methyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->3)-2,4-di-O-benzyl-β-D-quinovopyranoside

Base Information

• Chemical Name: methyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->3)-2,4-di-O-benzyl-β-D-quinovopyranoside
• CAS No.: 1106838-71-4
• Molecular Formula: C₃₃H₄₂O₁₂
• Molecular Weight: 630.689

Synonyms:methyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->3)-2,4-di-O-benzyl-β-D-quinovopyranoside

Chemical Property of methyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->3)-2,4-di-O-benzyl-β-D-quinovopyranoside

Chemical Property:

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Technology Process of methyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->3)-2,4-di-O-benzyl-β-D-quinovopyranoside

There total 1 articles about methyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->3)-2,4-di-O-benzyl-β-D-quinovopyranoside 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: 82.0%

ethyl 2,3,4-tri-O-acetyl-1-thio-α-L-rhamnopyranoside (125520-01-6) + methyl-2,4-di-O-benzyl-β-D-quinovopyranoside (134311-92-5) → methyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->3)-2,4-di-O-benzyl-β-D-quinovopyranoside (1106838-71-4)

Guidance literature:

With N-iodo-succinimide; trifluorormethanesulfonic acid; In dichloromethane; at -20 ℃; Molecular sieve;

DOI:10.1002/ejoc.200800696

Reference yield: 56.0%

methyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->3)-2,4-di-O-benzyl-β-D-quinovopyranoside (1106838-71-4) + acetic anhydride (108-24-7) → acetyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->3)-2,4-di-O-benzyl-β-D-quinovopyranoside + acetyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->3)-2,4-di-O-benzyl-α-D-quinovopyranoside (1106839-15-9)

Guidance literature:

With trifluoroacetic acid; In acetic acid; at 70 ℃; optical yield given as %de;

DOI:10.1002/ejoc.200800696

Reference yield: 43.0%

methyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->3)-2,4-di-O-benzyl-β-D-quinovopyranoside (1106838-71-4) + acetic anhydride (108-24-7) → acetyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->3)-5-O-acetyl-2-O-benzyl-β-D-quinovofuranoside + acetyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->3)-5-O-acetyl-2-O-benzyl-α-D-quinovofuranoside (1106839-19-3) + 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->3)-1,1,4,5-tetra-O-acetyl-2-O-benzyl-D-quinovose acetal (1106839-16-0)

Guidance literature:

With zinc(II) chloride; In acetic acid; at 5 ℃; optical yield given as %de;

DOI:10.1002/ejoc.200800696

upstream raw materials:

ethyl 2,3,4-tri-O-acetyl-1-thio-α-L-rhamnopyranoside

methyl-2,4-di-O-benzyl-β-D-quinovopyranoside

Downstream raw materials:

acetyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->3)-2,4-di-O-benzyl-α-D-quinovopyranoside

acetyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->3)-5-O-acetyl-2-O-benzyl-α-D-quinovofuranoside

2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->3)-1,1,4,5-tetra-O-acetyl-2-O-benzyl-D-quinovose acetal

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