Generic placeholder image

Letters in Organic Chemistry

Editor-in-Chief

ISSN (Print): 1570-1786
ISSN (Online): 1875-6255

Research Article

Synthesis of Monosulfated Lewis a Trisaccharide Library Through Sulfation of a Partial Protected Trisaccharide

Author(s): Yili Ding* and Bingyun Wang

Volume 14 , Issue 6 , 2017

Page: [446 - 449] Pages: 4

DOI: 10.2174/1570178614666170505113336

Price: $65

Abstract

Background: The biological significance of glycoconjugates has stimulated much synthetic activity in oligosaccharide synthesis, the sulfate group in sulfated oligosaccharides has been shown to be constitutively involved in the interaction of ligands with selectins, establishing combinatorial methods for the synthesis of sulfated oligosaccharide library may be useful for screening of ligands of selectins.

Results: Random sulfation of a partial benzyl protected Lewis A trisaccharide in pyridine provided a sulfated trisaccharide mixture. After hydrogenation with Pd/C and purification on Sephadex A-50 column, a monosulfated trisaccharide library was obtained as a mixture. The H-H COSY NMR spectrum of this mixture showed that this mixture contains all five possible monosulfated Lewis A trisaccharides with acceptable ratio.

Conclusion: Random sulfation of a partial protected oligosaccharide was demonstrated as the most efficient method so far for the synthesis of monosulfated oligosaccharide library.

Keywords: Combinatorial chemistry, lewis A trisaccharides, oligosaccharide, sulfated oligosaccharide library, sulfation, synthesis.

Graphical Abstract

Rights & Permissions Print Export Cite as
© 2022 Bentham Science Publishers | Privacy Policy