Issue 7, 2015

Synthesis of 7a-phenyl-1a,7a-dihydro-benzopyrano[2,3-b]azirin-7-ones via photoisomerization reaction

Abstract

A novel protocol has been developed for the synthesis of 7a-phenyl-1a,7a-dihydro-benzopyrano[2,3-b]azirin-7-ones via the photoisomerization of 4-phenyl-5-(2-hydroxyphenyl)isoxazoles. This procedure involves a photo-catalyzed ring opening of isoxazole and subsequent intramolecular nucleophilic addition between a 2H-azirine intermediate and a phenolic hydroxyl group. The synthetic method offers several notable advantages including operational simplicity, mild reaction conditions, moderate to high yields and environmental friendliness.

Graphical abstract: Synthesis of 7a-phenyl-1a,7a-dihydro-benzopyrano[2,3-b]azirin-7-ones via photoisomerization reaction

Supplementary files

Article information

Article type
Paper
Submitted
16 Oct 2014
Accepted
08 Dec 2014
First published
10 Dec 2014

RSC Adv., 2015,5, 4788-4794

Author version available

Synthesis of 7a-phenyl-1a,7a-dihydro-benzopyrano[2,3-b]azirin-7-ones via photoisomerization reaction

Q. Wang, Z. Zhang, X. Zhang, J. Zhang, Y. Kang and J. Peng, RSC Adv., 2015, 5, 4788 DOI: 10.1039/C4RA12542H

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