Abstract
The phosphorylated branched heptasaccharide beta-D-Galp-(1-->4)-alpha-D-Manp-(1-PO3H-6)-[beta-D-Glcp-(1-->3)]-beta-D-Galp-(1-->4)-alpha-D-Manp-(1-PO3H-6)-beta-D-Galp-(1-->4)-alpha-D-Manp-1-PO3H-O[CH2](8)CH=CH2, which is a fragment of the phosphoglycan portion of Leishmania mexicana phosphoglycan and proteophosphoglycan, has been synthesized using the thioglycoside and Helferich methods for the glycosylations and the glycosyl hydrogenphosphonate method for the successive introduction of the disaccharide phosphate and trisaccharide phosphate blocks.
| Original language | English |
|---|---|
| Pages (from-to) | 2587-2595 |
| Number of pages | 9 |
| Journal | Journal of the Chemical Society - Perkin Transactions 1 |
| Issue number | 16 |
| DOIs | |
| Publication status | Published - 21 Aug 1998 |
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Dive into the research topics of 'Parasite glycoconjugates: Part 8. Chemical synthesis of a heptaglycosyl triphosphate fragment of Leishmania mexicana lipo- and proteo-phosphoglycan and of a phosphorylated trisaccharide fragment of Leishmania donovani surface lipophosphoglycan'. Together they form a unique fingerprint.Cite this
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