Issue 15, 2015

Palladium-catalyzed dicarbonylative synthesis of tetracycle quinazolinones

Abstract

An interesting procedure for the synthesis of isoindolo[1,2-b]quinazolin-10(12H)-ones has been developed. Starting from commercially available 2-bromoanilines and 2-bromobenzyl amines, with the assistance of a palladium catalyst, the desired products were isolated in good yields. Notably, this procedure proceeded in a highly selective manner; two molecules of CO were incorporated into the substrates selectively.

Graphical abstract: Palladium-catalyzed dicarbonylative synthesis of tetracycle quinazolinones

Supplementary files

Article information

Article type
Communication
Submitted
24 Feb 2015
Accepted
12 Mar 2015
First published
12 Mar 2015

Org. Biomol. Chem., 2015,13, 4422-4425

Author version available

Palladium-catalyzed dicarbonylative synthesis of tetracycle quinazolinones

C. Shen, N. Y. T. Man, S. Stewart and X. Wu, Org. Biomol. Chem., 2015, 13, 4422 DOI: 10.1039/C5OB00368G

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