Issue 13, 1991

Facile trisulphide formation in the thermolysis of N,N′-diacetyl-L-cystine bismethylamide, an excellent model for protein-bound cystine

Abstract

The thermolysis of N,N′-diacetyl-L-cystine bismethylamide not only displays the known chemistry of protein-bound cystine, but also draws attention to the facile formation of trisulphides and, when conducted under alkaline conditions, allows the isolation of the simplest α,β-dehydropeptide.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1991, 903-904

Facile trisulphide formation in the thermolysis of N,N′-diacetyl-L-cystine bismethylamide, an excellent model for protein-bound cystine

M. Ghadimi and R. R. Hill, J. Chem. Soc., Chem. Commun., 1991, 903 DOI: 10.1039/C39910000903

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