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首页> 外文期刊>Organic & biomolecular chemistry >Pd(0)-catalyzed cross-coupling of allyl halides with α-diazocarbonyl compounds or N-mesylhydra zones: synthesis of 1,3-diene compounds
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Pd(0)-catalyzed cross-coupling of allyl halides with α-diazocarbonyl compounds or N-mesylhydra zones: synthesis of 1,3-diene compounds

机译:Pd(0)催化的烯丙基卤与α-重氮羰基化合物或N-甲磺酰基区域的交叉偶联:1,3-二烯化合物的合成

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摘要

With palladium catalysis, allyl bromides or chlorides react with a-diazocarbonyl compounds or N-mesyl-hydrazones to afford 1,3-diene derivatives. The reaction represents a novel and efficient method for the synthesis of 1,3-butadiene derivatives. Mechanistically, the reaction is proposed to follow a pathway involving the formation of a π-allylic palladium carbene complex and subsequent migratory insertion.
机译:在钯催化下,烯丙基溴或氯化物与α-重氮羰基化合物或N-甲磺酰基hydr反应生成1,3-二烯衍生物。该反应代表了一种合成1,3-丁二烯衍生物的新颖有效的方法。从机理上讲,建议该反应遵循包括形成π-烯丙基钯卡宾配合物和随后的迁移插入的途径。

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  • 来源
    《Organic & biomolecular chemistry 》 |2016年第15期| 3809-3820| 共12页
  • 作者单位

    Beijing National Laboratory of Molecular Sciences (BNLMS), Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College of Chemistry, Peking University, Beijing 100871, China;

    Beijing National Laboratory of Molecular Sciences (BNLMS), Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College of Chemistry, Peking University, Beijing 100871, China,College of Chemistry and Chemical Engineering, Inner Mongolia University, Hohhot 010021, China;

    Beijing National Laboratory of Molecular Sciences (BNLMS), Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College of Chemistry, Peking University, Beijing 100871, China;

    Beijing National Laboratory of Molecular Sciences (BNLMS), Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College of Chemistry, Peking University, Beijing 100871, China;

    Beijing National Laboratory of Molecular Sciences (BNLMS), Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College of Chemistry, Peking University, Beijing 100871, China;

    Beijing National Laboratory of Molecular Sciences (BNLMS), Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College of Chemistry, Peking University, Beijing 100871, China;

    Beijing National Laboratory of Molecular Sciences (BNLMS), Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College of Chemistry, Peking University, Beijing 100871, China;

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