Conducting C-C cross-coupling reactions under convenient and mild conditions remains extremely challenging in traditional organic synthesis. In this study, ZnCoO@g-CN@Cu exhibited extraordinary photocatalytic performance as a new visible light harvesting heterogeneous copper-based photocatalyst in cyanation and Mizoroki-Heck visible-light-driven cross-coupling reactions at room temperature and in air. Surprisingly, by this method, the cyanation and Mizoroki-Heck cross-coupling reactions of various iodo-, bromo- and also the challenging chloroarenes with respectively K[Fe(CN)]·3HO and olefins produced promising results in a sustainable and mild media. The significant photocatalytic performance of ZnCoO@g-CN@Cu arises from the synergistic optical properties of ZnCoO, g-CN, and Cu. These components can enhance the charge carrier generation and considerably reduce the recombination rate of photogenerated electron-hole pairs. No need to use heat or additives, applying an economical and benign light source, utilizing an environmentally compatible solvent, facile and low-cost photocatalytic approach, aerial conditions, high stability and convenient recyclability of the photocatalyst are the remarkable highlights of this methodology. Moreover, this platform exhibited the ability to be performed on a large scale, which is considered an important issue in industrial and pharmaceutical use. It is worth noting that this is the first time that a heterogeneous copper-based photocatalyst has been employed in visible light-promoted cyanation reactions of aryl halides.
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http://dx.doi.org/10.1039/d4ra04827j | DOI Listing |
Molecules
January 2025
Sustainable Chemistry for Metals and Molecules, Department of Chemistry, KU Leuven, Celestijnenlaan 200F, 3001 Leuven, Belgium.
A pyridine-fused triazapentalene shows weak fluorescence in solution and is readily accessible via nitrene-mediated cyclization. In this study, a modified Cadogan reaction was used to synthesize . Palladium-catalyzed reactions have been used as post-functionalization methods.
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December 2024
Institute of Organic and Analytical Chemistry (ICOA UMR 7311), CNRS, University of Orleans, F-45067 Orléans, France.
The emergence of RNA viruses driven by global population growth and international trade highlights the urgent need for effective antiviral agents that can inhibit viral replication. Nucleoside analogs, which mimic natural nucleotides, have shown promise in targeting RNA-dependent RNA polymerases (RdRps). Starting from protected 5-iodouridine, we report the synthesis of -substituted-(1,3-diyne)-uridines nucleosides and their phosphoramidate prodrugs.
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December 2024
Laboratoire de Chimie de Coordination, CNRS, Toulouse-INP, Université de Toulouse, 31000 Toulouse, France.
In recent years, there has been growing interest in the development of greener alternatives to traditional reagents used in carbon-carbon coupling reactions, particularly in response to environmental concerns. The commonly used aryl halides, despite being highly reactive in the Suzuki-Miyaura coupling (SMC), pose significant environmental risks. As a result, research has shifted towards exploring the use of phenols, which are widely accessible and environmentally benign.
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December 2024
College of Chemistry, Henan Key Laboratory of Chemical Biology and Organic Chemistry, Key Laboratory of Applied Chemistry of Henan Universities, Zhengzhou University, Zhengzhou 450052, China.
Isochroman and azole moieties are both present in a wide variety of biologically active molecules. Their efficient combination under mild reaction conditions is beneficial for obtaining small-molecule drug candidates. In this paper, we describe electrochemical α-C(sp)-H/N-H cross-coupling reactions between isochromans and azoles, yielding products in moderate to excellent yields.
View Article and Find Full Text PDFOrg Lett
January 2025
College of Materials Science and Engineering, Huaqiao University, Xiamen 361021, China.
The enantioselective synthesis of P(V)-stereogenic compounds has emerged as an interesting research topic primarily due to their significant biological activity and broad application prospects. Herein, we disclose a method for the construction of P(V)-stereogenic compounds from prochiral phosphinamides and aryl iodides via palladium- and chiral norbornene-catalyzed desymmetric annulation. The P(V)-stereogenic compounds were formed with a broad scope with excellent enantiomeric excesses.
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