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Compound - 4-hydroxy-1,7-dioxaspiroundecane


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Formula: C9H16O3 
MW: 172.22 

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

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Reference(s) for synthesis of 4-Hydroxy-1,7-dioxaspiro[5.5]undecane

Brinker, U.H., Haghani, A., and Gomann, K. 1985. Spiroacetal formation by carbene (carbenoid) insertion reaction: synthesis of the major constituent of the sex attractant of the olive fly (Dacus oleae). Z. Angew. Chem. Int. Ed. Engl. 24:230.
Kay, I.T., and Williams, E.X. 1983. Spiroketals: the synthesis of an olive fly pheromone component, 4-hydroxy-1,7dioxaspiro[5.5]undecane, via a novel cation-olefin cyclisation step. Tetrahedron Lett. 24:5915-5918.
Kocienski, P., and Yeates, C. 1983. A new synthesis of 1,7-dioxaspiro[5.5]undecanes. Application to a rectal gland secretion of the olive fruit fly (Dacus oleae). Tetrahedron Lett. 24:3905-3906.
Ley, S.V., Lygo, B., and Wonnacott, A. 1985. Preparation and reactions of 2-benzenesulphonyltetrahydropyran. Tetrahedron Lett. 26:535-538.
Ley, S.V., Lygo, B., Sternfeld, F., and Wonnacott, A. 1986. Alkylation reactions of anions derived from 2-benzene-sulphonyl tetrahydropyran and their application to spiroketal synthesis. Tetrahedron. 42:4333-4342.
Mori, K., Uematsu, T., Watanabe, H., Yanagi, K., and Minobe, M. 1984. Synthesis of the enantiomers of 1,7dioxaspiro[5.5]undecane and 4-hydroxy-1,7-dioxaspiro[5.5]undecane, the components of the olive fly pheromone. Tetrahedron Lett. 25:3875-3878.
Mori, K., Watanabe, H., Yanagi, K., and Minobe, M. 1985. Synthesis of the enantiomers of 1,7-dioxaspiro[5.5]undecane, 4-hydroxy-1,7-dioxaspiro[5.5]undecane and 3-hydroxy-1,7-dioxaspiro[5.5]undecane, the components of the olive fruit fly pheromone. Tetrahedron. 41:3663-3672.

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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