Issue 16, 1983

Redox-chain decomposition of hydroxylamine-O-sulphonic acid. A novel general source of nucleophilic radicals for the functionalization of heteroaromatic bases

Abstract

Protonated heteroaromatic bases react with formamide, N,N-dimethylformamide, cyclic ethers, and methanol in the presence of hydroxylamine-O-sulphonic acid and catalytic amounts of an iron(II) salt to afford selective substitution by a redox chain process.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1983, 916-917

Redox-chain decomposition of hydroxylamine-O-sulphonic acid. A novel general source of nucleophilic radicals for the functionalization of heteroaromatic bases

A. Citterio, A. Gentile, F. Minisci, M. Serravalle and S. Ventura, J. Chem. Soc., Chem. Commun., 1983, 916 DOI: 10.1039/C39830000916

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