Issue 6, 1984

Generation of thionitroso compounds by benzisothiazole ring opening

Abstract

Oxidation of 3-amino-2-phenylindazole (3) or thermolysis of 3-azido-2-phenylindazole (4) gives 2-cyanoazobenzene (5) quantitatively; thermolysis or photolysis of 3-azido-2, 1-benzisothiazoles (1) induces similar ring opening to give the transient 2-cyanothionitrosobenzenes (2).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1984, 374-375

Generation of thionitroso compounds by benzisothiazole ring opening

M. F. Joucla and C. W. Rees, J. Chem. Soc., Chem. Commun., 1984, 374 DOI: 10.1039/C39840000374

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