Nickel-catalyzed reductive coupling of secondary alkyl bromides with alkynes to construct allylic difluoromethyl alkenes

Abstract

We report a highly efficient and broadly applicable nickel-hydride-catalyzed reductive cross-coupling of unactivated CF2H-substituted electrophiles with diverse alkynes. The reaction proceeds with excellent catalytic efficiency and functional group tolerance, providing a powerful platform for the late-stage fluoroalkylation of complex drug molecules.

Graphical abstract: Nickel-catalyzed reductive coupling of secondary alkyl bromides with alkynes to construct allylic difluoromethyl alkenes

Supplementary files

Article information

Article type
Communication
Submitted
07 Nov 2025
Accepted
15 Dec 2025
First published
22 Dec 2025

Chem. Commun., 2026, Advance Article

Nickel-catalyzed reductive coupling of secondary alkyl bromides with alkynes to construct allylic difluoromethyl alkenes

J. Dong, X. Wen, Y. Xu, J. Chen, Y. Yuan and X. Zeng, Chem. Commun., 2026, Advance Article , DOI: 10.1039/D5CC06347G

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