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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
10
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pubmed:dateCreated |
2003-10-30
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pubmed:abstractText |
The enantiomers of 21-methyl-7-hentriacontanone (1), which might show weak bioactivity as the female sex pheromone of the screwworm fly (Cochliomyia hominivorax), were synthesized by starting from the enantiomers of citronellal. (+/-)-Citronellol was converted to a racemic and diastereomeric mixture of 5-acetoxy-19-methylnonacosane (2), which was considered to be a candidate for the female sex pheromone of C. hominivorax. Synthetic 2 exhibited no pheromone activity against male C. hominivorax.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0916-8451
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
67
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2224-31
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:14586112-Animals,
pubmed-meshheading:14586112-Diptera,
pubmed-meshheading:14586112-Female,
pubmed-meshheading:14586112-Hydrocarbons,
pubmed-meshheading:14586112-Ketones,
pubmed-meshheading:14586112-Magnetic Resonance Spectroscopy,
pubmed-meshheading:14586112-Male,
pubmed-meshheading:14586112-Molecular Structure,
pubmed-meshheading:14586112-Monoterpenes,
pubmed-meshheading:14586112-Sex Attractants,
pubmed-meshheading:14586112-Stereoisomerism,
pubmed-meshheading:14586112-Structure-Activity Relationship
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pubmed:year |
2003
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pubmed:articleTitle |
Synthesis of the enantiomers of 21-methyl-7-hentriacontanone and a stereoisomeric mixture of 5-acetoxy-19-methylnonacosane, candidates for the female sex pheromone of the screwworm fly Cochliomyia hominivorax.
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pubmed:affiliation |
Insect Pheromone and Traps Division, Fuji Flavor Co., Ltd., Midorigaoka, Hamura-City, Tokyo, Japan.
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pubmed:publicationType |
Journal Article
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