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1185974

CC(C)C[C@@H](C(=O)Nc1nc(N(C)C)ns1)N1CC(Oc2ccccc2Cl)=CC1=O
Reaction #47379
(S)-2-[4-(2-chloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-4-methyl-pentanoic acid (3-dimethylamino-[1,2,4]thiadiazol-5-yl)-amide
Ausbeute 36.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2cc(F)cc(F)c2)cc(C(=O)Nc2ncc(F)s2)n1
Reaction #183183
DOI: 10.1039/C8SC04228D
CON=C(C(=O)N[C@@H]1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=CCS[C@H]12)c1nc(NC(=O)OCc2ccccc2)sc1F
Reaction #214080
7β-[2-(2-carbobenzoxyamino-5-fluoro-4-thiazolyl)-2-methoxyiminoacetamido]-3-cephem-4-carboxylic acid diphenylmethyl ester
Ausbeute 70.9%DOI: 10.6084/m9.figshare.5104873.v1
CON=C(C(=O)N[C@@H]1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=CCS[C@H]12)c1nc(NC(=O)OCc2ccccc2)sc1F
Reaction #214084
7β-[2-(2-carbobenzoxyamino-5-fluoro-4-thiazolyl)-2-methoxyiminoacetamido]-3-cephem-4-carboxylic acid diphenylmethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCSc1ccc(C(=CC2CCCC2)C(=O)Nc2ncc(F)s2)cn1
Reaction #286902
DOI: 10.1039/C8SC04228D
—
Reaction #305259
desired acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(-c2nc(N3CCN(C)CC3)sc2F)cc1
Reaction #305268
title compound
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
COC1(OC)COC2C(Cl)CN(C(=O)C(CNC(=O)c3ccc(-c4nc(N5CCN(C)CC5)sc4F)cc3)C(C)C)C21
Reaction #305274
title compound
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(c1ncc(F)s1)C1CCNC1.O=C(O)C(F)(F)F
Reaction #340122
5-fluoro-N-methyl-N-(pyrrolidin-3-yl)thiazol-2-amine trifluoroacetate
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2cc(F)cc(F)c2)cc(C(=O)Nc2nc(C)c(F)s2)n1
Reaction #395831
DOI: 10.1039/C8SC04228D
CCOC(=O)C(C)(C)c1nc(N(Cc2ccc(OC)cc2)C(=O)OC(C)(C)C)sc1F
Reaction #611588
compound
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)(C)c1nc(N)sc1F
Reaction #611589
2-(2-Amino-5-fluoro-thiazol-4-yl)-2-methyl-propionic acid ethyl ester
Ausbeute 97.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2cc(F)cc(F)c2)cc(C(=O)Nc2nc(C)c(F)s2)n1
Reaction #639729
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2cc(F)cc(F)c2)cc(C(=O)Nc2ncc(F)s2)n1
Reaction #639730
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2cncc(F)c2)cc(C(=O)Nc2ncc(F)s2)n1
Reaction #639733
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ncc(F)s1)[C@H](C[C@H]1CCNC1)c1ccc(S(=O)(=O)C2CC2)cc1
Reaction #682004
(R)-2-(4-(cyclopropylsulfonyl)phenyl)-N-(5-fluorothiazol-2-yl)-3-((S)-pyrrolidin-3-yl)propanamide
Ausbeute 108.7%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)N1CC[C@H](C[C@@H](C(=O)Nc2ncc(F)s2)c2ccc(S(=O)(=O)C3CC3)cc2)C1
Reaction #682005
compound
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CC[C@H](C[C@@H](C(=O)Nc2ncc(F)s2)c2ccc(S(=O)(=O)C3CC3)cc2)C1
Reaction #682006
compound
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)N1CC[C@H](C[C@@H](C(=O)Nc2ncc(F)s2)c2ccc(S(=O)(=O)C3CC3)cc2)C1
Reaction #682007
compound
Ausbeute 99.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ncc(F)s1)[C@H](C[C@H]1CCN(C(=O)NO)C1)c1ccc(S(=O)(=O)C2CC2)cc1
Reaction #682008
compound
Ausbeute 54.3%DOI: 10.6084/m9.figshare.5104873.v1
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