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Synthesis 2013; 45(18): 2583-2592
DOI: 10.1055/s-0033-1338507
DOI: 10.1055/s-0033-1338507
paper
Synthesis of Functionalized Indanes via Palladium-Catalyzed Carboannulation of Diazabicyclic Olefins with o-Iodostyrenes
Weitere Informationen
Publikationsverlauf
Received: 13. Mai 2013
Accepted after revision: 26. Juni 2013
Publikationsdatum:
26. Juli 2013 (online)
![](https://www.thieme-connect.de/media/synthesis/201318/lookinside/thumbnails/10.1055-s-0033-1338507-1.jpg)
Abstract
Palladium-catalyzed carboannulation of bicyclic and tricyclic hydrazines with substituted o-iodostyrenes produced functionalized indanes in good to excellent yields. The methodology provides an important carbocyclic ring system under relatively mild conditions.
Key words
palladium - diazabicyclic olefins - carboannulation - o-iodostyrenes - functionalized indanesSupporting Information
- for this article is available online at http://www.thieme-connect.com/ejournals/toc/synthesis.
- Supporting Information
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