Substructure Search

5153

COC(=O)c1ccc([N+](=O)[O-])cc1S(=O)(=O)O
Reaction #1091
2-methoxycarbonyl-5-nitrobenzenesulfonic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc([N+](=O)[O-])cc1S(=O)(=O)Cl
Reaction #1092
2-Methoxycarbonyl-5-nitrobenzenesulfonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(N)cc1S(=O)(=O)NC(C)(C)C
Reaction #1093
N-tert-Butyl-5-amino-2-methoxycarbonylbenzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1NC(=O)c1ccc([N+](=O)[O-])cc1
Reaction #2517
title compound
Yield 87.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(NC(=O)c2ccc([N+](=O)[O-])cc2)c1
Reaction #2518
title compound
Yield 93.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(OC)c(NC(=O)c2ccc([N+](=O)[O-])cc2)c1
Reaction #2519
title compound
Yield 77.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(NC(=O)c2ccc([N+](=O)[O-])cc2)c(OC)c1
Reaction #2521
title compound
Yield 91.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccccc1)c1ccc([N+](=O)[O-])cc1
Reaction #2522
title compound
Yield 97.5%DOI: 10.6084/m9.figshare.5104873.v1
CSc1cccc(NC(=O)c2ccc([N+](=O)[O-])cc2)c1
Reaction #2523
title compound
Yield 85.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccccc1C(F)(F)F)c1ccc([N+](=O)[O-])cc1
Reaction #2524
title compound
Yield 15.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cccc(C(F)(F)F)c1)c1ccc([N+](=O)[O-])cc1
Reaction #2525
title compound
Yield 80.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cccnc1)c1ccc([N+](=O)[O-])cc1
Reaction #2526
title compound
Yield 49.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cccc([N+](=O)[O-])c1)c1ccc([N+](=O)[O-])cc1
Reaction #2528
title compound
Yield 83.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccccc1NC(=O)c1ccc([N+](=O)[O-])cc1
Reaction #2529
title compound
Yield 72.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(NC(=O)c2ccc([N+](=O)[O-])cc2)cc1
Reaction #2533
title compound
Yield 99.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(F)cc1)c1ccc([N+](=O)[O-])cc1
Reaction #2534
title compound
Yield 65.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(NC(=O)c2ccc([N+](=O)[O-])cc2)cc1C
Reaction #2539
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C)cc(NC(=O)c2ccc([N+](=O)[O-])cc2)c1
Reaction #2540
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(Cl)cc1)c1ccc([N+](=O)[O-])cc1
Reaction #2541
title compound
Yield 98.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc([N+](=O)[O-])c(Cn2cccc2C=O)c1
Reaction #3698
desired product
Yield 83.9%DOI: 10.6084/m9.figshare.5104873.v1
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