Silica supported palladium-phosphine complex: recyclable catalyst for Suzuki–Miyaura cross-coupling reactions at ambient temperature
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference85 articles.
1. For reviews, see:
2. Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds
3. Aryl−Aryl Bond Formation One Century after the Discovery of the Ullmann Reaction
4. Selected Patented Cross-Coupling Reaction Technologies
5. On the Nature of the Active Species in Palladium Catalyzed Mizoroki–Heck and Suzuki–Miyaura Couplings – Homogeneous or Heterogeneous Catalysis, A Critical Review
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1. Nitron analogs containing an N-arylcarbamoylmethyl group and Pd complexes derived therefrom: synthesis and catalytic activity in the Suzuki—Miyaura reaction;Russian Chemical Bulletin;2024-04
2. Suzuki–Miyaura cross-coupling reaction assisted by palladium nanoparticles-decorated zeolite 13X nanocomposite: a greener approach;Research on Chemical Intermediates;2022-01-10
3. Pd (II) Immobilized on Clinoptilolite as a Highly Active Heterogeneous Catalyst for Ullmann Coupling-type S-arylation of Thiols with Aryl Halides;Combinatorial Chemistry & High Throughput Screening;2020-10-05
4. Plasmonic heating using an easily recyclable Pd‐functionalized Fe 3 O 4 /Au core‐shell nanoparticle catalyst for the Suzuki and Sonogashira reaction;Applied Organometallic Chemistry;2020-04-17
5. Ligand-free, recyclable palladium-functionalized magnetite nanoparticles as a catalyst in the Suzuki-, Sonogashira, and Stille reaction;Journal of Organometallic Chemistry;2019-12
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