首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >A simple synthesis of functionalized 3-methyl-1-pyridinyl-1H-imidazolium salts as bidentate N-heterocycIic-carbene precursors and their application in Ir-catalyzed arene borylation
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A simple synthesis of functionalized 3-methyl-1-pyridinyl-1H-imidazolium salts as bidentate N-heterocycIic-carbene precursors and their application in Ir-catalyzed arene borylation

机译:作为双齿N-杂环卡宾前体的功能化3-甲基-1-吡啶基-1H-咪唑鎓盐的简单合成及其在Ir催化的芳烃硼化中的应用

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摘要

The selective alkylation of functionalized 2-(1H-imidazol-1-yl)pyridines 1 furnishes 3-methyl-1-pyridi-nyl-1H-imidazolium salts 2, which can be deprotonated to deliver strongly electron-donating bidentate N-heterocyclic carbene ligands (NHC). The synthesis of these ligands and their application in the iridium-catalyzed C-H activated borylation of arenes with its current scope and limitations are reported.
机译:官能化的2-(1H-咪唑-1-基)吡啶1的选择性烷基化提供了3-甲基-1-吡啶基-1H-咪唑鎓盐2,可以将其去质子化以提供强供电子的二齿N-杂环卡宾配体(NHC)。报道了这些配体的合成及其在铱催化的芳烃的C-H活化的硼化中的应用及其目前的范围和局限性。

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