PLOS ONE: Supported Palladium Nanoparticles Synthesized by Living Plants as a Catalyst for Suzuki-Miyaura Reactions
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Supported Palladium Nanoparticles that Catalyze Aminocarbonylation of Aryl Halides with Amines using Oxalic Acid as a Sustainable CO Source,Chemistry - A European Journal - X-MOL
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Catalysts | Free Full-Text | Microwave-Assisted Palladium-Catalyzed Cross-Coupling Reactions: Generation of Carbon–Carbon Bond | HTML
![A Pd-catalyzed, boron ester-mediated, reductive cross-coupling of two aryl halides to synthesize tricyclic biaryls - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C7OB01237C A Pd-catalyzed, boron ester-mediated, reductive cross-coupling of two aryl halides to synthesize tricyclic biaryls - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C7OB01237C](https://pubs.rsc.org/image/article/2017/OB/c7ob01237c/c7ob01237c-s1_hi-res.gif)
A Pd-catalyzed, boron ester-mediated, reductive cross-coupling of two aryl halides to synthesize tricyclic biaryls - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C7OB01237C
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Catalysts | Free Full-Text | Recent Advances in Metal-Catalyzed Alkyl–Boron (C(sp3)–C(sp2)) Suzuki-Miyaura Cross-Couplings | HTML
![Figure 1 from Palladium-Catalyzed Synthesis of (Hetero)Aryl Alkyl Sulfones from (Hetero)Aryl Boronic Acids, Unactivated Alkyl Halides, and Potassium Metabisulfite. | Semantic Scholar Figure 1 from Palladium-Catalyzed Synthesis of (Hetero)Aryl Alkyl Sulfones from (Hetero)Aryl Boronic Acids, Unactivated Alkyl Halides, and Potassium Metabisulfite. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/626be8e8e5c1178dd83cdca7c3491e7420865fd4/2-Table1-1.png)
Figure 1 from Palladium-Catalyzed Synthesis of (Hetero)Aryl Alkyl Sulfones from (Hetero)Aryl Boronic Acids, Unactivated Alkyl Halides, and Potassium Metabisulfite. | Semantic Scholar
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Palladium-catalyzed cross-coupling reactions of aryl boronic acids with aryl halides in water - PDF Free Download
![Table 1 from Fibrous nano-silica (KCC-1)-supported palladium catalyst: Suzuki coupling reactions under sustainable conditions. | Semantic Scholar Table 1 from Fibrous nano-silica (KCC-1)-supported palladium catalyst: Suzuki coupling reactions under sustainable conditions. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/d97cb13588ddf359fc5a61f7ef2977e8f505689a/3-Table1-1.png)
Table 1 from Fibrous nano-silica (KCC-1)-supported palladium catalyst: Suzuki coupling reactions under sustainable conditions. | Semantic Scholar
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Palladium-catalyzed cross-coupling reactions of aryl boronic acids with aryl halides in water - PDF Free Download
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Studies on Pd/NiFe 2 O 4 catalyzed ligand-free Suzuki reaction in aqueous phase: synthesis of biaryls, terphenyls and polyaryls – topic of research paper in Chemical sciences. Download scholarly article PDF and
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Reaction scope and mechanistic insights of nickel-catalyzed migratory Suzuki–Miyaura cross-coupling | Nature Communications
Pd-Catalyzed Suzuki coupling reactions of aryl halides containing basic nitrogen centers with arylboronic acids in water in the absence of added base - New Journal of Chemistry (RSC Publishing)
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Palladium(II)-catalyzed Heck reaction of aryl halides and arylboronic acids with olefins under mild conditions
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Palladium‐Catalyzed Direct Arylation of (Hetero)Arenes with Aryl Boronic Acids - Yang - 2008 - Angewandte Chemie International Edition - Wiley Online Library
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Palladium-catalyzed Suzuki cross-coupling of aryl halides with aryl boronic acids in the presence of glucosamine-based phosphines - [PDF Document]
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Novel pyridine-based Pd(II)-complex for efficient Suzuki coupling of aryl halides under microwaves irradiation in water | SpringerLink
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Suzuki-Miyaura cross-coupling of phenylboronic acid with aryl halides catalyzed by palladium and nickel species supported on alumina-based oxides - ScienceDirect
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i>N</i>-Doped porous carbon supported palladium nanoparticles as a highly efficient and recyclable catalyst for the Suzuki coupling reaction
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