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Palladium-catalyzed one-pot synthesis of diazoles via tert-butyl isocyanide insertion

机译:叔丁基异氰化物的钯催化一锅合成二唑

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摘要

An efficient one-pot palladium-catalyzed reaction for the synthesis of diazoles from readily available hydrazides and aryl halide via isocyanide insertion/cyclization sequence has been developed. This methodology efficiently constructs diazoles in good to excellent yields with the advantages of wide functional group tolerance and operational simplicity.
机译:已经开发了一种有效的一锅钯催化的反应,该反应可通过异氰化物的插入/环化顺序由易于获得的酰肼和芳基卤化物合成二唑。该方法有效地以良好至优异的产率构建了二唑,具有宽泛的官能团耐受性和操作简便性的优点。

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  • 来源
    《Organic & biomolecular chemistry》 |2015年第41期|10402-10408|共7页
  • 作者单位

    College of Pharmaceutical Sciences, Soochow University, Suzhou, 215123, China;

    College of Pharmaceutical Sciences, Soochow University, Suzhou, 215123, China;

    College of Pharmaceutical Sciences, Soochow University, Suzhou, 215123, China;

    College of Pharmaceutical Sciences, Soochow University, Suzhou, 215123, China;

    College of Pharmaceutical Sciences, Soochow University, Suzhou, 215123, China;

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