(5R)-5-hydroxy-1-(4-methoxybenzyloxy)-6-(R(S))-(phenylsulfinyl)hexan-3-one

Base Information

Chemical Name:(5R)-5-hydroxy-1-(4-methoxybenzyloxy)-6-(R(S))-(phenylsulfinyl)hexan-3-one
CAS No.:1173103-45-1
Molecular Formula:C₂₀H₂₄O₅S
Molecular Weight:376.474
Hs Code.:

Synonyms:(5R)-5-hydroxy-1-(4-methoxybenzyloxy)-6-(R(S))-(phenylsulfinyl)hexan-3-one

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Chemical Property of (5R)-5-hydroxy-1-(4-methoxybenzyloxy)-6-(R(S))-(phenylsulfinyl)hexan-3-one

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Technology Process of (5R)-5-hydroxy-1-(4-methoxybenzyloxy)-6-(R(S))-(phenylsulfinyl)hexan-3-one

There total 1 articles about (5R)-5-hydroxy-1-(4-methoxybenzyloxy)-6-(R(S))-(phenylsulfinyl)hexan-3-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: 70.0%

: 1173103-39-3
(2R,E)-6-(4-methoxybenzyloxy)-1-(R(S))-(phenylsulfinyl)hex-3-en-2-ol

: 1173103-45-1
(5R)-5-hydroxy-1-(4-methoxybenzyloxy)-6-(R(S))-(phenylsulfinyl)hexan-3-one

Guidance literature:: With oxygen; copper(l) chloride; palladium dichloride; In water; N,N-dimethyl-formamide; at 50 ℃; for 4h;
DOI:10.1016/j.tet.2009.09.062

Reference yield: 73.0%

: 1173103-45-1
(5R)-5-hydroxy-1-(4-methoxybenzyloxy)-6-(R(S))-(phenylsulfinyl)hexan-3-one

: 1173103-47-3
(2R,4R)-6-(4-methoxybenzyloxy)-1-(R(S))-(phenylsulfinyl)-hexane-2,4-diol

Guidance literature:: (5R)-5-hydroxy-1-(4-methoxybenzyloxy)-6-(R(S))-(phenylsulfinyl)hexan-3-one; With diethyl methoxy borane; In tetrahydrofuran; methanol; at -78 ℃; for 0.5h;

With sodium tetrahydroborate; In tetrahydrofuran; methanol; at -78 ℃; for 2h;

With dihydrogen peroxide; In tetrahydrofuran; methanol; phosphate buffer; at -78 - 20 ℃; pH=7; diastereoselective reaction;
DOI:10.1055/s-0029-1216722