
%0 Journal Article
%A Baker, KM 
%A Bell, KH 
%A Davis, BR 
%T Rearrangement of cross-conjugated methylenecyclohexadienes
%J Australian Journal of Chemistry
%D 1968/12/01
%V 21
%N 12
%P 2945-2950
%K 
%R https://doi.org/10.1071/CH9682945
%U https://www.publish.csiro.au/paper/CH9682945 
%X Acid-catalysed rearrangement of a number of polycyclic cross-conjugated   methylenecyclohexadienes possessing an angular methyl group (for example (I)) has led to the corresponding substituted 1,4-dimethylbenzenes. The reaction parallels the dienone-phenol rearrangement, but, unlike the latter, the course of the rearrangement is not sensitive to the reaction conditions. 
