吲哚唑增强了钌催化的不饱和键的氢化反应

Wenjun Jiang , Xiulin Li , Yaru Liu , Chunyan Zhang , Guoying Zhang , Ali Morsali
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引用次数: 0

摘要

催化加氢过程是非常令人垂涎的,具有很高的潜力,因为它有效地将关键分子转化为环境友好型醇,展示了卓越的原子效率和选择性。此外,这些酒精产品可作为合成各种药物的多功能前体。在此,我们开发了一种实用而有效的方法,利用钌催化吲唑主链PNN钳形配体对各种不饱和化合物进行加氢。该方法有效地解决了涉及CC/N/O和CC键的多功能氢化反应的化学选择性问题。Ru催化体系在可扩展合成PNN配体方面表现出优异的性能,在催化剂浓度低至0.001 mol%的情况下,实现了63 371的周转数和146.18 g的酒精。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Indazole enhances Ru-catalyzed hydrogenation of unsaturated bonds†

Indazole enhances Ru-catalyzed hydrogenation of unsaturated bonds†

Indazole enhances Ru-catalyzed hydrogenation of unsaturated bonds†
The catalytic hydrogenation process is highly coveted and holds high potential due to its efficient conversion of crucial molecules into environmentally friendly alcohols, showcasing exceptional atom efficiency and selectivity. Moreover, these alcohol products serve as versatile precursors for synthesizing various pharmaceuticals. Herein, we have developed a practical and efficient procedure for the hydrogenation of various unsaturated compounds using Ru-catalysis with an indazole backbone PNN pincer ligand. This method effectively tackles the challenge of chemoselectivity in multifunctional hydrogenation reactions involving CC/N/O and CC bonds. The Ru catalytic system exhibits exceptional performance in the scalable synthesis of PNN ligands, achieving a turnover number of 63 371 and producing 146.18 grams of alcohol with a catalyst concentration as low as 0.001 mol%.
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CiteScore
7.80
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