benzyl (3-O-tert-butyldiphenylsilyl-4,6-O-cyclohexylidene-β-D-mannopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside

Base Information

Chemical Name:benzyl (3-O-tert-butyldiphenylsilyl-4,6-O-cyclohexylidene-β-D-mannopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside
CAS No.:877669-88-0
Molecular Formula:C₆₃H₆₉NO₁₂Si
Molecular Weight:1060.33
Hs Code.:

Synonyms:benzyl (3-O-tert-butyldiphenylsilyl-4,6-O-cyclohexylidene-β-D-mannopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside

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Chemical Property of benzyl (3-O-tert-butyldiphenylsilyl-4,6-O-cyclohexylidene-β-D-mannopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside

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Technology Process of benzyl (3-O-tert-butyldiphenylsilyl-4,6-O-cyclohexylidene-β-D-mannopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside

There total 3 articles about benzyl (3-O-tert-butyldiphenylsilyl-4,6-O-cyclohexylidene-β-D-mannopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 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:

: C₇₂H₇₉NO₁₃SSi

: 877669-88-0
benzyl (3-O-tert-butyldiphenylsilyl-4,6-O-cyclohexylidene-β-D-mannopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside

Guidance literature:: With 2,6-di-tert-butyl-4-methylpyridine; methyl trifluoromethanesulfonate; In 1,2-dichloro-ethane; at 45 ℃; for 24h;
DOI:10.1016/j.bmcl.2005.10.100

Reference yield:

: 80035-36-5
benzyl 3,6-di-O-benzyl-2-deoxy-2-phthalimido-beta-D-glucopyranoside

: 877669-88-0
benzyl (3-O-tert-butyldiphenylsilyl-4,6-O-cyclohexylidene-β-D-mannopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: MS 4 Angstroem; DDQ / CH₂Cl₂ / 3 h / 0 - 20 °C

2: 72.4 mg / DTBMP; MS 4 Angstroem; MeOTf / 1,2-dichloro-ethane / 15 h / 45 °C

With 2,6-di-tert-butyl-4-methylpyridine; MS 4 Angstroem; 2,3-dicyano-5,6-dichloro-p-benzoquinone; methyl trifluoromethanesulfonate; In dichloromethane; 1,2-dichloro-ethane;
DOI:10.1016/j.carres.2006.12.022

Reference yield:

: 215721-98-5
methyl 4,6-O-cyclohexylidene-2-O-p-methoxybenzyl-3-O-tert-butyldiphenylsilyl-1-thio-α-D-mannopyranoside

: 877669-88-0
benzyl (3-O-tert-butyldiphenylsilyl-4,6-O-cyclohexylidene-β-D-mannopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: MS 4 Angstroem; DDQ / CH₂Cl₂ / 3 h / 0 - 20 °C

2: 72.4 mg / DTBMP; MS 4 Angstroem; MeOTf / 1,2-dichloro-ethane / 15 h / 45 °C

With 2,6-di-tert-butyl-4-methylpyridine; MS 4 Angstroem; 2,3-dicyano-5,6-dichloro-p-benzoquinone; methyl trifluoromethanesulfonate; In dichloromethane; 1,2-dichloro-ethane;
DOI:10.1016/j.carres.2006.12.022