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1.
J Chem Ecol ; 31(11): 2705-20, 2005 Nov.
Article in English | MEDLINE | ID: mdl-16273436

ABSTRACT

Four himachalene sesquiterpenes and (+)-gamma-cadinene, previously identified as possible pheromone components from males of a North American population of Phyllotreta cruciferae Goeze (Coleoptera, Chrysomelidae), were tested for attractiveness in field trapping experiments in Hungary. A mixture of the four synthetic racemic himachalene derivatives and (+)-gamma-cadinene from a botanical source was slightly attractive to beetles, but much more attractive when blended with the known host-plant-derived attractant allyl isothiocyanate. This result was consistent with a previous study in North America. In tests with optically pure synthetic compounds, a blend of the same himachalene enantiomers found from male beetles was equivalent to the corresponding blend of racemic compounds, whereas a blend of the opposite enantiomers was not active. Through subtraction tests, it was found that the single compound, (6R,7S)-2,2,6,10-tetramethylbicyclo[5.4.0.]undeca-9,11-diene [compound (+)-A in this study], was as active as the whole mixture, suggesting that this compound is the key pheromone component of the European population of P. cruciferae. During field trials, several congeneric species, including P. vittula, P. nemorum, P. nodicornis, and P. ochripes, also were caught, suggesting that the same compound(s) may be relatively widespread as pheromone components in this genus.


Subject(s)
Brassicaceae/chemistry , Coleoptera/drug effects , Isothiocyanates/pharmacology , Pheromones/pharmacology , Sesquiterpenes/pharmacology , Animals , Coleoptera/physiology , Feeding Behavior , Hungary , Isothiocyanates/chemistry , Pest Control, Biological , Pheromones/chemistry , Polycyclic Sesquiterpenes , Sesquiterpenes/chemistry , Species Specificity , Stereoisomerism
2.
Biosci Biotechnol Biochem ; 67(7): 1559-67, 2003 Jul.
Article in English | MEDLINE | ID: mdl-12913301

ABSTRACT

Four pheromone components of the female painted apple moth (Teia anartoides), an Australian insect pest, were synthesized. These were (Z)-6-henicosen-11-one (1), (6Z, 8E)-6,8-henicosadien-11-one (2), (Z)-cis-9,10-epoxy-6-henicosene (3), and (Z)-cis-9,10-epoxy-6-icosene (4). 2-Dodecanone was converted to 1 and 2, and both the enantiomers of 3 and 4 were synthesized from the enantiomers of 4-tert-butyldimethylsilyloxy-cis-2,3-epoxy-1-butanol.


Subject(s)
Moths/chemistry , Sex Attractants/chemistry , Sex Attractants/chemical synthesis , Animals , Epoxy Compounds/chemical synthesis , Female , Ketones/chemical synthesis , Ketones/chemistry , Molecular Structure , Stereoisomerism
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