首页> 外文期刊>Chemistry: A European journal >New Iridium Catalysts for the Selective Alkylation of Amines by Alcohols under Mild Conditions and for the Synthesis of Quinolines by Acceptor-less Dehydrogenative Condensation
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New Iridium Catalysts for the Selective Alkylation of Amines by Alcohols under Mild Conditions and for the Synthesis of Quinolines by Acceptor-less Dehydrogenative Condensation

机译:在温和条件下用醇选择性胺化胺和通过无受体脱氢缩合合成喹啉的新型铱催化剂

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摘要

A novel family of iridium catalysts stabilised by P,N-ligands have been introduced. The ligands are based on imidazo[1,5-b]pyridazin-7-amines and can be synthesised with a broad variety of substitution patterns. The catalysts were synthesised quantitatively from the protonated ligands and a commercially available iridium precursor. The catalysts mediate the alkylation of amines by alcohols under mild conditions (70°C). In addition, the synthesis of quinolines from secondary or primary alcohols and amino alcohols is reported. This sustainable synthesis proceeds through the liberation of two equivalents of water and two equivalents of dihydrogen. The investigations indicate that catalysts suitable for hydrogen autotransfer or borrowing hydrogen chemistry might also be suitable for acceptor-less dehydrogenative condensation reactions.
机译:引入了由P,N-配体稳定的新型铱催化剂。配体基于咪唑并[1,5-b]哒嗪-7-胺,可以合成多种取代方式。由质子化的配体和可商购的铱前体定量合成催化剂。催化剂在温和的条件下(70℃)介导醇的胺烷基化。另外,据报道由仲或伯醇和氨基醇合成喹啉。这种可持续的合成通过释放两当量的水和两当量的二氢来进行。研究表明,适用于氢自动转移或借用氢化学的催化剂也可能适用于无受体的脱氢缩合反应。

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