Stereoselective synthesis of the major component of a mosquito oviposition attractant pheromone from a β-lithiopropionate equivalent
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference22 articles.
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1. Bidirectional Synthesis of 6-Acetoxy-5-hexadecanolide, the Mosquito Oviposition Pheromone of Culex quinquefasciatus, from a C2-Symmetric Building Block Using Olefin Metathesis Reactions;The Journal of Organic Chemistry;2018-01-12
2. Diastereodivergent total synthesis of mosquito oviposition pheromone;RSC Adv.;2014
3. Facile total synthesis of (−)-(5R,6S)-6-acetoxy-5-hexadecanolide from carbohydrate, a mosquito oviposition attractant pheromone;Carbohydrate Research;2012-09
4. 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;Chinese Journal of Chemistry;2010-08-27
5. 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
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