
%0 Journal Article
%A Becker, H 
%A Ruge, B 
%A Skelton, BW 
%A White, AH 
%T On the Thermal Reversibility of the Photochemical Di-&#960;-methane Rearrangement of Bicyclo[2,2,2]octadienones. Confirmation of Regiospecificity and Stereochemistry by X-Ray Structure Analyses
%J Australian Journal of Chemistry
%D 1979/06/01
%V 32
%N 6
%P 1231-1240
%K 
%R https://doi.org/10.1071/CH9791231
%U https://www.publish.csiro.au/paper/CH9791231 
%X Thermolysis of the tricyclic photo-isomer obtained by di- &#960;-methane rearrangement of a t-butyl-substituted bicyclo[2,2,2]octadienone regenerates a new bicyclo[2,2,2]octadienone in which the oxo- substituted C2-bridge has undergone a 1,3-migration. The structures of the three isomers involved were established by X-ray analyses. 
