...
首页> 外文期刊>Journal of the American Chemical Society >Caution in the Use of Nonlinear Effects as a Mechanistic Tool for Catalytic Enantioconvergent Reactions: Intrinsic Negative Nonlinear Effects in the Absence of Higher-Order Species
【24h】

Caution in the Use of Nonlinear Effects as a Mechanistic Tool for Catalytic Enantioconvergent Reactions: Intrinsic Negative Nonlinear Effects in the Absence of Higher-Order Species

机译:使用非线性效应作为催化对映收敛反应的机理工具时的注意事项:没有高阶物种时的内在负性非线性效应

获取原文
获取原文并翻译 | 示例
           

摘要

Investigation of the dependence of product enantiometric excess (ee) on catalyst ee is a widely used tool to probe the mechanism of an enantioselective reaction; in particular, the observation of a nonlinear relationship is usually interpreted as an indication of the presence of one or more species that contain at least two units of the chiral entity. In this report, we demonstrate that catalytic enantioconvergent reactions can display an intrinsic negative nonlinear effect that originates purely from the kinetic characteristics of certain enantioconvergent processes and is independent of possible aggregation of the chiral entity. Specifically, this intrinsic negative nonlinear effect can arise when there is a kinetic resolution of the racemic starting material, and its magnitude is correlated with the selectivity factor and the conversion; the dependence on conversion provides a ready means to distinguish it from a more conventional nonlinear effect. We support our analysis with experimental data for two distinct enantioconvergent processes, one catalyzed by a chiral phosphine and the other by a chiral Pd/phosphine complex.
机译:产物对映体过量(ee)对催化剂ee的依赖性研究是广泛用于探索对映选择性反应机理的工具;特别是,观察到非线性关系通常被解释为一种或多种存在的指示。包含至少两个手性实体单元的物种。在这份报告中,我们证明催化对映体收敛反应可以显示出内在的负非线性效应,该效应完全源自某些对映体收敛过程的动力学特征,并且与手性实体的可能聚集无关。具体而言,当消旋起始原料具有动力学拆分时,这种内在的负非线性效应就会出现,并且其幅度与选择性因子和转化率相关;对转化的依赖性提供了一种将其与更常规的非线性方法区分开来的简便方法影响。我们用两种不同对映体收敛过程的实验数据来支持我们的分析,一种是由手性膦催化,另一种是由手性Pd /膦复合物催化。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2017年第11期|4225-4229|共5页
  • 作者

    Marcin Kalek; Gregory C. Fu;

  • 作者单位

    Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, United States, Department of Organic Chemistry, Arrhenius Laboratory, Stockholm University, 106 91 Stockholm, Sweden, Centre of New Technologies, University of Warsaw, 02-097 Warsaw, Poland;

    Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, United States;

  • 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
  • 关键词

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