Copper-Catalyzed Enantioselective Radical Esterification of Propargylic C–H Bonds

Author:

Zhu Xiaotao1,Bao HongliORCID,Xi Jiajia

Affiliation:

1. Key Laboratory of Coal to Ethylene Glycol and Its Related Technology, Center for Excellence in Molecular Synthesis, Fujian Institute of Research on the Structure of Matter

Abstract

AbstractThe copper-catalyzed enantioselective radical esterification of propargylic C–H bonds with tert-butyl peroxybenzoate (TBPB) as an oxidizing agent and an oxygenated nucleophile is reported. This variant of the Kharasch–Sosnovsky oxidation allows for the asymmetric esterification of open-chain carbon radicals without excessive amounts of alkyne substrates under mild reaction conditions, achieving a one-step conversion of simple alkynes into chiral propargylic esters.

Funder

National Natural Science Foundation of China

China Postdoctoral Science Foundation

Publisher

Georg Thieme Verlag KG

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