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Stereoselective synthesis of (5R,6S)-6-acetoxy hexadecanolide——The major component of the oviposition attractant pheromone of the mosquito Culex pipens fatigans and its enantiomer from L-glutamic acid 被引量:1
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作者 DING, Yu LI, Jia-Yao WANG, Zhi-Qin Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032 《Chinese Journal of Chemistry》 SCIE CAS CSCD 1992年第5期451-457,共0页
A concise synthesis of the mosquito oviposition attractant pheromone, (-)-(5R, 6S)- and (+)-(5S 6R)-6-acetoxy hexadecanolide from L-glutamic acid is described. The key steps are the inversion of the configuration at C... A concise synthesis of the mosquito oviposition attractant pheromone, (-)-(5R, 6S)- and (+)-(5S 6R)-6-acetoxy hexadecanolide from L-glutamic acid is described. The key steps are the inversion of the configuration at C-4 of 7, and the formation of δ-lactone from the γ-lactone through ring enlargement. 展开更多
关键词 Stereoselective synthesis of acetoxy hexadecanolide The major component of the oviposition attractant pheromone of the mosquito Culex pipens fatigans and its enantiomer from L-glutamic acid acid
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