Synthesis of a Neolactotetraose Glycoside Suitable for Enzymatic Elaboration to the Sialyl Lewis X Stage
- 1 March 1998
- journal article
- Published by Taylor & Francis in Journal of Carbohydrate Chemistry
- Vol. 17 (2) , 267-278
- https://doi.org/10.1080/07328309808002327
Abstract
No abstract availableThis publication has 25 references indexed in Scilit:
- Synthetic Studies on Sialoglycoconjugates 70: Synthesis of Sialyl and Sulfo Lewis × Analogs Containing a Ceramide or 2-(Tetradecyl)hexadecyl ResidueJournal of Carbohydrate Chemistry, 1995
- Synthesis of cluster sialoside inhibitors for influenza virusJournal of the American Chemical Society, 1991
- Enzyme-catalyzed synthesis of sialyl oligosaccharide with in situ regeneration of CMP-sialic acidJournal of the American Chemical Society, 1991
- Sticky sugars for selectinsNature, 1991
- The Synthesis and Glycosidation ofN-Acetylneuraminic AcidSynthesis, 1991
- High-efficiency synthesis of sialyloligosaccharides and sialoglycopeptidesJournal of the American Chemical Society, 1990
- Adhesion receptors of the immune systemNature, 1990
- Leukocyte adhesion to endothelium in inflammationCell, 1990
- Stereoselective synthesis of sialyl-lactotetraosylceramide and sialylneolactotetraosylceramideCarbohydrate Research, 1990
- A novel, reductive ring-opening of carbohydrate benzylidene acetalsCarbohydrate Research, 1982