Selective, radical-free activation of benzylic C–H bonds in methylarenes†
Abstract
We report rare examples of exclusive benzylic C–H oxidative addition in industrially important methylarenes using simple η4-arene iridium complexes. Mechanistic studies showed that coordinatively unsaturated η2-arene intermediates are responsible for the selective activation of benzylic, not aromatic C–H bonds and formation of stable benzyl complexes after trapping with a phosphine ligand.
- This article is part of the themed collection: Chemical Communications HOT articles