Issue 5, 2013

A new rapid multicomponent domino heteroannulation of heterocyclic keteneaminals: solvent-free regioselective synthesis of functionalized benzo[g]imidazo[1,2-a]quinolinediones

Abstract

A highly efficient and straightforward three-component cascade reaction was developed to synthesize benzo[g]imidazo[1,2-a]quinolinedione derivatives from heterocyclic ketene aminals (HKAs), aldehydes, and 2-hydroxy-1,4-naphthoquinone (HNQ) via Et3N-catalyzed tandem [3 + 2 + 1] annulation under solvent-free conditions. The reactions were very mild, convenient and highly regioselective to form new fused tetracyclic target molecules.

Graphical abstract: A new rapid multicomponent domino heteroannulation of heterocyclic ketene aminals: solvent-free regioselective synthesis of functionalized benzo[g]imidazo[1,2-a]quinolinediones

Supplementary files

Article information

Article type
Paper
Submitted
02 Aug 2012
Accepted
08 Nov 2012
First published
09 Nov 2012

Org. Biomol. Chem., 2013,11, 781-786

A new rapid multicomponent domino heteroannulation of heterocyclic ketene aminals: solvent-free regioselective synthesis of functionalized benzo[g]imidazo[1,2-a]quinolinediones

L. Wen, Q. Sun, H. Zhang and M. Li, Org. Biomol. Chem., 2013, 11, 781 DOI: 10.1039/C2OB27137K

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