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Development of Structurally Diverse N-Heterocyclic Carbene Ligands via Palladium-Copper-Catalyzed Decarboxylative Arylation of Pyrazolo[1,5-a]pyridine-3-carboxylic Acid

机译:吡咯并[1,5-a]吡啶-3-羧酸的钯-铜催化脱羧酰化反应制备结构多样的N-杂环碳配体

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摘要

A series of fused non-classical normal N-heterocyclic carbenes, Pyrpy-NHC precursors derived from pyrazolo[1,5-a]pyridines, has been prepared using palladium-copper-catalyzed decarboxylative arylation of pyrazolo[1,5-a]pyridine-3-carboxylic acid. Air-stable palladium and rhodium complexes of these ligands have been synthesized via mild transmetallation of Ag-Pyrpy-NHC. The structural properties of Rh(Pyrpy-NHC)(COD) Cl complexes were determined via X-ray analysis. The measurement of the CO stretching frequencies of dicarbonyl Rh-Pyrpy-NHC complexes revealed that the electron donating strength of Pyrpy-NHC could be tuned by varying the substituents of the aryl group. A catalytic study of the Pd-Pyrpy-NHC complexes revealed promising activity in the Suzuki-Miyaura reaction under ambient atmospheric conditions.
机译:使用吡咯并[1,5-a]吡啶的钯-铜催化脱羧芳基化反应制备了一系列稠合的非经典正杂环N-杂环卡宾,衍生自吡唑并[1,5-a]吡啶的Pyrpy-NHC前体。 -3-羧酸。这些配体的空气稳定的钯和铑配合物是通过Ag-Pyrpy-NHC的轻度金属过渡合成的。 Rh(Pyrpy-NHC)(COD)Cl配合物的结构性质通过X射线分析确定。对二羰基Rh-Pyrpy-NHC配合物的CO拉伸频率的测量表明,可以通过改变芳基的取代基来调节Pyrpy-NHC的给电子强度。 Pd-Pyrpy-NHC配合物的催化研究表明,在环境大气条件下,Suzuki-Miyaura反应具有良好的活性。

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