Asymmetric epoxidation of fujorinated allylic alcohols

C. Gosmini, T. Dubuffet, R. Sauvêtre, J. F. Normant

Research output: Contribution to journalArticlepeer-review

Abstract

The asymmetric epoxidation of an α,β-difluoro primary allylic alcohol, and of two α-fluoro secondary allylic alcohols follows the pattern known with non fluorinated analogs. The fluoro epoxides thus formed can be transformed into chiral α-ketols and into an α-fluoroacid.

Original languageEnglish
Pages (from-to)223-230
Number of pages8
JournalTetrahedron Asymmetry
Volume2
Issue number3
DOIs
Publication statusPublished - 1 Jan 1991
Externally publishedYes

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