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Synthesis from D-xylose of the salt marsh caterpillar moth pheromone (3Z,6Z,9S,10R)-epoxyheneicosadiene and its (3Z,6E)-stereoisomer.

✍ Scribed by J.R. Pougny; P. Rollin

Publisher: Elsevier Science
Year: 1987
Tongue: French
Weight: 132 KB
Volume: 28
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(00)96260-9

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Synthesis of optically active pheromones with an epoxy ring, (+)-disparlure and the saltmarsh caterpillar moth pheromone [(Z,Z)-3,6-cis-1-9,10-epoxyheneicosadiene]

✍ Kenji Mori; Takashi Ebata 📂 Article 📅 1981 🏛 Elsevier Science 🌐 French ⚖ 145 KB

+)-Disparlure \_2\_ and the saltmarsh caterpillar moth pheromone enantiomers l-were synthesized and the stereochemistry of the naturally occurring Lwas shown to be 92, 105.