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Insect phermones and their analogues XXXIX. Synthesis of 11RS-hydroxy- and 12-hydroxydodec-3Z-enoic acids — Acyclic precursors of the macrolide components of the pheromones of Cryptolestes ferrugineus and C. pusillus
- Source :
- Chemistry of Natural Compounds. 28:365-369
- Publication Year :
- 1992
- Publisher :
- Springer Science and Business Media LLC, 1992.
-
Abstract
- A new approach to the synthesis of 11RS-hydroxy- and 12-hydroxydodec-3Z-enoic acids has been developed with the use, in one of the key stages, of the partial ozonolysis of the acetates of the corresponding methylene-separated enynic alcohols.
Details
- ISSN :
- 15738388 and 00093130
- Volume :
- 28
- Database :
- OpenAIRE
- Journal :
- Chemistry of Natural Compounds
- Accession number :
- edsair.doi...........75fa8754a900b18608c1124089e6ae2c