87303-54-6

Upstream product

• 18439-60-6 methyl 2,3,4-tri-O-acetyl-6-O-p-toluenesulfonyl-α-D-mannopyranoside 
• 64-19-7 acetic acid 
• 51008-88-9 1,2,3,4-tetra-O-acetyl-D-mannopyranoside 
• 98-59-9 p-toluenesulfonyl chloride 
• 108-24-7 acetic anhydride 
• 6619-07-4 6-O-p-toluenesulfonyl-D-mannopyranose 
• 530-26-7 D-Mannose 
• 28154-37-2 1,2,3,4-tetra-O-acetyl-β-D-mannopyranose 

Relevant academic research and scientific papers

Pathways in the synthesis of functionalized glycolipids for liposomal preparations

We describe in this paper the synthesis of two glycolipids containing a mannosyl residue functionalized with malonic acid and azide groups at the C6 position. Two synthetic routes have been successfully implemented: the first one involves Schmidt's glycosylation procedure using functionalized carbohydrates, whereas the second one involves nucleophilic substitutions in the C6 position of an iodinated intermediate obtained using Koenigs-Knorr reaction. A comparative discussion of reactions and yields is realized. The two glycolipids served as material for the preparation of liposomes.

D - And L -Mannose-Containing glyco-Oligoamides Show Distinct Recognition Properties When Interacting with DNA

Mannose glyco-oligoamide β-D-Man-Py-γ-Py-Ind (β-D-Man, 1) and two new glyco-oligoamides, β-L-Man-Py-γ-Py-Ind (β-L-Man, 2) and 6-deoxy-β-D-Man-Py-γ-Py-Ind (6-deoxy-β-D-Man, 3), have been designed and synthesized to investigate the role of hydrogen-bonding

Building Units of Oligosaccharides, CX. - Synthesis of Potential Inhibitors of N-Acetylglucosaminyltransferase I

Modified derivatives of the trisaccharide octyl α-D-Man(1-->3)-6)>-β-D-Man were synthesized by attaching reactive groups via a pentyl spacer to the 4'-OH and 6'-OH group.Glycosylation steps were carried out by using the trichloroacetimidate m