A novel Fe-catalyzed fluorosulfonylation of alkenes with
Na2S2O4 and N-fluorobenzenesulfonimide
(NFSI) for assembling various lactam-functionalized alkyl sulfonyl
fluorides is disclosed. In this reaction, Na2S2O4 acts as both an SO2 source and a reductant.
Furthermore, the resulting products can be efficiently transformed
into valuable chemicals, including sulfonyl esters and sulfonamides,
via the sulfur(VI) fluoride exchange (SuFEx) click reaction. Preliminary
mechanistic studies suggest that the transformation proceeds through
intramolecular radical cyclization, SO2 insertion, sulfite
anion formation, and fluorination.