
%0 Journal Article
%A Hartshorn, MP 
%A Robinson, WT 
%A Sutton, KH 
%A Vaughan, J 
%A Wright, GJ 
%T An unexpected rearrangement of 1-Acetyl-3, t-5-dichloro-t-2,4-dimethyl- 2,5-dinitrocyclopent-3-en-r-1-ol; X-ray crystal structure of 3,t-5-Dichloro-t-6-hydroxy-2,4,6-trimethyl-r-2,5-dinitrocyclohex-3-enone
%J Australian Journal of Chemistry
%D 1983/02/01
%V 36
%N 2
%P 317-323
%K 
%R https://doi.org/10.1071/CH9830317
%U https://www.publish.csiro.au/paper/CH9830317 
%X 1-Acetyl-3,t-5-dichloro-t-2,4-dimethyl-2,5-dinitrocyclopent-3-en-r-1-ol (11) rearranges in acetone to give the C6-epimeric dinitrocyclohex-3-enone (13), the structure of which was determined by X-ray crystal analysis. The base-catalysed rearrangement of cyclohex-3-enone (13) is discussed. 
