4-nitrobenzyl (5R, 6S)-6-[(1R)-1-hydroxyethyl]-2-oxo-1-carbapenam-3-carboxylate

C[C@@H](O)[C@H]1C(=O)N2C(C(=O)[O-])=C(S[C@H]3CC[N+](C)(C)C3)C[C@H]12
Reaction #5155
title compound
المردود 18.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC[N+]1(C)C[C@@H](SC2=C(C(=O)[O-])N3C(=O)[C@H]([C@@H](C)O)[C@H]3C2)C[C@H]1C(=O)N(C)C
Reaction #5156
title compound
المردود 10.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)[O-])=C(S[C@H]3C[C@@H](C(=O)N(C)C)[N+](C)(C)C3)C[C@H]12
Reaction #5157
title compound
المردود 22.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)[O-])=C(S[C@H]3C[C@@H](C(N)=O)[N+](C)(C)C3)C[C@H]12
Reaction #5158
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)C(=O)C[C@H]12
Reaction #93089
(5R,6S) p-nitrobenzyl 6-[(R)-1-hydroxyethyl]-1-azabicyclo[3.2.0]heptan-3,7-dione-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)C(=O)C[C@H]12
Reaction #310870
(5R,6S) p-nitrobenzyl 6-[(R)-1-hydroxyethyl]-1-azabicyclo[3.2.0]heptan-3,7-dione-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_10
C=CC1=C(C(=O)OCc2ccc([N+](=O)[O-])cc2)N2C(=O)[C@H]([C@@H](C)O)[C@H]2C1
Reaction #343960
title compound
المردود 47.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_11
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)=C(/C=C/C(N)=O)C[C@H]12
Reaction #343964
title compound
المردود 34.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_11
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)C(=O)C[C@H]12
Reaction #442366
(5R,6S) p-nitrobenzyl 6-[(R)-1-hydroxyethyl]-1-azabicyclo[3.2.0]heptan-3,7-dione-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1983_03
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)C(=O)C[C@H]12
Reaction #522272
(5R,6S) p-nitrobenzyl 6-[(R)-1-hydroxyethyl]-1-azabicyclo[3.2.0]heptan-3,7-dione-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1983_08
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)O)=C(SCC(=N)N3CC[C@@H](OC(N)=O)C3)C[C@H]12
Reaction #709594
title product
المردود 17.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_09
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)O)=C(SCC(=N)N3CCC(=NO)CC3)C[C@H]12
Reaction #709597
title compound
المردود 6.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_09
CON=C1CCN(C(=N)CSC2=C(C(=O)O)N3C(=O)[C@H]([C@@H](C)O)[C@H]3C2)CC1
Reaction #709600
title compound
المردود 4.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_09
CON=C1CCN(C(=N)CSC2=C(C(=O)O)N3C(=O)[C@H]([C@@H](C)O)[C@H]3C2)C1
Reaction #709603
title compound
المردود 5.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_09
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)O)=C(SCC(=N)N3CCC(=NO)C3)C[C@H]12
Reaction #709606
title compound
المردود 3.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_09
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)O)=C(SCC(=N)N3CCC(OC(N)=O)CC3)C[C@H]12
Reaction #709609
title compound
المردود 19.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_09
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)C(=O)C[C@H]12
Reaction #735873
(5R,6S) p-nitrobenzyl 6-[(R)-1-hydroxyethyl]-1-azabicyclo[3.2.0]heptan-3,7-dione-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_04
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)[O-])=C(S[C@H]3CC[N+](C)(C)C3)C[C@H]12
Reaction #1117304
title compound
المردود 18.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_04
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)[O-])=C(SC3CC[N+](C)(C)CC3)C[C@H]12
Reaction #1117305
title compound
المردود 6.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_04
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)[O-])=C(S[C@H]3C[C@@H](C(=O)N(C)C)[N+](C)(C)C3)C[C@H]12
Reaction #1117306
title compound
المردود 22.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_04
الصفحة 1التالي