Use of the methylsulfenyl cation as an activator for glycosylation reactions with alkyl (aryl) l-thioglycopyranosides: synthesis of methyl O-(2-acetamido-2-deoxy-β-d-glucopyranosyl)-(1→ 2)-α-d-glucopyranoside, a derivative of the core trisaccharide of E. coli K12-Reference-Cited by-同舟云学术

Use of the methylsulfenyl cation as an activator for glycosylation reactions with alkyl (aryl) l-thioglycopyranosides: synthesis of methyl O-(2-acetamido-2-deoxy-β-d-glucopyranosyl)-(1→ 2)-α-d-glucopyranoside, a derivative of the core trisaccharide of E. coli K12

Published:1990-07 Issue: Volume:202 Page:225-238
ISSN:0008-6215
Container-title:Carbohydrate Research
language:en
Short-container-title:Carbohydrate Research

Author:

Dasgupta Falguni,Garegg Per J.

Publisher

Elsevier BV

Subject

Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry

Reference12 articles.

1. Alkyl sulfenyl triflate as activator in the thioglycoside-mediated formation of β-glycosidic linkages during oligosaccharide synthesis

2. Thioglycosides as glycosylating agents in oligosaccharide synthesis

3. Syntheses of a branched heptasaccharide having phytoalexin-elicitor activity

4. A novel promoter for the efficient construction of 1,2-trans linkages in glycoside synthesis, using thioglycosides as glycosyl donors

5. An efficient approach to O-glycosides through CuBr2-Bu4NBr mediated activation of glycosides

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