A novel chemical approach to biotinylated glycosulfopeptides

A symposium report. A novel chem. approach for the synthesis of biotinylated glycosulfopeptides uses two different chemoselective ligation reactions in the presence of the sulfate moiety. The strategy was applied to the synthesis of a peptide sequence derived from the N-terminal region of the P-selectin glycoprotein ligand 1 (PSGL-1), a major ligand of the selectin family involved in cell-cell adhesion. [on SciFinder (R)]


Published in:
Peptides 2000, Proceedings of the European Peptide Symposium, 26th, 303-304
Year:
2001
Laboratories:




 Record created 2006-02-09, last modified 2018-01-27


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