Diyne-steered switchable regioselectivity in cobalt(II)-catalysed C(sp2)-H activation of amides with unsymmetrical 1,3-diynes

Org Biomol Chem. 2023 Mar 1;21(9):1942-1951. doi: 10.1039/d2ob02193e.

Abstract

The regiochemical outcome of a cobalt(II) catalysed C-H activation reaction of aminoquinoline benzamides with unsymmetrical 1,3-diynes under relatively mild reaction conditions can be steered through the choice of diyne. The choice of diyne provides access to either 3- or 4-hydroxyalkyl isoquinolinones, paving the way for the synthesis of more highly elaborate isoquinolines.