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Presentation
Synthesis of Quinamide-Based Disaccharide Mimetics
Annual Conference of the Society for Glycobiology
  • Thuy Trang M. Nguyen
  • P. Phiasivongsa
  • Paul H. Gross, University of the Pacific
  • Andreas H. Franz, University of the Pacific
Document Type
Poster
Department
Chemistry
Organization
Society for Glycobiology
Location
San Diego, CA
Conference Dates
December 3-6, 2003
Date of Presentation
12-3-2003
Disciplines
Abstract
Oligosaccharides constitute important recognition motifs for fundamental biological processes such as cell-cell communication, immune response, and fertilization. Whereas most protein-carbohydrate interactions are weak, a pronounced increase in binding strength can be observed frequently if oligosaccharide clusters are involved. This “glycoside cluster effect” has been the foundation of efforts for the development of carbohydrate-based vaccines and drugs. This paper reports the synthesis and characterization of Small Cluster Oligosaccharide Mimetics (SCOM). The per-O-acetylated derivative of L-fucose was synthesized by an improved method. Tetra-O-acetyl-L-fucopyranose was converted to the glycosyl cyanide by HgBr2-promoted reaction with trimethylsilyl cyanide (Me3SiCN). Reduction of the fucosyl cyanide in the presence of t-butyloxycarbonyl anhydride (Boc)2O yielded the corresponding Boc-protected aminomethyl-C-glycoside and a disaccharidic analog. Both monomer and dimer were separated by flash column chromatography and were characterized by Nuclear Magnetic Resonance (NMR) spectroscopy and Electrospray-Ionization Mass Spectrometry (ESIMS). Removal of the acetyl groups and the Boc group towards fully deprotected aminomethyl-C-glycosides was investigated for both the C-glycoside monosaccharide and the disaccharide. The deprotected product was coupled with the previously synthesized 4,5-O-isopropylidene-1,3-lactone of quinic acid to yield the corresponding polyhydroxyl cluster qinamides. In separate experiments, the isopropylidenated quinic acid lactone was coupled with D-glucamine and with the previously synthesized benzyl-4,6-O-benzylidene-2-amino-2-deoxy-D-glucosamine to yield the corresponding quinamides. The identity of all products was confirmed by 1D-/2D-NMR spectroscopic techniques and mass spectrometry.
Citation Information
Thuy Trang M. Nguyen, P. Phiasivongsa, Paul H. Gross and Andreas H. Franz. "Synthesis of Quinamide-Based Disaccharide Mimetics" Annual Conference of the Society for Glycobiology (2003)
Available at: http://works.bepress.com/andreas-franz/72/