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« Previous CompoundE3E5E7E9-6,8-diethyl-4me-12Hy    Next Compound »E3Z13-18OH
 
Compound - E3Z13-18Ac
 


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(E,Z)-3,13-Octadecadienyl acetate
(E,Z)-3,13-Octadecadienyl acetate

Formula: C20H36O2 
CAS#: 53120-26-6 
MW: 308.5 

[MS]  [ NMR ]  [ Kovats ]  [Behavioural function]  [Chemdraw





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Reference(s) for synthesis of (E,Z)-3,13-Octadecadienyl acetate



Capdevila, A., Prasad, A.R., Quero, C., Petschen, I., Bosch, M.P., and Guerrero, A. 1999. A convergent and highly efficient synthesis of (E,Z)-2,13-octadecadienyl acetate and (E,Z)-3,13-octadecadienyl acetate, components of the sex pheromone of the leopard moth Zeuzera pyrina, through sulfones. Org. Lett. 1:845-848.
 
Doolittle, R.E., Proveaux, A.T., and Heath, R.R. 1980. Synthesis of sex pheromones of lesser peachtree borer and peachtree borer. J. Chem. Ecol. 6:271-284.
 
Ebata, T., and Mori, K. 1979. A convenient synthesis of a mixture of (Z,Z)-3,13-octadecadienyl acetate and its (E,Z)-isomer, the attractant for the cherrytree borer. Agric. Biol Chem. 43:1567.
 
Gardette, M., Alexis, A., and Normant, J.F. 1983. Synthesis of (Z,Z)-3,13-octadecadien-1-yl acetate. Component of the sex pheromone of Synanthedon tenuis. J. Chem. Ecol. 9:225-233.
 
Ivanova, N.M., Czeskis, B.A., Moiseenkov, A.M., and Nefedov, O.M. 1991. Bull. Acad. Sci. USSR Div. Chem. Sci. (Engl. Transl.). 40:2196-2204.
 
Svirskaya, P.I., and Leznoff, C.C. 1984. Synthesis of unconjugated (Z,Z)-diolefinic insect pheromones on insoluble polymer supports. J. Chem. Ecol. 10:321-333.
 
Tumlinson, J.H., Yonce, C.E, Doolittle, R.E., Heath, R.R., Gentry, C.R., and Mitchell, E.R. 1974. Sex pheromones and reproductive isolation of the lesser peachtree borer and the peachtree borer. Science. 185:614.
 
Uchida, M., Mori, K., and Matsui, M. 1978. Synthesis of (Z,Z)-3,13-octadienyl acetate and its (E,Z)-isomer, the attractant for the cherrytree borer. Agric. Biol. Chem. 42:1067.
 
Uchida, M., Nakagawa, K., and Mori, K. 1979. Stereoselective synthesis of (Z,Z)-3,13-octadecadienyl acetate the attractant for smaller clear wing moth. Agric. Biol. Chem. 43:1919.
 
Underhill, E.W., Steck, W., Chisholm, M.D., Worden, H.A., and Howe, J.A.G. 1978. A sex attractant for the cottonwood crownborer, Aegeria tibialis. Can. Entomol. 110:495-498.
 
Vinczer, P., Baan, G., Juvanez, Z., Novak, L., and Szantay, C. 1985. Simple and stereocontrolled synthesis of an optimal isomeric mixture of 3,13-octadecadien-1-yl acetates. Synth. Comm. 15:1257.
 
Voerman, S. 1979. Chemical conversion of 9-tetradecen-1-ol acetates to 3,13-octadecadien-1-ol acetates, sex attractants for male clearwing moths. J. Chem. Ecol. 5:759-766.
 
Zhang, X.-H., Guo, G -Z., Lin, G -Q., Wu, Y.-W, Wu, P.-X., Li, Z.-Y., and Wei, K.-N. 1986. Studies on identification and syntheses of insect pheromones. XXII. Sex pheromone of poplar twig clearwing moth Paranthrene tabaniformis Rott. - structure and synthesis. J. Chem. Ecol. 12:1263-1271.
 

 
Citation: El-Sayed AM 2014. The Pherobase: Database of Insect Pheromones and Semiochemicals. <http://www.pherobase.com>.
2003-2014 The Pherobase - Extensive Database of Insect Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 23-February-2014