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Sex pheromone of the pine sawflyDiprion pini (Hymenoptera: Diprionidae): Chemical identification,synthesis and biological activity
Authors:G Bergström  A -B Wassgren  O Anderbrant  J Fägerhag  H Edlund  E Hedenström  H -E Högberg  C Geri  M A Auger  M Varama  B S Hansson  J Löfqvist
Institution:(1) Chemical Ecology, Göteborg University, Carl Skottsbergs Gata 22, S-413 19 Göteborg, Sweden;(2) Department of Ecology, Lund University, Ecology Building, S-223 62 Lund, Sweden;(3) Chemistry, Department of Science and Engineering Mid Sweden University, S-851 70 Sundsvall, Sweden;(4) Centre de Recherches d'Orleans, Institut National de la Recherche Agronomique, Ardon, F-45160 Olivet, France;(5) Finnish Forest Research Institute, P.O. Box 18, FIN-01301 Vantaa, Finland;(6) Department of Plant Protection Sciences, Swedish University of Agricultural Sciences, P.O. Box 44, S-23053 Alnarp, Sweden
Abstract:The main component of the sex pheromone secretion of femaleDiprion pini L. (Hymenoptera: Diprionidae) from insects collected both in Finland and in France has been identified as athreo-3,7-dimethyl-2-tridecanol (8 ng per female) stereoisomer by GC-MS and synthesis. The secretion also contains lower and higher homologues in small amounts (1–4% of the main component). Combined gas chromatographic-electroantennographic detection showed activity in both natural and esterified extracts (acetates and propionates); the esters of the main component gave the largest responses. The acetates and propionates of the eight stereoisomers of 3,7-dimethyl-2-tridecanol were synthesized from enantiomerically highly enriched (>99% ee) building blocks. The stereochemistry of the main component was established to be (2S,3R,7R)-3,7-dimethyl-2-tridecanol by GC analysis of the natural material. It was purified by liquid chromatography prior to the GC analysis of both its pentafluorobenzoates and its isopropylcarbamates on a non-chiral polar column (ECD) and a chiral column (NPD), respectively. Field tests demonstrated that both the acetate and propionate of the main component (100 mgrg of each applied on cotton roll dispensers) were active in attracting males, with or without the presence of several of the minor compounds. Experiments with smaller amounts of the acetate and the propionate (1 mgrg in France and 50 mgrg in Finland) demonstrated that the propionate was more active than the acetate, and that it also caught more males than a blend of the two compounds.
Keywords:Diprion pini  semiochemicals  sex attractant  3  7-dimethyl-2-tridecanol  chiral synthesis  lipase  chiral analysis
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