100605-72-9

Upstream product

• 2595-07-5 allyl D-galactopyranoside 
• 100759-10-2 allyl 4,6-di-O-benzylidene-α-D-galactopyranoside 
• 100605-69-4 allyl 2,3-di-O-benzyl-α-D-galactopyranoside 
• 100759-11-3 allyl 2,3-di-O-benzyl-4,6-di-O-benzylidene-α-D-galactopyranoside 
• 100-39-0 benzyl bromide 
• 10257-28-0 D-Galactose 
• 100605-70-7 allyl 2,3-di-O-benzyl-6-O-p-tosyl-α-D-galactopyranoside 

Downstream Products

• 100605-73-0 Allyl-2,3-di-O-benzyl-6-desoxy-4-O-methyl-α-D-galactopyranosid 

Relevant academic research and scientific papers

In situ activating glycosylation of 6-deoxysugars: Synthesis of O- α-D- fucosyl(1→4)-O-α-D-fucosyl-(1→4)-O-α-D-quinovosyl-(1→4)-D-quinovose

The linear tetrasaccharide, α-D-fucopyranosyl-(1→4)-a-D-fucopyranosyl- (1→4)-α-D-quinovopyranosyl-(1→4)-D-quinovopyranose, the sugar cluster of asterosaponin A from the starfish, Asterias amurensis, was synthesized in a convergent manner. We employed an i

Syntheses of Methyl 4-O-(β-D-Curacosyl)-α-D-curamicoside, the Glycoside of the Disaccharide Moiety E-F of Flambamycin and Isomers

By application of the tetraisopropyldisiloxy function a five-step synthesis of the selectively protected 2,6-di-O-methylmannopyranoside 5a is achieved.Additionally several steps are used to transfer the galactopyranoside 7 into the α-bromide of 4-O-methyl