Preparation of acetylated C-(1-bromo-d-glycosyl) heterocycles and 1-bromo-d-glycosyl cyanides

L. Somsák, G. Batta, István Farkas

Research output: Contribution to journalArticle

35 Citations (Scopus)

Abstract

The reaction of acetylated C-(d-glycosyl) heterocycles and d-glycosyl cyanides with either N-bromosuccinimide in hot carbon tetrachloride or bromine under irradiation resulted in bromination at the anomeric carbon atom. The location of the bromine substituent and the conformations of these products were determined by n.m.r. spectroscopy. Absolute configurations of the bromo compounds were established.

Original languageEnglish
Pages (from-to)43-51
Number of pages9
JournalCarbohydrate Research
Volume124
Issue number1
DOIs
Publication statusPublished - Dec 10 1983

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Bromine
Cyanides
Bromosuccinimide
Carbon Tetrachloride
Halogenation
Conformations
Spectrum Analysis
Carbon
Irradiation
Spectroscopy
Atoms

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Organic Chemistry

Cite this

Preparation of acetylated C-(1-bromo-d-glycosyl) heterocycles and 1-bromo-d-glycosyl cyanides. / Somsák, L.; Batta, G.; Farkas, István.

In: Carbohydrate Research, Vol. 124, No. 1, 10.12.1983, p. 43-51.

Research output: Contribution to journalArticle

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