phenyl 2-acetamido-2-deoxy-4-O-α-L-fucopyranosyl-3-O-β-D-galactopyranosyl-β-D-glucopyranoside

Base Information

• Chemical Name: phenyl 2-acetamido-2-deoxy-4-O-α-L-fucopyranosyl-3-O-β-D-galactopyranosyl-β-D-glucopyranoside
• CAS No.: 81329-66-0
• Molecular Formula: C₂₆H₃₉NO₁₅
• Molecular Weight: 605.593
• Mol file: 81329-66-0.mol

Synonyms:phenyl 2-acetamido-2-deoxy-4-O-α-L-fucopyranosyl-3-O-β-D-galactopyranosyl-β-D-glucopyranoside

Chemical Property of phenyl 2-acetamido-2-deoxy-4-O-α-L-fucopyranosyl-3-O-β-D-galactopyranosyl-β-D-glucopyranoside

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of phenyl 2-acetamido-2-deoxy-4-O-α-L-fucopyranosyl-3-O-β-D-galactopyranosyl-β-D-glucopyranoside

There total 8 articles about phenyl 2-acetamido-2-deoxy-4-O-α-L-fucopyranosyl-3-O-β-D-galactopyranosyl-β-D-glucopyranoside which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 74.0%

phenyl 2-acetamido-2-deoxy-3-O-β-D-galactopyranosyl-4-O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-β-D-glucopyranoside (84333-53-9) → phenyl 2-acetamido-2-deoxy-4-O-α-L-fucopyranosyl-3-O-β-D-galactopyranosyl-β-D-glucopyranoside (81329-66-0)

Guidance literature:

With hydrogen; palladium on activated charcoal; In acetic acid; for 48h;

DOI:10.1016/0008-6215(83)88287-1

Reference yield:

phenyl 2-acetamido-2-deoxy-4,6-O-(p-methoxybenzylidene)-β-D-glucopyranoside (78489-49-3,117436-77-8) → phenyl 2-acetamido-2-deoxy-4-O-α-L-fucopyranosyl-3-O-β-D-galactopyranosyl-β-D-glucopyranoside (81329-66-0)

Guidance literature:

Multi-step reaction with 4 steps

1: 72 percent / mercuric cyanide / benzene; nitromethane / 52 h / 60 °C

2: 68 percent / 80 percent acetic acid / 0.33 h / 60 °C

3: 85 percent / 0.1 M sodium methoxide / CHCl₃; methanol / 1.) r.t., 6 h; 2.) 5 deg C, overnight

4: 1.) MES buffer, MnCl2, milk-enzyme; 2.) α-L-fucosidase(from human serum) / 1.) 37 deg C, 30 min, ethanol; 2.) 37 deg C, 6 h

With MES buffer; α-L-fucosidase(from human serum); milk-enzyme; sodium methylate; mercury(II) cyanide; acetic acid; manganese(ll) chloride; In methanol; nitromethane; chloroform; benzene;

DOI:10.1016/0008-6215(83)88287-1

Reference yield:

phenyl 2-acetamido-2-deoxy-3-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-β-D-glucopyranoside (84333-50-6) → phenyl 2-acetamido-2-deoxy-4-O-α-L-fucopyranosyl-3-O-β-D-galactopyranosyl-β-D-glucopyranoside (81329-66-0)

Guidance literature:

Multi-step reaction with 2 steps

1: 85 percent / 0.1 M sodium methoxide / CHCl₃; methanol / 1.) r.t., 6 h; 2.) 5 deg C, overnight

2: 1.) MES buffer, MnCl2, milk-enzyme; 2.) α-L-fucosidase(from human serum) / 1.) 37 deg C, 30 min, ethanol; 2.) 37 deg C, 6 h

With MES buffer; α-L-fucosidase(from human serum); milk-enzyme; sodium methylate; manganese(ll) chloride; In methanol; chloroform;

DOI:10.1016/0008-6215(83)88287-1

upstream raw materials:

phenyl 2-acetamido-2-deoxy-3-O-β-D-galactopyranosyl-4-O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-β-D-glucopyranoside

phenyl 2-acetamido-2-deoxy-3-O-β-D-galactopyranosyl-β-D-glucopyranoside

perbenzyl fucosyl bromide

phenyl 2-acetamido-2-deoxy-4,6-O-(p-methoxybenzylidene)-β-D-glucopyranoside