
%0 Journal Article
%A Gable, RW 
%A Parker, KJ 
%A Tsanaktsidis, J 
%T Selective Bromochlorination of <I>endo</I>-1,4-Dibromotricyclo[5.2.1.0<sup>2,6</sup>]deca-3,8-diene-5,10-dione 10-Ethylene Acetal at the Conjugated Carbon-Carbon Double Bond
%J Australian Journal of Chemistry
%D 1994/05/01
%V 47
%N 5
%P 963-968
%K 
%R https://doi.org/10.1071/CH9940963
%U https://www.publish.csiro.au/paper/CH9940963 
%X Exposure of (1) to bromine in thionyl chloride/ dimethylformamide produced (5), the result of regio- and stereo-selective addition of bromine chloride across the carbonyl-conjugated double bond. The structure of (5) was determined by X-ray crystallography, and its mode of formation is discussed in terms of the carbonyl attack mechanism. 
