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Synthesis 2014; 46(23): 3207-3212
DOI: 10.1055/s-0034-1378617
DOI: 10.1055/s-0034-1378617
paper
Domino Reaction of 2,2-Dihydroxyindene-1,3-dione with Aromatic Amines: Efficient Synthesis of Isochromeno[4,3-b]indol-5(11H)-one Derivatives
Weitere Informationen
Publikationsverlauf
Received: 15. April 2014
Accepted after revision: 17. Juli 2014
Publikationsdatum:
21. August 2014 (online)
![](https://www.thieme-connect.de/media/synthesis/201423/lookinside/thumbnails/10.1055-s-0034-1378617-1.jpg)
Abstract
An efficient approach to 16 examples of polyfunctionalized isochromeno[4,3-b]indol-5(1H)-one derivatives, obtained in 60–85% yield and with excellent regioselectivity, has been developed through a domino reaction of 2,2-dihydroxyindene-1,3-dione with aromatic amines under microwave irradiation. The atom- and step-economy and scope make this reaction a powerful tool for assembling polyheterocyclic scaffolds of general chemical and biomedical interest.
Key words
domino reactions - heterocycles - cyclizations - regioselectivity - isochromeno[4,3-b]indol-5(11H)-one - 2,2-dihydroxyindene-1,3-dione - aromatic aminesSupporting Information
- for this article is available online at http://www.thieme-connect.com/products/ejournals/journal/ 10.1055/s-00000084.
- Supporting Information
-
References
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