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Compound - E2-8OH


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Formula: C8H16O 
CAS#: 18409-17-1 
MW: 128.21 

[MS]  [ NMR ]  [ Kovats ]  [Behavioural function]  [Occurrence in plant]  [Chemdraw

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Reference(s) for synthesis of (E)-2-Octen-1-ol

Bonini, C., Federici, C., Rossi, L., and Righi, G. 1995. C-1 Reactivity of 2,3-epoxy alcohols via oxirane opening with metal halides: applications and synthesis of naturally occurring 2,3-octanediol, muricatacin, 3-octanol, and 4-dodecanolide. J. Org. Chem. 60:4803-4812.
Capon, R.J., and Barrow, R.A. 1998. Acid-mediated conversion of methylene-interrupted bisepoxides to tetrahydrofurans: a biomimetic transformation. J. Org. Chem. 63:75-83.
Gelin, R., and Albrand, M. 1976. C. R. Hebd. Seances Acad. Sci. Ser. C. 283:755-757.
Hamada, T., Zenkoh, T., Sato, H., and Yonemitsu, O. 1991. A chiral synthesis of (-)-cannabisativine: an application of the highly diastereo-selective hetero diels-alder reaction. Tetrahedron Lett. 32:1649-1652.
Ikeno, T., Kimura, T., Ohtsuka, Y., and Yamada, T. 1999. Selective 1,4-reduction of alpha,-unsaturated carbonyl compounds by combined use of bis(1,3-diketonato)cobalt(II) complex and diisobutylaluminum hydride. Syn. Lett. 1:96-98.
Matveeva, E.D., Erin, A.S., Mitroshin, D.B., and Kurts, A.L. 1995. Russ. J. Org. Chem. 31:1019-1022.
Mordini, A., Pecchi, S., Capozzi, G., Capperucci, A., and Degl'Innocenti, A. 1994. Heteroatom-assisted isomerization of oxiranes to allylic alcohols promoted by bases. J. Org. Chem. 59:4784-4790.
Morisaki, N., Funabashi, H., Furukawa, J., Shimazawa, R., Kanematsu, A. 1992. Chem. Pharm. Bull. 40:2945-2953.

Citation: El-Sayed AM 2018. The Pherobase: Database of Pheromones and Semiochemicals. <>.
2003-2018 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
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