
TY  - JOUR
A1  - Chai, CLL 
A1  - Hockless, DCR 
A1  - King, AR 
T1  - Reactivities of Piperazine-2,5-diones in Radical Bromination Reactions
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1996
VL  - 49
IS  - 11
SP  - 1229
EP  - 1233
KW  - 
UR  - https://doi.org/10.1071/CH9961229 
N2  - The reactivities of various N,N'- diacetylated piperazine-2,5-diones towards radical bromination reactions are reported. The studies show that glycyl  centres of piperazine-2,5-diones are more reactive towards radical bromination reactions compared to &#945;-substituted amino acid centres. In addition, large differences in reactivities were observed for the cis and trans isomers of N,N'-diacetylated alanine anhydride. Single-crystal structure determination of each isomer revealed that conformational effects may account for the difference in chemical reactivity. 
ER  -

