Jump to main content
Jump to site search

Issue 15, 2015
Previous Article Next Article

Palladium-catalyzed dicarbonylative synthesis of tetracycle quinazolinones

Author affiliations

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

Back to tab navigation

Supplementary files

Publication details

The article was received on 24 Feb 2015, accepted on 12 Mar 2015 and first published on 12 Mar 2015


Article type: Communication
DOI: 10.1039/C5OB00368G
Author version
available:
Download author version (PDF)
Citation: Org. Biomol. Chem., 2015,13, 4422-4425
  •   Request permissions

    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

Search articles by author

Spotlight

Advertisements