Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/118486
Title: Palladium-catalyzed chemoselective direct arylation of polyfluoroarenes with chloroaryl triflates at the C–Cl bond
Authors: Peng, Z 
Gu, C 
Yuen, OY 
Ng, SS 
So, CM 
Issue Date: 15-Dec-2025
Source: Chemistry, an Asian journal, 15 Dec. 2025, v. 20, no. 24, e00949
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.
Keywords: Chemoselectivity
Chloroaryl triflates
Direct arylation
Phosphine ligand
Polyfluoroarene
Publisher: Wiley-VCH
Journal: Chemistry, an Asian journal 
ISSN: 1861-4728
EISSN: 1861-471X
DOI: 10.1002/asia.202500949
Appears in Collections:Journal/Magazine Article

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