Pheromone synthesis. Part 244: Synthesis of the racemate and enantiomers of (11Z,19Z)-CH503 (3-acetoxy-11,19-octacosadien-1-ol), a new sex pheromone of male Drosophila melanogaster to show its (S)-isomer and racemate as bioactive

10.1016/j.tet.2010.06.080

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Main Authors: Mori, K., Shikichi, Y., Shankar, S., Yew, J.Y.
Other Authors: BIOLOGICAL SCIENCES
Format: Article
Published: 2014
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Online Access:http://scholarbank.nus.edu.sg/handle/10635/101373
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spelling sg-nus-scholar.10635-1013732023-10-25T20:10:50Z Pheromone synthesis. Part 244: Synthesis of the racemate and enantiomers of (11Z,19Z)-CH503 (3-acetoxy-11,19-octacosadien-1-ol), a new sex pheromone of male Drosophila melanogaster to show its (S)-isomer and racemate as bioactive Mori, K. Shikichi, Y. Shankar, S. Yew, J.Y. BIOLOGICAL SCIENCES (11Z,19Z)-3-Acetoxy-11,19-octacosadien-1-ol, (R)-, (S)-, and (±)- 3,4-Epoxy-1-butanol PMB ether, (R)-, and (S)- Drosophila melanogaster Jacobsen's hydrolytic kinetic resolution (HKR) of epoxide Pheromone 10.1016/j.tet.2010.06.080 Tetrahedron 66 35 7161-7168 TETRA 2014-10-27T08:36:31Z 2014-10-27T08:36:31Z 2010-08-28 Article Mori, K., Shikichi, Y., Shankar, S., Yew, J.Y. (2010-08-28). Pheromone synthesis. Part 244: Synthesis of the racemate and enantiomers of (11Z,19Z)-CH503 (3-acetoxy-11,19-octacosadien-1-ol), a new sex pheromone of male Drosophila melanogaster to show its (S)-isomer and racemate as bioactive. Tetrahedron 66 (35) : 7161-7168. ScholarBank@NUS Repository. https://doi.org/10.1016/j.tet.2010.06.080 00404020 http://scholarbank.nus.edu.sg/handle/10635/101373 000281298900015 Scopus
institution National University of Singapore
building NUS Library
continent Asia
country Singapore
Singapore
content_provider NUS Library
collection ScholarBank@NUS
topic (11Z,19Z)-3-Acetoxy-11,19-octacosadien-1-ol, (R)-, (S)-, and (±)-
3,4-Epoxy-1-butanol PMB ether, (R)-, and (S)-
Drosophila melanogaster
Jacobsen's hydrolytic kinetic resolution (HKR) of epoxide
Pheromone
spellingShingle (11Z,19Z)-3-Acetoxy-11,19-octacosadien-1-ol, (R)-, (S)-, and (±)-
3,4-Epoxy-1-butanol PMB ether, (R)-, and (S)-
Drosophila melanogaster
Jacobsen's hydrolytic kinetic resolution (HKR) of epoxide
Pheromone
Mori, K.
Shikichi, Y.
Shankar, S.
Yew, J.Y.
Pheromone synthesis. Part 244: Synthesis of the racemate and enantiomers of (11Z,19Z)-CH503 (3-acetoxy-11,19-octacosadien-1-ol), a new sex pheromone of male Drosophila melanogaster to show its (S)-isomer and racemate as bioactive
description 10.1016/j.tet.2010.06.080
author2 BIOLOGICAL SCIENCES
author_facet BIOLOGICAL SCIENCES
Mori, K.
Shikichi, Y.
Shankar, S.
Yew, J.Y.
format Article
author Mori, K.
Shikichi, Y.
Shankar, S.
Yew, J.Y.
author_sort Mori, K.
title Pheromone synthesis. Part 244: Synthesis of the racemate and enantiomers of (11Z,19Z)-CH503 (3-acetoxy-11,19-octacosadien-1-ol), a new sex pheromone of male Drosophila melanogaster to show its (S)-isomer and racemate as bioactive
title_short Pheromone synthesis. Part 244: Synthesis of the racemate and enantiomers of (11Z,19Z)-CH503 (3-acetoxy-11,19-octacosadien-1-ol), a new sex pheromone of male Drosophila melanogaster to show its (S)-isomer and racemate as bioactive
title_full Pheromone synthesis. Part 244: Synthesis of the racemate and enantiomers of (11Z,19Z)-CH503 (3-acetoxy-11,19-octacosadien-1-ol), a new sex pheromone of male Drosophila melanogaster to show its (S)-isomer and racemate as bioactive
title_fullStr Pheromone synthesis. Part 244: Synthesis of the racemate and enantiomers of (11Z,19Z)-CH503 (3-acetoxy-11,19-octacosadien-1-ol), a new sex pheromone of male Drosophila melanogaster to show its (S)-isomer and racemate as bioactive
title_full_unstemmed Pheromone synthesis. Part 244: Synthesis of the racemate and enantiomers of (11Z,19Z)-CH503 (3-acetoxy-11,19-octacosadien-1-ol), a new sex pheromone of male Drosophila melanogaster to show its (S)-isomer and racemate as bioactive
title_sort pheromone synthesis. part 244: synthesis of the racemate and enantiomers of (11z,19z)-ch503 (3-acetoxy-11,19-octacosadien-1-ol), a new sex pheromone of male drosophila melanogaster to show its (s)-isomer and racemate as bioactive
publishDate 2014
url http://scholarbank.nus.edu.sg/handle/10635/101373
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