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  • Stable fly  (2)
  • Springer  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Sex pheromone of the stable fly (1979)
    Springer
    Journal of chemical ecology 5 (1979), S. 353-361 
    Details
    ISSN: 1573-1561
    Keywords: Stable fly ; Stomoxys calcitrans (L) ; pheromone ; mating stimulants ; alkenes ; cuticular lipids ; copulatory behavior
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract The cuticular alkenes of the female stable fly,Stomoxys calcitrans (L), which were responsible for inducing male fly copulatory behavior are (Z)-9-hentriacontene, (Z)-9-tritriacontene, 13-methyl-1-hen-triacontene and 13-methyl-1-tritriacontene. The identifications of the branched alkenes and the synthesis of these four compounds are described. Bioassays indicate that these materials in combination with previously described methyl branched alkanes are more active than the individual components.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00987921
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  • 2
    Electronic Resource
    Electronic Resource
    Synthesis of the male stable fly polyene (Z,Z)-1,7,13-pentacosatriene and its geometrical isomers (1979)
    Springer
    Journal of chemical ecology 5 (1979), S. 415-422 
    Details
    ISSN: 1573-1561
    Keywords: Stable fly ; Stomoxys calcitrans (L.) ; pheromone ; sex pheromone ; polyene ; mating stimulant ; (Z,Z)-1,7,13-pentacosatriene
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract The four geometrical isomers of 1,7,13-pentacosatriene were synthesized from 1,7-octadiyne. Two of the required isomers were synthesized using known methodology. Hydrogenation of acetylenic linkages were employed to produce predominantly cis alkenes, and alkali metal/amine reduction was used to produce a trans alkene. It was thus possible to produce the (Z,Z) and the (Z,E) isomers. Methods for olefin inversion were then employed to obtain the other two isomers.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00987926
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    Paper (German National Licenses)
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