Issue 16, 2025

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

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.

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

Supplementary files

Article information

Article type
Paper
Submitted
26 Jan 2025
Accepted
25 Mar 2025
First published
26 Mar 2025
This article is Open Access
Creative Commons BY license

New J. Chem., 2025,49, 6666-6673

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

J. Wtulich, I. A. Nicholls and S. Kathiravan, New J. Chem., 2025, 49, 6666 DOI: 10.1039/D5NJ00359H

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements