Palladium-Catalyzed Linear Hydrothiocarbonylation of Unactivated Terminal Alkenes: Synthesis of Aliphatic Thioesters

A Pd-catalyzed hydrothiocarbonylation of unactivated terminal alkenes is presented. According to this protocol, aliphatic thioesters were synthesized with exclusive linear selectivity under mild reaction conditions. Good to excellent yields (up to 91% yield), broad substrate scope, broad functional group tolerance, and utility of the method demonstrated the advantages of this protocol.

Automated summary

This method utilizes palladium catalysis to synthesize aliphatic thioesters with exclusive linear selectivity, achieving good to excellent yields (up to 91%) and demonstrating broad substrate scope, functional group tolerance, and practicality, showcasing its advantages for various applications.