methyl 2,3,4-tri-O-benzyl-6-O-[3,4,6-tri-O-benzyl-2-O-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-α-D-mannopyranosyl]-α-D-mannopyranoside

Base Information

• Chemical Name: methyl 2,3,4-tri-O-benzyl-6-O-[3,4,6-tri-O-benzyl-2-O-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-α-D-mannopyranosyl]-α-D-mannopyranoside
• CAS No.: 313467-42-4
• Molecular Formula: C₈₂H₈₈O₁₆
• Molecular Weight: 1329.59

Synonyms:methyl 2,3,4-tri-O-benzyl-6-O-[3,4,6-tri-O-benzyl-2-O-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-α-D-mannopyranosyl]-α-D-mannopyranoside

Chemical Property of methyl 2,3,4-tri-O-benzyl-6-O-[3,4,6-tri-O-benzyl-2-O-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-α-D-mannopyranosyl]-α-D-mannopyranoside

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Technology Process of methyl 2,3,4-tri-O-benzyl-6-O-[3,4,6-tri-O-benzyl-2-O-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-α-D-mannopyranosyl]-α-D-mannopyranoside

There total 1 articles about methyl 2,3,4-tri-O-benzyl-6-O-[3,4,6-tri-O-benzyl-2-O-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-α-D-mannopyranosyl]-α-D-mannopyranoside 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: 83.7%

methyl 2,3,4-tri-O-benzyl-6-O-[3,4,6-tri-O-benzyl-2-O(2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-α-D-mannopyranosyl]-α-D-mannopyranoside → methyl 2,3,4-tri-O-benzyl-6-O-[3,4,6-tri-O-benzyl-2-O-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-α-D-mannopyranosyl]-α-D-mannopyranoside (313467-42-4)

Guidance literature:

With sodium; In methanol; at 25 ℃;

DOI:10.1016/S0008-6215(00)00137-3

Reference yield: 54.0%

tetra-O-benzyl-α-D-galactosyl bromide (53081-30-4) + methyl 2,3,4-tri-O-benzyl-6-O-[3,4,6-tri-O-benzyl-2-O-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-α-D-mannopyranosyl]-α-D-mannopyranoside (313467-42-4) → methyl 2,3,4-tri-O-benzyl-6-O-{3,4,6-tri-O-benzyl-2-O-[3,4,6-tri-O-benzyl-2-O-(2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl)-α-D-mannopyranosyl]-α-D-mannopyranosyl}-α-D-mannopyranoside

Guidance literature:

With 4 Angstroem MS; mercury(II) cyanide; In dichloromethane; at 25 ℃; for 24h;

DOI:10.1016/S0008-6215(00)00137-3

Reference yield: 45.0%

2,3,6,2',3',4',6'-hepta-O-acetyl-α-D-lactosyl trichloroacetimidate (92052-38-5,106256-89-7,126736-02-5,130703-21-8,132287-70-8,132287-71-9,139403-73-9,106256-81-9) + methyl 2,3,4-tri-O-benzyl-6-O-[3,4,6-tri-O-benzyl-2-O-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-α-D-mannopyranosyl]-α-D-mannopyranoside (313467-42-4) → methyl (2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->4)-(2,3,6-tri-O-acetyl-β-D-glucopyranosyl)-(1->2)-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1->2)-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1->6)-2,3,4-tri-O-benzyl-α-D-mannopyranoside

Guidance literature:

With trimethylsilyl trifluoromethanesulfonate; 4 Angstroem MS; In dichloromethane; at -15 ℃; for 5h;

DOI:10.1016/S0008-6215(00)00137-3

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