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

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@H](C)[C@H]12
Reaction #5154
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@H](C)[C@H]12
Reaction #65560
4-nitrobenzyl (4R, 5R, 6S)-6-[(1R)-1-hydroxyethyl]-4-methyl-3, 7-dioxo-1-azabicyclo[3.2.0]heptane-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)O)=C(S[C@@H]3CN[C@H](C(=O)NC(C)(C)C[NH+]4CCCC4)C3)[C@H](C)[C@H]12.O=S(=O)([O-])F
Reaction #65613
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)C(=O)[C@H](C)[C@H]12
Reaction #433559
4-nitrobenzyl (4R,5R,6S)-6-[(1R)-1-hydroxyethyl]-4-methyl-3,7-dioxo-1-azabicyclo[3.2.0]heptane-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_10
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)C(=O)[C@H](C)[C@H]12
Reaction #433563
4-nitrobenzyl (4R,5R,6S)-6-[(1R)-1-hydroxyethyl]-4-methyl-3,7-dioxo-1-azabicyclo[3.2.0]heptane-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_10
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)C(=O)[C@H](C)[C@H]12
Reaction #433567
4-nitrobenzyl (4R,5R,6S)-6-[(1R)-1-hydroxyethyl]-4-methyl-3,7-dioxo-1-azabicyclo[3.2.0]heptane-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_10
CC(=NC(=O)OCc1ccc([N+](=O)[O-])cc1)N1CCN(C(=O)[C@@H]2C[C@H](SC3=C(C(=O)OCc4ccc([N+](=O)[O-])cc4)N4C(=O)[C@H]([C@@H](C)O)[C@H]4[C@H]3C)CN2C(=O)OCc2ccc([N+](=O)[O-])cc2)CC1
Reaction #449176
title compound
Выход 21.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)=C(S[C@H]3C[C@@H](C(=O)N4CCCN(C(=O)OCc5ccc([N+](=O)[O-])cc5)CC4)N(C)C3)[C@H](C)[C@H]12
Reaction #449191
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)=C(S[C@H]3C[C@@H](C(=O)N4CCN(C)CC4)N(C)C3)[C@H](C)[C@H]12
Reaction #449194
title compound
Выход 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)=C(S[C@H]3C[C@@H](C(=O)N4CCN(CCOC(N)=O)CC4)N(C(=O)OCc4ccc([N+](=O)[O-])cc4)C3)[C@H](C)[C@H]12
Reaction #449198
title compound
Выход 28.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)=C(S[C@@H]3CN[C@H](C(=O)N4CCN(CC(=O)OCc5ccc([N+](=O)[O-])cc5)CC4)C3)[C@H](C)[C@H]12
Reaction #449199
title compound
Выход 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)=C(S[C@H]3C[C@@H](C(=O)N4CC[C@H](n5cncn5)C4)N(C(=O)OCc4ccc([N+](=O)[O-])cc4)C3)[C@H](C)[C@H]12
Reaction #449275
title compound
Выход 70.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)=C(S[C@@H]3CC(=S)N(C)C3)[C@H](C)[C@H]12
Reaction #552520
(1R, 5S, 6S)-2-[(4R)-N-methyl- pyrrolidine-2-thion-4-ylthio]-6-[(1R)-1-hydroxyethyl]-1-methylcarbapen -2-em-3-carboxylic acid 4-nitrobenzyl ester
Выход 68.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_10
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)=C(S[C@H]3CC(=S)N(C)C3)[C@H](C)[C@H]12
Reaction #552522
(1R, 5S, 6S)-2-[(4S)-N-methylpyrrolidine-2-thion-4-ylthio]-6-[(1R)-1-hydroxyethyl]-1-methylcarbapen-2-em-3-carboxylic acid 4-nitrobenzyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_10
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)=C(S[C@@H]3CCNC3=S)[C@H](C)[C@H]12
Reaction #552523
(1R, 5S, 6S)-2-[(3R)-pyrrolidine-2-thion-3-ylthio]-6-[(1R)-1-hydroxyethyl]-1-methylcarbapen-2-em-3-carboxylic acid 4-nitrobenzyl ester
Выход 39.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_10
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)C(=O)[C@H](C)[C@H]12
Reaction #707979
4-nitrobenzyl (4R,5R,6S)-6-[(1R)-1-hydroxyethyl]-4-methyl-3,7-dioxo-1-azabicyclo[3.2.0]-heptane-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_04
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)O)=C(SCC(=N)N3CCNC(=O)C3)[C@H](C)[C@H]12
Reaction #709615
title product
Выход 11.0%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)N3CC[C@@H](OC(N)=O)C3)[C@H](C)[C@H]12
Reaction #709616
title product
Выход 23.2%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@H](C)[C@H]12
Reaction #709617
title product
Выход 12.4%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)N3CCN(C)C(=O)C3)[C@H](C)[C@H]12
Reaction #709618
title compound
Выход 9.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_09
Страница 1Далее