Halogenation of N-substituted p-quinone monoimines and p-quinone monooxime ethers: XV. Synthesis and bromination of 4-(cinnamoyloxyimino)-cyclohexa-2,5-dienones

Resumo

New 4-(cinnamoyloxyimino)cyclohexa-2,5-dien-1-ones were synthesized, and their bromination afforded bromine addition products to the syn- and anti-C=C bonds of the quinoid ring. In all cases, bromine addition to the C=C double bond of the cinnamoyl fragment was observed.