	1.275	174.12	1.213	127.57	1.33	171.0218	0.735	83.13	0.013656470588235	0.010516900247321	0.012858781954887	0.011310204081633	0.61371396559894	C(=O)(C(CCl)(C)CCl)N(c1ccccc1Cl)C(c1ccc(C(F)(F)F)cc1)C(=O)NC(C)(C)C	Need Link
.	UCExp236-26	http://usefulchem.wikispaces.com/Exp236	No	No	5-Bromo-2-thiophenecarboxaldehyde	O=CC1=CC=C(Br)S1	Benzylamine	NCc1ccccc1	3,3'-dichloropivalic acid	ClCC(C(=O)O)(C)CCl	t-butylisocyanide	CC(C)(C)[N+]#[C-]		Khalid	methanol	0.1163	0.1	0.1	0.1	0.1	1.607	191.05	0.981	107.15	1.33	171.022	0.735	83.13	0.011888612321095	0.01092252803262	0.012858796992481	0.011310204081633	0.61244434948141	C(=O)(C(CCl)(C)CCl)N(Cc1ccccc1)C(c1sc(Br)cc1)C(=O)NC(C)(C)C	Need Link
.	UCExp236-07	http://usefulchem.wikispaces.com/Exp236	Yes	Yes	4-(trifluoromethyl)benzaldehyde	FC(F)(F)c1ccc(C=O)cc1	1-hexylamine	NCCCCCC	3,3'-dichloropivalic acid	ClCC(C(=O)O)(C)CCl	t-butylisocyanide	CC(C)(C)[N+]#[C-]		Khalid	methanol	0.1119	0.1	0.1	0.1	0.1	1.275	174.12	0.774	101.19	1.33	171.022	0.735	83.13	0.013656470588235	0.013073643410853	0.012858796992481	0.011310204081633	0.61425395313135	C(=O)(C(CCl)(C)CCl)N(CCCCCC)C(c1ccc(C(F)(F)F)cc1)C(=O)NC(C)(C)C	Need Link


.	UCExp236-15	http://usefulchem.wikispaces.com/Exp236	No	No	4-(trifluoromethyl)benzaldehyde	FC(F)(F)c1ccc(C=O)cc1	1-heptylamine	NCCCCCCC	3,3'-dichloropivalic acid	ClCC(C(=O)O)(C)CCl	t-butylisocyanide	CC(C)(C)[N+]#[C-]	Khalid	methanol	0.1103	0.1	0.1	0.1	0.1	1.275	174.12	0.777	115.22	1.33	171.022	0.735	83.13	0.013656470588235	0.014828828828829	0.012858796992481	0.011310204081633	0.61366898387204	C(=O)(C(CCl)(C)CCl)N(CCCCCCC)C(c1ccc(C(F)(F)F)cc1)C(=O)NC(C)(C)C	Need Link
.	UCExp241-35	http://usefulchem.wikispaces.com/Exp241	No	No	2,4-dimethylbenzaldehyde	O=CC1=CC=C(C)C=C1C	t-butylamine	NC(C)(C)C	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	t-butylisocyanide	CC(C)(C)[N+]#[C-]	Khalid	methanol	0.08719	0.1	0.1	0.1	0.1	0.962	134.18	0.696	73.14	1.406	180.15	0.735	83.13	0.013948024948025	0.010508620689655	0.012812944523471	0.011310204081633	0.7365408525344	C(=O)(Cc1ccc2OCOc2c1)N(C(C)(C)C)C(c1ccc(cc1C)C)C(=O)NC(C)(C)C
.	UCExp241-45	http://usefulchem.wikispaces.com/Exp241	No	No	5-Bromo-2-thiophenecarboxaldehyde	O=CC1=CC=C(Br)S1	t-butylamine	NC(C)(C)C	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	t-butylisocyanide	CC(C)(C)[N+]#[C-]	Khalid	methanol	0.08719	0.1	0.1	0.1	0.1	1.607	191.05	0.696	73.14	1.406	180.15	0.735	83.13	0.011888612321095	0.010508620689655	0.012812944523471	0.011310204081633	0.74788508410138	C(=O)(Cc1ccc2OCOc2c1)N(C(C)(C)C)C(c1sc(Br)cc1)C(=O)NC(C)(C)C
.	UCExp241-21	http://usefulchem.wikispaces.com/Exp241	No	No	p-tolualdehyde	Cc1ccc(C=O)cc1	Methylamine	NC	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	t-butylisocyanide	CC(C)(C)[N+]#[C-]	Khalid	methanol	0.13324	0.1	0.1	0.1	0.1	1.119	136.15	0.785	31.06	1.406	180.15	0.735	83.13	0.012167113494191	0.003956687898089	0.012812944523471	0.011310204081633	0.57641223159153	C(=O)(Cc1ccc2OCOc2c1)N(C)C(c1ccc(cc1)C)C(=O)NC(C)(C)C
.	UCExp241-18	http://usefulchem.wikispaces.com/Exp241	No	No	2,4-dimethylbenzaldehyde	O=CC1=CC=C(C)C=C1C	Methylamine	NC	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	t-butylisocyanide	CC(C)(C)[N+]#[C-]	Khalid	methanol	0.13324	0.1	0.1	0.1	0.1	0.962	134.18	0.785	31.06	1.406	180.15	0.735	83.13	0.013948024948025	0.003956687898089	0.012812944523471	0.011310204081633	0.57055525851688	C(=O)(Cc1ccc2OCOc2c1)N(C)C(c1ccc(cc1C)C)C(=O)NC(C)(C)C
.	UCExp241-22	http://usefulchem.wikispaces.com/Exp241	No	No	o-tolualdehyde	O=Cc1ccccc1C	Methylamine	NC	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	t-butylisocyanide	CC(C)(C)[N+]#[C-]	Khalid	methanol	0.13324	0.1	0.1	0.1	0.1	1.039	120.15	0.785	31.06	1.406	180.15	0.735	83.13	0.011564003849856	0.003956687898089	0.012812944523471	0.011310204081633	0.57842306022234	C(=O)(Cc1ccc2OCOc2c1)N(C)C(c1ccccc1C)C(=O)NC(C)(C)C
.	UCExp241-17	http://usefulchem.wikispaces.com/Exp241	No	No	5-Bromo-2-thiophenecarboxaldehyde	O=CC1=CC=C(Br)S1	Methylamine	NC	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	t-butylisocyanide	CC(C)(C)[N+]#[C-]	Khalid	methanol	0.13324	0.1	0.1	0.1	0.1	1.607	191.05	0.785	31.06	1.406	180.15	0.735	83.13	0.011888612321095	0.003956687898089	0.012812944523471	0.011310204081633	0.5773390425166	C(=O)(Cc1ccc2OCOc2c1)N(C)C(c1sc(Br)cc1)C(=O)NC(C)(C)C
.	UCExp241-46	http://usefulchem.wikispaces.com/Exp241	No	No	2,4-dimethylbenzaldehyde	O=CC1=CC=C(C)C=C1C	3-Chloroaniline	NC1=CC(Cl)=CC=C1	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	t-butylisocyanide	CC(C)(C)[N+]#[C-]	Khalid	methanol	0.08719	0.1	0.1	0.1	0.1	0.962	134.18	1.206	127.57	1.406	180.15	0.735	83.13	0.013948024948025	0.010577943615257	0.012812944523471	0.011310204081633	0.73616497283357	C(=O)(Cc1ccc2OCOc2c1)N(c1cccc(Cl)c1)C(c1ccc(cc1C)C)C(=O)NC(C)(C)C
.	UCExp241-33	http://usefulchem.wikispaces.com/Exp241	No	No	5-Bromo-2-thiophenecarboxaldehyde	O=CC1=CC=C(Br)S1	3-Chloroaniline	NC1=CC(Cl)=CC=C1	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	t-butylisocyanide	CC(C)(C)[N+]#[C-]	Khalid	methanol	0.08719	0.1	0.1	0.1	0.1	1.607	191.05	1.206	127.57	1.406	180.15	0.735	83.13	0.011888612321095	0.010577943615257	0.012812944523471	0.011310204081633	0.74749753965118	C(=O)(Cc1ccc2OCOc2c1)N(c1cccc(Cl)c1)C(c1sc(Br)cc1)C(=O)NC(C)(C)C
.	UCExp241-37	http://usefulchem.wikispaces.com/Exp241	No	No	4-(trifluoromethyl)benzaldehyde	FC(F)(F)c1ccc(C=O)cc1	cyclohexylamine	NC1CCCCC1	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	t-butylisocyanide	CC(C)(C)[N+]#[C-]	Khalid	methanol	0.08719	0.1	0.1	0.1	0.1	1.275	174.12	0.867	99.17	1.406	180.15	0.735	83.13	0.013656470588235	0.011438292964244	0.012812944523471	0.011310204081633	0.73309530523769	C(=O)(Cc1ccc2OCOc2c1)N(C1CCCCC1)C(c1ccc(C(F)(F)F)cc1)C(=O)NC(C)(C)C
.	UCExp241-39	http://usefulchem.wikispaces.com/Exp241	No	No	5-Bromo-2-thiophenecarboxaldehyde	O=CC1=CC=C(Br)S1	Aniline	Nc1ccccc1	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	t-butylisocyanide	CC(C)(C)[N+]#[C-]	Khalid	methanol	0.08719	0.1	0.1	0.1	0.1	1.18	216.23	1.022	93.13	1.406	180.15	0.735	83.13	0.018324576271186	0.00911252446184	0.012812944523471	0.011310204081633	0.72071942556516	C(=O)(Cc1ccc2OCOc2c1)N(c1ccccc1)C(c1sc(Br)cc1)C(=O)NC(C)(C)C
.	UCExp241-48	http://usefulchem.wikispaces.com/Exp241	No	No	2,4-dimethylbenzaldehyde	O=CC1=CC=C(C)C=C1C	Benzylamine	NCc1ccccc1	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	t-butylisocyanide	CC(C)(C)[N+]#[C-]	Khalid	methanol	0.08719	0.1	0.1	0.1	0.1	0.962	134.18	0.981	107.15	1.406	180.15	0.735	83.13	0.013948024948025	0.01092252803262	0.012812944523471	0.011310204081633	0.73430226110453	C(=O)(Cc1ccc2OCOc2c1)N(Cc1ccccc1)C(c1ccc(cc1C)C)C(=O)NC(C)(C)C
.	UCExp241-43	http://usefulchem.wikispaces.com/Exp241	No	No	4-(trifluoromethyl)benzaldehyde	FC(F)(F)c1ccc(C=O)cc1	furfurylamine	o1c(ccc1)CN	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	t-butylisocyanide	CC(C)(C)[N+]#[C-]	Khalid	methanol	0.08719	0.1	0.1	0.1	0.1	1.275	174.12	1.099	97.12	1.406	180.15	0.735	83.13	0.013656470588235	0.015843494085532	0.012812944523471	0.011310204081633	0.71016113252149	C(=O)(Cc1ccc2OCOc2c1)N(Cc1ccco1)C(c1ccc(C(F)(F)F)cc1)C(=O)NC(C)(C)C
.	UCExp241-40	http://usefulchem.wikispaces.com/Exp241	No	No	2,4-dimethylbenzaldehyde	O=CC1=CC=C(C)C=C1C	1-propylamine	NCCC	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	t-butylisocyanide	CC(C)(C)[N+]#[C-]	Khalid	methanol	0.08719	0.1	0.1	0.1	0.1	0.962	134.18	0.719	59.11	1.406	180.15	0.735	83.13	0.013948024948025	0.008221140472879	0.012812944523471	0.011310204081633	0.7491629189206	C(=O)(Cc1ccc2OCOc2c1)N(CCC)C(c1ccc(cc1C)C)C(=O)NC(C)(C)C
.	UCExp241-30	http://usefulchem.wikispaces.com/Exp241	No	No	5-Bromo-2-thiophenecarboxaldehyde	O=CC1=CC=C(Br)S1	butylamine	NCCCC	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	t-butylisocyanide	CC(C)(C)[N+]#[C-]	Khalid	methanol	0.08719	0.1	0.1	0.1	0.1	1.18	216.23	0.74	73.14	1.406	180.15	0.735	83.13	0.018324576271186	0.009883783783784	0.012812944523471	0.011310204081633	0.71673536905078	C(=O)(Cc1ccc2OCOc2c1)N(CCC)C(c1sc(Br)cc1)C(=O)NC(C)(C)C
.	UCExp241-47	http://usefulchem.wikispaces.com/Exp241	No	No	4-(trifluoromethyl)benzaldehyde	FC(F)(F)c1ccc(C=O)cc1	1-heptylamine	NCCCCCCC	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	t-butylisocyanide	CC(C)(C)[N+]#[C-]	Khalid	methanol	0.08719	0.1	0.1	0.1	0.1	1.275	174.12	0.777	115.22	1.406	180.15	0.735	83.13	0.013656470588235	0.014828828828829	0.012812944523471	0.011310204081633	0.71531552327493	C(=O)(Cc1ccc2OCOc2c1)N(CCCCCCC)C(c1ccc(C(F)(F)F)cc1)C(=O)NC(C)(C)C
.	UCExp241-36	http://usefulchem.wikispaces.com/Exp241	No	No	5-Bromo-2-thiophenecarboxaldehyde	O=CC1=CC=C(Br)S1	Benzylamine	NCc1ccccc1	3,4-methylenedioxyphenylacetic acid	O=C(O)Cc1ccc2OCOc2c1	t-butylisocyanide	CC(C)(C)[N+]#[C-]	Khalid	methanol	0.08719	0.1	0.1	0.1	0.1	1.607	191.05	0.981	107.15	1.406	180.15	0.735	83.13	0.011888612321095	0.01092252803262	0.012812944523471	0.011310204081633	0.74557711191821	C(=O)(CCC)N(C1CCCCC1)C(c1cc(cc(C(F)(F)F)c1)C(F)(F)F)C(=O)NC(C)(C)C
.	UCExp236-05	http://usefulchem.wikispaces.com/Exp236	No	No	4-(trifluoromethyl)benzaldehyde	FC(F)(F)c1ccc(C=O)cc1	t-butylamine	NC(C)(C)C	formic acid	O=CO	t-butylisocyanide	CC(C)(C)[N+]#[C-]	Khalid	methanol	0.1146	0.1	0.1	0.1	0.1	1.275	174.12	0.696	73.14	1.22	46.02	0.735	83.13	0.013656470588235	0.010508620689655	0.003772131147541	0.011310204081633	0.64999462305213	C(=O)N(C(C)