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Synthesis 2010(3): 486-492
DOI: 10.1055/s-0029-1217143
DOI: 10.1055/s-0029-1217143
PAPER
© Georg Thieme Verlag
Stuttgart ˙ New York
One-Pot Tandem Synthesis of Furo[3,2-h]quinolines by a Sonogashira Cross-Coupling and Cyclization Reaction Supported by Basic Alumina Under Microwave Irradiation
Further Information
Received
24 September 2009
Publication Date:
24 November 2009 (online)
Publication History
Publication Date:
24 November 2009 (online)
![](https://www.thieme-connect.de/media/synthesis/201003/lookinside/thumbnails/10.1055-s-0029-1217143-1.jpg)
Abstract
Acetylenic 8-quinolinols generated in situ by the Sonogashira cross-coupling reaction are efficiently converted into furo[3,2-h]quinolines by microwave-assisted, copper-catalyzed, intramolecular cyclization in the presence of basic alumina.
Key words
heterocycles - furoquinoline - cross-coupling - cyclizations - solid-phase synthesis - microwave irradiation
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