
%0 Journal Article
%A Brown, BT 
%A Phillips, JN 
%T Structure of 1-Acyl-2-alkyl-2-thiopseudoureas
%J Australian Journal of Chemistry
%D 1970/03/01
%V 23
%N 3
%P 553-559
%K 
%R https://doi.org/10.1071/CH9700553
%U https://www.publish.csiro.au/paper/CH9700553 
%X Deprotonation of 1-acyl-2-alkyl-2-thiopseudouronium salts has been shown to involve the loss of a proton from the 1 rather than the 3 position in those cases where both nitrogens carry at least one hydrogen atom. This results in an acylated 2-thiopseudourea in which the C=N is conjugated to the carbonyl group. 
