N-Directed, Radical Relay Enantioconvergent Sulfinylation of Distal C(sp³)–H Bonds via Cobalt Catalysis

Cobalt-catalyzed enantioconvergent cross-coupling of C(sp³)-H bonds with <i>in situ</i>-generated sulfenate anions is achieved to access chiral sulfoxides, which are found in the structures of many biologically active agents. The more challenging aliphatic C-H bonds as well as sterically hindered substrates containing tertiary C-H bonds could also be tolerated well. Mechanistic studies indicate that the transformation could undergo a Co^IIS(O)R-mediated single-electron transfer with <i>N</i>-fluorocarboxamides, followed by a 1,5-hydrogen atom transfer and then a pivotal organocobalt(IV)-controlled enantioselective cross-coupling process. This novel asymmetric radical reaction for C-S bond construction could open a new door for the synthesis of sulfur-centered chiral compounds.