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¦ « Previous CompoundE11Z13-16Ac    Next Compound »E11Z13-16OH ¦
 
Compound - E11Z13-16Ald
 


Bedoukain RussellIPM
 
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(E,Z)-11,13-Hexadecadienal
(E,Z)-11,13-Hexadecadienal

Formula: C16H28O 
CAS#: 73264-88-7 
MW: 236.4 

[MS]  [Behavioural function]  [Chemdraw





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Reference(s) for synthesis of (E,Z)-11,13-Hexadecadienal



Arai, K., Ando, T., Sakurai, A., Yamada, H., Koshihara, T., and Takahashi, N. 1982. Identification of the female sex pheromone of the cabbage webworm. Agric. Biol. Chem. 46:2395-2398.
 
Bishop, C.E., and Morrow, G.W. 1983. Synthesis of (Z,Z)-11,13-hexadecadienal, a principle component of navel orangeworm (Amyelois transitella) pheromone. J. Org. Chem. 48:657-660.
 
Coffelt, J.A., Vick, K.W., Sonnet, P.E., and Doolittle, R.E. 1979. Isolation, identification, and synthesis of a female sex pheromone of the navel orangeworm, Amyelois transitella (Lepidoptera: Pyralidae). J. Chem. Ecol. 5:955-966.
 
Furber, M., Taylor, J.K., and Burford, S.C. 1986. Stereospecific diene synthesis using acetylene carbocupration preparation of navel orangeworm pheromone and leukotriene analogues. J. Chem. Soc. Perkin Trans. 1:1809-1815.
 
Furber, M., Taylor, R.J.K., and Burford, S.C. 1985. Z,Z-dienes via acetylene carbocupration: synthesis of navel orangeworm pheromone. Tetrahedron Lett. 26:3285-3288.
 
Lo, V.M., and Shiao, M.-J. 1986. A convenient synthesis of (11E,13E)-11,13-hexadecadienal and (11Z,13E)-hexadecadienal. Synth. Comm. 16:1647-1656.
 
Michelot, D. 1983. Highly stereoselective synthesis of acetates of mono- and diunsaturated alcohols and analogous aldehydes, components of Lepidopteran sex pheromones, using tetrakis[triphenylphosphine]-palladium. Synthesis. 2:130-134.
 
Sonnet, P.E., and Heath, R.R. 1980. Stereospecific synthesis of (Z,Z)-11,13-hexadecadienal, a female sex pheromone of the navel orangeworm Amyelois transitella. J. Chem. Ecol. 6:221-228.
 
Yamada, S., Ohsawa, H., Suzuki, T., and Takayama, H. 1986. Stereoselective synthesis of (E)-, (E,Z)-, and (E,E)-conjugated dienes via alkylation of 3-sulfolenes as the key step. J. Org. Chem. 51:4934-4940.
 

 
Citation: El-Sayed AM 2023. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
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Page created on 15-October-2023