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« Previous Abstract[Historical study of separation technology innovation in the field of pharmaceutical science]    Next Abstract"Characterization of epoxytrienes derived from (3Z,6Z,9Z)-1,3,6,9-tetraenes, sex pheromone components of arctiid moths and related compounds" »

J Chem Ecol


Title:"Novel components of the sex pheromones produced by emerald moths: identification, synthesis, and field evaluation"
Author(s):Yamakawa R; Do ND; Kinjo M; Terashima Y; Ando T;
Address:"Tokyo University of Agriculture and Technology, Koganei, Tokyo, Japan"
Journal Title:J Chem Ecol
Year:2011
Volume:20101215
Issue:1
Page Number:105 - 113
DOI: 10.1007/s10886-010-9895-y
ISSN/ISBN:1573-1561 (Electronic) 0098-0331 (Linking)
Abstract:"The subfamily Geometrinae (Lepidoptera: Geometridae) includes many species called emerald moths. Based on our recent finding of novel polyenyl compounds, including a double bond at the 12-position from two geometrine species, Hemithea tritonaria and Thalassodes immissaria intaminata, (6Z,9Z,12Z)-6,9,12-trienes and (3Z,6Z,9Z,12Z)-3,6,9,12-tetraenes with a C(17)-C(20) straight chain were synthesized and analyzed by GC-MS. The 6,9,12-trienes, which were prepared by a double Wittig reaction between two alkanals and an ylide derived from (Z)-1,6-diiodo-3-hexene, characteristically produced fragment ions at m/z 79, 150, and M-98. The 3,6,9,12-tetraenes, which were prepared by a coupling between (Z)-3-alkenal and an ylide derived from (3Z,6Z)-1-iodo-3,6-nonadiene, showed fragment ions at m/z 79, 148, and M-96. These diagnostic ions were useful to distinguish these compounds from other known polyenyl pheromones, such as 4,6,9- and 6,9,11-trienes and 1,3,6,9-tetraenes. With reference to the GC-MS data, pheromone extracts of other species in Geometrinae inhabiting the Iriomote Islands were analyzed, and the 6,9,12-trienes were identified in the pheromone gland extracts of Pamphlebia rubrolimbraria rubrolimbraria and Maxates versicauda microptera. Furthermore, a field evaluation of the synthetic polyenes in a mixed forest of Tokyo revealed the following new male attractants for emerald moths: Idiochlora ussuriaria by a C(17) 6,9,12-triene and Jodis lactearia by a C(20) 3,6,9,12-tetraene, indicating the characteristic chemical structures of Geometrinae pheromones. On the other hand, through reexamination of the pheromone extract of H. tritonaria, (3E,6E)-alpha-farnesene was identified as an electrophysiologically active component in addition to the C(17) 6,9,12-triene. The binary mixture attracted more males than the single component lure baited with the triene in the Iriomote Islands"
Keywords:"Animals Chromatography, High Pressure Liquid Gas Chromatography-Mass Spectrometry Magnetic Resonance Spectroscopy Moths/*metabolism Sex Attractants/biosynthesis/*metabolism;"
Notes:"MedlineYamakawa, Rei Do, Nguyen Duc Kinjo, Masakatsu Terashima, Yoshie Ando, Tetsu eng Research Support, Non-U.S. Gov't 2010/12/17 J Chem Ecol. 2011 Jan; 37(1):105-13. doi: 10.1007/s10886-010-9895-y. Epub 2010 Dec 15"

 
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Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
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