
TY  - JOUR
A1  - Carman, Raymond M. 
A1  - Hansford, Karl A. 
A1  - Kennard, Colin H. L. 
T1  - Halogenated Terpenoids. XXXI. Tribromides from the Bromination of Various Exocyclic Olefins
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 2000
VL  - 53
IS  - 5
SP  - 439
EP  - 442
KW  - Bromination; tribromide; exocyclic methylene; cyclohexyl; X-ray crystallography.
UR  - https://doi.org/10.1071/CH00041 
N2  - 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. 
ER  -

