Copper-Catalyzed ortho-Functionalization of Quinoline N-Oxides with Vinyl Arenes

Angew Chem Int Ed Engl. 2020 Oct 19;59(43):18975-18979. doi: 10.1002/anie.202007699. Epub 2020 Aug 20.

Abstract

An efficient copper-catalyzed regioselective C-H alkenylation and borylative alkylation of quinoline N-oxides with vinyl arenes in the presence of pinacol diborane has been developed. The reaction proceeds through the borylcupration of the vinyl arenes followed by nucleophilic attack of the resulting alkyl copper species to the quinoline N-oxides. Benzoquinone and KOt Bu were identified as the necessary additives at the second step of the reaction that are crucial for the success of the reaction. A wide range of C2-functionalizaed quinolines were obtained with good functional group tolerance, which may find utilities in pharmaceuticals and synthetic chemistry.

Keywords: alkenylation; borylative alkylation; borylcupration; copper catalysis; quinoline N-oxides.