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  • 1985-1989  (2)
  • 1880-1889
  • (E,Z)-10,12-tetradecadien-1-ol acetate  (1)
  • Polymer and Materials Science  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical ecology 12 (1986), S. 1239-1245 
    ISSN: 1573-1561
    Keywords: Amorbia cuneana ; Amorbia essigana ; sex pheromone ; sex pheromone component ratios ; Lepidoptera ; Tortricidae ; (E,E)-10,12-tetra-decadien-1-ol acetate ; (E,Z)-10,12-tetradecadien-1-ol acetate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract The most effective lure for maleAmorbia cuneana (Walsingham) in Orange, Ventura, and Riverside counties of California was previously found to be a 1∶1 ratio of (E,E)-10,12- and (E,Z)-10,12-tetradecadien-1-ol acetates. In subsequent field tests in San Diego and Santa Barbara counties, this lure was ineffective. Analysis of sex pheromone glands (SPG) of femaleA. cuneana from these two counties showed theEE:EZ ratio to be about 1∶9 and synthetic lures of this composition were highly attractive in these areas. Analysis of the SPG of a number of females from both areas showed that there were three population types: two in the low ratio areas possessed 37 and 58%EZ, and the third in the high ratio areas possessed 89%EZ.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0323-7648
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Durch die Synthese von cyclischen Acrylaten wurde eine Reihe von Monomeren erhalten, die hohe Reaktivitäten der Copolymerisation bei gleichzeitiger Fähigkeit zur radikalischen Ringöffnungspolymerisation aufweisen. Sie wurden polymerisiert, um einen Pyruvatester in die Polymerkette einzuführen. Eine Reihe von Spiromethylencyclohexadienen wurde hergestellt, um neben der Carbonylgruppe und gespannten Ringen weitere Gruppen zu finden, die die radikalische Ringöffnungspolymerisation fördern. Bei ihrer Polymerisation wurden Polymere mit einer p-Phenylengruppe in der Kette erhalten.
    Notes: In order to find a series of monomers with high reactivities in copolymerization and still undergo free radical ringopening polymerization, a series of cyclic acrylates were synthesized and polymerized to insert a pyruvate ester into the backbone of the polymer. In order to discover groups other than the carbonyl groups and strained rings that would promote free radical ring-opening polymerization, a series of spiro methylenecyclohexadienes were prepared and polymerized to give a polymer with a p-phenylene group in the backbone.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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