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
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