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260411

Cn1c(=O)n(-c2ccc(C3(C(=O)N4CCC5(C4)OC(=O)c4cnccc45)CC3)cc2)c2ccccc21
Reaction #211211
DOI: 10.1039/C8SC04228D
CC(C)c1ccc(-n2ccnc2O[C@H](C)[C@@]2(c3ccc(F)cc3F)CO2)cc1
Reaction #216307
(2R)-2-(2,4-difluorophenyl)-2-[(1R)-1-[1-(4-isopropylphenyl)-2-imidazolyloxy]ethyl] oxiran
Ausbeute 13.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C#N)c1ccc(-n2c(=O)[nH]c3cnc4ccc(Br)cc4c32)cc1
Reaction #563342
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C#N)c1ccc(-n2c(=O)[nH]c3cnc4ccc(Cl)cc4c32)cc1
Reaction #563343
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2ncc3[nH]c(=O)n(-c4ccc(C(C)(C)C#N)cc4)c3c2c1
Reaction #563344
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C#N)c1ccc(-n2c(=O)n(S(=O)(=O)c3ccc(OC(F)(F)F)cc3)c3cnc4ccc(Br)cc4c32)cc1
Reaction #563345
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C#N)c1ccc(-n2c(=O)n(S(=O)(=O)c3ccccc3C#N)c3cnc4ccc(Br)cc4c32)cc1
Reaction #563346
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(S(=O)(=O)n2c(=O)n(-c3ccc(C(C)(C)C#N)cc3)c3c4cc(Br)ccc4ncc32)c1
Reaction #563347
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc([N+](=O)[O-])cc1S(=O)(=O)n1c(=O)n(-c2ccc(C(C)(C)C#N)cc2)c2c3cc(Br)ccc3ncc21
Reaction #563348
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2c(=O)n(-c3ccc(C(C)(C)C#N)cc3)c3c4cc(Br)ccc4ncc32)cc1F
Reaction #563349
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C)cc(S(=O)(=O)n2c(=O)n(-c3ccc(C(C)(C)C#N)cc3)c3c4cc(Br)ccc4ncc32)c1
Reaction #563350
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C#N)c1ccc(-n2c(=O)n(S(=O)(=O)c3ccccc3)c3cnc4ccc(Br)cc4c32)cc1
Reaction #563351
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2c(=O)n(-c3ccc(C(C)(C)C#N)cc3)c3c4cc(Br)ccc4ncc32)cc1
Reaction #563352
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C#N)c1ccc(-n2c(=O)n(S(=O)(=O)c3cccs3)c3cnc4ccc(Br)cc4c32)cc1
Reaction #563353
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C#N)c1ccc(-n2c(=O)n(S(=O)(=O)c3cccc(F)c3)c3cnc4ccc(Br)cc4c32)cc1
Reaction #563354
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C#N)c1ccc(-n2c(=O)n(S(=O)(=O)c3cccc4cccnc34)c3cnc4ccc(Br)cc4c32)cc1
Reaction #563355
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc(S(=O)(=O)n2c(=O)n(-c3ccc(C(C)(C)C#N)cc3)c3c4cc(Br)ccc4ncc32)cc1
Reaction #563356
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C#N)c1ccc(-n2c(=O)n(S(=O)(=O)c3cccc(C(F)(F)F)c3)c3cnc4ccc(Br)cc4c32)cc1
Reaction #563357
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(S(=O)(=O)n2c(=O)n(-c3ccc(C(C)(C)C#N)cc3)c3c4cc(Br)ccc4ncc32)c1
Reaction #563358
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C#N)c1ccc(-n2c(=O)n(S(=O)(=O)c3cccc(Br)c3)c3cnc4ccc(Br)cc4c32)cc1
Reaction #563359
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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