Issue 64, 2021

Ni-Catalyzed C(sp2)–H alkylation of N-quinolylbenzamides using alkylsilyl peroxides as structurally diverse alkyl sources

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.

Graphical abstract: Ni-Catalyzed C(sp2)–H alkylation of N-quinolylbenzamides using alkylsilyl peroxides as structurally diverse alkyl sources

Supplementary files

Article information

Article type
Communication
Submitted
08 Jun 2021
Accepted
05 Jul 2021
First published
06 Jul 2021

Chem. Commun., 2021,57, 7942-7945

Ni-Catalyzed C(sp2)–H alkylation of N-quinolylbenzamides using alkylsilyl peroxides as structurally diverse alkyl sources

S. Tsuzuki, S. Sakurai, A. Matsumoto, T. Kano and K. Maruoka, Chem. Commun., 2021, 57, 7942 DOI: 10.1039/D1CC02983E

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