Facile access to multi-substituted trifluoromethyl alkenes via dehydroxyfluorination of 3,3-difluoroallyl alcohols

Abstract

The dehydroxyfluorination of allylic alcohols stands as one of the most direct and effective methods for synthesizing versatile allylic fluorides. However, regioselectivity control in this transformation remains challenging. Herein, we demonstrate a fluorine effect-induced regiospecific dehydroxyfluorination of 3,3-difluoroallyl alcohols using Olah's reagent under mild reaction conditions.

Graphical abstract: Facile access to multi-substituted trifluoromethyl alkenes via dehydroxyfluorination of 3,3-difluoroallyl alcohols

Supplementary files

Article information

Article type
Paper
Submitted
30 Jul 2025
Accepted
26 Aug 2025
First published
26 Aug 2025

Org. Biomol. Chem., 2025, Advance Article

Facile access to multi-substituted trifluoromethyl alkenes via dehydroxyfluorination of 3,3-difluoroallyl alcohols

Z. Li, Z. Wang, C. Wang, J. Zhang and C. Feng, Org. Biomol. Chem., 2025, Advance Article , DOI: 10.1039/D5OB01233C

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