Issue 5, 1977

Loss of nitrogen in acylation reactions of 5-amino-1,2,3,4-thiatriazole. A new series of heteropentalenes

Abstract

2,5-Diaryl-1,6-dioxa-6a-thia-3,4-diazapentalenes are obtained when 5-amino-1,2,3,4-thiatrizole is treated with aroyl chlorides and pyridine, but acetylation of 5-amino-1,2,3,4-thiatriazole yields 3,5-diacetamido-1,2,4-thiadiazole.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1977, 143-144

Loss of nitrogen in acylation reactions of 5-amino-1,2,3,4-thiatriazole. A new series of heteropentalenes

R. J. S. Beer and I. Hart, J. Chem. Soc., Chem. Commun., 1977, 143 DOI: 10.1039/C39770000143

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