Chromium(II)-Catalyzed Defluorinative Reductive Cross-Coupling of Acetals with α-Trifluoromethyl Alkenes

Abstract

We report here the chromium(II)-catalyzed defluorinative reductive cross-coupling reaction of acetals with α-trifluoromethyl alkenes. α-Alkoxyalkyl radicals are generated from acetals under the synergistic effect of catalytic chromium and trimethylsilyl chloride. Subsequent selective cross-coupling of the radicals with α-trifluoromethyl alkenes provides a synthetic route to gem-difluoroalkenes that contain an alkoxy-substituent at the homoallylic position.

Supplementary files

Article information

Article type
Communication
Submitted
02 Apr 2025
Accepted
06 May 2025
First published
07 May 2025

Org. Biomol. Chem., 2025, Accepted Manuscript

Chromium(II)-Catalyzed Defluorinative Reductive Cross-Coupling of Acetals with α-Trifluoromethyl Alkenes

Z. Li, M. Luo and X. Zeng, Org. Biomol. Chem., 2025, Accepted Manuscript , DOI: 10.1039/D5OB00547G

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