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A stereospecific synthesis of (+)-disparlure, sex attractant of the gypsy moth

✍ Scribed by Donald G. Farnum; Tarik Veysoglu; Anja M. Cardé; Barbara Duhl-Emswiler; Taylor A. Pancoast; Thomas J. Reitz; Ring T. Cardé

Publisher: Elsevier Science
Year: 1977
Tongue: French
Weight: 204 KB
Volume: 18
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(01)83412-2

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✦ Synopsis

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. 4 The elegant assignment of the absolute stereochemistry of all of the

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