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TEMPO-catalyzed oxidative homocoupling route to 3,2′-biindolin-2-ones via an indolin-3-one intermediate

机译:TEMPO催化吲哚-3-酮中间体氧化制取3,2′-联吲哚-2-酮的信号

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摘要

A combinative C2-selective arylation, and C3-selective carbonylation of free indole derivatives, by means of TEMPO catalysis and a silver oxidant under non-directing group conditions, was successful demonstrated. This new methodology is both atom and step efficient and is applicable to a broad scope of substrates, allowing the synthesis of a range of synthetically valuable 3,2′-biindolin-2-ones in moderate to excellent yields.
机译:在非定向基团条件下,通过TEMPO催化和银氧化剂,成功地证明了游离吲哚衍生物的C2选择性芳基化和C3选择性羰基化。这种新方法既原子又有效,并且适用于多种底物,从而可以中等至极高的产率合成一系列具有合成价值的3,2'-联吲哚-2-酮。

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