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¦ « Previous CompoundZ3Z5-14Acid    Next Compound »Z3Z6-21Hy ¦
 
Compound - Z3Z6-12OH [(Z,Z)-3,6-Dodecadien-1-ol]
 


Bedoukain RussellIPM
 
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(Z,Z)-3,6-Dodecadien-1-ol
(Z,Z)-3,6-Dodecadien-1-ol

Formula: C12H22O 
CAS#: 29125-78-8 
MW: 182.3 

[MS]  [ NMR ]  [ Kovats ]  [Behavioural function]  [Occurrence in flower





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Reference(s) for synthesis of (Z,Z)-3,6-Dodecadien-1-ol [Z3Z6-12OH]


Corey, E.J., and Lansbury, P.T. 1983. Stereochemical course of 5-lipoxygenation of arachidonate by rat basophil leukemic cell (RBL-1) and potato enzymes. J. Am. Chem. Soc. 105:4093-4094.
 
Hutzinger, M.W., and Oehlschlager, A.C. 1995. Stereoselective synthesis of 1,4-dienes. Application to the preparation of insect pheromones (3Z,6Z)-dodeca-3,6-dien-1-ol and (4E,7Z)-trideca-4,7-dienyl acetate. J. Org. Chem. 60:4595-4601.
 
Saha, G., Basu, M.K., Kim, S., Jung, Y.-J., Adiyaman, Y., Adiyaman, M., Powell, W.S., Fitzgerald, G.A., and Rokach, J. 1999. A convenient strategy for the synthesis of ß,gamma-unsaturated aldehydes and acids. A construction of skipped dienes. Tetrahedron Lett. 40:7179-7183.
 
Yadav, J.S., Nanda, S., and Rao, A.B. 2001. Soybean lipoxygenase and horseradish peroxidase catalysed asymmetric oxidation-reduction sequence for the synthesis of chiral (Z,E) diene-diols. Syn. Lett. 6:787-788.
 
Zamboni, R., and Rokach, J. 1983. Stereospecific synthesis of 5S-HETE, 5R-HETE and their transformation to 5(±)-HPETE. Tetrahedron Lett. 24:999-1002.
 
Zhu, Y. and Liu, I. 1980. Synthesis of Z,Z-3,6-dodecadien-1-ol. Hua Hsueh Tung Pao. 9:527.
 

 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
Ⓒ 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
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