Ruthenium-Catalyzed Stereo- and Site-Selective ortho- and meta-C−H Glycosylation and Mechanistic Studies

Abstract

C-aryl glycosides are popular basic skeletons in biochemistry and pharmaceutical chemistry. Herein, ruthenium-catalyzed highly stereo- and site-selective ortho- and meta-C_Ar−H glycosylation is described. A series of C-aryl pyranosides and furanosides were synthesized by this method. The strategy showed good substrate scope, and various N-heterocyclic directing groups were compatible with the reaction system. A mechanistic study suggested that the key pathway of ortho-C_Ar−H glycosylation might involve oxidative addition/reduction elimination, whereas aryl meta-C−H glycosylation was mediated by σ-activation. Density functional theory calculations also showed that the high stereoselectivity of meta-C_Ar−H glycosylation was due to steric hindrance.