Journal of Fluorine Chemistry p. 99 - 104 (1997)
Update date:2022-08-28
Topics:
Xiao, Ling
Kitazume, Tomoya
The stereoselective synthesis of 3-fluoro-2-alkenoic acids was achieved by the reaction of lithium 3,3,3-trifluoropropionate with Grignard reagents. 2,2,2-Trifluoroethyl alkyl ketones were prepared by the reaction of 3,3,3-trifluoropropionic acid chloride with either lithium dialkylcuprates or magnesium dialkylcuprates. Optically active 1,1,1-trifluoro-3-alkanols were obtained by the enzymatic hydrolysis of the corresponding acetates.
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