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. |
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| 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. |
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| 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. |
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| 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. |
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| 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. |
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| 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. |
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| 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. |
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| 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. |
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| 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. |
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| 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. |
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| 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. |
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| 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. |
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