Ruthenium-catalysed late-stage C–H alkynylation of carboxylic acids using sustainable deep eutectic solvents†

IF 2.5 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY New Journal of Chemistry Pub Date : 2025-03-26 DOI:10.1039/D5NJ00359H
Julia Wtulich, Ian A. Nicholls and Subban Kathiravan
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Abstract

The demand for sustainable and environmentally friendly chemical processes has led to the development of innovative catalytic systems and solvent designs. Herein, we report a novel approach utilizing ruthenium catalysis in deep eutectic solvents (DESs) for the selective alkynylation of C–H bonds. Ruthenium, known for its low toxicity and cost-effectiveness, serves as an excellent alternative to other transition metals in eutectic liquids. Moreover, the utilization of supramolecular β-cyclodextrin-based deep eutectic liquids enhances the eco-friendliness and recoverability of the solvent system. The late-stage functionalization of drugs exemplifies the practical applicability and versatility of this method in organic synthesis, offering a sustainable pathway towards the synthesis of valuable compounds.

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钌催化羧酸晚期C-H烷基化反应用可持续深共晶溶剂†
对可持续和环境友好的化学过程的需求导致了创新的催化系统和溶剂设计的发展。在此,我们报告了一种在深共晶溶剂(DESs)中利用钌催化选择性烷基化C-H键的新方法。钌以其低毒性和低成本效益而闻名,是共晶液体中其他过渡金属的极好替代品。此外,超分子β-环糊精基深共晶液体的利用提高了溶剂体系的环保性和可恢复性。药物的后期功能化体现了该方法在有机合成中的实用性和多功能性,为合成有价值的化合物提供了一条可持续的途径。
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来源期刊
New Journal of Chemistry
New Journal of Chemistry 化学-化学综合
CiteScore
5.30
自引率
6.10%
发文量
1832
审稿时长
2 months
期刊介绍: A journal for new directions in chemistry
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