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1410118

O=C(O)c1coc2c1C(=O)CCC2
Reaction #995
4-oxo-4,5,6,7-tetrahydrobenzofuran-3-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cn2c(Cl)cccc2n1
Reaction #5524
desired product
Выход 67.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1coc(N)n1
Reaction #42612
ethyl 2-amino-1,3-oxazole-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1csc(Nc2cnc(CNC(=O)OC(C)(C)C)c3c(OC)cc(OC)cc23)n1
Reaction #42928
2-[1-(tert-butoxycarbonylamino-methyl)-6,8-dimethoxy-isoquinolin-4-ylamino]thiazole-4-carboxylic acid ethyl ester
Выход 42.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1csc(Nc2cnc(CNC(=O)OC(C)(C)C)c3cc(OC)c(OC)cc23)n1
Reaction #42949
2-[1-(tert-butoxycarbonylamino-methyl)-6,7-dimethoxy-isoquinolin-4-ylamino]thiazole-4-carboxylic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c2c(CN3C(=O)c4ccccc4C3=O)ncc(Nc3nc(C(=O)O)cs3)c2c1
Reaction #42972
title compound
Выход 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1csc(-c2nc3c(C#N)c(C)c(-c4ccccc4)c(F)c3o2)n1
Reaction #45768
compound
Выход 91.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1csc(N2N=C(c3ccc([N+](=O)[O-])cc3)c3cc4c(cc3CC2C)OCO4)n1
Reaction #53345
title compound
Выход 85.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #58915
crystals
Выход 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)O[C@@H]1C[C@@H](c2nc(C(=O)O)cs2)N(C(=O)OCc2ccc([N+](=O)[O-])cc2)C1
Reaction #65553
(2S,4R)-2- (4-carboxythiazol-2-yl)-4-methanesulfonyloxy-1-(4-nitrobenzyloxycarbonyl) pyrrolidine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=CNCCc2c1[nH]c1ccccc21
Reaction #66190
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OC(=O)C(=O)CBr
Reaction #66192
iso-propyl 3-bromopyruvate
Выход 124.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCOC(=O)C1=CNC(C)Cc2c1[nH]c1ccccc21
Reaction #66194
2-Methyl-1,2,3,6-tetrahydroazepino[4,5-b]indole-5-carboxylic acid n-propyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCCOC(=O)C1=CNC(C)Cc2c1[nH]c1cc(F)ccc21
Reaction #66197
2-Methyl-8-fluoro-1,2,3,6-tetrahydroazepino[4,5-b]indole-5-carboxylic acid n-propyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCCOC(=O)C1=CNC(CC)Cc2c1[nH]c1ccccc21
Reaction #66198
2-Ethyl 1,2,3,6-tetrahydroazepino[4,5-b]indole-5-carboxylic acid n-propyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1c(O)cnc2ccc(I)cc12
Reaction #68576
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1coc(/C=C/c2ccccc2)n1
Reaction #71125
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)c1nc(N2CC[C@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](OC)C2)sc1CC
Reaction #71803
title compound
Выход 78.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)c1nc(N2CC[C@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](OCC)C2)sc1CC
Reaction #71810
title compound
Выход 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1coc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)n1
Reaction #71880
title compound
Выход 79.4%DOI: 10.6084/m9.figshare.5104873.v1
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