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首页> 外文期刊>Chemistry: A European journal >One-Pot Asymmetric Synthesis of Quaternary Pyrroloindolones through a Multicatalytic N-Allylation/Hydroacylation Sequence
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One-Pot Asymmetric Synthesis of Quaternary Pyrroloindolones through a Multicatalytic N-Allylation/Hydroacylation Sequence

机译:通过多催化N-烯丙基化/氢化酰化序列一锅不对称合成季吡咯并吲哚酮

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摘要

An intramolecular, quaternary carbon center forming hydroacylation of α-substituted acrylates has been discovered. This interesting transformation can be readily incorporated into a multicatalytic tandem process enabled by a combination of nucleophilic tertiary amine and N-heterocyclic carbene catalysis. With no additional stoichiometric base required, this transformation affords the quaternary pyrroloindolones with high levels of enantioselectivity.
机译:已经发现了α-取代的丙烯酸酯的分子内,季碳中心形成加氢酰化。通过将亲核叔胺和N-杂环卡宾催化相结合,可以轻松地将此有趣的转化合并到多催化串联过程中。无需额外的化学计量基础,该转化即可提供具有高对映选择性的季吡咯并吲哚酮。

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