The synthesis of 3,6-di-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-D-galactose, a branched trisaccharide reported as a hydrolysis product of blood-group substances-Reference-Cited by-同舟云学术

The synthesis of 3,6-di-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-D-galactose, a branched trisaccharide reported as a hydrolysis product of blood-group substances

Published:1975-03 Issue:1 Volume:40 Page:23-29
ISSN:0008-6215
Container-title:Carbohydrate Research
language:en
Short-container-title:Carbohydrate Research

Author:

David Serge,Veyrières Alain

Publisher

Elsevier BV

Subject

Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry

Reference17 articles.

1. Cycloaddition as a possible path to disaccharide synthesis: stereochemical course of the reaction of butyl glyoxylate with a chiral, protected dienyl ether of glucose

2. Derivatives of 1,2-O-isopropylidene-α-D-galactofuranose

3. 2-Amino Sugar-containing Oligosaccharides Isolated from Hydrazinolyzate of Blood Group A Mucopolysaccharide of Hog Gastric Mucus

4. Immunochemical studies on blood groups. XXXVIII. Structures and activities of oligosaccharides produced by alkaline degradation of blood-group Lewisa substance. Proposed structure of the carbohydrate chains of human blood-group A,B,H,Lea, and Leb substances

5. Über Glucosaminide

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