PARASITE GLYCOCONJUGATES .5. BLOCKWISE APPROACH TO OLIGO(GLYCOSYL PHOSPHATES) - CHEMICAL SYNTHESIS OF A TERMINAL TRIS(GLYCOBIOSYL PHOSPHATE) FRAGMENT OF LEISHMANIA-DONOVANI ANTIGENIC LIPOPHOSPHOGLYCAN

Authors
NIKOLAEV AV RUTHERFORD TJ FERGUSON MAJ BRIMACOMBE JS
Citation
Av. Nikolaev et al., PARASITE GLYCOCONJUGATES .5. BLOCKWISE APPROACH TO OLIGO(GLYCOSYL PHOSPHATES) - CHEMICAL SYNTHESIS OF A TERMINAL TRIS(GLYCOBIOSYL PHOSPHATE) FRAGMENT OF LEISHMANIA-DONOVANI ANTIGENIC LIPOPHOSPHOGLYCAN, Journal of the Chemical Society. Perkin transactions. I, (13), 1996, pp. 1559-1566
Citations number
14
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Journal of the Chemical Society. Perkin transactions. I → ACNP
ISSN journal
0300922X
Issue
13
Year of publication
1996
Pages
1559 - 1566
Database
ISI
SICI code
0300-922X(1996):13<1559:PG.BAT>2.0.ZU;2-K
Abstract
The model tetramannosyl triphosphate 7 and the hexaglycosyl triphospha te 8, which is a terminal fragment of the phosphoglycan portion of Lei shmania donovani lipophosphoglycan, have been synthesized. Elongation of the chain was performed using the glycosyl hydrogenphosphonate meth od to couple together two phosphodiester blocks.