octyl 3,4-di-O-benzyl-2-O-p-methoxybenzyl-α-L-fucopyranosyl-(1->2)-3,4,6-tri-O-benzyl-β-D-galactopyranoside

Base Information

Chemical Name:octyl 3,4-di-O-benzyl-2-O-p-methoxybenzyl-α-L-fucopyranosyl-(1->2)-3,4,6-tri-O-benzyl-β-D-galactopyranoside
CAS No.:283587-83-7
Molecular Formula:C₆₃H₇₆O₁₁
Molecular Weight:1009.29
Hs Code.:

Synonyms:octyl 3,4-di-O-benzyl-2-O-p-methoxybenzyl-α-L-fucopyranosyl-(1->2)-3,4,6-tri-O-benzyl-β-D-galactopyranoside

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Chemical Property of octyl 3,4-di-O-benzyl-2-O-p-methoxybenzyl-α-L-fucopyranosyl-(1->2)-3,4,6-tri-O-benzyl-β-D-galactopyranoside

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Technology Process of octyl 3,4-di-O-benzyl-2-O-p-methoxybenzyl-α-L-fucopyranosyl-(1->2)-3,4,6-tri-O-benzyl-β-D-galactopyranoside

There total 8 articles about octyl 3,4-di-O-benzyl-2-O-p-methoxybenzyl-α-L-fucopyranosyl-(1->2)-3,4,6-tri-O-benzyl-β-D-galactopyranoside 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: 67.0%

: 220911-76-2
octyl 3,4,6-tri-O-benzyl-β-D-galactopyranoside

: 283587-71-3
ethyl 3,4-di-O-benzyl-2-O-p-methoxybenzyl-1-thio-β-L-fucopyranoside

: 283587-83-7
octyl 3,4-di-O-benzyl-2-O-p-methoxybenzyl-α-L-fucopyranosyl-(1->2)-3,4,6-tri-O-benzyl-β-D-galactopyranoside

Guidance literature:: With 2,6-di-tert-butyl-4-methylpyridine; 4 A molecular sieve; dimethyl-(methylthio)-sulphonium trifluoromethanesulphonate; In dichloromethane; for 4h;
DOI:10.1016/S0008-6215(00)00003-3

Reference yield:

: 111-87-5
octanol

: 283587-83-7
octyl 3,4-di-O-benzyl-2-O-p-methoxybenzyl-α-L-fucopyranosyl-(1->2)-3,4,6-tri-O-benzyl-β-D-galactopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 74 percent / Hg(CN)2; molecular sieves 3 Angstroem; HgBr₂ / acetonitrile

2: 97 percent / NaOMe / methanol

3: 67 percent / DTBMP; DMTST; 4 Angstroem molecular sieves / CH₂Cl₂ / 4 h

With 2,6-di-tert-butyl-4-methylpyridine; 3 A molecular sieve; 4 A molecular sieve; sodium methylate; mercury(II) cyanide; dimethyl-(methylthio)-sulphonium trifluoromethanesulphonate; mercury dibromide; In methanol; dichloromethane; acetonitrile; 1: Glycosylation / 2: Deacetylation / 3: Glycosylation;
DOI:10.1016/S0008-6215(00)00003-3

Reference yield:

: 127501-41-1
ethyl 2,3,4-tri-O-acetyl-1-thio-β-L-fucopyranoside

: 283587-83-7
octyl 3,4-di-O-benzyl-2-O-p-methoxybenzyl-α-L-fucopyranosyl-(1->2)-3,4,6-tri-O-benzyl-β-D-galactopyranoside

Guidance literature:: Multi-step reaction with 6 steps

1: NaOMe / methanol

2: camphorsulfonic acid

3: 89 percent / NaH / dimethylformamide / 3 h

4: AcOH / H₂O / 2 h / 60 °C

5: NaH / dimethylformamide / 3 h / 20 °C

6: 67 percent / DTBMP; DMTST; 4 Angstroem molecular sieves / CH₂Cl₂ / 4 h

With 2,6-di-tert-butyl-4-methylpyridine; 4 A molecular sieve; camphor-10-sulfonic acid; sodium methylate; sodium hydride; acetic acid; dimethyl-(methylthio)-sulphonium trifluoromethanesulphonate; In methanol; dichloromethane; water; N,N-dimethyl-formamide; 1: Deacetylation / 2: Cyclization / 3: Alkylation / 4: Hydrolysis / 5: Benzylation / 6: Glycosylation;
DOI:10.1016/S0008-6215(00)00003-3