Substructure Search

Cc1cc(-c2ccccc2)cc(N)c1N

N#Cc1cc(F)cc(-c2cc(N)c3c(c2)C2(CCCCC2)C(=O)N3)c1
Reaction #7101
title compound
Yield 52.2%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
Yield 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
Yield 97.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C#N)c(N)c(NC(=O)C(C)(C)C)c(N2CC[C@H](N(C)C)C2)c1-c1ccccc1
Reaction #45833
compound
Yield 43.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)c(N2CC[C@H](N(C)C)C2)c2[nH]c(C(C)(C)C)nc2c1C#N
Reaction #45834
2-tert-Butyl-7-[(3S)-3-(dimethylamino)pyrrolidin-1-yl]-5-methyl-6-phenyl-1H-benzimidazole-4-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2ccccc2F)cc([N+](=O)[O-])c1NO
Reaction #175840
DOI: 10.1039/C8SC04228D
Nc1cc(-c2ccccc2C(F)(F)F)cc(C(F)(F)F)c1N
Reaction #258602
DOI: 10.1039/C8SC04228D
N#Cc1cc(F)cc(-c2cc(N)c3c(c2)C2(CCCCC2)C(=O)N3)c1
Reaction #402027
DOI: 10.1039/C8SC04228D
CCOC(=O)N1CCC2C(C1)c1cc(-c3ccc(Cl)cc3Cl)cc3c1N2CC(C)N3C(=O)OCC
Reaction #404402
DOI: 10.1039/C8SC04228D
CN1CCN2c3c(cc(-c4ccc(Cl)cc4Cl)cc31)[C@@H]1CN(C(=O)OC(C)(C)C)CC[C@@H]12
Reaction #437978
tert-butyl (6bR,10aS)-5-(2,4-dichlorophenyl)-3-methyl-2,3,6b,9,10,10a-hexahydro-1H-pyrido[3′,4′:4,5]pyrrolo[1,2,3-de]quinoxaline-8(7H)-carboxylate
Yield 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN2c3c(cc(-c4ccc(Cl)cc4Cl)cc31)[C@@H]1CNCC[C@@H]12
Reaction #437979
title compound
Yield 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC[C@H]2[C@@H](C1)c1cc(-c3ccc(Cl)cc3Cl)cc3c1N2CCN3
Reaction #437980
Tert-butyl (6bR,10aS)-5-(2,4-dichlorophenyl)-2,3,6b,9,10,10a-hexahydro-1H-pyrido[3′,4′:4,5]pyrrolo[1,2,3-de]quinoxaline-8(7H)-carboxylate
Yield 61.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1CCC2C(C1)c1cc(-c3ccc(Cl)cc3Cl)cc3c1N2CC(C)N3C(=O)OCC
Reaction #437998
diethyl 5-(2,4-dichlorophenyl)-2-methyl-6b,9,10,10a-tetrahydro-1H-pyrido[3′,4′:4,5]pyrrolo[1,2,3-de]quinoxaline-3,8(2H,7H)-dicarboxylate
Yield 29.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CN2c3c(cc(-c4ccc(Cl)cc4Cl)cc3C3CNCCC32)N1
Reaction #437999
5-(2,4-dichlorophenyl)-2-methyl-2,3,6b,7,8,9,10,10a-octahydro-1H-pyrido[3′,4′:4,5]pyrrolo[1,2,3-de]quinoxaline
Yield 45.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(F)cc(-c2cc(N)c3c(c2)C2(CCCCC2)C(=O)N3)c1
Reaction #483432
title compound
Yield 52.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2ccccc2)cc([N+](=O)[O-])c1N
Reaction #539354
4-amino-3-methyl-5-nitrobiphenyl
Yield 81.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2ccccc2)cc(N)c1N
Reaction #539355
3,4-diamino-5-methylbiphenyl
Yield 100.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2cc(-c3ccccc3)cc(C)c2[nH]1
Reaction #539356
title compound
Yield 96.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2ccccc2F)cc([N+](=O)[O-])c1NO
Reaction #732116
N-(2′-Fluoro-5-methyl-3-nitro-biphenyl-4-yl)-hydroxylamine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC2C(C1)c1cc(-c3ccc(Cl)cc3Cl)cc3c1N2CCN3
Reaction #762307
DOI: 10.1039/C8SC04228D
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