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Compound - 1S-beta-pinene [(1S)-6,6-Dimethyl-2-methylenebicyclo[3.1.1]heptane]
 


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(1S)-6,6-Dimethyl-2-methylenebicyclo[3.1.1]heptane
(1S)-6,6-Dimethyl-2-methylenebicyclo[3.1.1]heptane

Formula: C10H16 
CAS#: 18172-67-3 
MW: 136.24 

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





Dots surface:


Reference(s) for synthesis of (1S)-6,6-Dimethyl-2-methylenebicyclo[3.1.1]heptane [1S-beta-pinene]


Araki, S., Hetano, M., and Butsugan, Y. 1986. Regioselective conversion of allylic alcohols to 1-propenes via organoiron complexes. J. Org. Chem. 51:2126-2128.
 
Bourgeois, M.-J., Montaudon, E., and Maillard, B. 1993. Une nouvelle synthèse de peroxydes d'alkyle dissymétriques à partir d alcools tertiaires. Tetrahedron. 49:2477-2484.
 
Hirabe, T., Nojima, M., and Kusabayashi, S. 1984. Lithium aluminum hydride reduction of allylic substrates. Notable leaving group effects on the product regiochemistry. J. Org. Chem. 49:4084-4086.
 
Matawowski, A. 1980. Pol. J. Chem. 54:469-479.
 
Wallach. 1908. J. Liebigs Ann. Chem. 363:11.
 

 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
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Page created on 13-February-2024