phenyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->3)-4-O-benzoyl-2-O-levulinoyl-1-thio-β-L-arabinopyranoside

Base Information

Chemical Name:phenyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->3)-4-O-benzoyl-2-O-levulinoyl-1-thio-β-L-arabinopyranoside
CAS No.:952575-80-3
Molecular Formula:C₃₅H₄₀O₁₄S
Molecular Weight:716.76
Hs Code.:

Synonyms:phenyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->3)-4-O-benzoyl-2-O-levulinoyl-1-thio-β-L-arabinopyranoside

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Chemical Property of phenyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->3)-4-O-benzoyl-2-O-levulinoyl-1-thio-β-L-arabinopyranoside

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Technology Process of phenyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->3)-4-O-benzoyl-2-O-levulinoyl-1-thio-β-L-arabinopyranoside

There total 1 articles about phenyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->3)-4-O-benzoyl-2-O-levulinoyl-1-thio-β-L-arabinopyranoside 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: 91.0%

: 952575-73-4
phenyl 4-O-benzoyl-2-O-levulinoyl-1-thio-β-L-arabinopyranoside

: 122089-71-8
2,3,4-tri-O-acetyl-L-rhamnopyranosyl trichloroacetimidate

: 952575-80-3
phenyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->3)-4-O-benzoyl-2-O-levulinoyl-1-thio-β-L-arabinopyranoside

Guidance literature:: With trimethylsilyl trifluoromethanesulfonate; 4 A molecular sieve; In dichloromethane; at -70 - -10 ℃; for 1h;
DOI:10.1002/anie.200701750

Reference yield: 71.0%

: 952575-80-3
phenyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->3)-4-O-benzoyl-2-O-levulinoyl-1-thio-β-L-arabinopyranoside

: 3-azidopropyl 3,4-di-O-benzyl-2-O-methyl-α-L-fucopyranosyl-(1->2)-3,6-di-O-benzyl-β-D-galactopyranoside

: C₇₃H₈₇N₃O₂₄

Guidance literature:: With N-iodo-succinimide; trifluorormethanesulfonic acid; 4 A molecular sieve; In dichloromethane; at -20 - 0 ℃; for 1h;
DOI:10.1002/anie.200701750