Jump to main content
Jump to site search

Issue 96, 2012
Previous Article Next Article

A concise synthesis of 3-aroylflavones via Lewis base 9-azajulolidine-catalyzed tandem acyl transfer–cyclization

Author affiliations

Abstract

Lewis base-catalyzed tandem acyl transfer–cyclization of acylated o-alkynoylphenols leading to 3-aroylflavones was developed. 9-Azajulolidine smoothly promoted the reaction of the aroyl derivatives at ambient temperature, and the structure-diversed synthesis of 3-aroylflavones with distinct substituents was achieved in moderate to excellent yields.

Graphical abstract: A concise synthesis of 3-aroylflavones via Lewis base 9-azajulolidine-catalyzed tandem acyl transfer–cyclization

Back to tab navigation

Supplementary files

Publication details

The article was received on 27 Sep 2012, accepted on 23 Oct 2012 and first published on 31 Oct 2012


Article type: Communication
DOI: 10.1039/C2CC37015H
Citation: Chem. Commun., 2012,48, 11796-11798
  •   Request permissions

    A concise synthesis of 3-aroylflavones via Lewis base 9-azajulolidine-catalyzed tandem acyl transfer–cyclization

    M. Yoshida, K. Saito, Y. Fujino and T. Doi, Chem. Commun., 2012, 48, 11796
    DOI: 10.1039/C2CC37015H

Search articles by author

Spotlight

Advertisements