87470-80-2

Upstream product

• 3616-19-1 1',2',3',6',2,3,4,6-octa-O-acetyl-β-D-lactose 
• 100-52-7 benzaldehyde 
• 87508-19-8 phenyl 4',6'-O-benzylidene-1-thio-β-lactoside 
• 27891-73-2 β-phenylsulfanyl lactoside 
• 914772-36-4 (4aR,6S,7R,8S,8aS)-7,8-Bis-benzyloxy-6-((2R,3R,4S,5R,6S)-4,5-bis-benzyloxy-2-benzyloxymethyl-6-phenylsulfanyl-tetrahydro-pyran-3-yloxy)-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine 
• 87508-20-1 phenyl (2,3-di-O-benzyl-4,6-O-benzylidene-β-D-galactopyranosyl)-(1→4)-2,3,6-tri-O-benzyl-1-thio-β-D-glucopyranoside 
• 170208-77-2 phenyl 4-O-(4,6-benzylidene-β-D-galactopyranosyl)-1-thio-β-D-glycopyranoside 
• 5346-81-6 phenyl 2,3,6-tri-O-acetyl-4-O-(2',3',4',6'-tetra-O-acetyl-β-D-galactopyranosyl)-1-thio-β-D-glucopyranoside 
• 108-98-5 thiophenol 

Downstream Products

• 87470-82-4 phenyl 2,3,6,2',3',6'-hexa-O-benzyl-4'-O-methyl-1-thio-β-lactoside 

Relevant academic research and scientific papers

An efficient glycosylation reaction for the synthesis of asialo GM2 analogues

We investigated the coupling reaction of glycosyl donors N-trichloroethoxycarbonyl-galactosamine-O-trichloroacetimidate (2a) and N-p-nitrobenzyloxycarbonyl-galactosamine-O-trichloroacetimidate (2b) with the 4′-OH of lactose derivatives (3a-d) to synthesiz

HYDROGENOLYSIS OF THE BENZYLIDENE ACETALS OF THIOGLYCOSIDES WITH THE LiAlH4-AlCl3 REAGENT. SYNTHESIS OF PARTIALLY BENZYLATED THIOGLYCOSIDE DERIVATIVES

Reductive hydrogenolysis of phenyl 2,3-di-O-benzyl-4,6-O-benzylidene-1-thio-β-D-gluco- (4) and -galactopyranoside (8) and phenyl 2,3,6,2',3'-penta-O-benzyl-4',6'-O-benzylidene-1-thio-β-cellobioside (15) with the LiAlH4-AlCl3 reagent resulted in the corres