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159147

CC1C(C(C)(C)O)CCN1c1ccc(C#N)c(Cl)c1C#N
Reaction #243745
DOI: 10.1039/C8SC04228D
N#Cc1ccc(F)c(C#N)c1Cl
Reaction #256930
DOI: 10.1039/C8SC04228D
CC1C(C(C)(C)O)CCN1c1ccc(C#N)c(Cl)c1CO
Reaction #287721
DOI: 10.1039/C8SC04228D
CCCc1c(N[C@@H](C(=O)O)[C@H](C)O)ccc(C#N)c1Cl
Reaction #325747
crude product
Ausbeute 13.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(N[C@@H](C(=O)O)[C@H](OCc2ccccc2)C(F)(F)F)ccc(C#N)c1Cl
Reaction #325759
(2R,3S)-3-(benzyloxy)-2-(3-chloro-4-cyano-2-methylphenylamino)-4,4,4-trifluorobutanoic acid
Ausbeute 21.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(F)ccc(C#N)c1Cl
Reaction #332230
title compound
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1c(F)ccc(C#N)c1Cl
Reaction #332231
title compound
Ausbeute 28.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(N[C@H]2CCC[C@@]2(C)O)ccc(C#N)c1Cl
Reaction #332250
title compound
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(NC2CCCC2(C)O)ccc(C#N)c1Cl
Reaction #332251
2-Chloro-4-[[2-hydroxy-2-methyl-cyclopentyl]amino]-3-methyl-benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
CCc1c(N[C@H]2CCCC2(C)O)ccc(C#N)c1Cl
Reaction #332252
2-Chloro-3-ethyl-4-[[(1S)-2-hydroxy-2-methyl-cyclopentyl]amino]benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(N[C@@H]2COC[C@@H]2O)ccc(C#N)c1Cl
Reaction #332253
title compound
Ausbeute 19.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(N[C@@H]2CC[C@H](O)[C@@]2(C)O)ccc(C#N)c1Cl
Reaction #332255
title compound
Ausbeute 6.4%DOI: 10.6084/m9.figshare.5104873.v1
CCc1c(N[C@@H]2CC[C@@H](O)[C@@]2(C)O)ccc(C#N)c1Cl
Reaction #332256
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(N[C@@H]2CCCC[C@@H]2O)ccc(C#N)c1Cl
Reaction #332257
title compound
Ausbeute 29.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(N[C@H]2CCCC[C@H]2O)ccc(C#N)c1Cl
Reaction #332258
title compound
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1c(N2CCC(C(C)(C)O)C2C)ccc(C#N)c1Cl
Reaction #379758
DOI: 10.1039/C8SC04228D
Cc1c(N2CCC(C(C)(C)O)C2C)ccc(C#N)c1Cl
Reaction #389583
DOI: 10.1039/C8SC04228D
Cc1c(F)ccc(C#N)c1Cl
Reaction #407302
DOI: 10.1039/C8SC04228D
Cc1c(N[C@@H](C(=O)O)[C@H](C)O)ccc(C#N)c1Cl
Reaction #557915
(2R,3S)-2-(3-chloro-4-cyano-2-methylphenylamino)-3-hydroxybutanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(N[C@@H](C(=O)O)[C@@H](C)O)ccc(C#N)c1Cl
Reaction #557918
(2R,3R)-2-(3-chloro-4-cyano-2-methylphenylamino)-3-hydroxybutanoic acid
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1
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