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  • 1
    Electronic Resource
    Electronic Resource
    Isolement et identification de composés à activité phéromonale chez les femelles de l'arctiide Tyria jacobaeae: Détermination biologique de la configuration absolue du composé majoritaire (1988)
    Springer
    Entomologia experimentalis et applicata 46 (1988), S. 281-289 
    Details
    ISSN: 1570-7458
    Keywords: Lepidoptera ; Arctiidae ; Sex Pheronome ; Behaviour ; Electroantennography ; Physico-chemistry ; (Z,Z)-3,6-Cis-9S,10R-epoxyheneicosadiene ; (Z,Z)-3,6-Cis-9,10-epoxyeicosadiene ; (Z,Z,Z)-3,6,9-heneicosatriene ; Lépidoptère ; Arctiidae ; Phéromone sexuelle ; Comportement ; Electroantennographie ; Physicochimie ; Epoxy-9S,10R-(Cis) hénéicosadiène-3Z,6Z ; Epoxy-9,10-(Cis) éicosadiène-3Z,6Z ; Hénéicosatriène-3Z,6Z,9Z
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Description / Table of Contents: Abstract The hexanic extracts from pheronomal glands of T. jacobaeae virgin females have been studied. Gas-chromatographic and mass-spectrometric analyses of the main component (no 1) (98%) in combination with behavioral and electrophysiological bioassays allowed us to determine its structure and absolue configuration: (Z,Z)-3,6-Cis-(S,R)9,10-epoxyheneicosadiene previously described in other Arctiid moths. A minor constituent (no 2) (1.5%) was identified as (Z,Z)-3,6-Cis-(S,R)9,10-epoxyeicosadiene by comparison with synthetic compound. This structure is a new one for a lepidoptera sex pheromone. The third component (no 3) of the same extracts has the same physico-chemical data as those of a previously reported constituent of another Arctiid moth: (Z,Z,Z)-3,6,9 heneicosatriene.
    Notes: Abstract Les analyses physico-chimiques d'extraits hexaniques de glandes à phéromone de femelles vierges de T. jacobaeae, associées à des études du comportement sexuel et à l'électroantennographie, ont permis d'identifier le composé majoritaire (98%) comme étant l'époxy-9S,10R-(Cis)-hénéicosadiène-3Z,6Z (no 1) et de déterminer sa configuration absolue. Les analogies entre les spectres du composé no 2 (1,5%) et ceux de l'époxy-9S,10R éicosadiène-3Z,6Z de synthèse nous conduisent à proposer cette structure pour ce constituant minoritaire. Le troisième produit (0,5%) possède les caractéristiques physico-chimiques de l'hénéicosatriène-3Z,6Z,9Z (no 3). Les produits 1 et 3 ont déjà été identifiés comme constituants de phéromones d'Arctiidae tandis que le produit 2 est décrit ici pour la première fois dans une sécrétion phéromonale de Lépidoptère.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00364200
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  • 2
    Electronic Resource
    Electronic Resource
    Chemical analysis of the pheromone blends produced by males and females of the neotropical moth,Mocis megas (Guénée) (Lepidoptera, Noctuidae, Catocalinae) (1990)
    Springer
    Cellular and molecular life sciences 46 (1990), S. 536-539 
    Details
    ISSN: 1420-9071
    Keywords: Sex pheromone ; male secretion ; chemical analysis ; (Z,Z) 6,9 heneicosadiene ; (Z,Z,Z) 3,6,9 heneicosatriene ; (Z,Z)-3,6-cis-9S,10R-epoxyheneicosadiene ; Mocis megas
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Pheromonal secretions produced by females and males of the noctuid moth,Mocis megas (Guénée) have been analyzed by gas chromatography and mass spectrometry (EI (electron impact) and CI (chemical ionization)). The female sex pheromone was a blend of (Z,Z,Z) 3,6,9 heneicosatriene (55%) and (Z,Z) 3,6-cis-9S, 10R-epoxyheneicosadiene (45%). Male secretion produced at the level of a prothoracic organ was a blend of two unsaturated major hydrocarbons: (Z,Z) 6,9 heneicosadiene, (64%) and (Z,Z,Z) 3,6,9 heneicosatriene (24%) and C19, C20 and C22 homologues (total ratio 12%), as minor components. The trienic hydrocarbon was present in both sexes. The behavioral role of this male secretion has not yet been elucidated.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01954259
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  • 3
    Electronic Resource
    Electronic Resource
    Optimized production of the acylium diagnostic ions in the chemical ionization NO+ mass spectra of long-chain monoolefins (1990)
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 25 (1990), S. 49-52 
    Details
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A recent reinvestigation of the reactivity of NO+ towards straight-chain monoolefinic compounds revealed that the characteristic acylium ions, previously reported for alkenyl acetates and related compounds, could also be obtained from alkenes and alkenoic acids (or esters). In this study, the influence of the sample pressure and that of NO on the production of the acylium ions was investigated, leading to disappearance graphs indicative of a strong dependence on these experimental factors. This gives a further explanation for previous apparent discrepancies in the literature and the optimum conditions of use for double-bond location in a variety of substituted or unsubstituted monoolefins.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/oms.1210250111
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    Paper (German National Licenses)
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