Radical-mediated brominations at ring-positions of carbohydrates - 35 years later

Research output: Chapter in Book/Report/Conference proceedingChapter

6 Citations (Scopus)

Abstract

The unique ability of sugar derivatives to undergo bromination at ring positions by a radical mechanism is surveyed more than three decades after the discovery of the reaction. The range of substrates as well as their transformations have been enormously extended, and many of the ensuing products have proven valuable tools for chemical glycobiology.

Original languageEnglish
Title of host publicationCarbohydrate Chemistry
Pages1-37
Number of pages37
Volume39
DOIs
Publication statusPublished - 2013

Publication series

NameCarbohydrate Chemistry
Volume39
ISSN (Print)2041353X
ISSN (Electronic)14651963

Fingerprint

Glycomics
Halogenation
Sugars
Carbohydrates
Derivatives
Substrates

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry

Cite this

Radical-mediated brominations at ring-positions of carbohydrates - 35 years later. / Somsák, L.; Czifrák, K.

Carbohydrate Chemistry. Vol. 39 2013. p. 1-37 (Carbohydrate Chemistry; Vol. 39).

Research output: Chapter in Book/Report/Conference proceedingChapter

Somsák, L. ; Czifrák, K. / Radical-mediated brominations at ring-positions of carbohydrates - 35 years later. Carbohydrate Chemistry. Vol. 39 2013. pp. 1-37 (Carbohydrate Chemistry).
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