2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl-(1→6)-2,3,4-tri-O-benzyl-β-D-glucopyranosyl-(1→6)-3,4-di-O-benzyl-D-glucal

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Chemical Name:2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl-(1→6)-2,3,4-tri-O-benzyl-β-D-glucopyranosyl-(1→6)-3,4-di-O-benzyl-D-glucal
CAS No.:1563178-12-0
Molecular Formula:C₈₁H₈₄O₁₄
Molecular Weight:1281.55
Hs Code.:

Synonyms:2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl-(1→6)-2,3,4-tri-O-benzyl-β-D-glucopyranosyl-(1→6)-3,4-di-O-benzyl-D-glucal

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Chemical Property of 2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl-(1→6)-2,3,4-tri-O-benzyl-β-D-glucopyranosyl-(1→6)-3,4-di-O-benzyl-D-glucal

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Technology Process of 2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl-(1→6)-2,3,4-tri-O-benzyl-β-D-glucopyranosyl-(1→6)-3,4-di-O-benzyl-D-glucal

There total 1 articles about 2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl-(1→6)-2,3,4-tri-O-benzyl-β-D-glucopyranosyl-(1→6)-3,4-di-O-benzyl-D-glucal 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: 92.0%

: 100-39-0
benzyl bromide

: 121654-10-2
O-(2,3,4,6-Tetra-O-benzyl-β-D-glucopyranosyl)-(1->6)-O-(3,4-di-O-benzyl-β-D-glucopyranosyl)-(1->6)-1,5-anhydro-3,4-di-O-benzyl-2-deoxy-D-arabino-hex-1-enopyranose

: 1563178-12-0
2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl-(1→6)-2,3,4-tri-O-benzyl-β-D-glucopyranosyl-(1→6)-3,4-di-O-benzyl-D-glucal

Guidance literature:: With tetra-(n-butyl)ammonium iodide; sodium hydride; In N,N-dimethyl-formamide; mineral oil; at 0 - 20 ℃; for 12h; Inert atmosphere;
DOI:10.1021/jo500032k

Reference yield:

: 1563178-12-0
2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl-(1→6)-2,3,4-tri-O-benzyl-β-D-glucopyranosyl-(1→6)-3,4-di-O-benzyl-D-glucal

: 1603820-31-0
C₈₁H₈₄O₁₅

Guidance literature:: With 3,3-dimethyldioxirane; In dichloromethane; at -50 ℃; for 12h; diastereoselective reaction; Inert atmosphere;
DOI:10.1021/jo500032k