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Compound - 1E3E7,11-4me8me12me-13Hy
 


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(E,E)-4,8,12-Trimethyl-1,3,7,11-tridecatetraene
(E,E)-4,8,12-Trimethyl-1,3,7,11-tridecatetraene

Formula: C16H26 
CAS#: 62235-06-7 
MW: 218.38 

[MS]  [ NMR ]  [ Kovats ]  [Behavioural function]  [Occurrence in plant]  [Chemdraw





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Reference(s) for synthesis of (E,E)-4,8,12-Trimethyl-1,3,7,11-tridecatetraene



Dodd, D.S., and Oehlschlager, A.C. 1992. Synthesis of inhibitors of 2,3-oxidosqualene-lanosterol cyclase: conjugate addition of organocuprates to N-(carbobenzyloxy)-3-carbomethoxy-5,6-dihydro-4-pyridone. J. Org. Chem. 57:2794-2803.
 
Ishihara, K., Ishibashi, H., and Yamamoto, H. 2002. Enantio-and diastereoselective stepwise cyclization of polyprenoids induced by chiral and achiral LBAs. A new entry to (-)-ambrox, (+)-podocarpa-8,11,13-triene diterpenoids, and(-)-tetracyclic polyprenoid of sedimentary origin. J. Am. Chem. Soc. 124:3647-3655.
 
Julia, M. et al. 1960. Bull. Soc. Chim. Fr. 1072-1079.
 
Maurer, B., Hauser, A., and Froidevaux, J.-C. 1986. (E)-4,8-dimethyl-1,3,7-nonatriene and (E,E)-4,8,12-trimethyl-1,3,7,11-tridecatetraene, two unusual hydrocarbons from cardamom oil. Tetrahedron Lett. 27:2111-2112.
 
Sen, S.E., and Garvin, G.M. 1995. Substrate requirements for Lepidopteran farnesol dehydrogenase. J. Agric. Food Chem. 43:820-825.
 

 
Citation: El-Sayed AM 2014. The Pherobase: Database of Insect Pheromones and Semiochemicals. <http://www.pherobase.com>.
2003-2014 The Pherobase - Extensive Database of Insect Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 23-February-2014