首页> 外文期刊>European journal of organic chemistry >Selective, efficient and functional group-tolerant CuOAc-mediated N-arylation of 1H-indoles and 9H-carbazole with aryl iodides under base-free and ligandless conditions
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Selective, efficient and functional group-tolerant CuOAc-mediated N-arylation of 1H-indoles and 9H-carbazole with aryl iodides under base-free and ligandless conditions

机译:在无碱和无配体条件下,选择性,有效和官能团耐受的CuOAc介导的1H吲哚和9H-咔唑与芳基碘的N-芳基化

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摘要

CuOAc-Mediated N-arylation of 1H-indole derivatives and 1H-carbazole with aryl iodides under base-free and ligandless conditions provides the required N-arylazoles with complete N-selectivity and in moderate to good yields. The experimental conditions for this new version of the Ullmann reaction allow an unprecedented tolerance of functional groups and facilitate the workup of the reaction mixtures and isolation of the required chemically pure reaction products. ((C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007).
机译:在无碱和无配体条件下,CuOAc介导的1H-吲哚衍生物和1H-咔唑与芳基碘的N-芳基化反应提供了所需的N-芳基唑,具有完全的N-选择性,并且产率中等至良好。此新版本的Ullmann反应的实验条件允许对官能团进行空前的耐受,并有助于反应混合物的后处理和所需化学纯反应产物的分离。 ((C)Wiley-VCH Verlag GmbH&Co.KGaA,69451 Weinheim,Germany,2007)。

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