
TY  - JOUR
A1  - Gable, RW 
A1  - Parker, KJ 
A1  - Tsanaktsidis, J 
T1  - 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
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1994
VL  - 47
IS  - 5
SP  - 963
EP  - 968
KW  - 
UR  - https://doi.org/10.1071/CH9940963 
N2  - 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. 
ER  -

