(E)-1-((6S)-(((tetrahydro-2H-pyran-2-yl)oxy)methyl)-4-(4,8-dimethylnona-3,7-dien-1-yl)cyclohexa-1,3-dien-1-yl)-2-(phenylsulfonyl)ethan-1-one

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Chemical Name:(E)-1-((6S)-(((tetrahydro-2H-pyran-2-yl)oxy)methyl)-4-(4,8-dimethylnona-3,7-dien-1-yl)cyclohexa-1,3-dien-1-yl)-2-(phenylsulfonyl)ethan-1-one
CAS No.:1613055-57-4
Molecular Formula:C₃₁H₄₂O₅S
Molecular Weight:526.737
Hs Code.:

Synonyms:(E)-1-((6S)-(((tetrahydro-2H-pyran-2-yl)oxy)methyl)-4-(4,8-dimethylnona-3,7-dien-1-yl)cyclohexa-1,3-dien-1-yl)-2-(phenylsulfonyl)ethan-1-one

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Chemical Property of (E)-1-((6S)-(((tetrahydro-2H-pyran-2-yl)oxy)methyl)-4-(4,8-dimethylnona-3,7-dien-1-yl)cyclohexa-1,3-dien-1-yl)-2-(phenylsulfonyl)ethan-1-one

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Technology Process of (E)-1-((6S)-(((tetrahydro-2H-pyran-2-yl)oxy)methyl)-4-(4,8-dimethylnona-3,7-dien-1-yl)cyclohexa-1,3-dien-1-yl)-2-(phenylsulfonyl)ethan-1-one

There total 1 articles about (E)-1-((6S)-(((tetrahydro-2H-pyran-2-yl)oxy)methyl)-4-(4,8-dimethylnona-3,7-dien-1-yl)cyclohexa-1,3-dien-1-yl)-2-(phenylsulfonyl)ethan-1-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:

: 72019-02-4
(6E)-3,7,11-trimethyldodeca-2,6,10-trienal

: C₁₆H₂₀O₅S

: 1613055-57-4
(E)-1-((6S)-(((tetrahydro-2H-pyran-2-yl)oxy)methyl)-4-(4,8-dimethylnona-3,7-dien-1-yl)cyclohexa-1,3-dien-1-yl)-2-(phenylsulfonyl)ethan-1-one

: 1613055-59-6
(E)-1-((6R)-(((tetrahydro-2H-pyran-2-yl)oxy)methyl)-4-(4,8-dimethylnona-3,7-dien-1-yl)cyclohexa-1,3-dien-1-yl)-2-(phenylsulfonyl)ethan-1-one

Guidance literature:: With (R)-2-(diphenyl(trimethylsilyloxy)methyl)pyrrolidine; benzoic acid; In ethanol; at 20 ℃; for 48h; Overall yield = 33 %; Overall yield = 14.1 mg; enantioselective reaction;
DOI:10.1016/j.tet.2014.04.076