914772-34-2

Upstream product

• 56865-31-7 methyl 4,6-O-benzylidene-β-D-galactopyranosyl-(1,4)-β-D-glucopyranoside 
• 100-39-0 benzyl bromide 

Downstream Products

• 19474-56-7 methyl 2,3,6-tri-O-benzyl-4-O-(2',3',6'-tri-O-benzyl-β-D-galactopyranosyl)-β-D-glucopyranoside 
• 914772-40-0 acetic acid 3-acetoxy-2-acetoxymethyl-6-[4,5-bis-benzyloxy-2-benzyloxymethyl-6-(4,5-bis-benzyloxy-2-benzyloxymethyl-6-methoxy-tetrahydro-pyran-3-yloxy)-tetrahydro-pyran-3-yloxy]-5-(2,2,2-trichloro-ethoxycarbonylamino)-tetrahydro-pyran-4-yl ester 
• 116235-03-1 methyl 2,3,6-tri-O-benzyl-4-O-(2,3,6-tri-O-benzyl-4-deoxy-β-D-xylo-hexopyranosyl)-β-D-glucopyranoside 

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

Studies of the molecular recognition of synthetic methyl β-lactoside analogues by Ricinus communis agglutinin

The 2-, 3-, 6-, 2'-, 3'-, 4'-, and 6'-deoxy derivatives and the 3-O-methyl derivative of methyl β-lactoside have been synthesised and their binding to the galactose-specific agglutinin from Ricinus communis (RCA-120) has been investigated. The results ind