首页> 外文期刊>Journal of the American Chemical Society >Ni(Ⅱ)-Bis[(R,R)-N,N′-dibenzylcyclohexane-1,2-diamine]Br_2 Catalyzed Enantioselective Michael Additions of 1,3-Dicarbonyl Compounds to Conjugated Nitroalkenes
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Ni(Ⅱ)-Bis[(R,R)-N,N′-dibenzylcyclohexane-1,2-diamine]Br_2 Catalyzed Enantioselective Michael Additions of 1,3-Dicarbonyl Compounds to Conjugated Nitroalkenes

机译:Ni(Ⅱ)-双[[R,R)-N,N'-二苄基环己烷-1,2-二胺] Br_2催化1,3-二羰基化合物与共轭硝基烯烃的对映选择性迈克尔加成反应

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摘要

The continued interest in the development of direct catalytic addition processes such as the Michael reaction is based on the wide variety of synthetically useful chiral building blocks that are readily assembled in the event that such processes can be rendered enantioselective. Products resulting from the enantioselective addition of nucleophiles to conjugated nitroalkenes represent attractive targets largely due to the attributes of the nitro group associated with its range of subsequent transformations. Recent studies by others have led to the development of catalytic enantioselective additions of 1,3-dicarbonyl compounds to conjugated nitroalkenes. The purpose of this communication is to introduce a new, readily prepared, chiral Ni(Ⅱ) catalyst 1 that facilitates this enantioselective transformation at ambient temperatures (Scheme 1).
机译:对直接催化加成方法如迈克尔反应的开发的持续兴趣是基于多种合成上有用的手性结构单元,在这种方法可以使对映选择性的情况下,这些手性结构单元易于组装。将亲核体对映选择性加成到共轭硝基烯烃中所得到的产物代表了有吸引力的靶标,这主要是由于硝基的性质及其后续转化范围所致。其他人最近的研究已经导致将1,3-二羰基化合物催化对映选择性加成到共轭硝基烯烃上。该交流的目的是介绍一种易于制备的新型手性Ni(Ⅱ)催化剂1,该催化剂在环境温度下有利于这种对映选择性转化(方案1)。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2005年第28期|p.9958-9959|共2页
  • 作者

    David A. Evans; Daniel Seidel;

  • 作者单位

    Department of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts 02138;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

  • 入库时间 2022-08-18 03:24:04

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