
%0 Journal Article
%A Carman, Raymond M. 
%A Hansford, Karl A. 
%A Kennard, Colin H. L. 
%T Halogenated Terpenoids. XXXI. Tribromides from the Bromination of Various Exocyclic Olefins
%J Australian Journal of Chemistry
%D 2000/07/27
%V 53
%N 5
%P 439-442
%K Bromination; tribromide; exocyclic methylene; cyclohexyl; X-ray crystallography.
%R https://doi.org/10.1071/CH00041
%U https://www.publish.csiro.au/paper/CH00041 
%X Bromination of methylene groups exocyclic to cyclohexyl systems can afford, besides the expected trans-dibromo products, considerable quantities of a tribromide. For example, simple bromination of 4-t-butyl-1-methylidene-cyclohexane affords c. 20% yield of (r-1, t-2, c-4)-1,2-dibromo-1-bromomethyl-4-t-butylcyclohexane. 
