Abstract
We report a Cu(I)-photocatalyzed three-component coupling process to achieve the regioselective, vicinal 1,2-aminosulfonylations of alkenes. The critical aspect of this methodology is found in the utilization of in situ generated photoactive Cu(I)-amine substrate com-plexes, which facilitate the formal oxidation of Cu(I) to Cu(III) in a stepwise manner. In this way, the conceivable two-component chlorosulfonylation of alkenes is effectively suppressed, allowing the combination of styrenes, sulfonyl chlorides, and amines. Further-more, this protocol can be used to facilitate late-stage functionalization, thereby enabling the diversification of biomolecules
Supplementary materials
Title
Supporting Information
Description
Experimental Procedures, Spectroscopical Data, Copies of NMR spectra.
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