Sulfones feature prominently in biologically active molecules and are key functional groups for organic synthesis. We report a mild, photoredox-catalyzed reaction for sulfonylation of aniline derivatives with sulfinate salts, and demonstrate the utility of the method by the late-stage functionalization of drugs. Key features of the method are the straightforward generation of sulfonyl radicals from bench-stable sulfinate salts and the use of simple aniline derivatives as convenient readily available coupling partners.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5868301 | PMC |
http://dx.doi.org/10.1039/c7sc03891g | DOI Listing |
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