conophthorin and decane

Optically pure synthetic enantiomers of (E)-conophthorin [(E)-7-methyl-1,6-dioxaspiro[4.5]decane], one of the volatiles affecting coniferophagous bark beetles, were tested on antennae of Ips typographus, I. duplicatus, I. subelongatus, Dendroctonus micans, and five Scolytus spp. by using combined gas chromatography-electroantennographic detection (GC-EAD). EAD dose-responses indicated that all three Ips species perceived only the naturally occurring and quantitatively dominant (5S,7S)-enantiomer, while its antipode, (5R,7R)-(E)-conophthorin was antennally inactive. Response thresholds for the Ips species were estimated as between 0.1 ng and 1 ng, or lower. The antennal responses of the Ips species caused by 100 ng of the (5R,7R)-enantiomer might be due to 1% impurity-(the active (5S,7S)-enantiomer) in the (5R,7R)-sample. At the 50-ng level, D. micans and five angiosperm Scolytus species (S. intracatus, S. mali, S. ratzeburgi, S. rugulosus, and S. scolytus) responded strongly to the (5S,7S)-enantiomer, while the (5R,7R)-enantiomer was antennally inactive. Currently updated knowledge on the natural occurrence, and electrophysiological and behavioral activity of (E)-conophthorin is summarized.

Topics: Acetals; Alkanes; Animals; Chromatography, Gas; Coleoptera; Dose-Response Relationship, Drug; Electrophysiology; Olfactory Receptor Neurons; Smell; Species Specificity; Spiro Compounds; Stereoisomerism