Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
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A Chiral Synthesis of a Mosquito Oviposition Pheromone

  • Kang, Suk-Ku (Department of Chemistry, Sung Kyun Kwan University Natural Science Campus) ;
  • Shin, Dong-Soo (Department of Chemistry, Sung Kyun Kwan University Natural Science Campus)
  • Published : 1986.08.20
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Abstract

(+)-(5S,6R)-Erythro-6-acetoxy-5-hexadecanolide, an optically active form of them ajor component of an oviposition attractant pheromone of a mosquito Culex pipiens fatigans, was synthesized enantiospecifically from (-)-2-deoxy-D-ribose.

Keywords

References

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Cited by

  1. ChemInform Abstract: A Chiral Synthesis of a Mosquito Oviposition Pheromone. vol.18, pp.16, 1987, https://doi.org/10.1002/chin.198716373
  2. Enantiomerically Pure Insect Pheromones: The Carbohydrate Synthetic Approach vol.10, pp.2, 1986, https://doi.org/10.1080/07328309108543898
  3. A Concise Synthesis of the Natural Mosquito Oviposition Attractant Pheromone from D-Glucose vol.10, pp.2, 1991, https://doi.org/10.1080/07328309108543907
  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 vol.10, pp.5, 1986, https://doi.org/10.1002/cjoc.19920100512
  5. Syntheses of 5-Hexadecanolide, 6-Acetoxy-5-hexadecanolide and Tanikolide vol.48, pp.4, 2001, https://doi.org/10.1002/jccs.200100112
  6. A Concise Li/liq. NH3 Mediated Synthesis of (4E,10Z)-Tetradeca-4,10-dienyl Acetate: The Major Sex Pheromone of Apple Leafminer Moth, Phyllonorycter ringoniella vol.35, pp.1, 1986, https://doi.org/10.5012/bkcs.2014.35.1.261