Radical Promoted C(sp²)–S Formation and C(sp³)–S Bond Cleavage: Access to 2-Substituted Thiochromones

Abstract

A radical-promoted cyclization of methylthiolated alkynones with diverse radical precursors has been developed. This strategy occurred via a C(sp²)-S bond formation and C(sp³)-S cleavage sequence and allows an efficient synthesis of a variety of phosphoryl-, sulfenyl-, CF₂COOEt-, and acyl-containing thiochromone derivatives in moderate to good yields under mild conditions.