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首页> 外文期刊>Organic & biomolecular chemistry >Rh-catalysed [5 + 1] cycloaddition of allenylcyclopropanes and CO: reaction development and application to the formal synthesis of (-)-galanthamine
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Rh-catalysed [5 + 1] cycloaddition of allenylcyclopropanes and CO: reaction development and application to the formal synthesis of (-)-galanthamine

机译:Rh催化的[5 +1]烯丙基环丙烷与CO的环加成反应:反应开发及在正式合成(-)-加兰他敏中的应用

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摘要

A Rh-catalysed [5 + 1] cycloaddition of allenylcyclopropanes and CO has been developed to synthesize functionalized 2-methyl-idene-3,4-cyclohexenones. The scope of this methodology has been investigated, showing that various functional groups can be tolerated. Both di- and tri-substituted allenylcyclopropanes can be applied to this cycloaddition and the [5 + 1] cycloadducts with the E configuration were obtained as the major products. In addition, the present [5 + 1] cycloaddition reaction has been utilized as a key step in the formal synthesis of the natural product (-)-galanthamine.
机译:已开发了Rh催化的烯丙基环丙烷和CO的[5 +1]环加成反应,以合成官能化的2-甲基-亚乙基-3,4-环己烯酮。已经研究了这种方法的范围,表明可以容忍各种官能团。二取代和三取代的烯基环丙烷均可用于该环加成反应,并获得具有E构型的[5 +1]环加合物作为主要产物。此外,目前的[5 +1]环加成反应已被用作天然产物(-)-加兰他敏正式合成中的关键步骤。

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  • 来源
    《Organic & biomolecular chemistry》 |2016年第25期|5945-5950|共6页
  • 作者

    Cheng-Hang Liu; Zhi-Xiang Yu;

  • 作者单位

    Beijing National Laboratory for 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 for 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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