(2S,3R,6R)-6-(((2S,3R,6R)-6-(benzyloxy)-2-((((2R,5R,6S)-5-hydroxy-6-(hydroxymethyl)-5,6-dihydro-2H-pyran-2-yl)oxy)methyl)-3,6-dihydro-2H-pyran-3-yl)oxy)-2-(hydroxymethyl)-3,6-dihydro-2H-pyran-3-ol

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Chemical Name:(2S,3R,6R)-6-(((2S,3R,6R)-6-(benzyloxy)-2-((((2R,5R,6S)-5-hydroxy-6-(hydroxymethyl)-5,6-dihydro-2H-pyran-2-yl)oxy)methyl)-3,6-dihydro-2H-pyran-3-yl)oxy)-2-(hydroxymethyl)-3,6-dihydro-2H-pyran-3-ol
CAS No.:1385024-31-6
Molecular Formula:C₂₅H₃₂O₁₀
Molecular Weight:492.523
Hs Code.:

(2S,3R,6R)-6-(((2S,3R,6R)-6-(benzyloxy)-2-((((2R,5R,6S)-5-hydroxy-6-(hydroxymethyl)-5,6-dihydro-2H-pyran-2-yl)oxy)methyl)-3,6-dihydro-2H-pyran-3-yl)oxy)-2-(hydroxymethyl)-3,6-dihydro-2H-pyran-3-ol

Synonyms:(2S,3R,6R)-6-(((2S,3R,6R)-6-(benzyloxy)-2-((((2R,5R,6S)-5-hydroxy-6-(hydroxymethyl)-5,6-dihydro-2H-pyran-2-yl)oxy)methyl)-3,6-dihydro-2H-pyran-3-yl)oxy)-2-(hydroxymethyl)-3,6-dihydro-2H-pyran-3-ol

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Chemical Property of (2S,3R,6R)-6-(((2S,3R,6R)-6-(benzyloxy)-2-((((2R,5R,6S)-5-hydroxy-6-(hydroxymethyl)-5,6-dihydro-2H-pyran-2-yl)oxy)methyl)-3,6-dihydro-2H-pyran-3-yl)oxy)-2-(hydroxymethyl)-3,6-dihydro-2H-pyran-3-ol

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Technology Process of (2S,3R,6R)-6-(((2S,3R,6R)-6-(benzyloxy)-2-((((2R,5R,6S)-5-hydroxy-6-(hydroxymethyl)-5,6-dihydro-2H-pyran-2-yl)oxy)methyl)-3,6-dihydro-2H-pyran-3-yl)oxy)-2-(hydroxymethyl)-3,6-dihydro-2H-pyran-3-ol

There total 9 articles about (2S,3R,6R)-6-(((2S,3R,6R)-6-(benzyloxy)-2-((((2R,5R,6S)-5-hydroxy-6-(hydroxymethyl)-5,6-dihydro-2H-pyran-2-yl)oxy)methyl)-3,6-dihydro-2H-pyran-3-yl)oxy)-2-(hydroxymethyl)-3,6-dihydro-2H-pyran-3-ol 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: 91.0%

: 1385024-30-5
(2S,3R,6R)-6-(((2S,3R,6R)-6-(Benzyloxy)-2-((((2R,5R,6S)-6-(((tert-butyldimethylsilyl)oxy)methyl)-5-hydroxy-5,6-dihydro-2H-pyran-2-yl)oxy)methyl)-3,6-dihydro-2H-pyran-3-yl)oxy)-2-(((tert-butyldimethylsilyl)oxy)methyl)-3,6-dihydro-2H-pyran-3-ol

: 1385024-31-6
(2S,3R,6R)-6-(((2S,3R,6R)-6-(benzyloxy)-2-((((2R,5R,6S)-5-hydroxy-6-(hydroxymethyl)-5,6-dihydro-2H-pyran-2-yl)oxy)methyl)-3,6-dihydro-2H-pyran-3-yl)oxy)-2-(hydroxymethyl)-3,6-dihydro-2H-pyran-3-ol

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 0 ℃; for 2h;
DOI:10.1021/ja305321e

Reference yield:

: 302348-82-9
(2S)-2-(((tert-butyldimethylsilyl)oxy)methyl)-6-hydroxy-2H-pyran-3(6H)-one

: 1385024-31-6
(2S,3R,6R)-6-(((2S,3R,6R)-6-(benzyloxy)-2-((((2R,5R,6S)-5-hydroxy-6-(hydroxymethyl)-5,6-dihydro-2H-pyran-2-yl)oxy)methyl)-3,6-dihydro-2H-pyran-3-yl)oxy)-2-(hydroxymethyl)-3,6-dihydro-2H-pyran-3-ol

Guidance literature:: Multi-step reaction with 4 steps

1: dmap / dichloromethane / 1 h / -78 °C

2: tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; triphenylphosphine / dichloromethane / 6 h / 0 °C

3: sodium tetrahydroborate / methanol / 8 h / -78 °C

4: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 0 °C

With dmap; tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; sodium tetrahydroborate; tetrabutyl ammonium fluoride; triphenylphosphine; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1021/ja305321e

Reference yield:

: 623157-43-7
(2S,6S)-carbonic acid tert-butyl ester 6-(tert-butyl-dimethyl-silanyloxymethyl)-4-oxo-2,3-dihydro-6H-pyran-2-yl ester

: 1385024-31-6
(2S,3R,6R)-6-(((2S,3R,6R)-6-(benzyloxy)-2-((((2R,5R,6S)-5-hydroxy-6-(hydroxymethyl)-5,6-dihydro-2H-pyran-2-yl)oxy)methyl)-3,6-dihydro-2H-pyran-3-yl)oxy)-2-(hydroxymethyl)-3,6-dihydro-2H-pyran-3-ol

Guidance literature:: Multi-step reaction with 3 steps

1: tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; triphenylphosphine / dichloromethane / 6 h / 0 °C

2: sodium tetrahydroborate / methanol / 8 h / -78 °C

3: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 0 °C

With tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; sodium tetrahydroborate; tetrabutyl ammonium fluoride; triphenylphosphine; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1021/ja305321e