SYNTHESIS OF BOTH ENANTIOMERS OF ERYTHRO-6-ACETOXY-5-HEXADECANOLIDE, THE MAJOR COMPONENT OF A MOSQUITO OVIPOSITION ATTRACTANT PHEROMONE
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Reference10 articles.
1. Synthesis of both the enantiomers of erythro-6-acetoxy-5-hexadecanolide
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3. Synthesis of Sesquiterpene Anti-Tumor Lactones. IV1. A Stereoselective Synthesis oftrans-2,3-Epoxycyclohexanol
4. Stereospecific umpolung .alpha.' substitution of ketones via reactions of organocuprates with enol ethers of .alpha.,.beta.-epoxycyclohexanones
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