Biological Activities of the Analogs of the Aggregation Pheromone of Tribolium castaneum (Coleoptera: Tenebrionidae)

Abstract

The biological activities of seven optically active analogs of the aggregation pheromone of Tribolium castaneum stereoselectively synthesized from (R)-(+)-citronellic acid (100% e.e.) and/or (S)-( –)-2-methyl-l-butanol (93% e.e.) were tested and compared with those of their corresponding racemates and the four optical isomers of the pheromone. The 4S-analogs showed no activity at doses of not less than 1,000 ng, whereas all 4/?-analogs were active at 1.0-1,000 ng, especially (4R, 8RS)-4,8-dimethyldecanal (VII) had strong activity showing an 40.3% of attractiveness at a dose of 1.0 ng. The 8S-analog was rather repulsive. The presence of the 4R methyl group was indispensable for the activity. The aggregation activities of the two optical isomers of the pheromone, (4R, 8R)- and (4R, 8S)-4,8-dimethyldecanals were tested in various mixtures of them. A (8:2) mixture was most active and significant difference even at a dose of 0.1 ng, which was about ten times more attractive than (4R, 8R)-isomer alone. The (4R, 8S)-isomer had no activity at doses of not less than 10 ng when used alone. The (4R, 8S)-isomer acted as a synergist. This suggested the possibility that the natural pheromone of T. castaneum might be a mixture of (4R, 8R)- and (4R, 8S)-isomers. © 1984, JAPANESE SOCIETY OF APPLIED ENTOMOLOGY AND ZOOLOGY. All rights reserved.