INTRODUCTION OF CENTER OF CHIRALITY INTO FLUOROCOMPOUNDS BY MICROBIAL TRANSFORMATION OF 2,2,2-TRIFLUOROETHANOL
Chemistry LettersPublished 1 October 1984
Tomoya Kitazume, Nobuo Ishikawa
Citations39
SJR quartileQ3
SJR score0.37
SNIP0.40
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Abstract
Abstract 2,2,2-Trifluoroethanol is found to be a valuable synthetic tool proceeding to the chiral trifluoromethylated compounds via enantiotopic differentiating reaction and carbon-carbon bond formation with active fermenting baker’s yeast.
Keywords
Pharmacology, Toxicology and Pharmaceutics
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