(2R,6S)-6-(((2R,3R,4αS,5S,7R,8R,8αR)-7-(benzyloxy)-2,3-dimethoxy-2,3,5-trimethylhexahydro-2H-pyrano[3,4b]-[1,4]-dioxin-8-yl)oxy)-2-methyl-2H-pyran-3(6H)-one

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Chemical Name:(2R,6S)-6-(((2R,3R,4αS,5S,7R,8R,8αR)-7-(benzyloxy)-2,3-dimethoxy-2,3,5-trimethylhexahydro-2H-pyrano[3,4b]-[1,4]-dioxin-8-yl)oxy)-2-methyl-2H-pyran-3(6H)-one
CAS No.:1428345-55-4
Molecular Formula:C₂₅H₃₄O₉
Molecular Weight:478.54
Hs Code.:

Synonyms:(2R,6S)-6-(((2R,3R,4αS,5S,7R,8R,8αR)-7-(benzyloxy)-2,3-dimethoxy-2,3,5-trimethylhexahydro-2H-pyrano[3,4b]-[1,4]-dioxin-8-yl)oxy)-2-methyl-2H-pyran-3(6H)-one

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Chemical Property of (2R,6S)-6-(((2R,3R,4αS,5S,7R,8R,8αR)-7-(benzyloxy)-2,3-dimethoxy-2,3,5-trimethylhexahydro-2H-pyrano[3,4b]-[1,4]-dioxin-8-yl)oxy)-2-methyl-2H-pyran-3(6H)-one

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Technology Process of (2R,6S)-6-(((2R,3R,4αS,5S,7R,8R,8αR)-7-(benzyloxy)-2,3-dimethoxy-2,3,5-trimethylhexahydro-2H-pyrano[3,4b]-[1,4]-dioxin-8-yl)oxy)-2-methyl-2H-pyran-3(6H)-one

There total 3 articles about (2R,6S)-6-(((2R,3R,4αS,5S,7R,8R,8αR)-7-(benzyloxy)-2,3-dimethoxy-2,3,5-trimethylhexahydro-2H-pyrano[3,4b]-[1,4]-dioxin-8-yl)oxy)-2-methyl-2H-pyran-3(6H)-one 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: 85.0%

: 679412-06-7
tert-butyl ((2R,6R)-6-methyl-5-oxo-5,6-dihydro-2H-pyran-2-yl) carbonate

: (4aS,8R,8aS)-7-benzyloxyhexahydro-2,3-dimethoxy-2,3,5-trimethyl-2H-pyrano[3,4-b][1,4]dioxin-8-ol

: 1428345-55-4
(2R,6S)-6-(((2R,3R,4αS,5S,7R,8R,8αR)-7-(benzyloxy)-2,3-dimethoxy-2,3,5-trimethylhexahydro-2H-pyrano[3,4b]-[1,4]-dioxin-8-yl)oxy)-2-methyl-2H-pyran-3(6H)-one

Guidance literature:: With tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; triphenylphosphine; In dichloromethane; at 0 ℃; for 4h; diastereoselective reaction; Inert atmosphere;
DOI:10.1016/j.tet.2013.02.073

Reference yield:

: 1192-62-7,80145-44-4
1-(2-furyl)-1-ethanone

: 1428345-55-4
(2R,6S)-6-(((2R,3R,4αS,5S,7R,8R,8αR)-7-(benzyloxy)-2,3-dimethoxy-2,3,5-trimethylhexahydro-2H-pyrano[3,4b]-[1,4]-dioxin-8-yl)oxy)-2-methyl-2H-pyran-3(6H)-one

Guidance literature:: Multi-step reaction with 3 steps

1: sodium formate

2: N-Bromosuccinimide / water

3: tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; triphenylphosphine / dichloromethane / 4 h / 0 °C / Inert atmosphere

With tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; N-Bromosuccinimide; sodium formate; triphenylphosphine; In dichloromethane; water; 1: |Noyori Asymmetric Hydrogenation / 2: |Achmatowicz Reaction;
DOI:10.1016/j.tet.2013.02.073

Reference yield:

: 27948-61-4
(R)-(+)-1-(2-furyl)ethanol

: 1428345-55-4
(2R,6S)-6-(((2R,3R,4αS,5S,7R,8R,8αR)-7-(benzyloxy)-2,3-dimethoxy-2,3,5-trimethylhexahydro-2H-pyrano[3,4b]-[1,4]-dioxin-8-yl)oxy)-2-methyl-2H-pyran-3(6H)-one

Guidance literature:: Multi-step reaction with 2 steps

1: N-Bromosuccinimide / water

2: tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; triphenylphosphine / dichloromethane / 4 h / 0 °C / Inert atmosphere

With tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; N-Bromosuccinimide; triphenylphosphine; In dichloromethane; water; 1: |Achmatowicz Reaction;
DOI:10.1016/j.tet.2013.02.073