Synthesis of the trisaccharide repeating unit of the O-antigen related to the enterohemorrhagic Escherichia coli type O26

H

Kakali Sarkar, Indrani Mukherjee, Nirmolendu Roy

Research output: Contribution to journalArticle

Abstract

L-Fucose was converted to the 2-azido-2-deoxy-L-fucose derivative, which together with the monosaccharide synthons prepared from L-rhamnose and D-glucosamine hydrochloride were utilized for the synthesis of the p-ethoxyphenyl glycoside of the trisaccharide repeating unit of the antigen from enterohemorrhagic Escherichia coli type O26:H.

Original languageEnglish (US)
Pages (from-to)95-107
Number of pages13
JournalJournal of Carbohydrate Chemistry
Volume22
Issue number2
DOIs
StatePublished - 2003
Externally publishedYes

Fingerprint

Enterohemorrhagic Escherichia coli
Trisaccharides
Rhamnose
O Antigens
Fucose
Monosaccharides
Glucosamine
Glycosides
Escherichia coli
Derivatives
Antigens
2-deoxy-L-fucose

Keywords

  • Escherichia coli type O26:H
  • Synthesis
  • Trisaccharide

ASJC Scopus subject areas

  • Organic Chemistry
  • Biochemistry, Genetics and Molecular Biology(all)
  • Biochemistry

Cite this

Synthesis of the trisaccharide repeating unit of the O-antigen related to the enterohemorrhagic Escherichia coli type O26 : H. / Sarkar, Kakali; Mukherjee, Indrani; Roy, Nirmolendu.

In: Journal of Carbohydrate Chemistry, Vol. 22, No. 2, 2003, p. 95-107.

Research output: Contribution to journalArticle

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