首页> 外文期刊>Chemistry: A European journal >Negishi's Reagent Versus Rosenthal's Reagent in the Formation of Zirconacyclopentadienes
【24h】

Negishi's Reagent Versus Rosenthal's Reagent in the Formation of Zirconacyclopentadienes

机译:Negishi的试剂与Rosenthal的试剂在形成锆胞间旋律化必需

获取原文
获取原文并翻译 | 示例
           

摘要

Zirconacyclopentadienes are versatile precursors for a large number of heteroles, which are accessible by Zrelement exchange reactions. The vast majority of reports describe their preparation by the use of Negishi's reagent, which is a species that is formed in situ. The zirconacyclopentadiene is then formed by the addition of one equivalent of a diyne or two equivalents of a monoyne moiety to this Negishi species. Another route involves Rosenthal's reagent (Cp_2Zr(py)Me_3SiC/CSiMe_3), which then reacts with a diyne or monoyne moiety. In this work, the efficiency of both routes was compared in terms of reaction time, stability of the product in the reaction mixture, and yield. The synthetic implications of using both routes are evaluated. Novel zirconacyclopentadienes were synthesized, characterized directly from the reaction mixture, and crystal structures could be obtained in most cases.
机译:锆氰基丙二烯部分是大量异种的多功能前体,可通过Zrelement Exchange反应访问。 绝大多数报告通过使用Negishi的试剂来描述他们的准备,这是一种原位形成的物种。 然后通过向该Negishi物种中添加一种当量的二炔部分或二当量的单炔部分来形成锆氰基丙烯。 另一条路线涉及罗森特尔的试剂(CP_2ZR(PY)ME_3SIC / CSIME_3),然后用DIYNE或MONOORE部分反应。 在这项工作中,在反应时间,反应混合物中产物的稳定性进行比较两条途径的效率,并得到产率。 评估使用两个路线的合成影响。 合成了新型锆氰基丙二烯,直接从反应混合物中表征,并且在大多数情况下可以获得晶体结构。

著录项

  • 来源
    《Chemistry: A European journal》 |2019年第58期|共11页
  • 作者单位

    Institute for Organic and Analytical Chemistry/MAPEX Center for Materials and Processes University of Bremen Leobener Str. 7/ Bibliothekstr. 1 28359 Bremen (Germany);

    Institute for Organic and Analytical Chemistry/MAPEX Center for Materials and Processes University of Bremen Leobener Str. 7/ Bibliothekstr. 1 28359 Bremen (Germany);

    Institute for Inorganic Chemistry and Crystallography/ MAPEX Center for Materials and Processes University of Bremen Leobener Str. 7/Bibliothekstr. 1 28359 Bremen (Germany);

    Institute for Inorganic Chemistry and Crystallography/ MAPEX Center for Materials and Processes University of Bremen Leobener Str. 7/Bibliothekstr. 1 28359 Bremen (Germany);

    Otto-Diels-Institute for Organic Chemistry University of Kiel Otto-Hahn-Platz 4 24098 Kiel (Germany);

    Institute for Organic and Analytical Chemistry/MAPEX Center for Materials and Processes University of Bremen Leobener Str. 7/ Bibliothekstr. 1 28359 Bremen (Germany);

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 应用化学;
  • 关键词

    metallacycles; Negishi's reagent; Rosenthal's reagent; substituent effects; zirconium;

    机译:金属族;Negishi的试剂;罗森尔的试剂;取代基效应;锆;

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号