Substructure Search

10215

Cc1c([N+](=O)[O-])ccc2c1C(=O)NS2(=O)=O
Reaction #904
4-Methyl-5-nitrosaccharin
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C[C@H]1C[C@@H](COS(=O)(=O)c2ccc([N+](=O)[O-])cc2)OC(C)(C)O1
Reaction #6554
product
Yield 110.5%DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1ccc([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #7000
2,4-dinitrobenzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(S(=O)(=O)OCCc2cccc([N+](=O)[O-])c2)cc1
Reaction #44058
title compound
Yield 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)S(=O)(=O)c1ccc([N+](=O)[O-])cc1
Reaction #53229
4-nitrobenzenesulphonic acid-dimethylamide
DOI: 10.6084/m9.figshare.5104873.v1
CN([C@H]1CC[C@H](OCCCCBr)CC1)S(=O)(=O)c1ccc([N+](=O)[O-])cc1
Reaction #53835
trans-N-[4-(4-Bromo-butoxy)-cyclohexyl]-N-methyl-4-nitro-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1cccc(NS(=O)(=O)c2ccc([N+](=O)[O-])cc2)c1
Reaction #55643
3-[[(4-Nitrophenyl)sulfonyl]amino]benzamide
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(S(=O)(=O)Nc2cccc(O)c2)cc1
Reaction #55932
product
Yield 56.6%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(S(=O)(=O)Nc2ccc(O)cc2)cc1
Reaction #55933
material
Yield 73.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(O)ccc1NS(=O)(=O)c1ccc([N+](=O)[O-])cc1
Reaction #55934
pure intermediate
Yield 84.3%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(S(=O)(=O)Nc2cccc3ccc(O)cc23)cc1
Reaction #56363
green product
Yield 47.0%DOI: 10.6084/m9.figshare.5104873.v1
CNS(=O)(=O)c1ccc([N+](=O)[O-])cc1
Reaction #57325
N-methyl-4-nitrobenzenesulfonamide
Yield 98.4%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(S(=O)(=O)NOC2CCOCC2)cc1
Reaction #57475
white crystals
Yield 36.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(CC)ON(C[C@@H](O)[C@H](Cc1ccccc1)NC(=O)O[C@H]1CO[C@H]2OCC[C@H]21)S(=O)(=O)c1ccc([N+](=O)[O-])cc1
Reaction #57491
(3R,3aS,6aR)hexahydrofuro[2,3-b]furan-3-yl (1S,2R)-1-benzyl-3-{(1-ethylpropoxy)[(4-nitrophenyl)sulfonyl]amino}-2-hydroxypropylcarbamate
Yield 88.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](OS(=O)(=O)c1ccc([N+](=O)[O-])cc1)c1ccccc1Cl
Reaction #72585
methyl(R)-2-(4-nitrophenylsulfonyloxy)-2(2-chlorophenyl)acetate
Yield 98.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1=C(OS(=O)(=O)c2ccc([N+](=O)[O-])cc2)C(=O)O[C@@H]1C
Reaction #83733
(R)-2-(4-nitrobenzenesulphonyloxy)-3-methoxycarbonyl -2penten-4-olide
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
CC(C)(C)OC(=O)N1CCCC(OS(=O)(=O)c2ccc([N+](=O)[O-])cc2)C1
Reaction #183865
DOI: 10.1039/C8SC04228D
Cn1cc(NS(=O)(=O)c2ccc([N+](=O)[O-])cc2[N+](=O)[O-])cn1
Reaction #185510
DOI: 10.1039/C8SC04228D
COc1cc([N+](=O)[O-])ccc1S(=O)(=O)NC(C)(C)C
Reaction #198920
DOI: 10.1039/C8SC04228D
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