Pheromone synthesis, CXCII Synthesis of all the stereoisomers of 10,14-dimethyloctadec-1-ene, 5,9-dimethyloctadecane and 5,9-dimethylheptadecane, thesex pheromone components of the apple leafminer, Lyonetia prunifoliella

Authors
Tamagawa, H Takikawa, H Mori, K
Citation
H. Tamagawa et al., Pheromone synthesis, CXCII Synthesis of all the stereoisomers of 10,14-dimethyloctadec-1-ene, 5,9-dimethyloctadecane and 5,9-dimethylheptadecane, thesex pheromone components of the apple leafminer, Lyonetia prunifoliella, EUR J ORG C, (5), 1999, pp. 973-978
Citations number
10
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
ISSN journal
1434193X → ACNP
Issue
5
Year of publication
1999
Pages
973 - 978
Database
ISI
SICI code
1434-193X(199905):5<973:PSCSOA>2.0.ZU;2-E
Abstract
All of the stereoisomers of 10,14-dimethyloctadec-1-ene (1), 5,9-dimethyloc tadecane (2) and 5,9-dimethylheptadecane (3), the sex pheromone components of the apple leafminer (Lyonetia prunifoliella), were synthesized by starti ng from the enantiomers of citronellol (4) and methyl 3-hydroxy-2-methylpro panoate (11).