Stereoselective synthesis of (Z)-13-hexadecen-11-yn-1-yl acetate, the major component of the sex pheromone of the pine processionary moth (Thaumetopoea pityocampa)
Autor: | Shani, A., Klug, J. T., Skorka, J. |
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Zdroj: | Journal of Chemical Ecology; July 1983, Vol. 9 Issue: 7 p863-867, 5p |
Abstrakt: | A short and stereoselective synthesis of (Z)-13-hexadecen-1 1-yn-1-yl acetate is described. The main feature is a low-temperature Wittig reaction of a triphenylpropylphosphonium bromide with a long-chain alkylated propargyl aldehyde. |
Databáze: | Supplemental Index |
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