Abstract
Herein, we report the development of a FSO2 radical-initiated tandem cyclization reaction under visible light photoredox catalysis, which allows for a facile access to FSO2-functionalized oxindoles from N-aryl acrylamides. This reaction features mild reaction conditions, readily available starting materials, and SuFExable products. The introduction of sulfonyl fluoride groups into oxindoles could be of interest for the related study in the context of discovering new bioactive molecules.
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