
TY  - JOUR
A1  - Hartshorn, MP 
A1  - Martyn, RJ 
A1  - Vaughan, J 
A1  - Wright, GJ 
T1  - Some base-catalysed reactions of polysubstituted Cyclohexa-2,5-dienones
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1983
VL  - 36
IS  - 4
SP  - 839
EP  - 842
KW  - 
UR  - https://doi.org/10.1071/CH9830839 
N2  - Substituted 4-nitrocyclohexa-2,5-dienones (la), (lb) and (4a) give 6-hydroxycyclohexa-2,4-dienones on mild treatment with aqueous sodium bicarbonate. Reactions of cyclohexa-2,5-dienones (4a) and (5) with ammonia in ether give phenols (7a) and (7b) with the loss of bromine from C4. The preparations of the 4-nitro dienones (4a) and (4b) are described. 
ER  -

