Pd-Catalyzed Alkynylation of 2‑Chloroacetates and 2‑Chloroacetamides with Potassium Alkynyltrifluoroborates

Abstract

The synthesis of β,γ-alkynyl esters and amides using air-stable potassium alkynyltrifluoroborates as nucleophilic partners in a mild Suzuki–Miyaura cross-coupling reaction has been achieved. Propargyl esters and amides were obtained in high yields using a low catalyst loading, and the substrate scope of the reaction has been significantly improved over previous methods