Title of article :
Efficient preparation of 9-Z-11-methylretinal and 11-Z-11-methylretinal
Author/Authors :
Dawadi، نويسنده , , Prativa B.S. and Verhoeven، نويسنده , , Michiel A. and Lugtenburg، نويسنده , , Johan، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2011
Abstract :
[2-(β-Ionylidene)propyl]triphenylphosphonium bromide is reacted with 3-methyl-4-oxobut-2-enenitrile in refluxing 1,2-epoxybutane to give a mixture of 11-Z- and all-E-11-methylretinal via DIBAL-H reduction. In an analogous fashion, β-ionyl triphenylphosphonium bromide is reacted with 3,5-dimethyl-6-oxohexa-2,4-dienenitrile in 1,2-epoxybutane followed by subsequent DIBAL-H reduction to afford a mixture of new products consisting of 9-Z-11-methylretinal, its all-E isomer and 1-(2′,6′,6′-trimethylcyclohex-2′-en-1′-yl)-6-(buten-2″-al-3″-yl)-3,5-dimethylcyclohexa-1,3-diene. These molecules were obtained in pure form by HPLC.
Keywords :
Cyclohexadiene formation , 1-(2?6? , 6?-Trimethylcyclohex-2?-en-1?-yl)-6-(buten-2?-al-3?-yl)-3 , 5-dimethylcyclohexa-1 , 1 , 3-diene , 4-conjugated Wittig reaction
Journal title :
Tetrahedron Letters
Journal title :
Tetrahedron Letters