Issue 12, 1996

Addition of organolithium reagents to α-(trifluoromethyl)styrene: concise synthesis of functionalised gem-difluoroalkenes

Abstract

The treatment of α-(trifluoromethyl)styrene with organolithium reagents results in the selective formation of gem-difluoroalkenes in good-to-excellent yields. This reaction has been applied to the synthesis of 3-gem-difluoro-2-phenylallylic amines and other functionalised gem-difluoroalkenes.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1996, 1409-1413

Addition of organolithium reagents to α-(trifluoromethyl)styrene: concise synthesis of functionalised gem-difluoroalkenes

J. Bégué, D. Bonnet-Delpon and M. H. Rock, J. Chem. Soc., Perkin Trans. 1, 1996, 1409 DOI: 10.1039/P19960001409

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