#11206164

Nc1ccc(CNn2cnc3ccccc32)cc1
Reaction #47796
title compound
المردود 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=[N+]([O-])c1ccc(CN2CCC2)cc1
Reaction #53206
4-(Azetidin-1-yl-methyl)-nitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccc(-c2cc3ccccc3[nH]2)cc1NCc1ccc([N+](=O)[O-])cc1
Reaction #53802
product
المردود 38.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccc(-c2cc3cc(F)c(F)cc3[nH]2)cc1NCc1ccc([N+](=O)[O-])cc1
Reaction #53806
product
المردود 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=[N+]([O-])c1ccc(-c2cnco2)cc1
Reaction #56860
5-(4-nitro-phenyl)-oxazole
المردود 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C1NC(=O)C(=Cc2ccc([N+](=O)[O-])cc2)S1
Reaction #58920
5-(4-nitrobenzylidene)-1,3-thiazolidine-2,4-dione
المردود 59.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(O)CCc1ccc([N+](=O)[O-])cc1
Reaction #64698
3-(4-nitrophenyl)propionic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CC(C)(C)c1cc(C(c2ccc([N+](=O)[O-])cc2)N2CCCCC2)cc(C(C)(C)C)c1O
Reaction #81030
title compound
المردود 23.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COC(=O)c1cc2c(=O)[nH]c(-c3ccc([N+](=O)[O-])cc3)nn2c1
Reaction #92065
methyl 2-p-nitrophenyl-4-oxo-3,4-dihydropyrrolo[2,1-f][1,2,4]triazine-6-formate
المردود 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(OCc1ccccc1)C1CS[C@@H]2[C@H](N=Cc3ccc([N+](=O)[O-])cc3)C(=O)N12
Reaction #93041
Benzyl 6β-(4-nitrobenzylideneamino)penam-3-caboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
CCOC(=O)C(C)=Cc1ccc([N+](=O)[O-])cc1
Reaction #95081
title compound
المردود 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
O=C1NC(=O)C(=Cc2ccc([N+](=O)[O-])cc2)N1
Reaction #95434
5-(4'-nitrobenzylidene)-hydantoin
المردود 93.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
O=[N+]([O-])c1ccc(CN[C@H]2CC[C@@H](C(c3ccccc3)c3ccccc3)OC2)cc1
Reaction #166085
compound 16d
المردود 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C1NC(=O)C(=Cc2ccc([N+](=O)[O-])cc2)N1
Reaction #175499
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1CCC(C(C)C)C(OC(=O)C(=Cc2ccc([N+](=O)[O-])cc2)C(=O)OC2CC(C)CCC2C(C)C)C1
Reaction #178849
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)C(F)=Cc1ccc([N+](=O)[O-])cc1
Reaction #180163
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(-c2cc3cc(F)c(F)cc3[nH]2)cc1NCc1ccc([N+](=O)[O-])cc1
Reaction #184049
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC(=O)C(=Cc1ccc([N+](=O)[O-])cc1)C(=O)OCCC#N
Reaction #187821
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC(=O)C(=Cc1ccc([N+](=O)[O-])cc1)C(=O)CC
Reaction #189821
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(NN=Cc1ccc([N+](=O)[O-])cc1)c1sc2ccccc2c1Cl
Reaction #198310
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
الصفحة 1التالي