Acridone studies. VII. Mechanistic implications of bromination studies
RH Prager and HM Thredgold
Australian Journal of Chemistry
22(7) 1511 - 1516
Published: 1969
Abstract
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.https://doi.org/10.1071/CH9691511
© CSIRO 1969