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Enantiospecific synthesis of (3S,6R)-3-hydroxy-1,7-dioxaspiro[5.5]undecane and its (4R)-4-hydroxy isomer [minor components of olive fruit fly (Dacus oleae) sex pheromone]

✍ Scribed by Isidoro Izquierdo Cubero; Maria T. Plaza López-Espinosa; Rafael Acuña Castillo


Publisher
Springer
Year
1992
Tongue
English
Weight
482 KB
Volume
18
Category
Article
ISSN
0098-0331

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📜 SIMILAR VOLUMES


Application of the double intramolecular
✍ Junliang Hao; Craig J Forsyth 📂 Article 📅 2002 🏛 Elsevier Science 🌐 French ⚖ 53 KB

Application of a novel double intramolecular hetero-Michael addition (DIHMA) strategy to spiroketal synthesis was illustrated by a concise synthesis of (±)-(4S\*,6S\*)-4-hydroxy-1,7-dioxaspiro[5.5]undecane, a Dacus oleae olive fly pheromone.