Allyl O-(2,3,6-tri-O-benzyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

Base Information

Chemical Name:Allyl O-(2,3,6-tri-O-benzyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside
CAS No.:148979-88-8
Molecular Formula:C₅₇H₆₂O₁₁
Molecular Weight:923.113
Hs Code.:

Synonyms:Allyl O-(2,3,6-tri-O-benzyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

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Chemical Property of Allyl O-(2,3,6-tri-O-benzyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

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Technology Process of Allyl O-(2,3,6-tri-O-benzyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

There total 11 articles about Allyl O-(2,3,6-tri-O-benzyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-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: 65.0%

: 160593-12-4
(4aR,6S,7R,8S,8aS)-6-((2R,3R,4S,5R,6R)-6-Allyloxy-4,5-bis-benzyloxy-2-benzyloxymethyl-tetrahydro-pyran-3-yloxy)-7,8-bis-benzyloxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine

: 148979-88-8
Allyl O-(2,3,6-tri-O-benzyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

Guidance literature:: With hydrogenchloride; 3 A molecular sieve; sodium cyanoborohydride; In tetrahydrofuran;
DOI:10.1016/0008-6215(94)00189-8

Reference yield:

: 50256-34-3,97777-13-4,103136-39-6
allyl 2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl-(1->4)-2,3,6-tri-O-acetyl-β-D-glucopyranoside

: 148979-88-8
Allyl O-(2,3,6-tri-O-benzyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 4 steps

1: Na, MeOH

2: 92 percent / zinc chloride / 8 h / Ambient temperature

3: NaH / dimethylformamide

4: 65 percent / 3A molecular sieves, NaCNBH₃, HCl / tetrahydrofuran

With hydrogenchloride; methanol; 3 A molecular sieve; sodium; sodium hydride; sodium cyanoborohydride; zinc(II) chloride; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1016/0008-6215(94)00189-8

Reference yield:

: 52211-61-7
(2S,3R,4S,5R,6R)-2-(((2R,3S,4R,5R,6R)-6-(allyloxy)-4,5-dihydroxy-2-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol

: 148979-88-8
Allyl O-(2,3,6-tri-O-benzyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 92 percent / zinc chloride / 8 h / Ambient temperature

2: NaH / dimethylformamide

3: 65 percent / 3A molecular sieves, NaCNBH₃, HCl / tetrahydrofuran

With hydrogenchloride; 3 A molecular sieve; sodium hydride; sodium cyanoborohydride; zinc(II) chloride; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1016/0008-6215(94)00189-8