Busqueda de Subestructura

94576

Cc1cc2c(c([N+](=O)[O-])c1)N(c1ccccc1C(=O)O)CC2
Reaction #4119
product
Rendimiento 32.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2c(c([N+](=O)[O-])c1)N(c1ccccc1C(=O)O)CC2
Reaction #4177
product
Rendimiento 32.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(F)cc(-c2cc(N)c3c(c2)C2(CCCCC2)C(=O)N3)c1
Reaction #7101
title compound
Rendimiento 52.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(N)c([N+](=O)[O-])cc(-c2ccn(C)c(=O)c2)c1F
Reaction #40529
title compound
Rendimiento 25.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(C)C)cc1-c1ccc(C(F)(F)F)cc1CNCc1cc([N+](=O)[O-])cc(C(F)(F)F)c1
Reaction #45330
{[5′-isopropyl-2′-methoxy-4-(trifluoromethyl)biphenyl-2-yl]methyl}[3-nitro-5-(trifluoromethyl)benzyl]amine
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N(Cc1cc([N+](=O)[O-])cc(C(F)(F)F)c1)Cc1cc(C(F)(F)F)ccc1-c1cc(C(C)C)ccc1OC
Reaction #45331
methyl {[5′-isopropyl-2′-methoxy-4-(trifluoromethyl)biphenyl-2-yl]methyl}[3-nitro-5-(trifluoromethyl)benzyl]carbamate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C#N)c(N)c([N+](=O)[O-])c(N2CC[C@H](N(C)C)C2)c1-c1ccccc1
Reaction #45831
compound
Rendimiento 90.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C#N)c(N)c(N)c(N2CC[C@H](N(C)C)C2)c1-c1ccccc1
Reaction #45832
compound
Rendimiento 97.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(C(F)(F)F)cc([N+](=O)[O-])c1O
Reaction #56525
2-hydroxy-3-nitro-5-trifluoromethylbenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2c(c([N+](=O)[O-])c1)N(c1ccccc1C(=O)O)CC2
Reaction #63405
product
Rendimiento 32.0%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1c(-c2ccc(F)cc2)oc2cc([N+](=O)[O-])c(-c3cc(C(=O)NC(C)(C)C)cc([N+](=O)[O-])c3)cc12
Reaction #86034
5-(3-(tert-butylcarbamoyl)-5-nitrophenyl)-2-(4-fluorophenyl)-N-methyl-6-nitrobenzofuran-3-carboxamide
Rendimiento 75.7%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1c(-c2ccc(F)cc2)oc2cc(N)c(-c3cc(N)cc(C(=O)NC(C)(C)C)c3)cc12
Reaction #86035
6-amino-5-(3-amino-5-(tert-butylcarbamoyl)phenyl)-2-(4-fluorophenyl)-N-methylbenzofuran-3-carboxamide
Rendimiento 64.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(C(C)(C)C)c([N+](=O)[O-])cc1O
Reaction #161166
2,4-di-tert-butyl-5-nitro-phenol
Rendimiento 29.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(-c2nc3ccccc3o2)cc(C(F)(F)F)c1F
Reaction #161458
title compound
Rendimiento 54.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)c2cc(N)cc(C(F)(F)F)c2)CC1
Reaction #173000
DOI: 10.1039/C8SC04228D
CC(C)(C)c1cc(C(C)(C)C)c([N+](=O)[O-])cc1O
Reaction #173238
DOI: 10.1039/C8SC04228D
CCc1cc([N+](=O)[O-])cc(CC)c1-c1cc(S(N)(=O)=O)ccc1C
Reaction #175679
DOI: 10.1039/C8SC04228D
COc1c(-c2ccc(C(=O)O)s2)cc(C)cc1[N+](=O)[O-]
Reaction #177008
DOI: 10.1039/C8SC04228D
CN(C(=O)c1cc(C(=O)O)cc([N+](=O)[O-])c1)C(CO)(CO)CO
Reaction #180220
DOI: 10.1039/C8SC04228D
Nc1cc(C(=O)Nc2cc(S(=O)(=O)O)cc3cc(S(=O)(=O)O)cc(S(=O)(=O)O)c23)cc(C(=O)Nc2cc(S(=O)(=O)O)cc3cc(S(=O)(=O)O)cc(S(=O)(=O)O)c23)c1
Reaction #180659
DOI: 10.1039/C8SC04228D
Página 1Siguiente