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 |
Show full item record
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.



