77668-00-9

Upstream product

• 77667-99-3 O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1 → 2)-O-(6-O-benzoyl-3,4-O-isopropylidene-β-D-galactopyranosyl)-(1 → 4)-2,3:5,6-di-O-isopropylidene-D-glucose dimethyl acetal 
• 72200-51-2 2,3:5,6-Di-O-isopropylidene-4-O-(3',4'-O-isopropylidene-β-D-galactopyranosyl)-aldehydo-D-glucose dimethyl acetal 
• 167612-34-2 phenyl 6-deoxy-2,3,4-tri-O-acetyl-1-thio-β-L-galactopyranoside 
• 187233-24-5 phenyl 6-deoxy-1-thio-β-L-galactopyranoside 
• 167612-35-3 2,3,4-tri-O-benzyl-1-thio-β-L-fucopyranoside 
• 76946-04-8 perbenzyl fucosyl bromide 
• 1250436-12-4 4-O-(6-O-pivaloyl-3,4-O-isopropylidene-β-D-galactopyranosyl)-2,3:5,6-di-O-isopropylidene-D-glucose dimethyl acetal 
• 77-76-9 2,2-dimethoxy-propane 
• 73-34-7 6-deoxy-L-galactose 
• 7404-35-5 1,2,3,4-tetra-O-acetyl-L-fucopyranose 
• 77667-97-1 O-(6-O-acetyl-3,4-isopropylidene-β-D-galactopyranosyl)-(1->4)-2,3:5,6-di-O-isopropylidene-D-glucose dimethyl acetal 
• 5965-66-2 LACTOSE 
• 1250831-29-8 O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1→2)-O-(6-O-(4-benzamidobenzoyl)-3,4-isopropylidene-β-D-galactopyranosyl)-(1→4)-2,3:5,6-di-O-isopropylidene-D-glucose dimethyl acetal 
• 1250831-24-3 O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1→2)-O-(6-O-pivaloyl-3,4-isopropylidene-β-D-galactopyranosyl)-(1→4)-2,3:5,6-di-O-isopropylidene-D-glucose dimethyl acetal 

Downstream Products

• 1417612-63-5 C₃₉H₅₁NO₁₄ 

Relevant academic research and scientific papers

PROCESS FOR PRODUCING 2'-O-FUCOSYLLACTOSE

The present invention relates to a method for preparing 2′-O-fucosyllactose, the intermediates obtainable by this method and the use of these intermediates. The preparation comprises the reaction of a protected fucose of the general formula (I) with a tri

Kilogram scale chemical synthesis of 2′-fucosyllactose

A scalable synthetic procedure to high quality 2′-fucosyllactose, the most abundant oligosaccharide in human breast milk, has been designed and validated in kilogram scale. The synthetic route has been developed to suit industrial environment and contains

METHOD FOR THE SYNTHESIS OF A TRISACCHARIDE

The present invention relates to an improved synthesis of a trisaccharide of the formula (1), novel intermediates used in the synthesis and the preparation of the intermediates.

Bi- to tetravalent glycoclusters: Synthesis, structure-activity profiles as lectin inhibitors and impact of combining both valency and headgroup tailoring on selectivity

The emerging functional versatility of cellular glycans makes research on the design of synthetic inhibitors a timely topic. In detail, the combination of ligand (or headgroup or contact site) structure with spatial parameters that depend on topological a

Bi- to tetravalent glycoclusters: Synthesis, structure-activity profiles as lectin inhibitors and impact of combining both valency and headgroup tailoring on selectivity

The emerging functional versatility of cellular glycans makes research on the design of synthetic inhibitors a timely topic. In detail, the combination of ligand (or headgroup or contact site) structure with spatial parameters that depend on topological a

SYNTHESIS OF 2'-O-FUCOSYLLACTOSE

The present invention relates to an improved synthesis of a trisaccharide of the formula (1), novel intermediates used in the synthesis and the preparation of the intermediates.

SYNTHESIS OF O-α-L-FUCOPYRANOSYL-(1->2)-O-β-D-GALACTOPYRANOSYL-(1->4)-D-GLUCOPYRANOSE (2'-O-α-L-FUCOPYRANOSYL-LACTOSE)

Selective benzoylation of 2,3:5,6:3',4'-tri-O-isopropylidenelactose dimethyl acetal (1) with benzoyl chloride in dichloromethane afforded the 6'-O-benzoyl derivative (2).The constitution of 2 was inferred from its n.m.r. spectrum, and confirmed by methyla