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Stereoselective synthesis of the both enantiomers of disparlure, the pheromone of the gypsy moth

✍ Scribed by K. Mori; T. Takigawa; M. Matsui

Book ID
107857020
Publisher
Elsevier Science
Year
1979
Tongue
French
Weight
529 KB
Volume
35
Category
Article
ISSN
0040-4020

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A stereospecific synthesis of (+)-dispar
A stereospecific synthesis of (+)-disparlure, sex attractant of the gypsy moth
✍ Donald G. Farnum; Tarik Veysoglu; Anja M. CardΓ©; Barbara Duhl-Emswiler; Taylor A πŸ“‚ Article πŸ“… 1977 πŸ› Elsevier Science 🌐 French βš– 204 KB

Disparlure, cis-7,8-epoxy-2-methyloctadecane, was identified as the female-produced sex pheromone of the gypsy moth, Lymantria &spur L., by Bierl, Beroza and Collier.' The 7R,BS enantiomer of disparlure was synthesized by Marumo' and Mori 3 and found to be more attractive to males than the racemate.