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
Link To Document :
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