Substructure Search

1142256

COc1ccc(CN2CCN(Cc3ccc([N+](=O)[O-])cn3)CC2(C)C)cc1
Reaction #71427
title compound
Yield 80.2%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)OCc1ccc([N+](=O)[O-])cn1
Reaction #71428
title compound
Yield 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(O)CN(Cc2ccc([N+](=O)[O-])cn2)C1
Reaction #84167
desired compound
Yield 71.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(COS(C)(=O)=O)ccc1[N+](=O)[O-]
Reaction #263832
DOI: 10.1039/C8SC04228D
CS(=O)(=O)OCc1ccc([N+](=O)[O-])cn1
Reaction #760221
DOI: 10.1039/C8SC04228D
COc1ccc(CN2CCN(Cc3ccc([N+](=O)[O-])cn3)CC2(C)C)cc1
Reaction #1277017
title compound
Yield 80.2%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)OCc1ccc([N+](=O)[O-])cn1
Reaction #1277018
title compound
Yield 99.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(COS(C)(=O)=O)ccc1[N+](=O)[O-]
Reaction #1898772
(6-methyl-5-nitropyridin-2-yl)methyl methanesulfonate
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2CCN(Cc3ccc([N+](=O)[O-])cn3)CC2(C)C)cc1
Reaction #2431983
DOI: 10.1039/C8SC04228D
COc1ccc(CN2CCN(Cc3ccc([N+](=O)[O-])cn3)CC2(C)C)cc1
Reaction #2479045
title compound
Yield 80.2%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)OCc1ccc([N+](=O)[O-])cn1
Reaction #2479046
title compound
Yield 99.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2CCN(Cc3ccc([N+](=O)[O-])cn3)CC2(C)C)cc1
Reaction #2496894
title compound
Yield 80.2%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)OCc1ccc([N+](=O)[O-])cn1
Reaction #2496895
title compound
Yield 99.0%DOI: 10.6084/m9.figshare.5104873.v1