Palladium‐Catalyzed Chemoselective Direct Arylation of Polyfluoroarenes With Chloroaryl Triflates at the C–Cl Bond

This study describes a palladium-catalyzed chemoselective direct arylation of polyfluoroarenes with chloro(hetero)aryl triflates, achieving site-selective functionalization at the C-Cl bond for the first time. The recently developed alkyl-pyrazole-based phosphine ligand (BirdPhos) proved essential for the success of this transformation, affording excellent yields with high chemoselectivity. Moreover, the catalytic system enables the efficient synthesis of a broad range of functionalized polyfluoroarene derivatives under mild, additive-free conditions. Notably, the reaction retains the triflate group in the products, providing a versatile functional handle for further derivatization and highlighting the broad applicability and synthetic utility of this method.

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Journal
Chemistry - An Asian Journal
Published
2025-11-14
DOI
https://doi.org/10.1002/asia.202500949
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.00

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article

Palladium‐Catalyzed Chemoselective Direct Arylation of Polyfluoroarenes With Chloroaryl Triflates at the C–Cl Bond

On Ying Yuen, Shan Shan Ng, Zifang Peng, Changxue Gu et al.
Chemistry - An Asian Journal
Catalytic C–H Functionalization Methods
article

Palladium‐Catalyzed Chemoselective Direct Arylation of Polyfluoroarenes With Chloroaryl Triflates at the C–Cl Bond

On Ying Yuen, Shan Shan Ng, Zifang Peng, Changxue Gu, Chau Ming So
article en

Abstract

This study describes a palladium-catalyzed chemoselective direct arylation of polyfluoroarenes with chloro(hetero)aryl triflates, achieving site-selective functionalization at the C-Cl bond for the first time. The recently developed alkyl-pyrazole-based phosphine ligand (BirdPhos) proved essential for the success of this transformation, affording excellent yields with high chemoselectivity. Moreover, the catalytic system enables the efficient synthesis of a broad range of functionalized polyfluoroarene derivatives under mild, additive-free conditions. Notably, the reaction retains the triflate group in the products, providing a versatile functional handle for further derivatization and highlighting the broad applicability and synthetic utility of this method.

Chemistry - An Asian JournalVol. 20(24)
Hong Kong Polytechnic University (HK)
Hong Kong Polytechnic University
Openalex Percentile: Top 74%
Catalytic C–H Functionalization Methods
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