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Organotitanium Nucleophiles in Asymmetric Cross-Coupling Reaction: Stereoconvergent Synthesis of Chiral α-CF_3 Thioethers

机译:不对称交叉偶联反应中的有机钛亲核试剂:手性α-CF_3硫醚的立体收敛合成

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摘要

Asymmetric Ni-catalyzed cross-coupling reactions have become a very attractive tool for the stereoselective construction of valuable organic chiral materials. While various nucleophiles are used in such transformation, organotitanium(IV) has not been used before. Herein we demonstrate, for the first time, that organotitanium species can serve as efficient coupling partners in asymmetric cross-couplings, which have proven to be beneficial, compared to the commonly used organomagnesium and organozinc counterparts. This principle is exemplified by the first asymmetric catalytic synthesis of CF3-substituted thioethers via a Ni-catalyzed stereoconvergent cross-coupling reaction. Thioether moieties and their derivatives are common motifs in many biologically active compounds, and their enantioenriched fluorinated analogs should be of great interest in the search for novel drugs and agrichemicals.
机译:Ni的不对称催化交叉偶联反应已成为有价值的有机手性材料的立体选择结构的非常有吸引力的工具。尽管在这种转化中使用了各种亲核试剂,但以前并未使用有机钛(IV)。在此,我们首次证明,与常用的有机镁和有机锌对应物相比,有机钛物质可在不对称交叉偶联中充当有效的偶联伴侣,事实证明这是有益的。该原理通过经由Ni催化的立体收敛交叉偶联反应的CF 3取代的硫醚的第一不对称催化合成得到例证。硫醚部分及其衍生物是许多生物活性化合物中的常见基序,它们的对映体富集的氟化类似物在寻找新药和农药时应引起极大兴趣。

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  • 来源
    《Journal of the American Chemical Society》 |2019年第28期|10994-10999|共6页
  • 作者单位

    Technion Israel Inst Technol, IL-3200008 Haifa, Israel;

    Technion Israel Inst Technol, IL-3200008 Haifa, Israel;

  • 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
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