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238028

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
CCc1c(F)ccc(C#N)c1Cl
Reaction #332231
title compound
Ausbeute 28.2%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
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
CCCc1c(N2CCC(C(C)(C)O)C2C)ccc(C#N)c1Cl
Reaction #379758
DOI: 10.1039/C8SC04228D
CCc1c(N[C@@H](C(=O)O)[C@H](C)O)ccc(C#N)c1Cl
Reaction #557936
solid
Ausbeute 467.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(N[C@@H](C(=O)O)[C@@H](C)O)ccc(C#N)c1Cl
Reaction #558018
title compound
Ausbeute 47.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(F)c(CCO)c1Cl
Reaction #558073
2-chloro-4-fluoro-3-(2-hydroxyethyl)benzonitrile
Ausbeute 66.2%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(F)c(CCBr)c1Cl
Reaction #558074
title compound
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1c(NC(C(=O)O)C(C)O)ccc(C#N)c1Cl
Reaction #558075
title compound
Ausbeute 97.1%DOI: 10.6084/m9.figshare.5104873.v1
CCc1c(N[C@@H](C(=O)O)[C@H](C)O)ccc(C#N)c1Cl
Reaction #650381
solid
Ausbeute 467.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(N[C@@H](C(=O)O)[C@@H](C)O)ccc(C#N)c1Cl
Reaction #650474
title compound
Ausbeute 47.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(F)c(CCO)c1Cl
Reaction #650537
2-chloro-4-fluoro-3-(2-hydroxyethyl)benzonitrile
Ausbeute 66.2%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(F)c(CCBr)c1Cl
Reaction #650538
title compound
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1c(NC(C(=O)O)C(C)O)ccc(C#N)c1Cl
Reaction #650539
title compound
Ausbeute 97.1%DOI: 10.6084/m9.figshare.5104873.v1
CCc1c(N2CCC(C(C)(C)O)C2C)ccc(C#N)c1Cl
Reaction #782110
DOI: 10.1039/C8SC04228D
CCc1c(N2CCC(O)C2C)ccc(C#N)c1Cl
Reaction #1020245
DOI: 10.1039/C8SC04228D
N#Cc1ccc(F)c(CCO)c1Cl
Reaction #1213456
DOI: 10.1039/C8SC04228D
CCc1c(N[C@@H](C(=O)O)[C@H](C)O)ccc(C#N)c1Cl
Reaction #1341830
solid
Ausbeute 467.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(N[C@@H](C(=O)O)[C@@H](C)O)ccc(C#N)c1Cl
Reaction #1341923
title compound
Ausbeute 47.0%DOI: 10.6084/m9.figshare.5104873.v1
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