Issue 1, 1973

2-Phenylbenzazete, an azacyclobutadiene

Abstract

2-Phenylbenzazete (2), the first heterocyclic analogue of cyclobutadiene, is formed by vapour phase pyrolysis of 4-phenylbenzo-1,2,3-triazine; it dimerises and reacts with nucleophiles and dienes very rapidly but is surprisingly stable at –80°; 2-phenylnaphty[2,3-b]-azete (12), formed similarly, is even appreciably stable at room temperature.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1973, 19-20

2-Phenylbenzazete, an azacyclobutadiene

B. M. Adger, M. Keating, C. W. Rees and R. C. Storr, J. Chem. Soc., Chem. Commun., 1973, 19 DOI: 10.1039/C39730000019

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