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« Previous Abstract"Improved synthesis of (3E,6Z,9Z)-1,3,6,9-nonadecatetraene, attraction inhibitor of bruce spanworm, Operophtera bruceata, to pheromone traps for monitoring winter moth, Operophtera brumata"    Next AbstractDiscovery of the aggregation pheromone of the brown marmorated stink bug (Halyomorpha halys) through the creation of stereoisomeric libraries of 1-bisabolen-3-ols »

J Chem Ecol


Title:"Determination of the stereochemistry of the aggregation pheromone of harlequin bug, Murgantia histrionica"
Author(s):Khrimian A; Shirali S; Vermillion KE; Siegler MA; Guzman F; Chauhan K; Aldrich JR; Weber DC;
Address:"US Department of Agriculture, Agricultural Research Service, Invasive Insect Biocontrol and Behavior Laboratory, Beltsville, MD, 20705, USA, ashot.khrimian@ars.usda.gov"
Journal Title:J Chem Ecol
Year:2014
Volume:20141119
Issue:11-Dec
Page Number:1260 - 1268
DOI: 10.1007/s10886-014-0521-2
ISSN/ISBN:1573-1561 (Electronic) 0098-0331 (Linking)
Abstract:"Preparation of a complete stereoisomeric library of 1,10-bisaboladien-3-ols and selected 10,11-epoxy-1-bisabolen-3-ols was pivotal for the identification of the aggregation pheromone of the brown marmorated stink bug, Halyomorpha halys. Herein, we describe syntheses of the remaining 10,11-epoxy-1-bisabolen-3-ols, and provide additional evidence on the assignment of relative and absolute configurations of these compounds by single-crystal X-ray crystallography of an intermediate, (3S,6R,7R,10S)-1-bisabolen-3,10,11-triol. To demonstrate the utility of this stereoisomeric library, we revisited the aggregation pheromone of the harlequin bug, Murgantia histrionica, and showed that the male-produced pheromone consists of two stereoisomers of 10,11-epoxy-1-bisabolen-3-ol. Employment of eight cis-10,11-epoxy-1-bisabolen-3-ol stereoisomeric standards, two enantioselective GC columns, and NMR spectroscopy enabled the identification of these compounds as (3S,6S,7R,10S)-10,11-epoxy-1-bisabolen-3-ol and (3S,6S,7R,10R)-10,11-epoxy-1-bisabolen-3-ol, which are produced by M. histrionica males in 1.4:1 ratio"
Keywords:"Animals *Chemotaxis Chromatography, Gas Crystallography, X-Ray Heteroptera/growth & development/*physiology Male Pheromones/*metabolism Stereoisomerism;"
Notes:"MedlineKhrimian, Ashot Shirali, Shyam Vermillion, Karl E Siegler, Maxime A Guzman, Filadelfo Chauhan, Kamlesh Aldrich, Jeffrey R Weber, Donald C eng 2014/11/20 J Chem Ecol. 2014 Dec; 40(11-12):1260-8. doi: 10.1007/s10886-014-0521-2. Epub 2014 Nov 19"

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