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R E Doolittle

Showing results (1-10 of 14) with videos related to

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Journal of Chemical Ecology|November 21, 2013
Sex attractants for the white-barred groundling moth (Recurvaria leucatella clerck) and the lesser bud moth (R. nanella Hübner) (Lepidoptera: Gelechiidae)M Tòth, R E Doolittle
Journal of Chemical Ecology|December 6, 2013
Stereoselective synthesis of (Z,E)-3,5-tetradecadienyl acetate: Sex attractant for carpenterworm moth,Prionoxystus robiniae (Peck) (Lepidoptera: Cossidae) and effect of isomers and monounsaturated acetates on its attractivenessR E Doolittle, J D Solomon
Journal of Chemical Ecology|November 16, 2013
Synergism of an insect sex pheromone specialist neuron: Implications for component identification and receptor interactionsM S Mayer, R E Doolittle
Journal of Chemical Ecology|November 23, 2013
Sex pheromone ofManduca Sexta (L) Stereoselective synthesis of (10E,12E,14Z)-10,12,14-Hexadecatrienal and IsomersR E Doolittle, A Brabham, J H Tumlinson
Journal of Chemical Ecology|November 16, 2013
Quadrupole storage mass spectrometry of mono- and dimethylalkanesR E Doolittle, A T Proveaux, H T Alborn, et al.
Journal of Chemical Ecology|January 15, 2014
Japanese beetle (Coleoptera: Scarabaeidae) : Response to synthetic sex attractant plus phenethyl propionate: EugenolM G Klein, J H Tumlinson, T L Ladd, et al.
Journal of Chemical Ecology|November 22, 2013
Trimedlure enantiomers: Differences in attraction for mediterranean fruit fly,Ceratitis capitata (Wied.) (Diptera: Tephritidae)R E Doolittle, R T Cunningham, T P McGovern, et al.
Journal of Chemical Ecology|November 19, 2013
Field tests of syntheticManduca sexta sex pheromoneJ H Tumlinson, E R Mitchell, R E Doolittle, et al.
Journal of Chemical Ecology|November 16, 2013
Structure-activity relationship observations oftrans-trimedlure enantiomersJ D Warthen, W F Schmidt, R E Doolittle, et al.
Science (New York, N.Y.)|August 19, 1977
Identification of the female Japanese beetle sex pheromone: inhibition of male response by an enantiomerJ H Tumlinson, M G Klein, R E Doolittle, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Journal of Chemical Ecology|November 21, 2013
Sex attractants for the white-barred groundling moth (Recurvaria leucatella clerck) and the lesser bud moth (R. nanella Hübner) (Lepidoptera: Gelechiidae)M Tòth, R E Doolittle
Journal of Chemical Ecology|December 6, 2013
Stereoselective synthesis of (Z,E)-3,5-tetradecadienyl acetate: Sex attractant for carpenterworm moth,Prionoxystus robiniae (Peck) (Lepidoptera: Cossidae) and effect of isomers and monounsaturated acetates on its attractivenessR E Doolittle, J D Solomon
Journal of Chemical Ecology|November 16, 2013
Synergism of an insect sex pheromone specialist neuron: Implications for component identification and receptor interactionsM S Mayer, R E Doolittle
Journal of Chemical Ecology|November 23, 2013
Sex pheromone ofManduca Sexta (L) Stereoselective synthesis of (10E,12E,14Z)-10,12,14-Hexadecatrienal and IsomersR E Doolittle, A Brabham, J H Tumlinson
Journal of Chemical Ecology|November 16, 2013
Quadrupole storage mass spectrometry of mono- and dimethylalkanesR E Doolittle, A T Proveaux, H T Alborn, et al.
Journal of Chemical Ecology|January 15, 2014
Japanese beetle (Coleoptera: Scarabaeidae) : Response to synthetic sex attractant plus phenethyl propionate: EugenolM G Klein, J H Tumlinson, T L Ladd, et al.
Journal of Chemical Ecology|November 22, 2013
Trimedlure enantiomers: Differences in attraction for mediterranean fruit fly,Ceratitis capitata (Wied.) (Diptera: Tephritidae)R E Doolittle, R T Cunningham, T P McGovern, et al.
Journal of Chemical Ecology|November 19, 2013
Field tests of syntheticManduca sexta sex pheromoneJ H Tumlinson, E R Mitchell, R E Doolittle, et al.
Journal of Chemical Ecology|November 16, 2013
Structure-activity relationship observations oftrans-trimedlure enantiomersJ D Warthen, W F Schmidt, R E Doolittle, et al.
Science (New York, N.Y.)|August 19, 1977
Identification of the female Japanese beetle sex pheromone: inhibition of male response by an enantiomerJ H Tumlinson, M G Klein, R E Doolittle, et al.
Pageof 2