
%0 Journal Article
%A Prager, RH 
%A Thredgold, HM 
%T Acridone studies. VII. Mechanistic implications of bromination studies
%J Australian Journal of Chemistry
%D 1969/07/01
%V 22
%N 7
%P 1511-1516
%K 
%R https://doi.org/10.1071/CH9691511
%U https://www.publish.csiro.au/paper/CH9691511 
%X The function of alcohols in the addition of bromine to highly oxygenated acridones is discussed, and pathways proposed to explain the structure of the products. The most important factors appear to be the relief of ring strain by addition across a double bond substituted by a methylenedioxy group, and the intermediacy of bromonium ions. 
