85011-46-7

Upstream product

• 71117-16-3 2,3,4-tri-O-benzyl-β-D-glucopyranose 
• 88567-49-1 6-O-acetyl-2,3,4-tri-O-benzyl-D-glucopyranose 
• 10548-46-6 1,6-anhydro-2,3,4-tri-O-benzyl-β-D-glucopyranose 
• 4356-77-8 1,6-di-O-acetyl-2,3,4-tri-O-benzyl-D-glucopyranose 
• 58527-89-2 benzyl 1,2,3,6-tetra-O-benzyl-α-D-glucopyranoside 

Downstream Products

• 431899-02-4 benzyl 2,3,4-tri-O-benzyl-6-O-tertbutoxycarboxymethyl-β-D-galactopyranosyl-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 

Relevant academic research and scientific papers

Human milk oligosaccharides: An enzymatic protection step simplifies the synthesis of 3′- and 6′-O-sialyllactose and their analogues

We describe a chemo-enzymatic synthesis of 3′- and 6′-O-sialyllactose, two trisaccharides occurring in the 'acidic fraction' of the human milk oligosaccharides and endowed with potential antiadhesive activity. The key step is the highly regioselective 6′-

The Stereoselective Dehydrative α-Glucosylation Using 6-O-Acetyl- and 6-O-p-Nitrobenzoyl-2,3,4-tri-O-benzyl-D-glucopyranoses

The stereoselective synthesis of α-linked glucobiose derivatives using 6-O-acetyl- or 6-O-p-nitrobenzoyl-2,3,4-tri-O-benzyl-D-glucopyranose and a ternary mixture of p-nitrobenzenesulfonyl chloride, silver trifluoromethanesulfonate, and triethylamine in dichloromethane is described.