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


Bedoukain

 
Discuss this Compound    Help


(2S,6R,8S)-(E,E)-2,8-dimethyl-1,7-dioxaspiro[5.5]undecane
(2S,6R,8S)-(E,E)-2,8-dimethyl-1,7-dioxaspiro[5.5]undecane

Formula: C11H20O2 
CAS#:  
MW: 184.28 

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





Dots surface:


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. <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