Busqueda de Subestructura

664

COc1ccc([N+](=O)[O-])cc1Nc1ncc(Cl)c(-c2cnn3ccccc23)n1
Reaction #515
Rendimiento 4.0%
COc1ccc([N+](=O)[O-])cc1Nc1ncc(Cl)c(-c2cnn3ccccc23)n1
Reaction #516
Rendimiento 4.0%
O=[N+]([O-])c1ccc(OCc2cccc(F)c2)c(Br)c1
Reaction #6912
title compound
Rendimiento 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(Oc2cc(N)c([N+](=O)[O-])cc2Br)cc1
Reaction #41619
compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1cccc1-c1cc([N+](=O)[O-])c(N)cc1Oc1ccc(S(C)(=O)=O)cc1
Reaction #41620
t-butyl 2-(4-amino-2-(4-methanesulfonyl-phenoxy)-5-nitro-phenyl)-pyrrole-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(N)cc1Br
Reaction #48162
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(N)cc1Br
Reaction #67427
off-white solid
Rendimiento 92.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(N)cc1Br
Reaction #170895
off-white solid
Rendimiento 92.6%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)CCOc1ccc(N)cc1Br
Reaction #173879
DOI: 10.1039/C8SC04228D
Cc1cc(Oc2ccc(F)cc2F)c(Br)cc1N
Reaction #185925
DOI: 10.1039/C8SC04228D
COc1ccc([N+](=O)[O-])cc1C1=CCN(C(=O)OC(C)(C)C)CC1
Reaction #193222
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1ccc(OCCO)c(Br)c1
Reaction #209791
DOI: 10.1039/C8SC04228D
COc1ccc([N+](=O)[O-])cc1N1C[C@@H](C)N[C@@H](C)C1
Reaction #217579
title product ( D1 )
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c([N+](=O)[O-])cc1Br
Reaction #217593
1-Bromo-2,4-bis(methyloxy)-5-nitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c([N+](=O)[O-])cc(Br)c(Oc2ccc(O)c(C(C)C)c2)c1Br
Reaction #224629
DOI: 10.1039/C8SC04228D
Cc1cc(Oc2c(Br)cc(N)c(C(F)(F)F)c2Br)cc(C(C)C)c1O
Reaction #231644
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1ccc(OC(F)F)c(Br)c1
Reaction #232937
DOI: 10.1039/C8SC04228D
CCOc1ccc([N+](=O)[O-])cc1Br
Reaction #232940
DOI: 10.1039/C8SC04228D
O=Cc1ccc(OC(F)F)c(Oc2ccc([N+](=O)[O-])cc2Br)c1
Reaction #235263
DOI: 10.1039/C8SC04228D
COc1ccc(N)cc1Br
Reaction #236417
DOI: 10.1039/C8SC04228D
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