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Synthesis and structure-activity relationship of diene modified analogs of<Emphasis Type="Italic"> Matsucoccus</Emphasis> sex pheromones
Authors:Z?Mendel  Email author" target="_blank">E?DunkelblumEmail author  M?Branco  J?C?Franco  S?Kurosawa  K?Mori
Institution:(1) Department of Entomology, Volcani Center ARO, 50250 Bet Dagan, Israel;(2) Instituto Superior de Agronomia, 1349-017 Lisbon, Portugal;(3) Department of Chemistry, Faculty of Science, Science University of Tokyo, Kagurazaka 1-3, 162-8601 Shinjuku-ku, Tokyo, Japan;
Abstract:The biological activity of the Matsucoccus spp. sex pheromones and diene modified analogs has been tested in forests of Israel and Portugal in order to explore the structure-activity relationship of the pine bast scale pheromone/kairomone system. The response of the adult predatory bugs, Elatophilus hebraicus and E. crassicornis and of the brown lacewing, Hemerobius stigma is more selective than that of the conspecific Matsucoccus males. The removal of the terminal methyl group from the diene terminus of both pheromones 1 and 2 eliminates all kairomonal activity but retains moderate pheromonal activity. Addition of a methyl group to the diene terminus of pheromones 1 and 2 sustains full pheromonal and kairomonal activities of the Elatophilus spp. but eliminates entirely the kairomonal activity of H. stigma. Subtle designed alterations in the structure of the diene group, typical of all Matsucoccus pheromones, change the mode of the kairomonal activity markedly.
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