
%0 Journal Article
%A Dyall, LK 
%T Oxidative cyclizations. IV. Isokinetic relationship in the oxidation of orthosubstituted anilines with (diacetoxyiodo)benzene
%J Australian Journal of Chemistry
%D 1973/12/01
%V 26
%N 12
%P 2665-2670
%K 
%R https://doi.org/10.1071/CH9732665
%U https://www.publish.csiro.au/paper/CH9732665 
%X The rates of oxidative cyclization of 11 ortho-substituted anilines by (diacetoxyiodo)benzene have been measured in toluene-acetic acid solution. The activation parameters give a precise fit to an isokinetic relationship, which indicates that a common reaction mechanism is followed. This mechanism applies to amines from the benzene, naphthalene, and anthraquinone families, with nitro and various carbonyl and arylazo groups as the ortho substituents. 
