Abstract: A method for repelling arthropods involving treating a subject or an object with an arthropod repelling composition containing an arthropod repelling effective amount of at least one clerodane of the formula in which R1 is H, halogen, formyl, a straight chain or branched C1-4 saturated alkyl, a straight chain or branched C2-4 unsaturated alkyl, or an aryl containing 6-10 carbon atoms in the ring skeleton thereof, wherein R1 is unsubstituted or substituted with one or more substituents, which are the same or different, selected from the group consisting of oxo (?O), OR2, CO2R2, and OC(O)R2, wherein R2 is H, a straight chain or branched C1-30 saturated alkyl, a straight chain or branched C2-30 unsaturated alkyl, or an aryl comprising 6-10 carbon atoms in the ring skeleton thereof; wherein R2 is unsubstituted or substituted with one or more substituents selected from the group consisting of halogen, amino, hydroxyl, oxo (?O), thio, cyano and nitro; optionally a carrier, optionally an arthropod repellant, and

Abstract: A method for for repelling arthropods involving treating an object or area with an arthropod repelling effective amount of at least one isolongifolenone analog (and optionally a carrier or carrier material).

Abstract: A method for for repelling arthropods involving treating an object or area with an arthropod repelling effective amount of at least one isolongifolenone analog (and optionally a carrier or carrier material).

Abstract: A method for making isolongifolenone involving reaction (?)-isolongifolene with chromium hexacarbonyl and t-butyl hydroperoxide. Also the use of isolongifolenone to repel arthropods by treating an object or area with an arthropod repelling effective amount of isolongifolenone (and optionally a carrier or carrier material).

Abstract: A method for repelling arthropods involving treating a subject or an object with an arthropod repelling composition containing an arthropod repelling effective amount of at least one clerodane of the formula in which R1 is H, halogen, formyl, a straight chain or branched C1-4 saturated alkyl, a straight chain or branched C2-4 unsaturated alkyl, or an aryl containing 6-10 carbon atoms in the ring skeleton thereof, wherein R1 is unsubstituted or substituted with one or more substituents, which are the same or different, selected from the group consisting of oxo (?O), OR2, CO2R2, and OC(O)R2, wherein R2 is H, a straight chain or branched C1-30 saturated alkyl, a straight chain or branched C2-30 unsaturated alkyl, or an aryl comprising 6-10 carbon atoms in the ring skeleton thereof; wherein R2 is unsubstituted or substituted with one or more substituents selected from the group consisting of halogen, amino, hydroxyl, oxo (?O), thio, cyano and nitro; optionally a carrier, optionally an arthropod repellant, an

Abstract: A method for selecting the most effective arthropod repellent from stereoisomers of a compound, involving testing each stereoisomer of the compound for its effectiveness as an arthropod repellent against an arthropod of a particular genus and species, comparing the test results and selecting the most effective arthropod repellent stereoisomer from the stereoisomers of the compound, wherein the compound is a piperidine analog. A composition for repelling arthropods, containing a carrier material and an arthropod repelling effective amount of a stereoisomer of a compound, wherein said stereoisomer is selected by the above method. A method for repelling arthropods (e.g., Aedes aegypti or Aedes albopictus) from a mammal, involving treating the mammal with an arthropod with the above repelling composition (e.g., containing (1S,2′S) stereoisomer of 1-(3-cyclohexen-1-ylcarbonyl)-2-methylpiperidine).

Abstract: Addition of (Z,Z)-3,13 octadecadienyl acetate to the grape root borer, Vitacea polistiformis (Harris), pheromone (E,Z)-2,13 octadecadienyl acetate increases capture of males in sticky traps by three- to sevenfold. This new composition will provide and effective system for monitoring and controlling the grape root borer.

Abstract: The racemate of 1-methylbutyldecanoate is synthesized and found to be a powerful attractant under field conditions for male bagworm moths. It is also found to suppress or inhibit completely the mating of female bagworm moths when applied to trees and shrubs in an effective mating suppressant or inhibiting amount.

Abstract: A combination of (Z)-11-hexadecenal, (Z)-9-tetradecenal, (Z)-9-hexadecenal, (Z)-7-hexadecenal, (Z)-11-hexadecen-1-ol, tetradecanal, and hexadecanal is an effective attractant for adult male tobacco budworm moths.

Abstract: A combination of (Z)-11-hexadecenal and (Z)-9-hexadecenal is an effective attractant for adult male corn earworm moth.