Optically inactive 1-[3-cyclohexen-1-ylcarbonyl] piperidine and 1-[3-cycloh
exen-1-ylcarbonyl]-2-methylpiperidine are repellents against blood-feeding
arthropods. Pure stereoisomers of these compounds were synthesized. and cha
racterized for use in bioassays. Initial laboratory tests with the malaria
vector Anopheles stephensi Listen showed that this species was repelled dif
ferentially by the stereoisomers of 1-[3-cyclohexen-1-ylcarbonyl]-2-methylp
iperidine. Two stereoisomers were twice as repellent as the other stereoiso
mers. These results indicate that stereoisomerism influences repellent effi
cacy in this class of compounds.