β-イミダゾリルエノン類の合成と反応

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概要

• 論文の詳細を見る

• As the analogues of acylimidazoles and β-aminoenones, the synthesis and the chemical properties of β-imidazolylenones were reviewed. The synthetic routes from β-haloenones, ynones and α, β-dibromoketones were described. By the reaction with pyrrolidine, the titled compounds are reactive as much as the β-haloenones. The quaternarization of the titled compounds by the treatment with methyl iodide increases the reactivity to the nucleophiles. As the nucleophiles, primary alcohols, phenols, thiols, amines, Grignard reagents and sodium borohydride are employed, and the replaced produts are obtained regioselectively. Also the titled compounds were shown to be useful for the starting materials of the various heterocycles by the treatment with the ambident nucleophiles such as hydroxylamine, hydrazines and ureas. The application of the synthetic procedure for β-chloroenones β-benzimidazolylenones gives β, β-diazolylenones, which were demonstrated as the good precursor of the acylketene derivatives. In conclusion, the titled compounds were shown to be much useful for the syntheses of β-substituted enones and various heterocycles.

• 社団法人 有機合成化学協会の論文

著者

• 鹿島 長次

  筑波大学化学系

• 田陦 忠国

  筑波大学化学系

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• β-イミダゾリルエノン類の合成と反応

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