Cp*Rh(iii) catalyzed ortho-halogenation of N-nitrosoanilines by solvent-controlled regioselective C–H functionalization†
Abstract
We present a novel, efficient, and regioselective method for the rhodium-catalyzed direct C–H ortho-halogenation of anilines that involves a removable N-nitroso directing group. This method featured mild reaction conditions, wide substrate scope, good functional group tolerance and satisfactory yields. To maintain the high ortho-regioselectivity and conversion, increasing the steric hindrance of the solvent was critical. Preliminary mechanistic studies suggest that C–H activation may be involved in the rate-determining step.
- This article is part of the themed collection: Synthetic methodology in OBC