Recherche de Sous-structure

1310776

COC(=O)c1cc2ccc([N+](=O)[O-])cc2s1
Reaction #43707
Methyl6-nitro-1-benzothiophene-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(C=O)c(N)c1
Reaction #80241
2,4-diaminobenzaldehyde
Rendement 71.9%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cc(Br)c([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #91802
( iii )
Rendement 7.0%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cc(C2CC2)c([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #91803
( iv )
Rendement 78.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1c2cc(C3CC3)c([N+](=O)[O-])cc2[n+]([O-])n1-c1ccc(Cl)cc1
Reaction #91804
2-(4-chlorophenyl)-5-cyclopropyl-6-nitro-2H-indazole-3-carbonitrile 1-oxide
Rendement 108.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-n2cc3cc(C4CC4)c([N+](=O)[O-])cc3n2)nc1
Reaction #91810
( ii )
Rendement 43.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(C)c([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #161137
5-methyl-2,4-dinitro-benzoic acid ethyl ester
Rendement 25.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(C=CN(C)C)c([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #161138
5-(2-dimethylamino-vinyl)-2,4-dinitro-benzoic acid ethyl ester
Rendement 32.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc2cc[nH]c2cc1N
Reaction #161139
6-amino-1H-indole-5-carboxylic acid ethyl ester
Rendement 30.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(N(CCCl)CCCl)c([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #178511
DOI: 10.1039/C8SC04228D
O=C(NCCO)c1c([N+](=O)[O-])cc([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #194903
DOI: 10.1039/C8SC04228D
CCCCSc1cc([N+](=O)[O-])cc(C(O)=NC)c1C(=O)O
Reaction #237217
DOI: 10.1039/C8SC04228D
N#Cc1ccc([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #245232
DOI: 10.1039/C8SC04228D
N#Cc1ccc([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #268695
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1ccc(CO)c([N+](=O)[O-])c1
Reaction #280484
DOI: 10.1039/C8SC04228D
Cc1cc([N+](=O)[O-])c(Cl)c([N+](=O)[O-])c1C(N)=O
Reaction #287052
DOI: 10.1039/C8SC04228D
O=Cc1cc(Br)c([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #293875
DOI: 10.1039/C8SC04228D
COC1C=C(C)C(=O)CC(C)(C)C1OC(=O)c1ccc([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #300254
DOI: 10.1039/C8SC04228D
O=C(NC(=O)c1ccc([N+](=O)[O-])cc1[N+](=O)[O-])Nc1ccc(Oc2ccc(Br)nn2)c(Cl)c1
Reaction #318248
desired product
Rendement 40.7%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1ccc([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #322242
title compound
Rendement 89.0%DOI: 10.6084/m9.figshare.5104873.v1
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