Transition Metals Catalyzed Direct C─H Chalcogentaion of Arenes and Heteroarenes

Abstract

Transition metals catalyzed C─H bond activation reactions have appeared as an emerging field to introduce different functional groups in the inactivated saturated and unsaturated C-H bonds. C─S and C─Se bond constructions in aromatic scaffolds are very interesting due to the important applications of organochalcogen reagents in pharmaceutical chemistry and the material world. The introduction of sulphur or selenium moiety to an inert C─H functionality of an arene under transition metal catalysis has become one of the prime challenges and targets in recent years. In this perspective, various transition metals such as Cu, Ni, Co, Pd, Rh, Ru etc. have been extensively studied. Aromatic arenes owning bearing suitable directing groups appeared as the most promising coupling partners to selectively synthesize differently substituted aryl sulfones and aryl sulfides/selenides. The synthetic strategies were highly convenient owing to the regioselectivity of products, broad substrate scope, mild reaction conditions and excellent functional group tolerance. The current review article comprehensively summarizes the extent of C─S/Se bond formation via transition metal-catalyzed C─H bond activation with the assistance of directing groups to govern the site selectivity.