Palladium-catalyzed transformation enhances functionalization in polyfluoroarenes, suggesting broad utility for new compounds.
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.
No takes yet. Share an insight, caveat, or question.
Peng et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: