The snythesis of disaccharides by the ferric chloride-catalyzed coupling of 2-acylamido-2-deoxy-β-D-glucopyranose 1-acetates to protect sugar acceptors-Reference-Cited by-同舟云学术

The snythesis of disaccharides by the ferric chloride-catalyzed coupling of 2-acylamido-2-deoxy-β-D-glucopyranose 1-acetates to protect sugar acceptors

Published:1979-07 Issue: Volume:72 Page:C15-C17
ISSN:0008-6215
Container-title:Carbohydrate Research
language:en
Short-container-title:Carbohydrate Research

Author:

Kiso Makoto,Anderson Laurens

Publisher

Elsevier BV

Subject

Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry

Reference9 articles.

1. The ferric chloride-catalyzed glycosylation of alcohols by 2-acylamido-2-deoxy-β-D-glucopyranose 1-acetates

2. Preparation of benzyl ethers of 1,2-dideoxy-2′-methyl-α-D-glucopyranoso-[2,1-d]-Δ2′-oxazoline for use in oligosaccharide synthesis

3. The synthesis and properties of benzylated oxazolines derived from 2-acetamido-2-deoxy-D-glucose

4. O-Benzylated thio sugars. Derivatives of 2,3,6-tri-O-benzyl-1-thio-d-galactopyranose suitable for use in oligosaccharide synthesis

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