Halogenation of <Emphasis Type="Italic">N</Emphasis>-substituted <Emphasis Type="Italic">p</Emphasis>-quinone monoimines and <Emphasis Type="Italic">p</Emphasis>-quinone monooxime ethers: XV. Synthesis and bromination of 4-(cinnamoyloxyimino)-cyclohexa-2,5-dienones期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

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

Authors:	S. A. Konovalova A. P. Avdeenko S. A. Goncharova

Abstract:	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.

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