Stereoselective syntheses of a di-, tri-, and tetra-saccharide fragment of shigella dysenteriae type 1 O-antigen using 3,4,6-tri-O-acetyl-2-azido-2-deoxy-α-d-glucopyranosyl chloride as a glycosyl donor-Reference-Cited by-同舟云学术

Stereoselective syntheses of a di-, tri-, and tetra-saccharide fragment of shigella dysenteriae type 1 O-antigen using 3,4,6-tri-O-acetyl-2-azido-2-deoxy-α-d-glucopyranosyl chloride as a glycosyl donor

Published:1992-05 Issue:1 Volume:229 Page:103-116
ISSN:0008-6215
Container-title:Carbohydrate Research
language:en
Short-container-title:Carbohydrate Research

Author:

Pavliak Viliam,Kováč Pavol,Glaudemans Cornelis P.J.

Publisher

Elsevier BV

Subject

Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry

Reference26 articles.

1. A short synthesis of 1,3,4,6-tetra-O-acetyl-2-azido-2-deoxy-β-d-glucopyranose and the corresponding α-glucosyl chloride from d-mannose

2. A small plasmid in Shigella dysenteriae 1 specifies one or more functions essential for O antigen production and bacterial virulence

3. Enteric infections

4. Somatic Antigens of Shigella. Structural Investigation on the O-Specific Polysaccharide Chain of Shigella Dysenteriae Type 1 Lipopolysaccharide

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