Nickel(II)–aryl complexes as catalysts for the Suzuki cross-coupling reaction of chloroarenes and arylboronic acids
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference45 articles.
1. The Palladium-Catalyzed Cross-Coupling Reaction of Phenylboronic Acid with Haloarenes in the Presence of Bases
2. Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds
3. Catalytic cross-coupling reactions in biaryl synthesis
4. Recent advances in the cross-coupling reactions of organoboron derivatives with organic electrophiles, 1995–1998
5. Recent applications of the Suzuki–Miyaura cross-coupling reaction in organic synthesis
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1. Suzuki-Miyaura Cross-Coupling using convenient and accessible Nickelocene/Phosphine precatalyst;Journal of Catalysis;2024-08
2. A nickel-catalyzed Suzuki-Miyaura coupling reaction of aryl halides facilitated by pyridine derivatives;Tetrahedron Letters;2024-06
3. Bench-stable Nickel(II)–aryl Complex-Catalyzed cyclotrimerisation of diynes and alkynes to synthesis multisubstituted benzene derivatives;Results in Chemistry;2024-01
4. A new β-cyclodextrin-based nickel as green and water-soluble supramolecular catalysts for aqueous Suzuki reaction;Scientific Reports;2023-12-02
5. Implanted mixed ligand Ni complex of phenolic Schiff base and 2, 2’ bipyridine on MCM-41 as an efficient catalyst for Suzuki–Miyaura cross-coupling reactions: a greener approach;Research on Chemical Intermediates;2022-08-01
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