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
Author:
Publisher
Wiley
Subject
General Chemistry
Reference21 articles.
1. Laurence , B. R. Pickett , J. A. J. Chem. Soc., Chem. Commun. 59 1982
2. Absolute configuration of mosquito oviposition attractant pheromone, 6-acetoxy-5-hexadecanolide
3. Fuganti , C. Grasselli , P. Servi , S. J. Chem. Soc., Chem. Commun. 1285 1982
4. Synthesis of both the enantiomers of erythro-6-acetoxy-5-hexadecanolide
5. Masaki , Y. Nagata , K. Kaji , K. Chem. Lett. 1835 1983
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. A Facile Synthesis of Both Enantiomers of 6-Acetoxy-5-hexadecanolide, a Major Component of Mosquito Oviposition Attractant Pheromones;European Journal of Organic Chemistry;2009-03-05
2. Enzymes in organic synthesis. 27. Lipase-Catalyzed Synthesis of (5R,6S)-6-Acetoxyalkan-5-olides - homologues of the mosquito oviposition attractant pheromone;Journal für Praktische Chemie/Chemiker-Zeitung;1997
3. Enzymes in organic synthesis, 23. Chemo-enzymatic synthesis of (5R,6S)-6-acetoxyhexadecan-5-olide — the major component of the mosquito oviposition attractant pheromone;Liebigs Annalen;1995-05
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