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)
- 1 July 1983
- journal article
- research article
- Published by Springer Nature in Journal of Chemical Ecology
- Vol. 9 (7) , 863-867
- https://doi.org/10.1007/bf00987810
Abstract
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.Keywords
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