This study unveils a new catalytic crossover reaction of sulfinamides. Leveraging mild acid catalysis, the reaction demonstrates a high tolerance to structural variations, yielding equimolar products across diverse sulfinamide substrates. Notably, small sulfinamide libraries can be selectively oxidized to sulfonamides, providing a new platform for ligand optimization and discovery in medicinal chemistry. This crossover chemotype provides a new tool for high-throughput experimentation in discovery chemistry.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11165587 | PMC |
http://dx.doi.org/10.1021/acs.joc.4c00572 | DOI Listing |
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