
%0 Journal Article
%A Hartshorn, MP 
%A Robinson, WT 
%A Vaughan, J 
%A White, JM 
%T The Nitration of 4,6-Disubstituted 2-Phenylphenols. Some Structural Studies
%J Australian Journal of Chemistry
%D 1985/04/01
%V 38
%N 4
%P 575-585
%K 
%R https://doi.org/10.1071/CH9850575
%U https://www.publish.csiro.au/paper/CH9850575 
%X 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). 
