Transition-metal-free sulfonylations of methylthiolated alkynones to synthesize 3-sulfonylated thioflavones

A set of transition-metal-free NaI/TBHP-mediated sulfonylation cyclization reactions of methylthiolated alkynones with sulfonyl hydrazides was developed, by which various 3-sulfonylated thioflavones were prepared under mild reaction conditions. The features of this procedure included metal-free reaction conditions, ease of reagent handling, short reaction times, and a broad functional group tolerance. A set of transition-metal-free NaI/TBHP-mediated sulfonylation cyclization reactions of methylthiolated alkynones with sulfonyl hydrazides was developed, by which various 3-sulfonylated thioflavones were prepared under mild reaction conditions.