Issue 7, 1996

Synthesis of 1H- and 5H-1,3-diazepines from azido- and tetrazolo-pyridines

Abstract

Stable 1H-1,3-diazepines 7–9,10,13,14,17 and 19 are obtained, often in high yields, by photolysis of triflouoromethyl-substituted azido- or tetrazolo-pyridines in the presence of alcohols or amines; in some cases 5H-1,3-diazepines are also formed(11,21 and 23).

Article information

Article type
Paper

Chem. Commun., 1996, 813-814

Synthesis of 1H- and 5H-1,3-diazepines from azido- and tetrazolo-pyridines

A. Reisinger and C. Wentrup, Chem. Commun., 1996, 813 DOI: 10.1039/CC9960000813

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.

Social activity

Spotlight

Advertisements