
TY  - JOUR
A1  - Prager, RH 
A1  - Thredgold, HM 
T1  - Acridone studies. VII. Mechanistic implications of bromination studies
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1969
VL  - 22
IS  - 7
SP  - 1511
EP  - 1516
KW  - 
UR  - https://doi.org/10.1071/CH9691511 
N2  - The function of alcohols in the addition of bromine to highly oxygenated acridones is discussed, and pathways proposed to explain the structure of the products. The most important factors appear to be the relief of ring strain by addition across a double bond substituted by a methylenedioxy group, and the intermediacy of bromonium ions. 
ER  -

