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Synthesis 2014; 46(06): 752-756
DOI: 10.1055/s-0033-1338590
DOI: 10.1055/s-0033-1338590
paper
Oxidation of 1-Amidoalkyl-2-naphthols Using (Diacetoxyiodo)benzene: Unusual Formation of 1-Arylnaphtho[1,2-d]isoxazoles
Further Information
Publication History
Received: 30 September 2013
Accepted after revision: 08 January 2014
Publication Date:
07 February 2014 (online)
![](https://www.thieme-connect.de/media/synthesis/201406/lookinside/thumbnails/10.1055-s-0033-1338590-1.jpg)
Abstract
The reactions of 1-amidoalkyl-2-naphthols with (diacetoxyiodo)benzene results in the unusual formation of 1-arylnaphtho[1,2-d]isoxazoles. This procedure demonstrates a useful application of (diacetoxyiodo)benzene for the oxidative formation of an N–O bond.
Key words
1,2-benzisoxazole - hypervalent iodine - 1-amidoalkyl-2-naphthols - 2-hydroxyaryl ketoximes - phenolic oxidationSupporting Information
- for this article is available online at http://www.thieme-connect.com/ejournals/toc/synthesis.
- Supporting Information
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