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首页> 外文期刊>Synthesis: International Journal of Methods in Synthetic Organic Chemistry >Stereoselective Synthesis of 3,4-trans-Disubstituted γ-Lactams by Cerium(IV) Ammonium Nitrate Mediated Radical Cyclization of Cinnamamides
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Stereoselective Synthesis of 3,4-trans-Disubstituted γ-Lactams by Cerium(IV) Ammonium Nitrate Mediated Radical Cyclization of Cinnamamides

机译:硝酸铈(IV)铵介导的肉桂酰胺自由基环化立体选择性合成3,4-反式-双取代的γ-内酰胺

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摘要

A facile synthesis of 3,4-trans-disubstituted γ-lactams was developed, consisting of the radical cyclization of cinnam-amides mediated by cerium(IV) ammonium nitrate. The single-electron-transfer (SET) reaction of the methoxystyrenyl moiety mediated by cerium(IV) ammonium nitrate gives rise to a cation radical, whose cyclization followed by reaction with oxygen and methanol generates 3,4-trans-disubstituted γ-lactams.
机译:开发了一种简便的合成3,4-反式二取代γ-内酰胺的方法,该方法由硝酸铈(IV)铵介导的肉桂酰胺的自由基环化组成。硝酸铈(IV)铵介导的甲氧基苯乙烯基部分的单电子转移(SET)反应产生一个阳离子自由基,其环化作用随后与氧和甲醇反应生成3,4-反式-二取代的γ-内酰胺。

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