A novel and versatile glycosyl donor for the preparation of glycosides of N-acetylneuraminic acid

This publication has 9 references indexed in Scilit:

• A highly convergent synthesis of a hexasaccharide derived from the oligosaccharide of group B type III Streptococcus
  Tetrahedron Letters, 1997
• Recent developments in chemical oligosaccharide synthesis
  Contemporary Organic Synthesis, 1996
• N,N-diacetyl-glucosamine and -galactosamine derivatives as glycosyl donors
  Tetrahedron Letters, 1995
• A facile, large-scale preparation of the methyl 2-thioglycoside of N-acetylneuraminic acid, and its usefulness for the α-stereoselective synthesis of sialoglycosides
  Carbohydrate Research, 1991
• Communication: Synthetic Studies on Sialoglycoconjugates 25: Reactivity of Glycosyl Promoters in α-Glycosylation of N-Acetyl-Neuraminic Acid with the Primary and Secondary Hydroxyl Groups in the Suitably Protected Galactose and Lactose Derivatives
  Journal of Carbohydrate Chemistry, 1991
• Stereoselective synthesis of sialyl-lactotetraosylceramide and sialylneolactotetraosylceramide
  Carbohydrate Research, 1990
• Immunization of Pregnant Women with a Polysaccharide Vaccine of Group B Streptococcus
  New England Journal of Medicine, 1988
• Long-Term Outcome of Group B Streptococcal Meningitis
  Pediatrics, 1986
• Immunodeterminant specificity of human immunity to type III group B streptococcus.
  The Journal of Experimental Medicine, 1979