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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
(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





Dots surface:


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.
 

 
Citation: El-Sayed AM 2014. The Pherobase: Database of Insect Pheromones and Semiochemicals. <http://www.pherobase.com>.
2003-2014 The Pherobase - Extensive Database of Insect Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 23-February-2014