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CCOC(=O)C=O

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)C(=O)c1csc(N)n1
Reaction #2724
Ethyl 2-amino-thiazol-4-yl-glyoxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cn2c(Cl)cccc2n1
Reaction #5524
desired product
Ausbeute 67.7%DOI: 10.6084/m9.figshare.5104873.v1
CCC(NC(=O)C1CCCC1)c1nnc(-c2ccccc2)[nH]c1=O
Reaction #7643
N-[1-(5-Oxo-3-phenyl-4,5-dihydro-1,2,4-triazin-6-yl)propyl]cyclopentanecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)C(CC)NC(=O)C1CCCC1
Reaction #7645
Ethyl 3-[(cyclopentylcarbonyl)amino]-2-oxopentanoate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc([C@@H](Oc2ccc3c(cnn3-c3ccc(F)cc3)c2)[C@H](C)NC(=O)C(=O)OC(C)C)c1
Reaction #41365
Propan-2-yl[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-(3-methoxyphenyl)propan-2-yl]carbamoylformate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)c1nc(NC=O)sc1Cl
Reaction #41810
title intermediate
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
Ausbeute 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
C[C@H]1CN([C@H](c2cc(F)c(F)c(F)c2)[C@@H](C)O[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)C(=O)C(=O)O1
Reaction #44610
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1CN([C@H](c2cc(F)c(F)c(F)c2)[C@@H](C)O[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)C(=O)[C@@H](O)O1
Reaction #44611
title compound
Ausbeute 97.5%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CN([C@H](c2cc(F)c(F)c(F)c2)[C@@H](C)O[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)C(=O)C(=O)O1
Reaction #44638
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1CN([C@H](c2cc(F)c(F)c(F)c2)[C@@H](C)O[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)C(=O)[C@@H](O)O1
Reaction #44639
title compound
Ausbeute 97.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1csc(-c2nc3c(C#N)c(C)c(-c4ccccc4)c(F)c3o2)n1
Reaction #45768
compound
Ausbeute 91.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OC(=O)[C@H](C)Nc1ccc(Cl)c(Cl)c1
Reaction #51306
title compound
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
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)c1cc(N)c(C2CCCCC2)c(Cl)c1
Reaction #54836
ethyl 3-amino-5-chloro-4-cyclohexylphenylglyoxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)c1csc(NC=O)n1
Reaction #56560
ethyl 2-(2-formylaminothiazol-4-yl)glyoxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=CNc1nc(C(=O)C(=O)O)cs1
Reaction #56561
2-(2-formylaminothiazol-4-yl)glyoxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)c1ccc(O)cc1O
Reaction #57513
solid
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
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