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Intermolecular Palladium(0)-Catalyzed Atropo-enantioselective C-H Arylation of Heteroarenes

机译:分子间钯(0)催化杂芳烃的对映体对映选择性C-H芳基化

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摘要

Atropisomeric (hetero)biaryls are motifs with increasing significance in ligands, natural products, and biologically active molecules. The straightforward construction of the stereogenic axis by efficient C—H functionalization methods is extremely rare and challenging. An intermolecular and highly enantioselective C—H arylation of relevant heteroarenes providing an efficient access to atropisomeric (hetero)biaryls is reported. The use of a Pd(0) complex equipped with H_8-BINAPO as a chiral ligand enables the direct functionalization of a broad range of 1,2,3-triazoles and pyrazoles in excellent yields and selectivities of up to 97.5:2.5 er. The method also allows for an atroposelective double C—H arylation for the construction of two stereogenic axes with >99.5:0.5 er.
机译:阻转异构(杂)联芳基是在配体,天然产物和生物活性分子中具有越来越重要意义的基序。通过高效的CH功能化方法对立体轴的直接构建极为罕见且具有挑战性。据报道,相关杂芳烃的分子间和高度对映选择性的CH芳基化提供了对阻转异构(杂)联芳基的有效利用。使用配有H_8-BINAPO作为手性配体的Pd(0)配合物,可以直接官能化各种1,2,3-三唑和吡唑,且产率高,选择性高达97.5:2.5 er。该方法还允许对映体选择性双重CH芳基化,以构建两个立体异构轴,其> 99.5:0.5 er。

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  • 来源
    《Journal of the American Chemical Society》 |2020年第5期|2161-2167|共7页
  • 作者

  • 作者单位

    Laboratory of Asymmetric Catalysis and Synthesis Institute of Chemical Sciences and Engineering Ecole Polytechnique Federale de Lausanne (EPFL) 1015 Lausanne Switzerland;

    Department of Chemistry University of Basel 4056 Basel Switzerland;

    Laboratory of Asymmetric Catalysis and Synthesis Institute of Chemical Sciences and Engineering Ecole Polytechnique Federale de Lausanne (EPFL) 1015 Lausanne Switzerland;

  • 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);
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  • 正文语种 eng
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