Direct sulfamidation of 1,4-naphthoquinones using -methoxy sulfonamides under metal-free conditions in water was developed. Base-mediated nucleophilic addition of -methoxy sulfonamides, followed by N-O bond cleavage allowed the formation of enesulfonamides. Further, the synthesis of pyrrolonaphthoquinones proved the practicability of the current approach.

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http://dx.doi.org/10.1021/acs.joc.3c01409DOI Listing

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