Issue 19, 1979

Oxidation of 2,4-dinitrobenzenesulphenamide in the presence of alkenes: formation of aziridines

Abstract

Oxidation of 2,4-dinitrobenzenesulphenamide in the presence of electron-rich alkenes yields N-2,4-dinitrophenylthioaziridines which have been converted into the corresponding N–H aziridines by reduction.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1979, 832-833

Oxidation of 2,4-dinitrobenzenesulphenamide in the presence of alkenes: formation of aziridines

R. S. Atkinson and B. D. Judkins, J. Chem. Soc., Chem. Commun., 1979, 832 DOI: 10.1039/C39790000832

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