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.
Authors
- On Ying Yuen (ORCID: https://orcid.org/0000-0002-4330-0543)
- Shan Shan Ng
- Zifang Peng
- Changxue Gu
- Chau Ming So (ORCID: https://orcid.org/0000-0001-6268-651X)
Institutions
- Hong Kong Polytechnic University (HK)
Publication Details
- 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
Funders
- Hong Kong Polytechnic University