Synlett 2006(11): 1671-1674  
DOI: 10.1055/s-2006-944229
LETTER
© Georg Thieme Verlag Stuttgart · New York

A Multicomponent Domino Reaction and in situ Aerobic Oxidation Sequence for the First One-Pot Synthesis of Polycyclic Benzimidazoles from 1,3-Dicarbonyl Derivatives

Frédéric Liéby-Muller, Céline Simon, Katja Imhof, Thierry Constantieux*, Jean Rodriguez*
Université Paul Cézanne (Aix-Marseille III), CNRS UMR 6178 ‘SYMBIO’, Faculté des Sciences et Techniques, Case D12, 13397 Marseille Cedex 20, France
Fax: +33(4)91288841; e-Mail: jean.rodriguez@univ-cezanne.fr;
Further Information

Publication History

Received 3 April 2006
Publication Date:
04 July 2006 (online)

Abstract

A facile one-pot synthesis of functionalized pyrido[1,2-a]benzimidazoles is described via a molecular-sieves-promoted three-component domino reaction and in situ aerobic oxidation sequence from 1,3-dicarbonyls, aromatic o-diamines and unsaturated aldehydes. This environmentally friendly sequence does not require any harmful reagents, and liberates water as the only by-product. The desired products are obtained in good to excellent yields and generally with high purity, after simple filtration.