Abstract

AbstractA novel and regioselective ammonium iodide mediated C−S bond formation protocol involving flavones and sulfonyl chlorides to generate different ArS‐substituted flavone derivatives in high yields was developed. Different from existing metal‐free C−S bond formation protocols with the use of PPh3 or I2 as the catalyst, this method provides an alternative way of constructing C−S bonds through the use of NH4I as a catalyst, which makes it highly valuable for the efficient synthesis of thioether compounds.

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