
TY  - JOUR
A1  - Ghisalberti, L 
A1  - Jefferies, P 
A1  - Stuart, A 
T1  - The Absolute Configuration of a Sesquiterpene Enone From <I>Stevia purpurea</I> and a Phenol From <I>Lasianthaea podocephala</I>
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1979
VL  - 32
IS  - 7
SP  - 1627
EP  - 1630
KW  - 
UR  - https://doi.org/10.1071/CH9791627 
N2  - (6S,1'R)-6-(1',5'-Dimethylhex-4'-enyl)-3-methylcyclohex-2-enone (1a) has been prepared and found to be the enantiomer of an enone obtained from Stevia purpurea. Oxidation of enone (1a) gives (R)-2-(1',5'-dimethylhex-4'-enyl)-5-methylphenol, identical with a natural product from Lasianthaea podocephala. 
ER  -

