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Compound - trans-nerolidol [(E)-3,7,11-Trimethyl-1,6,10-dodecatrien-3-ol]
 


Bedoukain RussellIPM
 
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(E)-3,7,11-Trimethyl-1,6,10-dodecatrien-3-ol
(E)-3,7,11-Trimethyl-1,6,10-dodecatrien-3-ol

Formula: C15H26O 
CAS#: 40716-66-3 
MW: 222.37 

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





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Reference(s) for synthesis of (E)-3,7,11-Trimethyl-1,6,10-dodecatrien-3-ol [trans-nerolidol]


Cane, D.E., Iyengar, R., and Shiao, M.-S. 1981. Cyclonerodiol biosynthesis and the enzymic conversion of farnesyl to nerolidyl pyrophosphate. J. Am. Chem. Soc. 103:914-931.
 
Cuvigny, T., Julia, M., and Rolando, C. 1988. Alkylation du linalol sur les carbones C8 (et C6). J. Organomet. Chem. 344:9-28.
 
Gordon, E.M., and Pluscec, J. 1992. Chemistry of isoprenylated cysteinyl containing peptides. [2,3]. Sigmatropic rearrangement of S-farnesylcysteinyl sulfoxides. Studies toward a mild method of deprenylating lipopeptides. J. Am. Chem. Soc. 114:1521-1523.
 
Morizawa, Y., Mori, I., Hiyama, T., and Nozaki, H. 1981. Bis[trimethylsilyl] sulfate-catalyzed alcohol protection with dihydropyran, deprotection, and transesterification. Synthesis. 11:899-901.
 

 
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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