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.
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