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« Previous Compound3me7me-E2,7-8-propionate    Next Compound »3me7me-E2-octen-1,8-diol
 
Compound - 3me7me-E2E6-1,10-diol
 


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(E,E)-3,7-Dimethyl-2,6-decadien-1,10-diol
(E,E)-3,7-Dimethyl-2,6-decadien-1,10-diol

Formula: C12H22O2 
CAS#: 24048-35-9 
MW: 198.3 

[MS]  [ NMR ]  [Behavioural function]  [Chemdraw





Dots surface:


Reference(s) for synthesis of (E,E)-3,7-Dimethyl-2,6-decadien-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.
 

 
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.
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