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Compound - Y11Z13-16Ac
 


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(Z)-13-Hexadecen-11-yn-1-ol acetate
(Z)-13-Hexadecen-11-yn-1-ol acetate

Formula: C18H30O2 
CAS#: 78617-58-0 
MW: 278.43 

[MS]  [ NMR ]  [Behavioural function]  [Chemdraw





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Reference(s) for synthesis of (Z)-13-Hexadecen-11-yn-1-ol acetate



Camps, F., Coll, J., Canela, R., Guerrero, A., and Riba, M. 1981. Synthesis of the two isomers of the potential sex pheromone of Thaumetopoea pityocampa and related model compounds. Chem. Lett. 703-706.
 
Camps, F., Coll, J., Guerrero, A., and Riba, M. 1983. Simple and stereoselective synthesis of sex pheromone of processionary moth, Thaumetopoea pityocampa (Denis and Schiff.). J. Chem. Ecol. 9:869.
 
Camps, F., Fabrias, G., and Guerrero, A. 1986. Synthesis of a fluorinated analog of the sex pheromone of the processionary moth Thaumetopoea pityocampa (Denis & Schiff.). Tetrahedron. 42:3623-3629.
 
Cardillo, G., Cugola, A., Orena, M., and Sandri, S. 1982. A stereoselective synthesis of (Z)-13-hexadecen-11-ynyl acetate, the sex pheromone of Thaumetopoea pityocampa. Gaz. Chim. Ital. 112:231-234.
 
Carpita, A., Quaglia, F., Rossi, E., and Rossi, R. 1983. Synthesis and bioactivity of (Z)-13-hexadecen-11-yn-yl acetate, the proposed sex pheromone of Thaumetopoea pityocampa, and its (E)-stereoisomer. Frustula Entomol. 6:327.
 
Gardette, M., Alexakis, A., and Normant, J.F. 1983. Synthesis of (Z)-13-hexadecen-11-yn-1-yl acetate. Major component of sex pheromone of the processionary moth. J. Chem. Ecol. 9:219-223.
 
Kang, J., Kim, Y.H., Lee, C.S., and Pyun, C. 1983. Total synthesis of 13Z-hexadecen-11-yl-1-ol acetate, pheromone of processionary moth of pine tree. Bull. Korean Chem. Soc. 4:257.
 
Michelot, D., Guerrero, A., and Ratovelomanana, V. 1982. Efficient stereoselective synthesis of (Z)-hexadec-13-en-11-ynyl acetate, a sex attractant of Thaumetopoea pityocampa (Denis and Schiff.). J. Chem. Res. 4:1043-1051.
 
Rossi, R., and Carpita, A. 1983. Stereospecific synthesis of (Z)-13 hexadecen-11-yn-1-yl acetate, the sex pheromone of the processionary moth, and of (5Z,7E)-5,7-dodecadien-1-ol, a sex pheromone component of the forest tent caterpillar. Tetrahedron. 39:287-290.
 
Rossi, R., Carpita, A., and Piccardi, P. 1983. Insect sex pheromones: transition metal-catalyzed stereoselective syntheses of internal conjugated (E)-enynes. In Pesticide Chemistry: Human Welfare Environment, Proc. 5th International Congress of Pesticide Chemistry, Miyamoto, J., and Kearney, P.C., Eds., Pergamon Press. Oxford. 129.
 
Shani, A., Klug, J.T., and Skorka, J. 1983. 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). J. Chem. Ecol. 9:863.
 
Stille, J.K., and Simpson, J.H. 1987. Stereospecific palladium-catalyzed coupling reactions of vinyl iodides with acetylenic tin reagents. J. Am. Chem. Soc. 109:2138-2152.
 

 
Citation: El-Sayed AM 2014. The Pherobase: Database of Insect Pheromones and Semiochemicals. <http://www.pherobase.com>.
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