ArticleScientific reports2025
Copper catalyzed carbon-selenium bond formation via the coupling reaction of aryl halides, phenylboronic acid and Se.
Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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Who cites it
2 citing papers in PubMed.
- Unlocking Selenium Chemical Space via a Programmable Synthesis Platform Bearing Cannabinoid Receptor Recognition Motifs.Journal of the American Chemical Society · 2026Article
- A Comprehensive Review of Magnetic Nanocatalysts for C-S, C-Se Bond Formation.ChemistryOpen · 2025Review
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Authors and funding
3 authors.
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Abstract
This is the first report for C-Se bond formation involving the reaction of aryl halides with arylboronic acid and selenium powder to synthesis of unsymmetrical diaryl selenides in the presence of CuI as a homogeneous catalyst. A wide range of aryl halides react with various substituted groups under optimal conditions to provide the desired unsymmetrical diaryl selenides with good to high yields. Also, the same reactions were investigated in the presence of M-MCF@Gua-Cu as a reusable magnetic nanocatalyst under optimal conditions. The M-MCF@Gua-Cu catalyst allows for simpler (easy work-up) and greener methodology. In addition, the advantages of the presented method include the use of arylboronic acid/Se as a safe and cost-effective arylselenating system, the simplicity of operation, and green and cheap solvent.
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