Sulfoxidation of alkenes and alkynes with NFSI as a radical initiator and selective oxidant

Chem Commun (Camb). 2016 Dec 20;53(1):184-187. doi: 10.1039/c6cc08631d.

Abstract

Sulfoxides are important functional molecules. We develop a short-route (one-pot) synthesis of this class of molecules by reacting thiols with alkenes or alkynes under mild and metal-free conditions. N-Fluorobenzenesulfonimide (NFSI) is used to play dual roles: as a radical initiator for a thiol-ene/-yne reaction to form sulfide adducts, and as efficient oxidant for conversion of the sulfides formed in situ to sulfoxides. Over-oxidation of the sulfoxides to sulfones is avoided in our approach.

Publication types

  • Research Support, Non-U.S. Gov't