Issue 16, 2021

Palladium-catalyzed carbonylative cyclization of benzyl chlorides with anthranils for the synthesis of 3-arylquinolin-2(1H)-ones

Abstract

An efficient carbonylative procedure for the synthesis of 3-arylquinoin-2(1H)-ones has been established. Through a palladium-catalyzed aminocarbonylation of benzyl chlorides with anthranils, a variety of 3-arylquinoin-2(1H)-one products were obtained in moderate to excellent yields with good functional group tolerance.

Graphical abstract: Palladium-catalyzed carbonylative cyclization of benzyl chlorides with anthranils for the synthesis of 3-arylquinolin-2(1H)-ones

Supplementary files

Article information

Article type
Communication
Submitted
17 Feb 2021
Accepted
26 Mar 2021
First published
26 Mar 2021

Org. Biomol. Chem., 2021,19, 3584-3588

Palladium-catalyzed carbonylative cyclization of benzyl chlorides with anthranils for the synthesis of 3-arylquinolin-2(1H)-ones

J. Liu, R. Xu, W. Wang, X. Qi and X. Wu, Org. Biomol. Chem., 2021, 19, 3584 DOI: 10.1039/D1OB00298H

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