Title of article
Synthesis of all the stereoisomers of 6-methyl-2-octadecanone, 6,14-dimethyl-2-octadecanone, and 14-methyl-2-octadecanone, the components of the female-produced sex pheromone of a moth, Lyclene dharma dharma
Author/Authors
Kenji Mori، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2009
Pages
8
From page
2798
To page
2805
Abstract
All of the stereoisomers of the components of the female-produced sex pheromone of a moth, Lyclene dharma dharma, were synthesized. They are (R)- and (S)-6-methyl-2-octadecanone, (6R,14R)-, (6R,14S)-, (6S,14R)-, and (6S,14S)-6,14-dimethyl-2-octadecanone, and (R)- and (S)-14-methyl-2-octadecanone. Enantiomers of citronellal and methyl (S)-3-hydroxy-2-methylpropanoate were the starting materials, and olefin cross metathesis was employed as the key reaction.
Keywords
citronellal , (R) and (S) , Methyl-branched ketones , Pheromone , Methyl (S)-3-hydroxy-2-methylpropanoate , Olefin cross metathesis
Journal title
Tetrahedron
Serial Year
2009
Journal title
Tetrahedron
Record number
1095274
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