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Compound - 1S2R4S5R-alpha-multistriatin

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(1S,2R,4S,5R)-5-Ethyl-2,4-dimethyl-6,8-dioxabicyclo[3.2.1]octane Formula:  C10H18O2  CAS#:    MW:  170.25  [MS]  [Behavioural function]  [Chemdraw]

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Reference(s) for synthesis of (1S,2R,4S,5R)-5-Ethyl-2,4-dimethyl-6,8-dioxabicyclo[3.2.1]octane Cernigliaro, G.J., and Kocienski, P.J. 1977. A synthesis of (-)-alpha-multistriatin. J. Org. Chem. 42:3622-3624.   Fitzsimmons, B.J., Plaumann, D.E., and Fraser-Reid, B. 1979. Chiral synthons for the multistriatins. Tetrahedron Lett. 20:3925-3928.   Gore, W.E., Pearce, G.T., and Silverstein, R.M. 1975. Relative stereochemistry of multistriatin (2,4-dimethyl-5-ethyl-6,8-dioxabicyclo[3.2.1]octane). J. Org. Chem. 40:1705-1708.   LaGrange, A., Olesker, A., Costa, S.S., and Lukacs, G. 1982. A route from D-galactose to the aggregation pheromone component (-)-alpha-multistriatin. Carbohydrate Res. 110:159-164.   Larcheveque, M., and Henrot, S. 1987. A stereospecific synthesis of optically pure (-)-alpha-multistriatin. Tetrahedron. 43:2303-2310.   Mori, K. 1976. Pheromone synthesis. Synthesis, of (1S,2R,4S,5R)-(-)-alpha-multistriatin the pheromone in the smaller European elm bark beetle Scolytus multistriatus. Tetrahedron. 32:1979-1981.   Sum, P.-E., and Weiler, L. 1978. Stereospecific synthesis of (-)-alpha-multistriatin from D-glucose. Can. J. Chem. 56:2700.