The chemical synthesis of Leishmania donovani phosphoglycan via polycondensation of a glycobiosyl hydrogenphosphonate monomer

TY - JOUR

T1 - The chemical synthesis of Leishmania donovani phosphoglycan via polycondensation of a glycobiosyl hydrogenphosphonate monomer

AU - Nikolaev, Andrei V.

AU - Chudek, John Alexander

AU - Ferguson, Michael A. J.

N1 - Medline is the source for the MeSH terms of this document.

PY - 1995/1/1

Y1 - 1995/1/1

N2 - A polycondensation of 2,3,6-tri-O-benzoyl-4-O-(2,3,4-tri-O-benzoyl-ß-D-galactopyranosyl)-a -D-mannopyranosyl hydrogenphosphonate in the presence of trimethylacetyl chloride has been used to synthesize a linear poly[ß-D-galactopyranosyl-(1?4)-a-D-mannopyranosyl phosphate] representing the phosphoglycan part of the lipophosphoglycan from Leishmania donovani.

AB - A polycondensation of 2,3,6-tri-O-benzoyl-4-O-(2,3,4-tri-O-benzoyl-ß-D-galactopyranosyl)-a -D-mannopyranosyl hydrogenphosphonate in the presence of trimethylacetyl chloride has been used to synthesize a linear poly[ß-D-galactopyranosyl-(1?4)-a-D-mannopyranosyl phosphate] representing the phosphoglycan part of the lipophosphoglycan from Leishmania donovani.

UR - https://www.scopus.com/pages/publications/0029021946

U2 - 10.1016/0008-6215(95)00067-4

DO - 10.1016/0008-6215(95)00067-4

M3 - Article

AN - SCOPUS:0029021946

SN - 0008-6215

VL - 272

SP - 179

EP - 189

JO - Carbohydrate Research

JF - Carbohydrate Research

IS - 2

ER -