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Compound - 4S5S-ferrugineol
 


Bedoukain

 
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(4S,5S)-4-Methylnonan-5-ol
(4S,5S)-4-Methylnonan-5-ol

Formula: C10H22O 
CAS#:  
MW: 158.28 

[MS]  [ NMR ]  [Behavioural function]  [Chemdraw





Dots surface:


Reference(s) for synthesis of (4S,5S)-4-Methylnonan-5-ol



Mori, K., Kiyota, H., Malosse, C., and Rochat, D. 1993. Synthesis of the enantiomers of syn-4-methyl-5-nonanol to determine the absolute configuration of the naturally occurring (4S,5S) isomer isolated as the male-produced pheromone compound of Rynchophorus vulneratus and Metamasius hemipterus. Liebigs Ann. Chem: 1201-1204.
 
Odriozola, J.M., García, J.M., González, A., and Gil, P. 1999. Asymmetric synthesis of phoenicol, ferrugineol and cruentol, aggregation pheromones of Rhynchophorus spp.Tetrahedron: Asymmetry. 10:4627-4632.
 
Oehlschlager, A.C., Prior, R.N.B., Perez, A.L., Gries, R., Gries, G., Pierce, H.D., Jr., and Laup, S. 1995. Structure, chirality, and field testing of a male-produced aggregation pheromone of Asian palm weevil Rhynchophorus bilineatus (Montr.) (Coleoptera: Curculionidae). J. Chem. Ecol. 21:1619-1630.
 

 
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.
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