EtOAc

Cc1nn2cc[nH]c2c1-c1ccc(N)cc1.Cl
Reaction #1168
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(NCc1ccccc1)C1CCNCC1
Reaction #1171
N-benzyl-4-piperidinecarboxamide
Выход 35.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=COC(C)=O
Reaction #1188
vinyl acetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc(C(=O)O)ccc1I
Reaction #1232
3-methyl-4-iodobenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)OC(=O)[C@H](CCCCN)NC(=O)OCc1ccccc1
Reaction #1270
Nα-CBZ-O-t-butyl L-lysine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)CN1Cc2ccccc2C[C@H](NC(=O)OCc2ccccc2)C1=O
Reaction #1282
(S)-1,3,4,5-Tetrahydro-4-[[(phenylmethoxy)carbonyl]amino]-3-oxo-2H-2-benzazepine-2-acetic acid, ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)CN1C(=O)[C@@H](NC(=O)OCc2ccccc2)CSC[C@H]1c1ccccc1
Reaction #1284
(3R-cis)-Tetrahydro-5-oxo-3-phenyl-6-[[(phenylmethoxy)carbonyl]amino]-1,4-thiazepine-4(5H)-acetic acid, ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)[C@H](CCCCO)N1C(=O)c2ccccc2C1=O
Reaction #1294
title product
Выход 196.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)CN1Cc2ccccc2C[C@H](NC(=O)OCc2ccccc2)C1=O
Reaction #1414
(S)-1,3,4,5-Tetrahydro-4-[[(phenylmethoxy)carbonyl]amino]-3-oxo-2H-2-benzazepine-2-acetic acid, ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)[C@H](CCCCNC(=O)OCc1ccccc1)NC(=O)OC(C)(C)C.N#N
Reaction #1416
N2 [(1,1-Dimethylethoxy)carbonyl]-N6 -[(phenylmethoxy)carbonyl]-L-lysine, methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)CN1C(=O)[C@@H](NC(=O)OCc2ccccc2)CSC[C@H]1c1ccccc1
Reaction #1418
(3R-cis)-Tetrahydro-5-oxo-3-phenyl-6-[[(phenylmethoxy)carbonyl]amino]-1,4-thiazepine-4(5H)-acetic acid, ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)OC(=O)C1CCN(C(=O)OCc2ccccc2)N1
Reaction #1426
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)[C@H](CCCCO)N1C(=O)c2ccccc2C1=O
Reaction #1430
title product
Выход 196.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)C1(c2ccccc2)CCCC1
Reaction #1448
1-phenylcyclopentanecarboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
—
Reaction #1472
crude material
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)c1ccc2cc(-c3ccc4c(c3)C(=O)CCC4(C)C)ccc2c1
Reaction #1474
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)c1ccc2cc(C3CC(C)(C)c4ccccc4C3OCOC)ccc2c1
Reaction #1475
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1(C)CCC(=O)c2cc(N)ccc21
Reaction #1480
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)c1ccc(OC(=O)c2ccc3c(c2)C(c2cccs2)=CCC3(C)C)cc1
Reaction #1489
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1(C)CC=C(c2cccs2)c2cc(C(=O)Oc3ccc(C(=O)O)cc3)ccc21
Reaction #1491
4-[[(5,5-Dimethyl-5,6-dihydro-8-(2-thienyl)-naphthalen-2-yl)carbonyl]oxy]-benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
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