
%0 Journal Article
%A Francis, CL 
%A Ward, AD 
%T Attempted Heterocyclic Syntheses Through Electrophilic Ring Closure Reactions of 2-Allylaniline Systems Containing Larger Side Chains
%J Australian Journal of Chemistry
%D 1994/11/01
%V 47
%N 11
%P 2109-2117
%K 
%R https://doi.org/10.1071/CH9942109
%U https://www.publish.csiro.au/paper/CH9942109 
%X The electrophile-initiated cyclization of some 2-allylanilines and their amide derivatives has been further investigated. Although 2-allylanilines with small, allylic  substituents such as methyl reacted with iodine to yield 3-iodo-1,2,3,4-tetrahydroquinolines the 2-allylanilines with larger substituents related to those of virantmycin provided low yields of the tetrahydroquinoline as part of a complex product mixture. 
