Title of article :
Iridodials: enantiospecific synthesis and stereochemical assignment of the pheromone for the golden-eyed lacewing, Chrysopa oculata
Author/Authors :
Chauhan، نويسنده , , Kamlesh R. and Zhang، نويسنده , , Qing-He and Aldrich، نويسنده , , Jeffrey R.، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2004
Pages :
2
From page :
3339
To page :
3340
Abstract :
1R,2S,5R,8R; 1R,2S,5R,8S; 1S,2S,5R,8R; and 1S,2S,5R,8S-Iridodials have been prepared in five steps from 4aS,7S,7aR and 4aS,7S,7aS-nepetalactones, major components of catnip oil. 1R,2S,5R,8R-Iridodial has been identified as a male-produced male-aggregation pheromone for Chrysopa oculata, the first pheromone of any kind identified for lacewings.
Keywords :
Nepetalactone , Lacewing , Iridodials
Journal title :
Tetrahedron Letters
Serial Year :
2004
Journal title :
Tetrahedron Letters
Record number :
1841365
Link To Document :
بازگشت