Pheromone synthesis. Part 250: Determination of the stereostructure of CH503, a sex pheromone of male Drosophila melanogaster, as (3R,11Z,19Z)-3- acetoxy-11,19-octacosadien-1-ol by synthesis and chromatographic analysis of its eight isomers

Tetrahedron

Volumn 68, Issue 19, 2012, Pages 3750-3760

  Shikichi, Yasumasa ^a   Akasaka, Kazuaki ^b   Tamogami, Shigeyuki ^c   Shankar, Shruti ^d   Yew, Joanne Y ^d   Mori, Kenji ^a  

^a TOYO GOSEI CO LTD   (Japan)

^b SHOKEI GAKUIN UNIVERSITY   (Japan)

^c T Hasegawa Co   (Japan)

^d NATIONAL UNIVERSITY OF SINGAPORE   (Singapore)

Author keywords

Chemical ecology; Drosophila melanogaster; HPLC separation of E Z isomers; HPLC separation of enantiomers; Pheromone

Indexed keywords

3 ACETOXY 11,19 OCTACOSADIEN 1 OL; SEX PHEROMONE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; DROSOPHILA MELANOGASTER; ESTERIFICATION; MALE; NONHUMAN; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; REVERSED PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; STEREOCHEMISTRY; STEREOISOMERISM; SYNTHESIS;

DROSOPHILA MELANOGASTER;

EID: 84859603664     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2012.03.002     Document Type: Article

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