methyl 3-O-acetyl-5-O-benzoyl-2-O-(2,3-di-O-acetyl-5-O-benzoyl-β-D-ribofuranosyl)-β-D-ribofuranoside

Base Information

Chemical Name:methyl 3-O-acetyl-5-O-benzoyl-2-O-(2,3-di-O-acetyl-5-O-benzoyl-β-D-ribofuranosyl)-β-D-ribofuranoside
CAS No.:120090-40-6
Molecular Formula:C₃₁H₃₄O₁₄
Molecular Weight:630.603
Hs Code.:

Synonyms:methyl 3-O-acetyl-5-O-benzoyl-2-O-(2,3-di-O-acetyl-5-O-benzoyl-β-D-ribofuranosyl)-β-D-ribofuranoside

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Chemical Property of methyl 3-O-acetyl-5-O-benzoyl-2-O-(2,3-di-O-acetyl-5-O-benzoyl-β-D-ribofuranosyl)-β-D-ribofuranoside

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Technology Process of methyl 3-O-acetyl-5-O-benzoyl-2-O-(2,3-di-O-acetyl-5-O-benzoyl-β-D-ribofuranosyl)-β-D-ribofuranoside

There total 4 articles about methyl 3-O-acetyl-5-O-benzoyl-2-O-(2,3-di-O-acetyl-5-O-benzoyl-β-D-ribofuranosyl)-β-D-ribofuranoside 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: 71.0%

: 120090-36-0
methyl 3-O-acetyl-5-O-benzoyl-2-O-trityl-β-D-ribofuranoside

: 120090-32-6
3-O-acetyl-5-O-benzoyl-1,2-O-<(1-endo-cyano)ethylidene>-α-D-ribofuranose

: 120090-40-6
methyl 3-O-acetyl-5-O-benzoyl-2-O-(2,3-di-O-acetyl-5-O-benzoyl-β-D-ribofuranosyl)-β-D-ribofuranoside

Guidance literature:: triphenylmethyl perchlorate; In dichloromethane; Ambient temperature; dark;
DOI:10.1016/0008-6215(88)80081-8

Reference yield:

: 5517-61-3
methyl 3'-O-benzoyl-β-D-apiofuranoside

: 120090-40-6
methyl 3-O-acetyl-5-O-benzoyl-2-O-(2,3-di-O-acetyl-5-O-benzoyl-β-D-ribofuranosyl)-β-D-ribofuranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 36 percent / 2,4,6-trimethylpyridine / CH₂Cl₂ / 4 h / Ambient temperature

2: 96 percent / 4-dimethylaminopyridine / pyridine / 2 h / Ambient temperature

3: 71 percent / triphenylmethylium perchlorate / CH₂Cl₂ / Ambient temperature; dark

With 2,4,6-trimethyl-pyridine; dmap; triphenylmethyl perchlorate; In pyridine; dichloromethane;
DOI:10.1016/0008-6215(88)80081-8

Reference yield:

: 120090-34-8
methyl 5-O-benzoyl-2-O-trityl-β-D-ribofuranoside

: 120090-40-6
methyl 3-O-acetyl-5-O-benzoyl-2-O-(2,3-di-O-acetyl-5-O-benzoyl-β-D-ribofuranosyl)-β-D-ribofuranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 96 percent / 4-dimethylaminopyridine / pyridine / 2 h / Ambient temperature

2: 71 percent / triphenylmethylium perchlorate / CH₂Cl₂ / Ambient temperature; dark

With dmap; triphenylmethyl perchlorate; In pyridine; dichloromethane;
DOI:10.1016/0008-6215(88)80081-8