Conference paper

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)]


    • LCBP-CONF-2001-007

    Record created on 2006-02-09, modified on 2016-08-08


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