Anwendbarkeit von Borkenkäferpheromonen: Konfiguration und Konsequenzen1,2
Author:
Publisher
Wiley
Subject
General Agricultural and Biological Sciences
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1439-0418.1976.tb03378.x/fullpdf
Reference19 articles.
1. Comparison of sex pheromone inhibitor for disruption of pheromone communication in Rhyacionia buoliana;Daterman;Environ. Entomol.,1975
2. Synthesis of exo-brevicomin, the pheromone of western pine beetle, to obtain optically active forms of known absolute configuration;Mori;Tetrahodron,1974
3. Synthesis of optically active forms of frontalin, the pheromone of Dendroctonus bark beetles;Mori;Tetrahedron,1975a
4. Synthesis and absolute configuration of (-)-ipsenol (2-methyl-6-methylene-7-octene-5-ol), the pheromone of Ips paraconfusus Lanier;Mori;Tetrahedron Letters,1975b
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2. The Synthesis of Insect Pheromones;Total Synthesis of Natural Products;2007-02-20
3. Determination of Interconversion Barriers by Dynamic Gas Chromatography: Epimerization of Chalcogran;Chemistry;2001-04-01
4. Quantitative Separation of the Enantiomeric Pairs of the Pheromone 2-Ethyl-1,6-dioxaspiro[4.4]nonane by Complexation Chromatography on an Optically Active Metal Complex;Angewandte Chemie International Edition in English;1980-06
5. Quantitative Trennung der Enantiomerenpaare des Pheromons 2-Ethyl-1,6-dioxaspiro[4,4]nonan durch Komplexierungschromatographie an einem optisch aktiven Metallkomplex;Angewandte Chemie;1980-06
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