Issue 5, 1981

Photolysis and thermolysis of phenyl azide in acetic acid

Abstract

The photolysis and thermolysis of phenyl azide in acetic acid gave 2,3-dihydro-1H-azepin-2-one via 1-aza-cyclohepta-1,2,4,6-tetraene, and ring-disubstituted products via a resonance-stabilized ion formed by attack of singlet phenylnitrene on acetic acid

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1981, 202-204

Photolysis and thermolysis of phenyl azide in acetic acid

H. Takeuchi and K. Koyama, J. Chem. Soc., Chem. Commun., 1981, 202 DOI: 10.1039/C39810000202

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements