INTRODUCTION OF CENTER OF CHIRALITY INTO FLUOROCOMPOUNDS BY MICROBIAL TRANSFORMATION OF 2,2,2-TRIFLUOROETHANOL

DOI: 10.1246/cl.1984.1815

Source and publish data:

Chemistry Letters p. 1815 - 1818 (1984)

Update date:2022-07-30

Topics:

Authors:

Kitazume, Tomoya

Ishikawa, Nobuo

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Article abstract of DOI:10.1246/cl.1984.1815

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.

Full text of DOI:10.1246/cl.1984.1815

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