Author(s) Wang, X.; Wang, B.; Yin, X.; Yu, W.; Liao, Y.; Ye, J.; Wang, M.; Hu, L.; Liao, J.
Journal Angew Chem Int Ed Engl
Date Published 2019 08 26
Abstract

A highly enantioselective thiocarbonylation of styrenes with CO and thiols has been achieved by Pd catalysis, providing highly enantioenriched thioesters in good to excellent yields. Key to the successful execution of this reaction is the use of a chiral sulfoxide-(P-dialkyl)-phosphine (SOP) ligands. This thiocarbonylation proceeds smoothly under mild reaction conditions (1 atm CO and 0 °C) and displays broad substrate scope. Also demonstrated is that this transformation can be conducted using surrogates of CO, greatly increasing the safety aspects of running the reaction. The generality and utility of the method is manifested by its application to the synthetic transformations of thioester products and the direct acylation of cysteine-containing dipeptides. A primary mechanism was investigated and a plausible catalytic cycle was proposed.

DOI 10.1002/anie.201905905
ISSN 1521-3773
Citation Angew Chem Int Ed Engl. 2019;58(35):1226412270.