
%0 Journal Article
%A Gash, DM 
%A Woodgate, PD 
%T Formation of <I>ortho</I> Diol Diacetates in the Acid-Catalysed Rearrangement of 4-Aryl-4-hydroxycyclohexa-2,5-dienones. A Structural Reassignment
%J Australian Journal of Chemistry
%D 1979/08/01
%V 32
%N 8
%P 1863-1867
%K 
%R https://doi.org/10.1071/CH9791863
%U https://www.publish.csiro.au/paper/CH9791863 
%X Treatment of the p-quinols 2,6-di-t-butyl-4-hydroxy-4-phenylnaphthalen-1(4H)-one, 2,6-di-t-butyl-4-hydroxy-4-phenylcyclohexa-2,5-dienone and 2,6-di-t-butyl-4-hydroxy-4-(4'-methoxyphenyl)cyclohexa-2,5-dienone with acetic anhydride and sulfuric acid affords, as the major product, an aromatic ortho diol diacetate. 
