Issue 21, 1970

Synthesis and reactions of 5,6-dehydrobenzimidazoles

Abstract

Lead tetra-acetate oxidation of 5-amino-1,2-dimethyltriazolo[4,5-d]benzimidazole gave 5,6-dehydro-1,2-dimethylbenzimidazole, which underwent subsequent cyclo-addition with a variety of dienophiles and dipolarophiles; other 5,6-dehydrobenzimidazoles have been prepared by this method, and also by aprotic diazotisation of the appropriate 6-aminobenzimidazole-5-carboxylic acid.

Article information

Article type
Paper

J. Chem. Soc. D, 1970, 1458-1459

Synthesis and reactions of 5,6-dehydrobenzimidazoles

R. C. Perera and R. K. Smalley, J. Chem. Soc. D, 1970, 1458 DOI: 10.1039/C29700001458

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