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

机译:在不对称交叉偶联反应中的有机钛核酸:手性α-CF_3硫醚的立体CONGEGGENT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:不对称的Ni催化的交叉偶联反应已成为有价值的有机手性材料的立体选择性结构的非常有吸引力的工具。虽然各种核酸用于这种转化,但之前未使用有机钛(IV)。在此,我们首次证明了有机钛物种可以用作不对称的交叉偶联中的有效偶联伴侣,其被证明是有益的,而与常用的有机镁和有机抑制对应物相比。该原理通过Ni催化的立体CONECONGENT联偶联反应的第一不对称催化合成CF3取代的硫醚的第一非对称催化合成。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,它们的对母语含氟类似物应该对寻求新型药物和农业的致力感兴趣。

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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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