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C[N+](=O)[O-]

O=C(O)c1c([N+](=O)[O-])cccc1S(=O)(=O)O
Reaction #1090
2-Carboxy-nitrobenzenesulfonic acid
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(C(=O)N2Cc3cccn3Cc3ccccc32)cc1
Reaction #3602
desired product
Ausbeute 97.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(=O)N2Cc3cccn3Cc3ccccc32)ccc1N
Reaction #3613
desired product
Ausbeute 85.2%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1cc([N+](=O)[O-])ccc1C1=NC2=NC=NC(=O)C2=N1
Reaction #3959
8-(2-Dimethylamino-4-nitro-phenyl)-purin-6-one
DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1cc([N+](=O)[O-])ccc1NC1CC1
Reaction #46116
2-cyclopropylamino-5-nitrobenzenesulphonamide
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc2c(c1)S(=O)(=O)N=CN2C1CC1
Reaction #46117
4-cyclopropyl-7-nitro-4H-1,2,4-benzothiadiazine 1,1-dioxide
DOI: 10.6084/m9.figshare.5104873.v1
CNS(=O)(=O)c1ccc([N+](=O)[O-])cc1
Reaction #57325
N-methyl-4-nitrobenzenesulfonamide
Ausbeute 98.4%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #57326
solid
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc([N+](=O)[O-])ccc1N1CCOCC1)N1CCN(c2ccccc2F)CC1
Reaction #60992
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(CCc2ccc([N+](=O)[O-])cc2S(=O)(=O)[O-])c(S(=O)(=O)[O-])c1
Reaction #64586
4,4'-dinitrobibenzyl-2,2'-disulfonate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(Nc2ncnc3cc([N+](=O)[O-])ccc23)c1
Reaction #80311
4-(3'-methylanilino)-7-nitroquinazoline
DOI: 10.6084/m9.figshare.5104873.v1
Cn1nc(-c2c(F)cccc2Cl)nc1-c1cccc([N+](=O)[O-])c1Cl
Reaction #80483
desired compound
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1c(C(F)(F)F)cc(Cl)c2[nH]c(=O)c(=O)[nH]c12
Reaction #82040
title compound
Ausbeute 93.9%DOI: 10.6084/m9.figshare.5104873.v1
Nc1c(C(F)(F)F)cc(Cl)c2[nH]c(=O)c(=O)[nH]c12
Reaction #82628
title compound
Ausbeute 93.9%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(C(=O)N2Cc3cccn3Cc3ccccc32)cc1
Reaction #83432
desired product
Ausbeute 97.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(=O)N2Cc3cccn3Cc3ccccc32)ccc1N
Reaction #83442
desired product
Ausbeute 85.2%DOI: 10.6084/m9.figshare.5104873.v1
CNS(=O)(=O)c1ccc([N+](=O)[O-])cc1
Reaction #85508
4-nitrobenzenesulfonic acid methylamide
DOI: 10.6084/m9.figshare.5104873.v1
COCCOc1ccc(Nc2cc(N(C)C(=O)Nc3c(Cl)c(OC)cc(OC)c3Cl)ncn2)c([N+](=O)[O-])c1
Reaction #86457
title compound
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Nc1ccc(-c2cccs2)cc1[N+](=O)[O-]
Reaction #90943
tert-butyl (2-nitro-4-(thiophen-2-yl)phenyl)carbamate
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Nc1ccc(-c2cccs2)cc1N
Reaction #90944
tert-butyl (2-amino-4-(thiophen-2-yl)phenyl)carbamate
Ausbeute 69.4%DOI: 10.6084/m9.figshare.5104873.v1
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