Palladium-Catalyzed Defluorinative Coupling of Indoles with α,α-Difluoro-β,γ-Unsaturated Ketones: Direct Access to Functionalized α-Fluoroenones

Abstract

A palladium-catalyzed defluorinative coupling of indoles with α,α-difluoro-β,γ-unsaturated ketones is reported.This method provides direct access to a diverse range of functionalized (Z)-α-fluoroenones in moderate to excellent yields under mild conditions. The reaction exhibits broad substrate scope and functional group tolerance for both coupling partners, including electron-rich, electron-deficient, and sterically hindered indoles, as well as aryl, heteroaryl, and alkyl-substituted fluorinated ketones. It is operationally simple, scalable, and proceeds under ambient atmosphere.

Supplementary files

Article information

Article type
Communication
Submitted
10 Feb 2026
Accepted
31 Mar 2026
First published
02 Apr 2026

Org. Biomol. Chem., 2025, Accepted Manuscript

Palladium-Catalyzed Defluorinative Coupling of Indoles with α,α-Difluoro-β,γ-Unsaturated Ketones: Direct Access to Functionalized α-Fluoroenones

C. Chen, H. Zhu, Z. Luo, J. Hu, Z. Xiong, F. Zhou and J. Wu, Org. Biomol. Chem., 2025, Accepted Manuscript , DOI: 10.1039/D6OB00246C

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