Journal of the Indian Chemical Society, Journal Year: 2025, Volume and Issue: unknown, P. 101787 - 101787
Published: May 1, 2025
Language: Английский
Journal of the Indian Chemical Society, Journal Year: 2025, Volume and Issue: unknown, P. 101787 - 101787
Published: May 1, 2025
Language: Английский
Frontiers in Chemistry, Journal Year: 2025, Volume and Issue: 13
Published: March 3, 2025
In the last 10 years, synthesis of anthracene scaffolds has attracted considerable interest because their distinctive electronic characteristics and various uses in organic electronics, photovoltaics, therapeutics. Anthracene, a polycyclic aromatic hydrocarbon, is valued for its lightweight, stability, electron transport capabilities, making it key building block advanced materials. Traditional methods often face challenges such as low selectivity harsh conditions. However, recent advancements transition metal-catalyzed reactions have transformed field, offering more efficient versatile approaches. This review examines methodologies utilizing metal catalysts like palladium, zinc, indium, cobalt, gold, iridium, rhodium ruthenium, which enabled novel synthetic pathways selective formation substituted anthracenes through cross-coupling reactions. The function ligands, including phosphines N-heterocyclic carbenes, improving reaction efficiency also examined. shift towards greener noted, with focus on minimizing waste reducing toxic reagents. Several case studies demonstrate successful application these techniques, highlighting structural diversity functional potential derivatives applications.
Language: Английский
Citations
4Catalysis Surveys from Asia, Journal Year: 2025, Volume and Issue: unknown
Published: March 11, 2025
Language: Английский
Citations
3Journal of Molecular Structure, Journal Year: 2025, Volume and Issue: unknown, P. 142050 - 142050
Published: March 1, 2025
Language: Английский
Citations
0ChemistryOpen, Journal Year: 2025, Volume and Issue: unknown
Published: March 27, 2025
Abstract This review manuscript examines magnetic nanocatalysts and their pivotal role in forming carbon‐sulfur (C−S) carbon‐selenium (C−Se) bonds. The study delves into the latest advancements synthesis, characterization, application of nanocatalysts, highlighting unique advantages, including enhanced catalytic activity, superior selectivity, easy recovery through separation, which align with principles green chemistry. Through a critical analysis recent research findings, this also explores mechanistic pathways facilitated by these offering insights operational efficiency potential for recyclability. aims not only to catalog current achievements burgeoning field but identify challenges propose future directions developing more efficient, sustainable, versatile systems C−S C−Se bond formation. By encompassing broad spectrum ranging from bare magnets functionalized composite materials, is comprehensive resource researchers engaged organic catalysis, sustainable
Language: Английский
Citations
0Journal of Organometallic Chemistry, Journal Year: 2025, Volume and Issue: unknown, P. 123654 - 123654
Published: April 1, 2025
Language: Английский
Citations
0Polyhedron, Journal Year: 2025, Volume and Issue: unknown, P. 117564 - 117564
Published: April 1, 2025
Language: Английский
Citations
0Research on Chemical Intermediates, Journal Year: 2025, Volume and Issue: unknown
Published: April 25, 2025
Language: Английский
Citations
0Nanoscale Advances, Journal Year: 2025, Volume and Issue: unknown
Published: Jan. 1, 2025
The study presents a new nanocatalyst, AlFe 2 O 4 @SiO -SO 3 H, designed to improve the efficiency and sustainability of A3 coupling reaction, which is important for synthesizing 2-thioarylbenzoazoles.
Language: Английский
Citations
0Journal of Inorganic and Organometallic Polymers and Materials, Journal Year: 2025, Volume and Issue: unknown
Published: May 19, 2025
Language: Английский
Citations
0Journal of the Indian Chemical Society, Journal Year: 2025, Volume and Issue: unknown, P. 101787 - 101787
Published: May 1, 2025
Language: Английский
Citations
0