58527-89-2

Upstream product

• 58527-86-9 Benzyl 2,3-di-O-benzyl-α-D-glucopyranoside 
• 100-39-0 benzyl bromide 
• 83236-84-4 benzyl 4-O-allyl-3-O-benzyl-α-D-glucopyranoside 
• 100-44-7 benzyl chloride 

Downstream Products

• 120269-13-8 O-(2,3,4-tri-O-benzyl-α-L-rhamnopyranosyl)-(1->1)-2,3,4-tri-O-benzyl-α-L-rhamnopyranoside 
• 91233-23-7 (E)-4-((2R,3R,4S,5R,6S)-4,5,6-Tris-benzyloxy-2-benzyloxymethyl-tetrahydro-pyran-3-yloxy)-but-3-en-2-one 
• 91233-26-0 (E)-2-Methyl-1-((2R,3R,4S,5R,6S)-4,5,6-tris-benzyloxy-2-benzyloxymethyl-tetrahydro-pyran-3-yloxy)-pent-1-en-3-one 
• 125219-26-3 benzyl 2,3,6-tri-O-benzyl-α-D-xylo-hex-4-ulopyranoside 
• 124813-93-0 benzyl 2,3,6-tri-O-benzyl-4-O-(2,4,6-tri-O-acetyl-3-O-benzyl-β-D-glucopyranosyl)-α-D-glucopyranoside 
• 173977-53-2 Benzyl O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-α-D-glucopyranoside 
• 173977-54-3 Benzyl O-(2,3-di-O-acetyl-4,6-O-benzylidene-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-α-D-glucopyranoside 
• 1034139-92-8 benzyl O-(3,4,6-tri-O-acetyl-2-azido-2-deoxy-α-D-glucopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-α-D-glucopyranoside 
• 1344024-95-8 (4-deoxy-4-methyl-(1,2,3,6-tetra-O-benzyl-α-D-glucopyranosyl))-(2,3,4,6-tetra-O-benzyl)-α-D-glucopyranoside 
• 1344024-94-7 (4-deoxy-4-methyl-(1,2,3,6-tetra-O-benzyl-α-D-glucopyranosyl))-(2,3,4,6-tetra-O-acetyl)-β-D-galactopyranoside 
• 1344024-93-6 (4-deoxy-4-methyl-(1,2,3,6-tetra-O-benzyl-α-D-glucopyranosyl))-(2,3,4,6-tetra-O-acetyl)-β-D-glucopyranoside 
• 1334774-11-6 1,2,3,6-tetra-O-benzyl-4-O-[12-(tetrahydropyranyloxy)dodecyl]-α-D-glucopyranose 
• 1334774-26-3 1,2,3,6-tetra-O-benzyl-4-O-[9-[(2R,3R,4R,5S)-3,4,5-tribenzyloxy-2-benzyloxymethylpiperidino]nonyl]-α-D-glucopyranose 
• 1334774-24-1 1,2,3,6-tetra-O-benzyl-4-O-[6-[(2R,3R,4R,5S)-3,4,5-tribenzyloxy-2-benzyloxymethylpiperidino]hexyl]-α-D-glucopyranose 

Relevant academic research and scientific papers

DISACCHARIDES

A disaccharide having the structure (Formula I), and a disaccharide having the structure (Formula II) exhibit immunomodulatory activity.

Synthesis of Branched-Chain Oligosaccharides in Sarsasapogenins by Dehydrative Glycosylation

The branched-chain oligosaccharides, 6-O-(β-D-glucopyranosyl)-4-O-(α-L-rhamnopyranosyl)-D-glucopyranose, and 2,6-di-O-(β-D-glucopyranosyl)-4-O-(α-L-rhamnopyranosyl)-D-glucopyranose, which compose sarsasapogenins, as well as the structurally related 2-O-(β

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.

A Mild Procedure for the Regiospecific Benzylation and Allylation of Polyhydroxy-compounds via their Stannylene Derivatives in Non-polar Solvents

The reactions of benzyl and allylbromides on the stannylene derivatives of polyhydroxy-compounds, which normally proceed only at insignificant speed in refluxing benzene solution, are greatly accelerated in the presence of quaternary ammonium halides.Thes