
TY  - JOUR
A1  - Hartshorn, MP 
A1  - Robinson, WT 
A1  - Vaughan, J 
A1  - White, JM 
T1  - The Nitration of 4,6-Disubstituted 2-Phenylphenols. Some Structural Studies
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1985
VL  - 38
IS  - 4
SP  - 575
EP  - 585
KW  - 
UR  - https://doi.org/10.1071/CH9850575 
N2  - Nitration of the bromophenols (4a) and (5a) give products of nitro-debromination . Reaction of 6-methyl-4-nitro-2-phenylphenol (5c) with nitrogen dioxide gives 2-hydroxy-2-phenylcyclohex-3-enones (8) and (9), and probably stereoisomers (10), (20), (21) and (22). The mode of ormation of these compounds is discussed. X-ray crystal structure determinations are reported for compounds (8) and (9). 
ER  -

