Chemoselective Cu-catalyzed acylsilylation of vinyl arenes using silylboronates and acyl fluorides.

We report the chemoselective copper-catalyzed acylsilylation of vinyl arenes using bench-stable silylboronates and acyl fluorides, which enables efficient access to β-silyl ketones under mild conditions. The reaction proceeds without the need for photochemical activation and exhibits a broad substrate scope, tolerating a wide range of electron-deficient and heteroaromatic vinyl arenes, as well as electronically diverse acyl fluorides, including drug-derived motifs. A key to this success is the LUMO-lowering effect of the electron-withdrawing substituents on the aryl ring, which enhances nucleophilic attack by a silylcopper(i) species. Mechanistically, the transformation proceeds via a PCy3-ligated copper catalyst, mediating Si-B σ-bond transmetalation, alkene insertion, and nucleophilic substitution with acyl fluoride. Notably, acyl fluorides outperform commonly used acid chlorides and acyl imidazoles, offering both improved reactivity and catalyst turnover through the formation of a reactive Cu-F intermediate, which regenerates the active silylcopper species with the concomitant formation of F-Bpin. It is worth noting that this system enables clear discrimination between electronically similar vinyl arenes. The method should be a promising platform for site-selective and chemoselective alkene functionalization in complex settings.