Synthese von Disparlure durch Kolbe‐Elektrolyse
- 19 January 1978
- journal article
- Published by Wiley in Angewandte Chemie
- Vol. 90 (1), 48-49
- https://doi.org/10.1002/ange.19780900108
Abstract
Disparlure (1), der Sexuallockstoff des Waldschädlings Lymantria dispar, konnte jetzt durch doppelte Kolbe‐Elektrolyse in konfigurativ reiner Form gewonnen werden. „Verunreinigung”︁ durch geometrische Isomere setzt die Lockwirkung synthetischer Pheromone stark herab. magnified imageThis publication has 8 references indexed in Scilit:
- Synthese von ( Z )‐7‐Dodecenylacetat (Looplure) durch Kolbe‐ElektrolyseEuropean Journal of Inorganic Chemistry, 1977
- Pheromone, X. Eine stereoselektive Synthese des (Z)‐7,8‐Epoxy‐2‐methyloctadecans (Disparlure)European Journal of Inorganic Chemistry, 1976
- Isolation, Identification, and Synthesis of the Gypsy Moth Sex Attractant1Journal of Economic Entomology, 1972
- Novel Total Synthesis of the Sex Attractant ofPorthetria dispar (7,8-cis-Epoxy-2-methyloctadecane)Angewandte Chemie International Edition in English, 1972
- Neue Totalsynthese des Sexuallockstoffes von Porthetria dispar (7,8-cis-Epoxy-2-methyloctadecan)Angewandte Chemie, 1972
- Potent Sex Attractant of the Gypsy Moth: Its Isolation, Identification, and SynthesisScience, 1970
- Sex Pheromone of the Pink Bollworm Moth: Biological Masking by Its Geometrical IsomerScience, 1969
- Sex Pheromone PerceptionNature, 1968