123809-58-5

Upstream product

• 108-24-7 acetic anhydride 
• 40592-72-1 O³-α-D-Galactopyranosyl-D-glucose 
• 27607-77-8 trimethylsilyl trifluoromethanesulfonate 
• 27086-14-2 1,2,4,6-tetra-O-acetyl-β-D-glucopyranose 
• 604-69-3 β-D-glucose pentaacetate 
• 63064-54-0 allyl 2-acetamido-3,6-di-O-benzyl-2-deoxy-α-D-glucopyranoside 
• 71216-86-9 O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-(1<*>3)-O-(2,4,6-tri-O-acetyl-β-D-mannopyranosyl)-(1<*>4)-2-methyl-(2-acetamido-3,6-di-O-acetyl-1,2-dideoxy-α-D-glucopyrano)-<2,1-d>2-oxazoline 
• 55287-49-5 benzyl 2-acetamido-3,6-di-O-benzyl-2-deoxy-α-D-glucopyranoside 
• 22352-62-1 O¹,O²,O⁴,O⁶-Tetraacetyl-O³-(tetra-O-acetyl-α-D-galactopyranosyl)-ξ-D-glucopyranose 

Downstream Products

• 22352-62-1 O¹,O²,O⁴,O⁶-Tetraacetyl-O³-(tetra-O-acetyl-ξ-D-galactopyranosyl)-ξ-D-mannopyranose 

Relevant academic research and scientific papers

The Synthesis of Active-Site Directed Inhibitors of Some β-Glucan Hydrolases

The 2,3-epoxypropyl, 3,4-epoxybutyl and 4,5-epoxypentyl β-glycosides of D-glucose, cellobiose and laminaribiose have been prepared.As well, the 4,5-epoxypentyl β-glycosides of cellotriose, laminaritriose and two other trisaccharides have been synthesized. 3,4-Epoxybutyl β-cellobioside has also been prepared with a 14C-label in the cellobiose residue.

OLIGOSACCHARIDE OXAZOLINES: PREPARATION, AND APPLICATION TO THE SYNTHESIS OF GLYCOPROTEIN CARBOHYDRATE STRUCTURES

O-α-D-mannopyranosyl-(1->3)-O-β-D-mannopyranosyl-(1->4)-2-acetamido-2-deoxy-D-glucopyranose, isoleted from mannosidosis urine, was converted, via the per-O-acetylglycosyl chloride, into O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-(1->3)-O-(2,4,6-tri-O-a