Issue 17, 1999

Photodegradation of aryl sulfonamides: N-tosylglycine

Abstract

Continuing uncertainty about pathways and consequences of the photolability of aryl sulfonamides is partly resolved by the results of comprehensive product analysis in the photolysis of aqueous N-tosylglycine, which indicate that intramolecular electron or hydrogen transfer (according to conditions) promote the widely reported S–N cleavage and reveal the nature of subsequent and competing processes.

Article information

Article type
Paper

Chem. Commun., 1999, 1735-1736

Photodegradation of aryl sulfonamides: N-tosylglycine

R. R. Hill, G. E. Jeffs, D. R. Roberts and S. A. Wood, Chem. Commun., 1999, 1735 DOI: 10.1039/A905358A

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