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 - http://www.scopus.com/inward/record.url?scp=0029021946&partnerID=8YFLogxK
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 -