scholarly journals Biological Activity of (R)- and (S)-14-Methyl-1-Octadecene, as the Chiral Component of the Sex Pheromone of the Peach Leafminer Moth, Lyonetia clerkella LINNE(Lepidoptera : Lyonetiidae)

1985 ◽  
Vol 20 (4) ◽  
pp. 411-415 ◽  
Author(s):  
Rikio SATO ◽  
Noriyosi ABE ◽  
Philip SONNET ◽  
Hajime SUGIE ◽  
Yoshio TAMAKI
2003 ◽  
Vol 51 (10) ◽  
pp. 2987-2991 ◽  
Author(s):  
Carmen Quero ◽  
Josep Bau ◽  
Angel Guerrero ◽  
Michael Breuer ◽  
Arnold De Loof ◽  
...  

1976 ◽  
Vol 40 (2) ◽  
pp. 391-394
Author(s):  
Tetsuo Sato ◽  
Ritsuo Nishida ◽  
Yasumasa Kuwahara ◽  
Hiroshi Fukami ◽  
Shoziro Ishii

ChemInform ◽  
1988 ◽  
Vol 19 (35) ◽  
Author(s):  
S.-K. KANG ◽  
C.-H. LEE ◽  
J. H. KIM ◽  
J.-O. LEE

2002 ◽  
Vol 57 (7-8) ◽  
pp. 739-752 ◽  
Author(s):  
Wittko Francke ◽  
Stephan Franke ◽  
Jan Bergmann ◽  
Till Tolasch ◽  
Mitko Subchev ◽  
...  

Mass spectrometric investigations confirmed the structure of the female produced sex pheromone of the horse-chestnut leafminer Cameraria ohridella Desch. and Dim. to be (8E,10Z)-8,10-tetradecadienal. Pure samples, prepared in a straightforward synthesis, were highly attractive in field tests and proved to be suitable for monitoring of flight activities and population dynamics. In mixtures with the synthetic pheromone, analogues like 9-tridecynal and 7-dodecynyl formate were shown to reduce trap catches. In electroantennographic experiments, pheromone analogues were less active than the pheromone. 9-Tridecynal was the most EAG active analogue tested, followed by 7-dodecyn-1-yl formate and 7-undecyn-1- yl formate.


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