首页> 外文期刊>The Journal of Organic Chemistry >Allylic amination and N-arylation-based domino reactions providing rapid three-component strategies to fused pyrroles with different substituted patterns
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Allylic amination and N-arylation-based domino reactions providing rapid three-component strategies to fused pyrroles with different substituted patterns

机译:烯丙基胺化和基于N-芳基化的多米诺骨牌反应为具有不同取代模式的稠合吡咯提供了快速的三组分策略

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摘要

New three-component domino reaction providing divergent approaches to multifunctionalized fused pyrroles with different substituted patterns have been established (40 examples). The direct C(sp ~3)-N bond formation was achieved through intermolecular allylic amination in a one-pot operation, and N-arylation of amines was realized by varying N-amino acid enaminones. The reaction is easy to perform simply by mixing three common reactants in acetic acid under microwave heating. The reaction proceeds at fast rates and can be finished within 30 min, which makes workup convenient to give good chemical yields.
机译:已经建立了新的三组分多米诺反应,该反应为具有不同取代模式的多功能化稠合吡咯提供了多样化的方法(40个实例)。通过一锅操作通过分子间烯丙基胺化反应实现直接的C(sp〜3)-N键形成,通过改变N-氨基酸烯胺酮实现胺的N-芳基化。在微波加热下,将三种常见的反应物在乙酸中混合即可轻松进行反应。反应以快速进行,可以在30分钟内完成,这使得后处理方便,从而获得了良好的化学收率。

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