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205498

CC(C)(C)OC(=O)NCc1nnc(-c2ccc(OCc3cccc(F)c3)cc2)s1
Reaction #532581
tert-butyl((5-(4-((3-fluorobenzyl)oxy)phenyl)-1,3,4-thiadiazol-2-yl)methyl)carbamate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCc1nnc(-c2ccc([C@@H](O)[C@@H](CF)NC(=O)C(Cl)Cl)cc2)s1
Reaction #612691
title compound
Ausbeute 7.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc([C@H]2C[C@@H]2COc2cc(N(Cc3nnc(C)s3)C(=O)OC(C)(C)C)c(=O)n(C)n2)nc1
Reaction #617971
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCc1nnc(SCC2=C(C(=O)O)N3C(=O)C(N)[C@H]3SC2)s1
Reaction #1482954
7-amino-3-(5-tert-butoxycarbonylaminomethyl-1,3,4-thiadiazol-2-yl)thiomethyl-3-cephem-4-carboxylic acid
Ausbeute 56.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCc1nnc(S)s1
Reaction #1482966
5-t-butoxycarbonylaminomethyl-1,3,4-thiadiazole-2-thiol
Ausbeute 65.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCc1nnc(-c2ccc([C@@H](O)[C@@H](CF)NC(=O)C(Cl)Cl)cc2)s1
Reaction #1574624
title compound
Ausbeute 7.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCc1nnc(-c2ccc([C@@H](O)[C@@H](CF)NC(=O)C(Cl)Cl)cc2)s1
Reaction #1607622
title compound
Ausbeute 7.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1sc(CNC(=O)OC(C)(C)C)nc1C(=O)O
Reaction #1670090
2-(N-Boc-Aminomethyl)-5-methylthiazole-4-carboxylic Acid
DOI: 10.6084/m9.figshare.5104873.v1
Cc1sc(CNC(=O)OC(C)(C)C)nc1C(N)=O
Reaction #1670091
2-(N-Boc-Aminomethyl)-5-methylthiazole-4-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1sc(CNC(=O)OC(C)(C)C)nc1C#N
Reaction #1670092
4-Cyano-2-(N-Boc-aminomethyl)-5-methylthiazole
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(CNC(=O)OC(C)(C)C)sc1C#N
Reaction #1670093
2-(N-BOC-Aminomethyl)-5-cyano-4-methylthiazole
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCc1nnc(SCC2=C(C(=O)O)N3C(=O)C(N)[C@H]3SC2)s1
Reaction #1766081
7-amino-3-(5-tert-butoxycarbonylaminomethyl-1,3,4-thiadiazol-2-yl)thiomethyl-3-cephem-4-carboxylic acid
Ausbeute 56.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nnc(CNC(=O)OC(C)(C)C)s1
Reaction #1981896
title compound
Ausbeute 79.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nnc(CN)s1.Cl
Reaction #1981897
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc([C@H]2C[C@@H]2COc2cc(N(Cc3nnc(C)s3)C(=O)OC(C)(C)C)nc(C)n2)nc1
Reaction #2262586
2-2
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nnc(CNC(=O)OC(C)(C)C)s1
Reaction #2262595
product
Ausbeute 261.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nnc(CN(C(=O)OC(C)(C)C)c2cc(OC[C@H]3C[C@@H]3c3ccc(C)cn3)nc(C)n2)s1
Reaction #2262596
syrup
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(OC[C@H]2C[C@@H]2c2ccc(C(C)(C)O)cn2)cc(N(Cc2nnc(C)s2)C(=O)OC(C)(C)C)n1
Reaction #2262599
crude product
Ausbeute 99.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C2C(COc3cc(N(Cc4nnc(C)s4)C(=O)OC(C)(C)C)nc(C)n3)C2OC(C)(C)C)nc1
Reaction #2262606
solid
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCc1nnc(C(C)(C)C)s1
Reaction #2262609
title compound
Ausbeute 92.6%DOI: 10.6084/m9.figshare.5104873.v1
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