Recherche de Sous-structure

Nc1cc(-c2ccccc2)ccc1O

COC(=O)c1cc(-c2ccccc2)c(F)c(N)c1OC
Reaction #45800
compound
Rendement 92.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C#N)cc(-c2ccccc2)c(F)c1N
Reaction #45801
compound
Rendement 92.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(N)c(F)c(-c2ccccc2)c(Br)c1C#N
Reaction #45802
compound
Rendement 89.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(N)c(F)c(-c2ccccc2)c(C)c1C#N
Reaction #45803
5-Amino-6-fluoro-4-methoxy-2-methylbiphenyl-3-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C#N)c(C)c(-c2ccccc2)c(F)c1NC(=O)C(C)(C)C
Reaction #45804
N-(5-Cyano-2-fluoro-4-methoxy-6-methylbiphenyl-3-yl)-2,2-dimethylpropionamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C#N)c(O)c(NC(=O)C(C)(C)C)c(F)c1-c1ccccc1
Reaction #45805
compound
Rendement 65.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)c(F)c2nc(C(C)(C)C)oc2c1C#N
Reaction #45806
compound
Rendement 90.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2ccc(I)c3c2CNC3=O)cc([N+](=O)[O-])c1O
Reaction #49380
7-iodo-4-(4-hydroxy-3-methoxy-5-nitrophenyl)isoindolinone
Rendement 31.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2cccc(-c3cccc(C(F)(F)F)n3)c2)cc([N+](=O)[O-])c1O
Reaction #70919
3-methoxy-5-nitro-3′-(6-(trifluoromethyl)pyridin-2-yl)biphenyl-4-ol
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(-c2cccc(-c3cccc(C(F)(F)F)n3)c2)cc(O)c1O
Reaction #70920
5-nitro-3′-(6-(trifluoromethyl)pyridin-2-yl)biphenyl-3,4-diol
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2cccc(-c3cccc(C(F)(F)F)n3)c2)cc([N+](=O)[O-])c1O
Reaction #90265
3-methoxy-5-nitro-3′-(6-(trifluoromethyl)pyridin-2-yl)biphenyl-4-ol
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(-c2cccc(-c3cccc(C(F)(F)F)n3)c2)cc(O)c1O
Reaction #90266
5-nitro-3′-(6-(trifluoromethyl)pyridin-2-yl)biphenyl-3,4-diol
DOI: 10.6084/m9.figshare.5104873.v1
CCC(C)COc1ccc(-c2ccc(C(=O)O)cc2)cc1[N+](=O)[O-]
Reaction #175883
DOI: 10.1039/C8SC04228D
CCCCCCC(C)Oc1ccc(-c2ccc(C(=O)OC)cc2)cc1N
Reaction #178615
DOI: 10.1039/C8SC04228D
O=C(Nc1cc(-c2ccccc2)ccc1O)c1ccc(C(C(=O)Nc2ccccc2)C(=O)Nc2ccccc2)cc1
Reaction #189628
DOI: 10.1039/C8SC04228D
CC1Oc2ccc(-c3ccccc3)cc2N=C1N
Reaction #192996
DOI: 10.1039/C8SC04228D
CCCCCCC(C)Oc1ccc(OCc2ccccc2)c([N+](=O)[O-])c1
Reaction #197135
DOI: 10.1039/C8SC04228D
CCCCCCC(C)Oc1cc([N+](=O)[O-])c(-c2ccc(C(=O)OC)cc2)cc1N(C)C
Reaction #198317
DOI: 10.1039/C8SC04228D
COC(=O)CCCCCOc1ccc(-c2ccc(C#N)cc2)cc1N
Reaction #202378
DOI: 10.1039/C8SC04228D
O=C(Nc1cc(-c2ccccc2)ccc1O)c1ccc(Cl)c([N+](=O)[O-])c1
Reaction #204677
DOI: 10.1039/C8SC04228D
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