Ni-Catalyzed C(sp<sup>2</sup>)–H alkylation of <i>N</i>-quinolylbenzamides using alkylsilyl peroxides as structurally diverse alkyl sources
Saori Tsuzuki, Shunya Sakurai, Akira Matsumoto, Taichi Kano, Keiji Maruoka
Abstract
A Ni-catalyzed direct C-H alkylation of N-quinolylbenzamides using alkylsilyl peroxides as alkyl-radical precursors is described. The reaction forms a new C(sp3)-C(sp2) bond via the selective cleavage of both C(sp3)-C(sp3) and C(sp2)-H bonds. This transformation shows a high functional-group tolerance and, due to the structural diversity of alkylsilyl peroxides, a wide range of alkyl chains including functional groups and complex structures can be introduced at the ortho-position of readily available N-quinolylbenzamide derivatives. Mechanistic studies suggest that the reaction involves a radical mechanism.
Topics & Concepts
AlkylationAlkylCatalysisChemistryMedicinal chemistryHalideOrganic chemistryCatalytic C–H Functionalization MethodsRadical Photochemical ReactionsOxidative Organic Chemistry Reactions