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« Previous CompoundE,E-2me8me-1,7-dioxaspiroundecane    Next Compound »E,E-alpha-farnesene
Compound - E,E-2Sme6R8Sme-1,7-dioxaspiroundecane


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Formula: C11H20O2 
MW: 184.28 

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

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Reference(s) for synthesis of (2S,6R,8S)-(E,E)-2,8-dimethyl-1,7-dioxaspiro[5.5]undecane

Enders, D., Dahmen, W., Dederichs, E., Gatzweiler, W., and Weuster, P. 1990. Synthesis of spiroacetal pheromones via metalated hydrazones. Synthesis. 11:1013-1019.
Giese, B., Bartmann, D., and Hasskerl, T. 1987. Synthesis of pheromones with acetal structures via C-C bond formation. Liebigs Ann. Chem. 427-430.
Kitching, W., Lewis, J.A., Perkins, M.V., Drew, R., Moore, C.J., Schurig, V., Koenig, W.A., and Francke, W. 1989. Chemistry of fruit flies. Composition of the rectal gland secretion of (male) Dacus cucumis (cucumber fly) and Dacus halfordiae. Characterization of (Z,Z)-2,8-dimethyl-1,7-dioxaspiro[5.5]undecane. J. Org. Chem. 54:3893-3902.
Pothier, N., Goldstein, S., and Deslongchamps, P. 1992. Cyclization of hydroxyenol ethers into spiroacetals. Evidence for the position of the transition state and its implication on the stereoelectronic effects in acetal formation. Helv. Chim. Acta. 75:604-620.

Citation: El-Sayed AM 2014. The Pherobase: Database of Insect Pheromones and Semiochemicals. <>.
2003-2014 The Pherobase - Extensive Database of Insect Pheromones and Semiochemicals. Ashraf M. El-Sayed.
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