99388-33-7

Upstream product

• 18404-72-3 benzyl 4-O-β-D-galactopyranosyl-β-D-glucopyranoside 
• 100-44-7 benzyl chloride 
• 105165-62-6 benzyl O-(3-O-allyl-β-D-galactopyranosyl)-(1->4)-β-D-glucopyranoside 
• 100-39-0 benzyl bromide 
• 67310-53-6 (2R,3S,4S,5R,6S)-2-(acetoxymethyl)-6-(((2R,3R,4S,5R,6R)-4,5-diacetoxy-2-(acetoxymethyl)-6-(benzyloxy)tetrahydro-2H-pyran-3-yl)oxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate 
• 105165-63-7 benzyl 3'-O-allyl-2,6,2',4',6'-penta-O-benzyl-β-lactoside 

Downstream Products

• 105165-64-8 benzyl 2,6,2',4',6'-penta-O-benzyl-3,3'-O-(3,6,9-trioxaundecane-1,11-diyl)-β-lactoside 

Relevant academic research and scientific papers

CHIRAL MACROCYCLIC COMPOUNDS FROM LACTOSE DERIVATIVES

The reaction of benzyl 2,6,6'-tri-O-benzyl-3',4'-O-isopropylidene-β-lactoside with 1,11-ditosyloxy-3,6,9-trioxaundecane gave benzyl 2,6,6'-tri-O-benzyl-3',4'-O-isopropylidene-3,2'-O-(3,6,9-trioxaundecane-1,11-diyl)-β-lactoside (2,47percent).Acid hydrolysi

4-O-beta-D-Galactopyranosyl-3-O-methyl-D-glucose: a new synthesis and application to the evaluation of intestinal lactase.

4-O-beta-D-Galactopyranosyl-3-O-methyl-D-glucose (1, 3-O-methyl-lactose) has been prepared from benzyl 2,6-di-O-benzyl-4-O-(2,6-di-O-benzyl-3, 4-O-isopropylidene-beta-D-galactopyranosyl)-beta-D-glucopyranoside (5) and from benzyl 2,6-di-O-benzyl-4-O-(2,3,