
TY  - JOUR
A1  - Hamilton, RJ 
A1  - Mander, LN 
T1  - Approaches to the Synthesis of Quassinoids
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1991
VL  - 44
IS  - 7
SP  - 927
EP  - 938
KW  - 
UR  - https://doi.org/10.1071/CH9910927 
N2  - A range of hydrophenanthrene methyl ethers were subjected to Birch reduction, and the products converted into the epoxides (21), (26) and (27). These were treated with diethylaluminium cyanide, but useful products were not obtained from (21) or (26). However, epoxide (27) was converted into the hydroxy nitrile (28) and thence enone (30), a potentially useful intermediate for the synthesis of quassinoids. 
ER  -

