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¦ « Previous CompoundE8-11Ac    Next Compound »E8-12OH ¦
 
Compound - E8-12Ac [(E)-8-Dodecenyl acetate]
 


Bedoukain RussellIPM
 
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(E)-8-Dodecenyl acetate
(E)-8-Dodecenyl acetate

Formula: C14H26O2 
CAS#: 38363-29-0 
MW: 226.36 

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





Dots surface:


Reference(s) for synthesis of (E)-8-Dodecenyl acetate [E8-12Ac]


Angelini, A., Descoins, C., Le Rumeur, C., and Lhoste, J. 1980. Nouveaux resultats obtenus avec un attractif sexuel de Cryptophlebia leucotreta Meyr. Cot. Fib. Trop. 35:277.
 
Aukrust, A., Rongved, P., and Skatteboll, L. 1985. The synthesis of (Z)-8-dodecen-1-ol and its acetate, pheromone components of the oriental fruit moth (Grapholitha molesta). Acta Chem. Scand. B39:267.
 
Brovko, V.V., Mazur, V.G., Vlasov, A.A., Shishmakova, T.G., Strepkova, L.S., and Evstifeev, A.V. 1980. Synthesis of sex pheromones of codling and plum fruit moths and the housefly. Khim. Sel'sk. Khoz. 18:30.
 
Burger, B.V., Roux, M.l., Mackenroth, W.M., Spies, H.S.C., and Hofmeyr, J.H. 1990. 7-vinyldecyl acetate, novel inhibitor of pheromonal attraction in the false codling moth, Cryptophlebia leucotreta. Tetrahedron Lett. 31:5771-5772.
 
Chan, T.H., and Koumaglo, K. 1985. Silicon in organic synthesis. Stereoselective synthesis of some insect sex pheromones. J. Organomet. Chem. 285:109-120.
 
Holan, G., and O'Keefe, D.F. 1973. An improved synthesis of insect sex attractant: cis-8-dodecen-1-ol acetate. Tetrahedron Lett. 14:673-674.
 
Horiike, M., Tanouchi, M., and Hirano, C. 1980. A convenient method for synthesizing (Z)-alkenols and their acetates. Agric. Biol. Chem. 44:257-262.
 
Ishmuratov, G.Y., Ishmuratova, N.M., Odinokov, V.N., and Tolstikov, G.A. 1997. Use of enyne compounds in the synthesis of insect pheromones. Chem. Nat. Comp. (Engl. Transl.). 33:25-30.
 
Julia, M., and Stacino, J.-P. 1986. Syntheses a l'aide de sulfones. XXXVII. Synthese de trois pheromones a une double liaison Z: Z,8-DDA; Z,9-DDA; Z,9-TDA. Tetrahedron. 42:2469-2474.
 
Kovaleva, A.S., Ivanov, L.L., Tashlykova, T.M, Bulina, V.M., Bekh, A.K., Shkolina, L.A., Pyatnova, Y.B., Terekhova, A.I., and Razin, V.A. 1976. Synthesis and results of biological tests of the sex pheromone of the plum moth. Khim. Sredstva. Zashch. Rast. 7:82.
 
Leal, W.S., Bento, J.M.S., Murata, Y., Ono, M., Parra, J.R.P., and Vilela, E.F. 2001. Identification, synthesis, and field evaluation of the sex pheromone of the citrus fruit borer Ecdytolopha aurantiana. J. Chem. Ecol. 27:2041-2051.
 
Leznoff, C.C., and Fyles, T.M. 1976. Synthesis of insect sex attractants on solid phases. J. Chem. Soc. Chem. Comm. 7:251-252.
 
Mithran, S., and Mamdapur, V.R. 1986. A facile synthesis of the oriental fruit moth sex pheromone. Chem. Ind. (London). 711.
 
Mori, K., Uchida, U., and Matsui, M. 1977. Synthesis of aliphatic insect pheromones from alicyclic starting materials. (Z)-6-heneicosen-11-one and (Z)-8-dodecenyl acetate. Tetrahedron. 33:385-387.
 
Odinokov, V.N., Ishmuratov, G.U., Baleetsia, G.G., and Tolstikov, G.A. 1985. Pheromones of insects and their analogs. XIII. The synthesis of (E)-8-dodecenyl and (Z)-8-dodecenyl acetates as components of sex pheromones of Grapholitha funebrana and Grapholitha molesta. Khim. Prir. Soedin. 398-400.
 
Persoons, C.J., Ritter, F.J., Hainaut, D., and Demoute, J.P. 1976. Sex pheromone of the false codling moth Cryptophlebia (=Argyroploce) leucotreta trans-8-dodecenyl acetate, a corrected structure. Med. Fac. Landbouww. Rijksuniv. Gent. 41:937.
 
Popovici, N., Botar, A.A., Barabas, A., Oprean, I., and Hodosan, F. 1983. Exo- and endohormones. V. Syntheses of the sex pheromone of the European pine shoot moth (Rhyacionia bouliana). The Grignard route. J. Prak. Chem. 325:17.
 
Schwarz, M., and Waters, R.M. 1972. Insect sex attractants. XII. An efficient procedure for the preparation of unsaturated alcohols and acetates. Synthesis. 10:567-568.
 

 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
Ⓒ 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
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