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1141881

CS(=O)(=O)OC1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)[C@@H](NC(=O)Cc3ccccc3)[C@H]2SC1
Reaction #56681
title compound
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)OC1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)[C@@H](NC(=O)Cc3ccccc3)[C@H]2SC1
Reaction #56682
title compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccccc1)N[C@@H]1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=C(Sc3nc(-c4ccncc4)cs3)CS[C@H]12
Reaction #56683
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccccc1)N[C@@H]1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=C(Sc3nc(-c4ccncc4)cs3)CS[C@H]12
Reaction #56684
title compound
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccccc1)N[C@@H]1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=C(Sc3nc(-c4ccncc4)cs3)CS[C@H]12
Reaction #56686
benzhydryl 7β-[(phenylacetyl)amino]-3-[4-(4-pyridyl)-2-thiazolylthio]-3-cephem-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #460531
crude product
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #463757
cephems
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #699470
cephems
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)OC1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)[C@@H](NC(=O)Cc3ccccc3)[C@H]2SC1
Reaction #1158494
title compound
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)OC1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)[C@@H](NC(=O)Cc3ccccc3)[C@H]2SC1
Reaction #1158495
title compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccccc1)N[C@@H]1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=C(Sc3nc(-c4ccncc4)cs3)CS[C@H]12
Reaction #1158496
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccccc1)N[C@@H]1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=C(Sc3nc(-c4ccncc4)cs3)CS[C@H]12
Reaction #1158497
title compound
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccccc1)N[C@@H]1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=C(Sc3nc(-c4ccncc4)cs3)CS[C@H]12
Reaction #1158499
Benzhydryl 7β-[(phenylacetyl)amino]-3-[4-(4-pyridyl)-2-thiazolylthio]-3-cephem-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)OC1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)Cc3ccccc3)[C@H]2S(=O)C1
Reaction #1349933
benzhydryl 7-phenylacetamido-3-mesyloxy-3-cephem-4-carboxylate-1-oxide
Ausbeute 80.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)OC2=C(C(=O)OC(c3ccccc3)c3ccccc3)N3C(=O)C(N)[C@H]3SC2)cc1
Reaction #1349936
benzhydryl 7-amino-3-tosyloxy-3-cephem-4-carboxylate
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #1508982
cephems
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C2=C(C(=O)OC(c3ccccc3)c3ccccc3)N3C(=O)C(NC(=O)Cc4ccccc4)[C@H]3SC2)cc1
Reaction #1695553
diphenylmethyl 7-phenylacetamido-3-(p-methoxyphenyl)-3cephem-4-carboxylate
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CC1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)Cc3ccccc3)[C@H]2SC1
Reaction #1695554
Diphenylmethyl 7-phenylacetamido-3-ethenyl-3-cephem-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccccc1)N[C@@H]1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=C(c3ccc4c(c3)-c3ccc(CO)cc3C4=O)CS[C@H]12
Reaction #1824091
desired product
Ausbeute 61.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccccc1)N[C@@H]1C(=O)N2C(C(=O)O)=C(OS(=O)(=O)C(F)(F)F)CS[C@H]12
Reaction #1945695
7β-(2-phenylacetamido)-3-trifluoromethanesulfonyloxy-3-cephem-4-carboxylic acid
Ausbeute 113.8%DOI: 10.6084/m9.figshare.5104873.v1
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