Suzuki-Miyaura cross-coupling of phenylboronic acid with aryl halides catalyzed by palladium and nickel species supported on alumina-based oxides
Author:
Funder
National Science Centre
Publisher
Elsevier BV
Subject
Materials Chemistry,Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Reference32 articles.
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1. Palladium-Decorated Covalent Organic Framework Supported on Zinc Ferrite as Magnetic Catalyst for Suzuki Reaction and p-nitrophenol Reduction;Catalysis Letters;2022-11-07
2. Heterogenization of Pd(II) complexes as catalysts for the Suzuki-Miyaura reaction;Applied Catalysis A: General;2021-10
3. Zeolite enslaved transition metal complexes as novel heterogeneous catalysts for synthesis of polycyclic heterocycles using suzuki--miyaura cross coupling reaction under greener conditions;Inorganic Chemistry Communications;2020-12
4. Fe 3 O 4 ‐Lignin@Pd‐NPs: A highly efficient, magnetically recoverable and recyclable catalyst for Mizoroki‐Heck reaction under solvent‐free conditions;Applied Organometallic Chemistry;2020-07-15
5. Nb2O5 supported catalysts for cross-coupling reactions;Journal of Coordination Chemistry;2020-05-18
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