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J Chem Ecol

Title:		"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)"
Author(s):		Shani A; Klug JT; Skorka J;
Address:		"Department of Chemistry and Applied Research Institute, Ben-Gurion University of the Negev, 84120, Beer-Sheva, Israel"
Journal Title:		J Chem Ecol
Year:		1983
Volume:		9
Issue:		7
Page Number:		863 - 867
DOI:		10.1007/BF00987810
ISSN/ISBN:		0098-0331 (Print) 0098-0331 (Linking)
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:
Notes:		"PubMed-not-MEDLINEShani, A Klug, J T Skorka, J eng 1983/07/01 J Chem Ecol. 1983 Jul; 9(7):863-7. doi: 10.1007/BF00987810"