303752-87-6

Upstream product

• 168037-64-7 2,3-Bis-O-(phenylmethyl)-4,6-O-(phenylmethylene)-D-galactopyranose 
• 545-06-2 trichloroacetonitrile 
• 303752-88-7 Allyl 2,3-Bis-O-(phenylmethyl)-4,6-O-(phenylmethylene)-D-galactopyranoside 
• 20746-64-9 (2S,4aR,7R,8R,8aR)-6-Allyloxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine-7,8-diol 
• 3006-41-5 4,6-O-benzylidene-α,β-D-galactopyranose 
• 100-39-0 benzyl bromide 

Downstream Products

• 303752-86-5 (2S,3S,4R)-2-azido-1-(((2S,4aS,6S,7R,8S,8aR)-7,8-bis(benzyloxy)-2-phenylhexahydropyrano[3,2-d][1,3]dioxin-6-yl)oxy)octadecane-3,4-diol 
• 1200762-61-3 (2,3-di-O-benzyl-4,6-O-benzylidene-β-D-galactopyranosyl)-(1->6)-O-1,2:3,4-di-O-isopropylidene-α-D-galactopyranose 
• 1177264-14-0 (2,3-di-O-benzyl-4,6-O-benzylidene-α-D-galactopyranosyl)-(1->6)-O-1,2:3,4-di-O-isopropylidene-α-D-galactopyranose 
• 1352408-15-1 3,4-di-O-benzyl-1-O-(2,3,4-tri-O-benzyl-α-D-galactopyranosyl)-2-(6-phenylhexanoyl)aminooctadecane-1,3,4-triol 
• 1352408-14-0 2-azido-3,4-di-O-benzyl-1-O-(2,3,4-tri-O-benzyl-α-D-galactopyranosyl)octadecane-1,3,4-triol 
• 1352408-21-9 C₃₆H₆₁NO₁₀ 
• 1352408-20-8 3,4-dihydroxy-1-O-(3,4,5-trihydroxy-α-D-galactopyranosyl)-2-(6-phenylhexanoyl)aminooctadecane-1,3,4-triol 
• 1352408-19-5 3,4-di-O-benzyl-1-O-(2,3,4-tri-O-benzyl-α-D-galactopyranosyluronate)-2-(6-phenylhexanoyl)aminooctadecane-1,3,4-triol 
• 1352408-17-3 3,4-di-O-benzyl-1-O-(2,3,4-tri-O-benzyl-6-hydroxy-6-iodo-α-D-galactopyranosyl)-2-(6-phenylhexanoyl)aminooctadecane-1,3,4-triol 
• 951767-71-8 2-azido-3,4-di-O-benzyl-1-O-(2,3-di-O-benzyloxyl-4,6-O-benzyllidene-α-D-galactopyranosyl)-D-ribooctadecane-1,3,4-triol 
• 1242144-15-5 (2S,3R,4R)-2-tert-butyldimethylsilyloxy-3,4-O-isopropylideneoctadecyl-2,3-di-O-benzyl-4,6-O-benzylidene-β-D-galactopyranoside 
• 1215176-83-2 (2S,3R,4R)-2-tert-butyldimethylsilyloxy-3,4-O-isopropylideneoctadecyl-2,3-di-O-benzyl-4,6-O-benzylidene-α-D-galactopyranoside 
• 303752-91-2 1-O-(2,3-di-O-benzyl-4,6-O-benzylidene-α-D-galactopyranosyl)-2-O-methanesulfonyl-D-arabino-1,2,3,4-octadecantetrol 

Relevant academic research and scientific papers

Glycosylation catalyzed by a chiral bronsted acid

"Chemical equation presented" The use of a chiral Bronsted acid catalyst for the activation of trichloroacetimidate glycosyl donors has been demonstrated for the first time. In toluene the chirality of the acid catalyst is seen to influence the stereochem

Total synthesis of α-galactosyl cerebroside

A highly convergent synthetic approach was developed to obtain α- galactosyl cerebroside O-(α-D-galactopyranosyl)-2-hexacosylamino-D-ribo- 1,3,4-octadecantriol, which has previously been demonstrated to have immunostimulatory activity. Known 4,6-O-benzyli