Issue 15, 1982

New syntheses of C-mercuriated sugars and rapid conversion into bromo-sugars by reaction with bromine chloride from sodium bromide and chloramine-T

Abstract

New C-mercuriated sugars have been synthesised via hydroboration–transmetallation sequences; the bis(glycosyl)mercury compound (4) reacts very repidly with bromine chloride generated in situ from sodium bromide and chloramine-T, to give a high isolated yields of bromo-sugar (5)(87%).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1982, 887-888

New syntheses of C-mercuriated sugars and rapid conversion into bromo-sugars by reaction with bromine chloride from sodium bromide and chloramine-T

L. D. Hall and J. Neeser, J. Chem. Soc., Chem. Commun., 1982, 887 DOI: 10.1039/C39820000887

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