Issue 18, 1980

[4 + 6]π Cycloadditions of thiadiazole 1,1-dioxides to 6-dimethylaminofulvene: a synthesis of a diaza-azulene

Abstract

Treatment of 2,5-bis(alkylsulphinyl)-1,3,4-thiadiazole 1,1-dioxides with 6-dimethylaminofulvene in acetone gave 5,6-diaza-azulenes in good yields; solvent effects support a concerted mechanism for the formation of the cycloadducts.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1980, 873-874

[4 + 6]π Cycloadditions of thiadiazole 1,1-dioxides to 6-dimethylaminofulvene: a synthesis of a diaza-azulene

M. Mori and K. Kanematsu, J. Chem. Soc., Chem. Commun., 1980, 873 DOI: 10.1039/C39800000873

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