58527-86-9

Upstream product

• 2280-44-6 D-Glucose 
• 100-39-0 benzyl bromide 
• 784179-19-7 benzyl 4,6-O-benzylidene-2,3-tri-O-benzyl-α,β-D-glucopyranoside 
• 142698-31-5 benzyl 2,3-di-O-benzyl-4,6-O-benzylidene-α-D-glucopyranoside 
• 100-51-6 benzyl alcohol 
• 79549-73-8 benzyl 4,6-O-(phenylmethylene)-α-D-glucopyranoside 
• 34246-23-6 benzyl D-glucopyranoside 

Downstream Products

• 84073-57-4 Benzyl 2,3-di-O-benzyl-6-O-phenyl-α-D-glucopyranoside 
• 84073-56-3 Benzyl 2,3-di-O-benzyl-4-O-phenyl-α-D-glucopyranoside 
• 58527-89-2 benzyl 1,2,3,6-tetra-O-benzyl-α-D-glucopyranoside 
• 4132-31-4 penta‐O‐benzyl-α-D‐glucopyranoside 
• 59935-49-8 benzyl 2,3,4-tri-O-benzyl-α-D-glucopyranoside 
• 78727-78-3 benzyl 2,3-di-O-benzyl-6-O-methoxymethyl-α-D-glucopyranoside 
• 356047-14-8 benzyl 2,3-di-O-benzyl-4-O-(4-methoxybenzyl)-α-D-glucopyranoside 
• 356047-12-6 benzyl 2,3-di-O-benzyl-6-O-tert-butyldiphenylsilyl-4-O-(4-methoxybenzyl)-α-D-glucopyranoside 
• 245527-13-3 Benzyl 2,3-di-O-benzyl-4,6-di-O-(3-hydroxypropyl)-α-D-glucopyranoside 
• 55281-50-0 benzyl 2,3-di-O-benzyl-6-deoxy-α-D-glucopyranoside 
• 77977-09-4 benzyl 2,3-di-O-benzyl-6-deoxy-α-D-xylo-hexopyranosid-4-ulose 
• 1034140-22-1 benzyl 2,3-di-O-benzyl-6-bromo-6-deoxy-α-D-glucopyranoside 
• 1034140-24-3 benzyl 2,3-di-O-benzyl-6-O-thexyldimethylsilyl-α-D-glucopyranoside 

Relevant academic research and scientific papers

Synthesis of Bradyrhizose from d -Glucose

We describe the synthesis of the unusual bicyclic sugar bradyrhizose in 14 steps and a 6% overall yield from d-glucose. The synthesis involves the elaboration of a trans-fused carbocyclic ring onto the preexisting glucopyranose framework followed by adjus

TANNIN INHIBITORS OF HIV

The invention provides a method to prevent or treat HIV-infection with synthetic tannins, and pharmaceutical compositions comprising synthetic tannins.

Regioselective removal of the anomeric O-benzyl from differentially protected carbohydrates

A mild, regioselective deprotection of the anomeric O-benzyl from multi-functionally protected carbohydrates via catalytic transfer hydrogenation is described. The protocol is tolerant of O-benzyl and O-benzylidene protections at non-anomeric positions, g

Synthesis of monosaccharide-fused azetidines

Primary amines reacted upon 4,6-ditosylates of glucopyranosides to give an azetidine ring fused on C-4 and C-6 of the pyranose ring. On the other hand, the 4,6-ditosylate of benzyl mannopyranoside led to the 4,6-diamino-4,6-dideoxy derivative in a good yield. All the compounds and their precursors were identified by 1H and 13C NMR spectroscopy. Assignments of proton signals were made unambiguously using homodecoupling experiments.