136848-08-3Relevant articles and documents
Synthesis of the Two Enantiomers of 1-Chloro-1,1-difluoro-3-(p-tolylsulphonyl)propan-2-ol by Microbial Reduction of the Parent Propanone and Transformation into 3,3-Difluorotetrahydrofuran Derivatives
Arnone, Alberto,Bernardi, Rosanna,Bravo, Pierfrancesco,Cardillo, Rosanna,Ghiringhelli, Dario,Cavicchio, Giancarlo
, p. 1887 - 1892 (2007/10/02)
Both R and S enantiomers of 1-chloro-1,1-difluoro-3-(p-tolylsulphonyl)propan-2-ol were obtained with high enantioselection by microbial reduction of 1-chloro-1,1-difluoro-3-(p-tolylsulphonyl)-propan-2-one.The enantiomerically pure R-alcohol was obtained a