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Compound - Z7-16OH [(Z)-7-Hexadecen-1-ol]

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(Z)-7-Hexadecen-1-ol Formula:  C16H32O  CAS#:  24880-48-6  MW:  240.42  [MS]  [ NMR ]  [ Kovats ]  [Behavioural function]

Dots surface:

Reference(s) for synthesis of (Z)-7-Hexadecen-1-ol [Z7-16OH] Brown, H.C., Basavaiah, D., and Bhat, N.G. 1986. Vinylic organoboranes. 4. A general, one-pot synthesis of 6- and 7-alkyn-1-ols via boracyclanes. Influence of steric effects in the iodination of lithium alkynyl ate complexes of dialkylborinates. J. Org. Chem. 51:4518-4521.   Horiike, M., and Hirano, C. 1980. A facile synthesis of the sex pheromones (Z)-7-dodecen-1-yl acetate and its homologs. Agric. Biol. Chem. 44:2229-2230.   Periasamy, M., Prasad, A.S.B., and Suseela, Y. 1995. Synthesis of Z-alkenes from alkenylcatecholboranes through reaction with RMgX and I2 induced rearrangement. Tetrahedron. 51:2743-2748.   Rossi, R., and Carpita, A. 1977. Insect pheromones. Stereoselective reduction of beta- or omega- alkynols to the corresponding (E)-alkenols by lithium tetrahydroaluminate. Synthesis. 8:561-562.   Schaub, B., Blaser, G., and Schlosser, M. 1985. Omega-hydroxyalkyl-phosphonium salts as "instant-ylid" components: extremely convenient and highly cis-selective synthesis of alkenol-type pheromones. Tetrahedron Lett. 26:307-310.   Seidel, W., and Schaefer, H.J. 1980. Kolbe-synthese ungesaettigter pheromone durch coelektrolyse mit 5-alkinsaeuren. Chem. Ber. 113:3898-3903.