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Synthesis 2013; 45(1): 53-64
DOI: 10.1055/s-0032-1316822
DOI: 10.1055/s-0032-1316822
paper
Thermal [3+2] Cycloaddition of Aromatic Azomethine Imines with Allenoates
Weitere Informationen
Publikationsverlauf
Received: 05. Oktober 2012
Accepted after revision: 09. November 2012
Publikationsdatum:
06. Dezember 2012 (online)
![](https://www.thieme-connect.de/media/synthesis/201301/lookinside/thumbnails/10.1055-s-0032-1316822-1.jpg)
Abstract
The thermal [3+2] cycloadditions of two classes of aromatic azomethine imines with allenoates have been investigated. The reactions are operationally simple and proceed smoothly under mild reaction conditions to provide a variety of dinitrogen-fused heterocycles in moderate to excellent yields.
Supporting Information
- for this article is available online at http://www.thieme-connect.com/ejournals/toc/synthesis.
- Supporting Information
-
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For recent reviews on Et743, see:
Hisamine:
RIR-4-95:
Synthesis:
For examples of the cycloaddition of azomethine imines, see:
For reviews, see: