
%0 Journal Article
%A Bapat, JB 
%A Black, DSC 
%A Newland, G 
%T Nitrones and oxaziridines. XII. Vinylogous hydroxamic acid structures of the reduction products from &#947;-nitro (o- and p-hydroxyphenyl) ketones
%J Australian Journal of Chemistry
%D 1974/07/01
%V 27
%N 7
%P 1591-1595
%K 
%R https://doi.org/10.1071/CH9741591
%U https://www.publish.csiro.au/paper/CH9741591 
%X Vinylogous hydroxamic acid structures (4) and (5) are assigned to the products of the zinc and ammonium chloride reduction of the &#947;-nitro (o- and p-hydroxyphenyl) ketones (lc) and (1d) respectively. Similar reduction of the related &#947;-nitro (m-hydroxyphenyl) ketone (le) afforded the nitrone (2e). 
