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Compound - 3me7me-E2E6-1,10-diol [(E,E)-3,7-Dimethyl-2,6-decadien-1,10-diol]

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(E,E)-3,7-Dimethyl-2,6-decadien-1,10-diol Formula:  C12H22O2  CAS#:  24048-35-9  MW:  198.3  [MS]  [ NMR ]  [Behavioural function]

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Reference(s) for synthesis of (E,E)-3,7-Dimethyl-2,6-decadien-1,10-diol [3me7me-E2E6-1,10-diol] Katzenellenbogen, J.A., and Cristy, K.J. 1974. Stereoselectivity of the rearrangement of allylsiloxyvinyl ethers. A highly stereoselective synthesis of a diol found in the pheromonal secretion of the queen butterfly. J. Org. Chem. 39:3315-3318.   Masaki, Y., Sakuma, K., and Kaji, K. 1980. A new stereoselective synthesis of a terpenoid diol component of the pheromonal secretion of the queen butterfly. Chem. Lett. 1061.   Masaki, Y., Sakuma, K., and Kaji, K. 1985. Regio- and stereoselective terminal allylic carboxymethylation of gem-dimethyl olefins. Synthesis, of biologically important linear degraded terpenoids. Chem. Pharm Bull. 33:1930-1940.   Miles, D.H., Loew, P., Johnson, W.S., Kluge, A.F., and Meinwald, J. 1972. A short stereoselective synthesis of some terpenes from the pheromonal secretion of the queen and Monarch butterflies. Tetrahedron Lett. 30:3019-3022.   Nystroem, J.-E., and Baeckvall, J.-E. 1983. Synthesis of the major pheromonal component of the Monarch butterfly (Danaus plexippus) via palladium-catalyzed 1,4-functionalization of isoprene. J. Org. Chem. 48:3947-3950.   Odinokov, B.N., Kukovinets, O.S., Sakharova, N.I., and Tolstikov, G.A. 1989. J. Org. Chem. USSR (Engl. Transl.). 25:25-28.   Zakharkin, L.I., and Petrushkina, E.A. 1984. Stereospecific synthesis of (E)-3,7-dimethyl-2-octene-1,8-diol from a telomer of isoprene with diethylamine. Zh. Org. Khim. 20:2073.