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Synlett 2006(11): 1671-1674
DOI: 10.1055/s-2006-944229
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
Further Information
Received
3 April 2006
Publication Date:
04 July 2006 (online)
Publication History
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.
Key words
multicomponent reaction - 1,3-dicarbonyls - benzimidazoles - heterogeneous catalysis - aerobic oxidation
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