𝔖 Bobbio Scriptorium
✦   LIBER   ✦

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

✍ Scribed by G.A. Tolstikov; V.N. Odinokov; R.I. Galeeva; R.S. Bakeeva


Publisher
Elsevier Science
Year
1978
Tongue
French
Weight
111 KB
Volume
19
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


A stereospecific synthesis of (+)-dispar
✍ 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.

A convenient stereoselective synthesis o
✍ Shigefumi Kuwahara; Daisuke Itoh; Walter S. Leal; Osamu Kodama πŸ“‚ Article πŸ“… 1998 πŸ› Elsevier Science 🌐 French βš– 132 KB

rs,3'S,4'R,2Z)-(-)-2-(Y,4'-Epoxy-4'-methylcyelohexyl)-6-methyl-2,5-heptadiene, a sex pheromone component of the southern green stink bug (Nezara viridula (L.)), was synthesized stereoselectively in four steps and 18% overall yield from (S)-4-methyl-3-cyclohexene-l-carboxylie acid.