Synthesis of all four isomers of disparlure using osmium-catalyzed asymmetric dihydroxylation.

This publication has 15 references indexed in Scilit:

• Total synthesis of (+)-disparlure
  Tetrahedron Letters, 1987
• Diastereoselective α-alkylation of β-hydroxy sulfoxides and its application to the synthesis of (+)- and (3)-disparlure
  Tetrahedron Letters, 1987
• Synthesis of chiral 1,2-diols and related compounds of biological activities via stepwise ring fission of 5-alkyl-6,8-dioxabicyclo[3.2.1]octane skeleton
  Tetrahedron Letters, 1986
• An enantiospecific synthesis of (+)-disparlure from carbohydrate precursors
  Carbohydrate Research, 1986
• Studies on the identification and syntheses of insect pheromones: XX. Synthesis of (7R, 8S)-(+)-sex pheromone of gypsy moth through the kinetic resolution of (±) allylic alcohol by Sharpless asymmetric epoxidation
  Acta Chimica Sinica, 1985
• Synthesis of optically active pheromones with an epoxy ring, (+)-disparlure and the saltmarsh caterpillar moth pheromone [(Z,Z)-3,6-cis-1-9,10-epoxyheneicosadiene]
  Tetrahedron Letters, 1981
• Asymmetric epoxidation provides shortest routes to four chiral epoxy alcohols which are key intermediates in syntheses of methymycin, erythromycin, leukotriene C-1, and disparlure
  Journal of the American Chemical Society, 1981
• Synthesis and activity of optically active disparlure
  Journal of the American Chemical Society, 1974
• Potent Sex Attractant of the Gypsy Moth: Its Isolation, Identification, and Synthesis
  Science, 1970
• .alpha.-Methoxy-.alpha.-trifluoromethylphenylacetic acid, a versatile reagent for the determination of enantiomeric composition of alcohols and amines
  The Journal of Organic Chemistry, 1969