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750513

CCS(=O)C1=C(C(=O)OCc2ccccc2)N2C(=O)CC2C1
Reaction #56014
benzyl 3-ethylsulphinyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate
المردود 94.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NCCS(=O)C1=C(C(=O)OCc2ccccc2)N2C(=O)CC2C1
Reaction #56015
benzyl 3-(2-acetamidoethylsulphinyl)-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate
المردود 76.8%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)C1=C(C(=O)OCc2ccccc2)N2C(=O)C(Cc3ccccc3)C2C1
Reaction #56017
benzyl 6-benzyl-3-ethylsulphinyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate
المردود 87.1%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)C1=C(C(=O)OCc2ccccc2)N2C(=O)CC2C1
Reaction #96210
benzyl 3-ethylsulphinyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate
المردود 94.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NCCS(=O)C1=C(C(=O)OCc2ccccc2)N2C(=O)CC2C1
Reaction #96211
benzyl 3-(2-acetamidoethylsulphinyl)-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate
المردود 76.8%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)C1=C(C(=O)OCc2ccccc2)N2C(=O)C(Cc3ccccc3)C2C1
Reaction #96213
benzyl 6-benzyl-3-ethylsulphinyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate
المردود 87.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NCCS(=O)C1=C(C(=O)OCc2ccccc2)N2C(=O)CC2C1
Reaction #189778
DOI: 10.1039/C8SC04228D
CCS(=O)C1=C(C(=O)OCc2ccccc2)N2C(=O)CC2C1
Reaction #1638490
DOI: 10.1039/C8SC04228D
CCS(=O)C1=C(C(=O)OCc2ccccc2)N2C(=O)CC2C1
Reaction #1665052
benzyl 3-ethylsulphinyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate
المردود 94.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NCCS(=O)C1=C(C(=O)OCc2ccccc2)N2C(=O)CC2C1
Reaction #1665053
benzyl 3-(2-acetamidoethylsulphinyl)-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate
المردود 76.8%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)C1=C(C(=O)OCc2ccccc2)N2C(=O)C(Cc3ccccc3)C2C1
Reaction #1665055
benzyl 6-benzyl-3-ethylsulphinyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate
المردود 87.1%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)=C(S[C@H]3C[C@@H](C(=O)N(C)C)N(C(=O)OCc4ccc([N+](=O)[O-])cc4)C3)[C@H](C)[C@H]12
Reaction #1824107
title compound
المردود 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)C1=C(C(=O)OCc2ccccc2)N2C(=O)C(Cc3ccccc3)C2C1
Reaction #2229717
DOI: 10.1039/C8SC04228D