nitro methane

O=[N+]([O-])/C=C/c1ccc2c(c1)OCO2
Reaction #3096
E-2-(3,4-methylenedioxy)-nitrostyrene
Rendement 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=[N+]([O-])C=Cc1ccc2c(c1)OCO2
Reaction #3102
3,4-Methylenedioxy-1-(2-nitroethenyl)-benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=[N+]([O-])C=Cc1ccccc1
Reaction #3401
title compound
Rendement 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=[N+]([O-])C=Cc1cccc(Cl)c1
Reaction #6489
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)c1ccc2c(c1)C(C)(C)CCO2
Reaction #6640
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)c1ccc2c(c1)C(C)(C)CC(C)(C)O2
Reaction #6644
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)c1cc2c(cc1C)OC(C)(C)CC2(C)C
Reaction #6647
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COC(=O)c1ccc(C=C[N+](=O)[O-])cc1
Reaction #6827
4-(2-nitro-vinyl)-benzoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)CC(C[N+](=O)[O-])c1ccc(OC)cc1
Reaction #6832
3-(4-methoxyphenyl)-4-nitrobutyric acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C(O)COc1ccccc1)[N+](=O)[O-]
Reaction #41354
subtitle compound
Rendement 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc(C=C[N+](=O)[O-])cc1F
Reaction #43137
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=[N+]([O-])C=Cc1ccc2[nH]ccc2c1
Reaction #43201
5-(2-nitro-vinyl)-1H-indole
Rendement 11.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1C2CCN(CC2)C1C(C[N+](=O)[O-])c1cccnc1
Reaction #43656
oil
Rendement 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=[N+]([O-])C=Cc1ccc(Cl)c(F)c1
Reaction #48054
1-chloro-2-fluoro-4-(2-nitro-vinyl)-benzene
Rendement 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
—
Reaction #48606
crude oil
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=[N+]([O-])CC(O)c1cccc(O)c1
Reaction #48622
desired compound
Rendement 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=[N+]([O-])/C=C/c1cc(F)cc(Cl)c1
Reaction #48637
desired compound
Rendement 58.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCc1ccccc1CC[N+](=O)[O-]
Reaction #48709
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCOc1cc(F)cc(/C=C/[N+](=O)[O-])c1
Reaction #48715
desired compound
Rendement 69.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=[N+]([O-])/C=C/c1cc(F)cc(OCc2ccccc2)c1
Reaction #48719
desired compound
Rendement 68.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
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