A new stereoselective synthesis of racemic disparlure, the sex pheromone of gypsy moth (porthetria dispar L.)

This publication has 6 references indexed in Scilit:

• The synthesis of alkenes from carbonyl compounds and carbanions α to silicon V. Stereoselective synthesis of E- and Z-disubstituted alkenes.
  Tetrahedron Letters, 1976
• Stereoselective synthesis of optically active disparlure, the pheromone of the gypsy moth (Porthetriadispar L.)
  Tetrahedron Letters, 1976
• Pheromone, X. Eine stereoselektive Synthese des (Z)‐7,8‐Epoxy‐2‐methyloctadecans (Disparlure)
  European Journal of Inorganic Chemistry, 1976
• Neue Totalsynthese des Sexuallockstoffes von Porthetria dispar (7,8‐cis‐Epoxy‐2‐methyloctadecan)
  Angewandte Chemie, 1972
• Coupling of Grignard Reagents with Organic Halides
  Synthesis, 1971
• Potent Sex Attractant of the Gypsy Moth: Its Isolation, Identification, and Synthesis
  Science, 1970