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  • 1980-1984  (3)
  • 1955-1959
  • Organic Chemistry  (2)
  • Hymenoptera  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical ecology 6 (1980), S. 895-903 
    ISSN: 1573-1561
    Keywords: Dasymutilla occidentalis ; Dasymutilla ; Timulla ; Pseudomethoca ; Smicromyrme ; Traumatomutilla ; Pappognatha ; Hymenoptera ; Mutillidae ; 4-methyl-3-heptanone ; 4,6-dimethyl-3-nonanone ; 4,6-dimethyl-3-octanone ; allomones
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract The mandibular gland secretion of the mutillid wasp,Dasymutilla occidentalis, possesses three short-chained ketones-4-methyl-3-heptanone (4MH), 4,6-dimethyl-3-nonanone (4,6DMN), 4,6-dimethyl-3-octanone (4,6DMO)—and several unidentified compounds. This is the first report of 4,6DMN as a natural product and its synthesis is described. These ketones, which are either known to be ant alarm pheromones or are structurally very similar to ant alarm pheromones, appear to function as allomones against ants, major potential predators of mutillid wasps. The major secretory component, 4-methyl-3-heptanone, which was identified in females and/ or males of the species analyzed within the generaDasymutilla, Timulla, Traumatomutilla, andPappognatha, appears to constitute a chemical character of the defensive secretions of these genera.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 323 (1981), S. 654-660 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Mass Spectroscopy of Natural Products. XIII. Mass Spectroscopic Investigations of A-nor-AllobetulanesThe mass spectroscopic fragmentation behaviour of A-nor-allobetulanes with several substituents at C-2 is discussed. The skeleton fragmentation is comparable to that of C-3-substituted allobetulanes. The nature of the substituent at C-2 influences both the abundance of typical skeleton fragments and the formation of specific ions.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 322 (1980), S. 695-700 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Mass Spectroscopy of Natural Products. VII. Mass Spectroscopic Studies of C-3-substituted Nitrogen Containing Friedelanes
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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