Incorporation of the CF group into arenes has found increasing importance in drug discovery. Herein, we report the first photoredox-catalyzed cross-coupling of aryl thianthrenium salts with a copper-based trifluoromethyl reagent, which enables a site-selective late-stage trifluoromethylation of arenes. The reaction proceeds with broad functional group tolerance, even for complex small molecules on gram scale. The method was further extended to produce pentafluoroethylated derivatives.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7754511 | PMC |
http://dx.doi.org/10.1002/anie.201906672 | DOI Listing |
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