Abstract
A short, blockwise, 2+2-glycosylation approach to the synthesis of a tetrasaccharide component of Trypanosoma cruzi mucin is reported. Despite the use of a 1,2-linked disaccharide donor, high yield (79%) and good stereocontrol (>10:1, β:α) were achieved in the key glycosylation step. Preliminary studies indicate that this branched tetrasaccharide can serve as a substrate for enzymatic sialylation by the parasite cell surface trans-sialidase.
| Original language | Undefined |
|---|---|
| Pages (from-to) | 2175-2177 |
| Number of pages | 3 |
| Journal | SYNLETT |
| Volume | 14 |
| DOIs | |
| Publication status | Published - 5 Aug 2008 |
Keywords
- oligosaccharide
- synthesis
- parasite
- mucin
- trans-sialidase
- drug target
Research Highlights, Institutes and Platforms
- Manchester Institute of Biotechnology
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