Bedoukian     Laser Vibrometer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa

Synthesis

Control
Invasive spp.
References
Abstract
Guide
Print
Email to a Friend
Kindly Donate for The Pherobase
« Previous CompoundE4Z9-14Ald    Next Compound »E5-10OH
 
Compound - E5-10Ac
 


Bedoukain

 
Discuss this Compound    Help


(E)-5-Decenyl acetate
(E)-5-Decenyl acetate

Formula: C12H22O2 
CAS#: 38421-90-8 
MW: 198.3 

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





Dots surface:


Reference(s) for synthesis of (E)-5-Decenyl acetate



Botar, A.A., Oprean, B.I., Csonka-Horvai, J., and Hodosan, F. 1983. Exo- and endohormones. Vl. Syntheses of the sex pheromones of some Lepidoptera. Rev. Roum. Chim. 28:741.
 
Buss, A.D., Greeves, N., Levin, D., Wallace, P., and Warren, S. 1984. Synthesis of single isomers (E or Z) of unsaturated alcohols by the Horner-Wittig reaction. Tetrahedron Lett. 25:357-360.
 
Chattopadhyay, A., Mamdapur, V.R., and Chadha, M.S. 1983. A convenient synthesis of (E)-9-tetradecen-1-yl acetate, a sex pheromone of gelechiid moth & (E)-5-decenol, a sex pheromone of peach twig borer. Ind. J. Chem. 22B:12211223.
 
Chauret, D.C., and Chong, J.M. 1993. Reactions of alpha-epoxysilanes with organocopper reagents. A stereoselective route to alkenes. Tetrahedron Lett. 34:3695-3698.
 
Odinokov, V.N., Baletsia, G.G., Ishmuratov, G.U., Vaxitov, R.S., and Tolstikov, C.A. 1985. Pheromones of insects and their analogs. XII. Synthesis, of isomers of 5-decenylacetate, pheromone of Anarsia lineatella and Agrotis segetum. Khim. Prir. Soedin. 395-398.
 
Vig, O.P., Sharma, M.L., Gakhar, M., and Malik, N. 1980. Synthesis of (E)-5-decen-1-ol, a sex pheromone isolated from peach twig borer moth, Anarsia lineatella. Ind. J. Chem. B. 19:755.
 
Wakamura, J. 1980. Sex attractant pheromone of the common cutworm moth Agrotis fucosa Butler: field evaluation. Appl. Entomol. Zool. 15:167.
 
Wenkert, E., Ferreira, V.F., Michelotti, E.L., and Tingoli, M. 1985. Synthesis of acyclic, cis olefinic pheromones by way of Nickel-catalyzed Grignard reactions. J. Org. Chem. 50:719-721.
 
Yu, H., Zang, B., and Han, X. 1983. Scientific notes on the synthesis of sex pheromone of Euxoa segetum (Schiffermuller) and activity test in the field. K'un Ch'ung Chih. Shih. 20:105.
 
Zakharkin, L.I., and Petrushkina, E.A. 1985. Stereoselective synthesis of E-5-decen-1-ol from E-1,6-undecadiene. Izv. Akad. Nauk. SSSR. Ser. Khim. 205.
 

 
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