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首页> 外文期刊>Organic & biomolecular chemistry >Palladium-catalyzed double coupling reaction of terminal alkynes with isocyanides: a direct approach to symmetrical N-aryl dialkynylimines
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Palladium-catalyzed double coupling reaction of terminal alkynes with isocyanides: a direct approach to symmetrical N-aryl dialkynylimines

机译:用异氰酸酯的末端炔烃的钯催化的双偶联反应:对称N-芳基二烷基二氨基的直接方法

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摘要

A novel and efficient one-pot synthesis of symmetrical N-aryl dia-Ikynylimines via palladium-catalyzed and copper-promoted iso-cyanide insertion, cross-coupling and elimination has been developed. This method features readily available starting materials, mild reaction conditions and high atom efficiency as well as simple one-pot operation, which make this strategy highly attractive. Moreover, 2-iodobenzo[f]quinoline derivatives can be obtained via electrophilic cyclization of N-aryl dialkynylimines.
机译:通过钯催化和铜促进的异氰化物插入,交叉偶联和消除,开发了一种新颖的和有效的单钾合成对称的N-芳基二酰胺。该方法采用易于可用的原料,温和的反应条件和高原子效率以及简单的单锅操作,使这一策略具有高度吸引力。此外,可以通过N-芳基二氧化胺的亲电环化获得2-碘苯并[F]喹啉衍生物。

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  • 来源
    《Organic & biomolecular chemistry》 |2020年第40期|8089-8093|共5页
  • 作者单位

    National Demonstration Center for Experimental Chemistry Education Hunan Engineering Laboratory for Analyse and Drugs Development of Ethnomedicine in Wuling Mountains Jishou University Jishou 416000 P. R. China;

    Shanghai Key Laboratory of Functional Materials Chemistry Key Laboratory for Advanced Materials State Key Laboratory of Chemical Engineering and School of Chemistry & Molecular Engineering East China University of Science and Technology 130 Meilong Road Shanghai 200237 China;

    National Demonstration Center for Experimental Chemistry Education Hunan Engineering Laboratory for Analyse and Drugs Development of Ethnomedicine in Wuling Mountains Jishou University Jishou 416000 P. R. China;

    National Demonstration Center for Experimental Chemistry Education Hunan Engineering Laboratory for Analyse and Drugs Development of Ethnomedicine in Wuling Mountains Jishou University Jishou 416000 P. R. China;

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