Oxidant-controlled regioselectivity in the oxidative arylation of N-acetylindoles

Tetrahedron Lett. 2008 Jun 16;49(25):4050-4053. doi: 10.1016/j.tetlet.2008.04.073.

Abstract

N-Acetylindoles can be oxidatively coupled with arenes such as benzene or pentafluorobenzene in dioxane. The use of Cu(OAc)(2) as the stoichiometric oxidant produces selective arylation at the 3-position of indole while AgOAc produces selective arylation at indole's 2-position.