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Synthesis of all the four stereoisomers of (1′S)-1-ethyl-2-methylpropyl 3,13-dimethylpentadecanoate, the major component of the sex pheromone of Paulownia bagworm, Clania variegata

✍ Scribed by Kenji Mori; Takuya Tashiro


Book ID
108285417
Publisher
Elsevier Science
Year
2009
Tongue
French
Weight
321 KB
Volume
50
Category
Article
ISSN
0040-4039

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Pheromone Synthesis, CLXXVI. Synthesis o
✍ Takikawa, Hirosato ;Shirai, Yasuo ;Kobayashi, Makoto ;Mori, Kenji 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 621 KB

## 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).