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

Base Information Edit
  • Chemical Name:octyl 3-O-acetyl-2,4-di-O-benzyl-α-L-fucopyranosyl-(1->2)-3,4,6-tri-O-benzyl-β-D-galactopyranoside
  • CAS No.:283587-78-0
  • Molecular Formula:C57H70O11
  • Molecular Weight:931.176
  • Hs Code.:
  • Mol file:283587-78-0.mol
octyl 3-O-acetyl-2,4-di-O-benzyl-α-L-fucopyranosyl-(1->2)-3,4,6-tri-O-benzyl-β-D-galactopyranoside

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

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

There total 9 articles about octyl 3-O-acetyl-2,4-di-O-benzyl-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:
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
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: 71 percent / DMTST; DTBMP; 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
Guidance literature:
Multi-step reaction with 7 steps
1: NaOMe / methanol
2: camphorsulfonic acid
3: 93 percent / NaH / dimethylformamide
4: 84 percent / AcOH / 70 °C
5: 600 mg / Bu4NHSO4; NaOH / CH2Cl2; H2O / 48 h / 20 °C
6: 89 percent / pyridine
7: 71 percent / DMTST; DTBMP; 4 Angstroem molecular sieves / CH2Cl2 / 4 h
With pyridine; sodium hydroxide; 2,6-di-tert-butyl-4-methylpyridine; 4 A molecular sieve; camphor-10-sulfonic acid; sodium methylate; tetra(n-butyl)ammonium hydrogensulfate; 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: Alkylation / 6: Acetylation / 7: Glycosylation;
DOI:10.1016/S0008-6215(00)00003-3
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