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Pheromone Synthesis, CLXXVI. Synthesis of the Four Stereoisomers of 3,13-Dimethylheptadecane, the Major Sex Pheromone Component of the Western False Hemlock Looper

✍ Scribed by Takikawa, Hirosato ;Shirai, Yasuo ;Kobayashi, Makoto ;Mori, Kenji

Publisher
John Wiley and Sons
Year
1996
Tongue
English
Weight
621 KB
Volume
1996
Category
Article
ISSN
0947-3440

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✦ Synopsis

Abstract

All of the four stereoisomers of 3,13‐dimethylheptadecane (1), the female‐produced sex pheromone of the western false hemlock looper (Nepytia freemani), were synthesized by starting from the enatiomers of citronellol (2a) and 2‐methyl‐1‐butanol (4a).

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