An efficient and stereoselective synthesis of beta-D-Arap-(1-->2)-beta-D-Galp-(1-->3)-beta-D-Galp-(1-->4)-alpha-D-Manp, a tetrasaccharide fragment of Leishmania major lipophosphoglycan

A tetrasaccharide fragment of Leishmania major lipophosphoglycan (which seems to be involved in a biological mechanism for the parasite transmission) has been synthesised using the thioglycoside, trichloroacetimidate and halide-exchange glycosylation procedures and step-wise chain elongation strateg...

Full description

Saved in:
Bibliographic Details
Published in:Carbohydrate research 2001-12, Vol.336 (4), p.243-248
Main Authors: Yashunsky, D V, Higson, A P, Ross, A J, Nikolaev, A V
Format: Article
Language:English
Subjects:
Animals
Carbohydrate Sequence
Glycosphingolipids - chemistry
Glycosylation
Leishmania major - chemistry
Oligosaccharides - chemical synthesis
Oligosaccharides - chemistry
Stereoisomerism
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:A tetrasaccharide fragment of Leishmania major lipophosphoglycan (which seems to be involved in a biological mechanism for the parasite transmission) has been synthesised using the thioglycoside, trichloroacetimidate and halide-exchange glycosylation procedures and step-wise chain elongation strategy.
ISSN:0008-6215
DOI:10.1016/S0008-6215(01)00274-9