616861-59-7

Upstream product

• 98-88-4 benzoyl chloride 
• 162466-65-1 allyl 3,4,6-tri-O-benzyl-β-D-galactopyranoside 
• 616861-58-6 allyl 2-O-acetyl-3,4,6-tri-O-benzyl-β-D-galactopyranoside 
• 616861-57-5 3,4,6-tri-O-benzyl-1,2-O-(allyloxyethylidene)-α-D-galactopyranose 
• 616861-56-4 3,4,6-tri-O-acetyl-α-D-galactopyranose-1,2-O-diyl allyl orthoacetate 
• 25878-60-8 D-galactose pentaacetate 
• 100-39-0 benzyl bromide 

Downstream Products

• 616861-60-0 2-O-benzoyl-3,4,6-tri-O-benzyl-β-D-galactopyranosyl trichloroacetimidate 
• 616861-61-1 2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-galactopyranosyl trichloroacetimidate 
• 616861-53-1 methyl (3,4,6-tri-O-benzyl-β-D-galactopyranosyl)-(1->2)-(allyl 3,4-di-O-methoxymethyl-β-D-glucopyranosid)uronate 
• 616861-51-9 methyl (2-O-benzoyl-3,4,6-tri-O-benzyl-β-D-galactopyranosyl)-(1->2)-(allyl 3,4-di-O-methoxymethyl-β-D-glucopyranosid)uronate 
• 148926-02-7 2-O-benzoyl-3,4,6-tri-O-benzyl-D-galactopyranose 

Relevant academic research and scientific papers

Is acyl migration to the aglycon avoidable in 2-acyl assisted glycosylation reactions?

This report unequivocally separates orthoester formation from acyl transfer for the first time and indicates possible routes to eliminate 2-O-acyl transfer during glycosylation reactions. Experimental evidence is shown that acyl transfer from 2-O-acyl-3,4

Synthesis of the trisaccharide portion of soyasaponin βg: Evaluation of a new glucuronic acid acceptor

The synthesis of the trisaccharide portion of soyasaponin βg was successfully achieved using a new glucuronic acid acceptor: methyl 1-O-allyl-3,4-di-O-methoxymethyl-β-D-glucuronate (9). This compound and methyl 1-O-allyl-3,4-di-O-tert-butyldimethylsilyl-β