Bedoukian   RussellIPM   Laser Vibrometer

Animal Taxa
Plant Taxa
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa


Invasive spp.
Email to a Friend
Kindly Donate for The Pherobase
« Previous Compound7Rme-27Hy    Next Compound »7Sme11Rme-17Hy
Compound - 7S8R-disparlure


Discuss this Compound    Help


Formula: C19H38O 
CAS#: 42991-03-7 
MW: 282.51 

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

Dots surface:

Reference(s) for synthesis of (7S,8R)-cis-7,8-Epoxy-2-methyloctadecane

Brown, H.C., and Basavaiah, D. 1983. Pheromone synthesis via organoboranes: a convenient stereospecific synthesis of racemic disparlure, the sex pheromone of the gypsy moth (Porthetria dispar L.). Synthesis. 4:283-284.
Bykov, V.I., Goletiani, A.R., Butenko, T.A., and Finkelshtein, E.Sh. 2002. Stereoselective cometathesis of 1,5-cyclooctadiene with ethylene as an efficient pathway to Z-ene biologically active natural products. Dokl. Chem. (Engl. Transl.). 384:163-166.
Chan, T.H., and Koumaglo, K. 1985. Silicon in organic synthesis. Stereoselective synthesis of some insect sex pheromones. J. Organomet. Chem. 285:109-120.
Friesen, R.W., and Giroux, A. 1994. Can. J. Chem. 72:1857-1865.
Jonas, J., Slanina, P., Humpa, O., and Mazal, C. 1988. Collect. Czech. Chem. Comm. 53:857-859.
Kel'in, A.V., and Kulinkovich, O.G. 1998. New synthesis of ()-cis-disparlure, pheromone of female gypsy moth (Porthetria dispar) species. Russ. J. Org. Chem. 34:1446-1448.
Koumaglo, K., and Chan, T.H. 1984. Regioselection in the alkylation of trimethylsilylallyl anion - stereoselective synthesis of disubstituted alkenes. Tetrahedron Lett. 25:717-720.
Koumbis, A.E., and Chronopoulos, D.D. 2005. A short and efficient synthesis of (+)-disparlure and its enantiomer. Tetrahedron Lett. 46:4353-4355.
Marshall, J.A., Jablonowski, J.A., and Jiang, H. 1999. Total synthesis of the gypsy moth pheromones (+)- and (-)-disparlure from a single nonracemic alpha-silyloxy allylic stannane. J. Org. Chem. 64:2152-2154.
Prestwich, G.D., Mc Graham, S., Kuo, J.-W., and Vogt, R.G. 1989. Tritium-labeled enantiomers of disparlure. Synthesis and in vitro metabolism. J. Am. Chem. Soc. 111:636-642.
Sonnet, P.E. 1980. Olefin inversion. 3. Preparations and reductions of vic-halohydrin trifluoroacetates. J. Org. Chem. 45:154-157.
Vig, O.P., Sharma, M.L., Kumari, S., and Vohra, N. 1985. A new synthesis of (Z)-7,8-epoxy-2-methyloctadecane (disparlure). Indian J. Chem. Sect. B. 24:860-861.
Wang, K.K., and Chu, K.-H. 1984. Preparation of (Z)-alkenes, ketones and alkynes via trialkyltin chloride induced intramolecular transfer reaction of lithium 1-alkynyltrialkylborates. Stereoselective synthesis of the sex pheromones of the Douglas fir tussock moth, the gypsy moth, and the wild silkmoth Antheraea polyphemus. J. Org. Chem. 49:5175-5178.

Citation: El-Sayed AM 2018. The Pherobase: Database of Pheromones and Semiochemicals. <>.
2003-2018 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 5-January-2018