¦ « Previous Compoundserricornin    Next Compound »seudenone ¦

Compound - seudenol

¦ Discuss this Compound    Help ¦

3-Methyl-2-cyclohexen-1-ol Formula:  C7H12O  CAS#:  21378-21-2  MW:  112.17  [MS]  [ NMR ]  [ Kovats ]  [Behavioural function]  [Chemdraw]

Dots surface:

Reference(s) for synthesis of 3-Methyl-2-cyclohexen-1-ol Barnier, J.-P., Morisson, V., Volle, I., and Blanco, L. 1999. Chemo-enzymatic preparation of optically active endo-bicyclo[4.1.0]heptan-2-ols. Tetrahedron: Asymmetry. 10:1107-1117.   De Bruyn, M., De Vos, D.E., and Jacobs, P.A. 2002. Chemoselective hydrogen transfer reduction of unsaturated ketones to allylic alcohols with solid Zr and Hf catalysts. Adv. Synth. Catal. 344:1120-1125.   Mori, K., Hazra, B.G., Pfeiffer, R.J., Gupta, A.K., and Lindgren, B.S. 1987. Synthesis and bioactivity of optically active forms of 1-methyl-2-cyclohexen-1-ol, an aggregation pheromone of Dendroctonus pseudotsugae. Tetrahedron. 43:2249-2254.   Mori, K., Tamada, S, Uchida, M., Mizumachi, N., Tachibana, Y., and Matsui, M. 1978. Synthesis of optically active forms of seudenol, the pheromone of Douglas fir beetle. Tetrahedron. 34:1901-1905.   Plummer, E.L., Stewart, T.E., Byrne, K., Pearce, G.T., and Silverstein, R.M. 1976. Determination of the enantiomeric composition of several insect pheromone alcohols. J. Chem. Ecol. 2:307.   Sreekumar, R., Padmakumar, R., and Rugmini, P. 1998. Regioselective reduction of epoxides and conjugated carbonyl compounds using zeolite supported zinc borohydride. Tetrahedron Lett. 39:5151-5154.   Wenkert, E., Michelotti, E.L., Swindell, C.S., and Tingoli, M. 1984. Transformation of carbon-oxygen in carbon-carbon bonds mediated by low-valent nickel species. J. Org. Chem. 49:4894-4899.