
%0 Journal Article
%A Pasaribu, SJ 
%A Williams, LR 
%T Synthesis of phenethanolamine derivatives with potential &#946;-adrenergic antagonistic activity
%J Australian Journal of Chemistry
%D 1975/05/01
%V 28
%N 5
%P 1023-1030
%K 
%R https://doi.org/10.1071/CH9751023
%U https://www.publish.csiro.au/paper/CH9751023 
%X The mass spectra of bromonitroacetophenones, intermediates in the synthesis of phenethanolamine derivatives containing a nitro and bromo group in the aryl ring, have been studied. The acetophenones were converted into the corresponding &#945;,&#946;-epoxystyrenes, which were then treated with various amines, and proton magnetic resonance and mass spectral studies were used to confirm the direction of ring opening and purity of the products. 
