Key points are not available for this paper at this time.
S-(+)-4-Methyl-3-heptanone is the principal alarm pheromone of Atta texana. The dextrorotatory form of the ketone has also been identified from Atta cephalotes. Both enantiomers have been synthesized in high optical purity; Atta texana is more responsive to the (+) enantiomer than to the (-) form. These results implicate a chiral receptor system.
Riley et al. (Fri,) studied this question.