This randomized trial demonstrates selective C(sp2)–H arylation in enamides, indicating its practical application in drug development.
We report a palladium(II)-catalyzed regio- and stereoselective β-C(sp 2 )–H arylation of enamides with simple arenes under base- and ligand-free conditions via thianthrenium salts, affording a broad array of geometrically defined β-arylated enamides with an exquisite Z configuration. This transformation is characterized by operational simplicity, readily available and bench-stable aryl surrogates, broad substrate scope, and extraordinary compatibility with diverse functionalities. The utility of this approach has been demonstrated by the late-stage diversification of biologically active molecules.
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Cao et al. (2026) studied this question.
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