
%0 Journal Article
%A Kasum, B 
%A Prager, RH 
%T A 'Classical' approach to the synthesis of perloline
%J Australian Journal of Chemistry
%D 1983/07/01
%V 36
%N 7
%P 1455-1467
%K 
%R https://doi.org/10.1071/CH9831455
%U https://www.publish.csiro.au/paper/CH9831455 
%X An approach to the synthesis of perloline by the reaction of (2-bromophenyl)(3',4'-dimethoxy- phenyl)amine with a suitably 4-substituted 2-oxo-1,2-dihydropyridine-3-carboxylic acid was unsuccessful due to the inability to form the amide bond. The diphenylamine was efficiently synthesized from the nitrone of dimethoxybenzylidene-2-bromoaniline via the oxaziridine, the thermal rearrangement of which was investigated. Conjugate additions of a diphenylamine dianion to unsaturated esters are reported. 
