142329-80-4

Upstream product

• 142329-79-1 4-nitrophenyl O-<3,4-O-isopropylidene-2-O-(4-methoxybenzyl)-α-L-fucopyranosyl>-(1->3)-2-acetamido-2-deoxy-4,6-O-isopropylidene-β-D-glucopyranoside 
• 66347-26-0 β-L-fucopyranosyl azide 
• 3459-18-5 4-nitrophenyl N-acetyl-β-D-glucosaminide 
• 10231-84-2 (4-nitro-phenyl)-α-L-fucopyranoside 
• 142329-94-0 4-nitrophenyl 2-acetamido-2-deoxy-4,6-O-isopropylidene-β-D-glucopyranoside 
• 130572-02-0 Methyl 3,4-O-Isopropylidene-2-O-(4-methoxybenzyl)-1-Thio-β-L-Fucopyranoside 
• 130572-04-2 methyl 3,4-O-isopropylidene-1-thio-β-L-fucopyranoside 

Relevant academic research and scientific papers

β-Glycosyl Azides as Substrates for α-Glycosynthases: Preparation of Efficient α-L-Fucosynthases

Fucose-containing oligosaccharides play a central role in physio-pathological events, and fucosylated oligosaccharides have interesting potential applications in biomedicine. No methods for the large-scale production of oligosaccharides are currently avai

Glycosidase-catalyzed synthesis of fucosyl di- and trisaccharide derivatives using α-L-fucosidase from Alcaligenes sp.

p-Nitrophenyl glycosides of di-and trisaccharides containing a (1→2)-, (1→3)-, (1→4)-, or (1→6)-linked α-L-fucosyl group were synthesized using the transglycosylation reaction mediated by α-L-fucosidase from Alcaligenes sp. with p-nitrophenyl glycosides of N-acetyllactosamine, lactose, D-GlcNAc, and D-Glc as acceptors. The enzymatic process for preparing these compounds is simple, and the yield is sufficiently high to make the method practical.

A facile synthesis of nitrophenyl oligosaccharides containing the O-α-L-fucopyranosyl-(1 → 3)-2-acetamido-2-deoxy-β-D-glucopyranosyl unit at their nonreducing end

A facile approach towards the synthesis of 4-nitrophenyl O-α-L-fucopyranosyl-(1 → 3)-2-acetamido-2-deoxy-β-D-glucopyranoside, 2-nitrophenyl O-α-L-fucopyranosyl-(1 → 3)-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1 → 6)-2-acetamido-2-deoxy-α-D-galactopyran