Sugar bromoimino derivatives: New sugar derivatives readily prepared from β-D-glycosyl azides

Jean Pierre Praly, Carméla Di Stéfano, L. Somsák, Gérard Descotes

Research output: Contribution to journalArticle

13 Citations (Scopus)

Abstract

The treatment of two protected β-D-glycosyl azides by N-bromosuccinimide in refluxing carbon tetrachloride under free-radical conditions leads to efficient preparations of the corresponding bromoimino derivatives via an unprecedented reaction of organic azides leading, in the present case, to new sugar derivatives.

Original languageEnglish
Pages (from-to)200-201
Number of pages2
JournalJournal of the Chemical Society, Chemical Communications
Issue number2
DOIs
Publication statusPublished - 1992

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Azides
Sugars
Bromosuccinimide
Derivatives
Carbon tetrachloride
Carbon Tetrachloride
Free radicals
Free Radicals

ASJC Scopus subject areas

  • Molecular Medicine

Cite this

Sugar bromoimino derivatives : New sugar derivatives readily prepared from β-D-glycosyl azides. / Praly, Jean Pierre; Di Stéfano, Carméla; Somsák, L.; Descotes, Gérard.

In: Journal of the Chemical Society, Chemical Communications, No. 2, 1992, p. 200-201.

Research output: Contribution to journalArticle

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