Abstract
The syntheses of monodisperse lysine dendrimers, capped with two to sixty-four mono-, di- and tri-α-d-mannopyranosyl residues are described. These syntheses used reactive N-hydroxysuccinimide esters to ensure complete reaction of dendrimer amines with the mannosylating reagents. The purities of the dendrimers were established by RP-HPLC and MALDI-TOF mass spectrometry and were found to be excellent. The relative ability of these glycodendrimers to induce dendritic cell maturation was measured, however, no significant trends were observed.
| Original language | English |
|---|---|
| Pages (from-to) | 2939-2950 |
| Journal | Tetrahedron |
| Volume | 65 |
| Issue number | 15 |
| DOIs | |
| Publication status | Published - 2009 |
Keywords
- Organic Chemical Synthesis
- Cellular Immunology
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