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Mechanistic Aspects of the Palladium‐Catalyzed Suzuki‐Miyaura Cross‐Coupling Reaction

https://doi.org/10.1002/chem.202101880

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inferredcites →https://doi.org/10.1021/ja00781a070openalex-snapshot

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C2-Symmetric Bis-Hydrazones as Ligands in the Asymmetric Suzuki−Miyaura Cross-Coupling

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Alkylboranes in the Suzuki−Miyaura Coupling: Stereochemical and Mechanistic Studies

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Electronic Nature of N-Heterocyclic Carbene Ligands: Effect on the Suzuki Reaction

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The Importance of Ligand Steric Effects on Transmetalation

inferredcites →https://doi.org/10.1021/om060380iopenalex-snapshot

A DFT Study of the Full Catalytic Cycle of the Suzuki−Miyaura Cross-Coupling on a Model System

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Oxidative Addition of Aryl Chlorides to Monoligated Palladium(0): A DFT-SCRF Study

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Determination of N-Heterocyclic Carbene (NHC) Steric and Electronic Parameters using the [(NHC)Ir(CO)2Cl] System

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An overview of N-heterocyclic carbenes

inferredcites →https://doi.org/10.1038/nature14615openalex-snapshot

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Well-defined nickel and palladium precatalysts for cross-coupling

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Room-temperature activation of aryl chlorides in Suzuki–Miyaura coupling using a [Pd(μ-Cl)Cl(NHC)]2 complex (NHC = N-heterocyclic carbene)

inferredcites →https://doi.org/10.1039/b814973aopenalex-snapshot

Theoretical aspects of palladium-catalysed carbon–carbon cross-coupling reactions

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Percent buried volume for phosphine and N-heterocyclic carbene ligands: steric properties in organometallic chemistry

inferredcites →https://doi.org/10.1039/c1dt10983aopenalex-snapshot

Phosphine and solvent effects on oxidative addition of CH3Br to Pd(PR3) and Pd(PR3)2 complexes

inferredcites →https://doi.org/10.1039/c2cy20311aopenalex-snapshot

A latent ruthenium based olefin metathesis catalyst with a sterically demanding NHC ligand

inferredcites →https://doi.org/10.1039/c2sc20103hopenalex-snapshot

Theoretical study of Pd(0)-catalyzed carbohalogenation of alkenes: mechanism and origins of reactivities and selectivities in alkyl halide reductive elimination from Pd(ii) species

inferredcites →https://doi.org/10.1039/c3972000144aopenalex-snapshot

Activation of Grignard reagents by transition-metal complexes. A new and simple synthesis of trans-stilbenes and polyphenyls

inferredcites →https://doi.org/10.1039/c39790000866openalex-snapshot

Stereoselective synthesis of arylated (E)-alkenes by the reaction of alk-1-enylboranes with aryl halides in the presence of palladium catalyst

inferredcites →https://doi.org/10.1039/c3cc47404fopenalex-snapshot

Palladium monophosphine Pd(PPh 3 ): is it really accessible in solution?

inferredcites →https://doi.org/10.1039/c3cs35521gopenalex-snapshot

Transition-metal-catalyzed Suzuki–Miyaura cross-coupling reactions: a remarkable advance from palladium to nickel catalysts

inferredcites →https://doi.org/10.1039/c3cs60197hopenalex-snapshot

Selection of boron reagents for Suzuki–Miyaura coupling

inferredcites →https://doi.org/10.1039/c3dt32980aopenalex-snapshot

How does the addition of steric hindrance to a typical N-heterocyclic carbene ligand affect catalytic activity in olefin metathesis?

inferredcites →https://doi.org/10.1039/c4cs00061gopenalex-snapshot

Experiment and computation: a combined approach to study the reactivity of palladium complexes in oxidation states 0 to iv

inferredcites →https://doi.org/10.1039/c4dt01758gopenalex-snapshot

Computed ligand effects on the oxidative addition of phenyl halides to phosphine supported palladium(0) catalysts

inferredcites →https://doi.org/10.1039/c6ob00084copenalex-snapshot

Palladium-catalyzed Suzuki–Miyaura coupling of amides by carbon–nitrogen cleavage: general strategy for amide N–C bond activation

inferredcites →https://doi.org/10.1039/c7sc02692gopenalex-snapshot

Suzuki–Miyaura cross-coupling of amides and esters at room temperature: correlation with barriers to rotation around C–N and C–O bonds

inferredcites →https://doi.org/10.1039/c8cp07671eopenalex-snapshot

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inferredcites →https://doi.org/10.1039/c9cp02844gopenalex-snapshot

Quantifying electronic similarities between NHC–gold( i ) complexes and their isolobal imidazolium precursors

inferredcites →https://doi.org/10.1039/c9cs00866gopenalex-snapshot

Stable abnormal N-heterocyclic carbenes and their applications

inferredcites →https://doi.org/10.1039/c9cy02080bopenalex-snapshot

Buchwald–Hartwig cross-coupling of amides (transamidation) by selective N–C(O) cleavage mediated by air- and moisture-stable [Pd(NHC)(allyl)Cl] precatalysts: catalyst evaluation and mechanism

inferredcites →https://doi.org/10.1039/c9sc03169copenalex-snapshot

Palladium-catalyzed decarbonylative Suzuki–Miyaura cross-coupling of amides by carbon–nitrogen bond activation

inferredcites →https://doi.org/10.1039/d0qi01133aopenalex-snapshot

Comparative study of aryl halides in Pd-mediated reactions: key factors beyond the oxidative addition step

inferredcites →https://doi.org/10.1055/s-1994-22773openalex-snapshot

Synthesis of Allenes by Palladium-Catalyzed Cross-Coupling Reaction of Organoboron Compounds with Propargylic Carbonates: Transmetallation of Organoboron Compounds with (Alkoxo)palladium Complexes Under Neutral Conditions

inferredcites →https://doi.org/10.1055/s-2008-1067225openalex-snapshot

Pd-NHC (PEPPSI) Complexes: Synthetic Utility and Computational Studies into Their Reactivity

inferredcites →https://doi.org/10.1246/bcsj.44.581openalex-snapshot

Arylation of Olefin with Aryl Iodide Catalyzed by Palladium

inferredcites →https://doi.org/10.1246/bcsj.46.1505openalex-snapshot

Arylation of Olefin with Iodobenzene Catalyzed by Palladium

inferredcites →https://doi.org/10.1246/bcsj.49.1958openalex-snapshot

Nickel-Phosphine Complex-Catalyzed Grignard Coupling. I. Cross-Coupling of Alkyl, Aryl, and Alkenyl Grignard Reagents with Aryl and Alkenyl Halides: General Scope and Limitations

inferredcites →https://doi.org/10.1246/bcsj.80.233openalex-snapshot

Transition Metal-Catalyzed Organometallic Reactions that Have Revolutionized Organic Synthesis

inferredcites →https://doi.org/10.1595/205651316x690925openalex-snapshot

“New Trends in Cross-Coupling: Theory and Applications”

inferredcites →https://doi.org/10.24820/ark.5550190.p011.451openalex-snapshot

Aminomethylpyridinequinones as new ligands for PEPPSI-type complexes

inferredcites →https://doi.org/10.3390/catal9010053openalex-snapshot

Recent Advances in Acyl Suzuki Cross-Coupling

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Evaluation of Hemilabile Pd(Ii) Nns and Nnse Non-Symmetric Pincers in Suzuki-Miyaura Cross-Coupling: Unexpected Selective Nitrile Hydration of 4-Bromonitrobenzene in Mild Conditions

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Ligand‐Promoted Catalyzed Reactions

inferred← citeshttps://doi.org/10.1002/9783527844258.ch4openalex-snapshot

Atroposelective Suzuki–Miyaura Coupling Toward Axially Chiral Biaryls: Mechanistic Insight

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Nickel‐Catalyzed Cross‐Coupling of Aryl Alkyl Selenides with Aryl Bromides: Cross‐Coupling Between Two Electrophiles

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Decoding Transmetalation in Miyaura Borylation: The Hidden Chemistry of Bis(pinacolato) Diboron and Base Effects

inferred← citeshttps://doi.org/10.1002/adsc.70631openalex-snapshot

Orthogonal One‐Pot Dual Catalysis Enabled by a Hybrid Chiral Diene/Phosphine Ligand

inferred← citeshttps://doi.org/10.1002/adsc.70700openalex-snapshot

The Synthesis of [Pd(NHC)(acac)Cl]·(HFIP) Adducts and Their Catalytic Activity in the α‐Arylation of Ketones

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A Generalized Approach for Distal C–H Arylation of Organic Building Blocks: Unveiling the Role of Counter Anion

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The Core‐Shell Magnetic Mesoporous Microspheres Immobilized NHC‐Palladacycles: An Efficient and Recyclable Catalyst for Suzuki‐Miyaura Cross‐Coupling of Pharmaceutical Synthesis

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Halogen‐Substituted Mesoionic‐Carbene/Palladium Complexes for Catalytic Arylation of Aldehydes

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Highly Ordered Mesoporous Polymer‐Supported Phosphine as the Ligand for Organometallic Reaction: Suzuki‐Miyaura Cross‐Coupling of Aryl Chlorides at Room Temperature

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Advanced Pd–NAPA Precatalysts for Broad‐Scope Kumada–Tamao–Corriu Couplings of Challenging Aryl Chlorides

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Expanding the Horizons of Suzuki Reactions: Pd‐PEPPSI–Mediated Traditional and Decarbonylative Couplings With Diverse Assure Analogues

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Nano‐Multiactive Sites Pd/PdO/CuO/PdCu 3 Formed In Situ on the Surface Hetero‐Organometallic Pd(II)/Cu(II) Nanosheet: Investigation on the Formation of Active Sites, Synergistic, and Catalytic Activity

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Synthesis, Structural Analysis, and Catalysis for Suzuki–Miyaura Coupling Reactions of Tetradentate N ^ C ^ C ^ N and Tetracarbene C ^ C ^ C ^ C Nickel– N ‐Heterocyclic Carbene Complexes

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Reactivity‐Tunable Palladium Precatalysts with Favorable Catalytic Properties in Suzuki–Miyaura Cross‐Coupling Reactions

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A Well‐Defined Pd‐NHC Pre‐Catalyst for the Borylation of Aryl Chlorides

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Recent Progress in Homogeneous and Heterogeneous Pd Catalyst Systems for Suzuki‐Miyaura Coupling in the Absence of Added Base

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Unravelling Enzymatic Features in a Supramolecular Iridium Catalyst by Computational Calculations

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One‐Pot Tandem Coupling Method for the Short‐Step Formal Synthesis of Riccardin C

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A Non Expected Alternative Ni(0) Species in the Ni‐Catalytic Aldehyde and Alcohol Arylation Reactions Facilitated by a 1,5‐Diaza‐3,7‐diphosphacyclooctane Ligand

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Continuous Direct Mechanocatalytic Suzuki‐Miyaura Coupling via Twin‐Screw Extrusion

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Rationalization of a Streptavidin Based Enantioselective Artificial Suzukiase: An Integrative Computational Approach

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Interrogating Explicit Solvent Effects on the Mechanism and Site‐Selectivity of Aryl Halide Oxidative Addition to L 2 Pd(0)

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Efficient and Rapid Arylation of NH₂‐Unprotected Bromobisindole Ethanamines via Suzuki‐Miyaura Coupling: Generating New Leads Against Leishmania

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Transmetalation From Boron to Beryllium in Phosphorus‐Based Scorpionate Complexes

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Late‐Stage Modification of Halotryptophan‐Containing Peptides Via Negishi Cross‐Coupling

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Recent Insights in Multi‐Target Drugs in Pharmacology and Medicinal Chemistry

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From In Situ Monitoring to Better Understanding of the Suzuki‐Miyaura Cross Coupling in the Solid State

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9,9‐Bis[4‐(N‐aryl)phenyl]methylidene‐xanthylidene Derivatives Displaying Mechano‐, Crystallo‐, and Thermochromism

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1,2,3,4‐Tetrafluorobiphenylene: A Prototype Janus‐Headed Scaffold for Ambipolar Materials

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Mechanochemistry: New Tools to Navigate the Uncharted Territory of “Impossible” Reactions

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Ni/PiNe Heterogeneous Catalyst from Biomass Waste: Low‐Loading, Ligand‐Free Suzuki‐Miyaura Cross‐Coupling

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Durable Heterogeneous Pd‐PNP Pincer Complex for CarbonCarbon Bond Formation in Continuous‐Flow Systems

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Design, Synthesis, and Biological Evaluation of 8‐Phenyl‐THIQ as Antidepressive Agents

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Anionic Boraza‐Crown Ethers

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A Bis‐Thiosemicarbazone Pd(II) SiO2 Nanoparticle Conjugate for CC Coupling Catalysis

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Formation of Pd Pincer Complexes through CH Bond Activation: Mass Spectrometric Analyses and Application in the Suzuki–Miyaura Reaction

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Supramolecular Catalysts for Organic Synthesis: Preparation and Applications of Cyclodextrins and Calixarenes in C−C Cross‐Coupling Reactions

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Mechanochemical Nickel‐Catalyzed Suzuki–Miyaura Cross‐Coupling of Phenol‐Derived Cyanate Esters

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Palladium‐Catalyzed Suzuki–Miyaura Cross‐Coupling of Heteroaryl‐2‐Boronic Acids with Nitroaryl Halides

inferred← citeshttps://doi.org/10.1002/ejoc.202501209openalex-snapshot

Carbonylative Suzuki–Miyaura Coupling of 1‐Iodoglycals Mediated by the N ‐Heterocyclic Carbene Catalyst PEPPSI: Preparation of C ‐Acyl Glycosides

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Gold‐Catalyzed Synthesis of Spirocycles: Recent Advances

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Organocatalytic Decarboxylation of 2‐phenylbutanoic Acid and 1,4‐dicyanobenzene: A DFT Investigation

inferred← citeshttps://doi.org/10.1002/slct.202301058openalex-snapshot

Synthesis of a Water‐Soluble Pd‐Based Catalyst with a Thymine‐Modified β ‐Cyclodextrin Ligand for Suzuki Coupling Reactions

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Cross‐Coupling Reactions between Arenediazonium o ‐Benzenedisulfonimides and Organolithium Reagents in a Deep Eutectic Solvent

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Energy‐Efficient Synthesis of Haloquinazolines and Their Suzuki Cross‐Coupling Reactions in Propylene Carbonate

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Synthesis and Characterization of Air‐Stable Palladium(II) and Copper(I) Ph‐Garphos Complexes and their Applications to Asymmetric Catalysis

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Pd Nanoparticles Supported on Luffa Sponge as a Heterogenous Catalyst for C−O and C−C Coupling Reaction: From Waste to Use

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Perimidine‐2‐chalcogenone Ligand‐Supported Palladium(II) Complex: A Potent Catalyst in Suzuki–Miyuara Cross‐Coupling Reaction and Nitroarene Reduction

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Palladium‐Catalyzed Denitrogenative Suzuki Coupling of Benzotriazinones with Potassium (Hetero)Aryl Trifluoroborates

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Green Approach to Aerobic Suzuki Coupling Reaction in Water Based on Heterogeneous Palladium Nanoparticles (PdNPs@VRP) Catalyst Synthesized from Vetiver Root Powder

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Ligand‐Free Transition‐Metal‐Catalyzed Suzuki–Miyaura Cross‐Coupling: Advances in Homogeneous and Heterogeneous Catalysis (2016–2025)

inferred← citeshttps://doi.org/10.1002/tcr.202200099openalex-snapshot

Recent Advances in Synthesis of Multiply Arylated/Alkylated Pyridines

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Recent Advances in Homogeneous Catalysis with Platinum Group Pincer Complexes: Hydrogen‐Mediated Transformations and Cross‐Coupling Reactions

inferred← citeshttps://doi.org/10.1002/wcms.1590openalex-snapshot

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Recent advances on palladium incorporated clay-based heterogeneous catalyst for carbon–carbon coupling reactions

inferred← citeshttps://doi.org/10.1007/s00706-025-03396-4openalex-snapshot

Recent advances in the design and synthesis of coumarins and their derivatives via Suzuki–Miyaura reaction (2002–2024)

inferred← citeshttps://doi.org/10.1007/s10562-022-04160-7openalex-snapshot

Modified Boron Nitride Nanosheets-Loaded Palladium Nanoparticles: An Air-Stable, Highly Active, and Recyclable Multiphase Catalyst for the Suzuki Reaction

inferred← citeshttps://doi.org/10.1007/s10570-023-05323-4openalex-snapshot

Biomacromolecule supported N-heterocyclic carbene-palladium(II) as a novel catalyst for Suzuki–Miyaura and Mizoroki–Heck cross-coupling reactions

inferred← citeshttps://doi.org/10.1007/s10593-026-03453-8openalex-snapshot

Synthesis of arylpyridines by Pd(II) coordination polymer catalyzed C–C coupling

inferred← citeshttps://doi.org/10.1007/s10853-025-11993-1openalex-snapshot

Palladium on ionic liquid–phosphine-modified magnetic nanoparticles for aqueous Suzuki–Miyaura reaction at room temperature

inferred← citeshttps://doi.org/10.1007/s11144-024-02777-wopenalex-snapshot

N-heterocyclic carbene-palladium complex immobilized on Co-MOF 74 microrods as a highly selective catalyst for Suzuki–Miyaura cross-coupling

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Novel Pd(II) complex of Schiff base encapsulated on ferrite–titania core [Pd@SB/Fe3O4–TiO2]: a recyclable nanocatalyst for Suzuki coupling and hydrogenation of aromatic nitro compounds

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Design and synthesis of a new heterogeneous metal–organic framework-based nanocatalyst (Pd@TMU-17-NH2-Glu-Mla) with excellent performance toward Suzuki coupling reactions

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Catalytic Properties of the Palladium(II) Coordination Polymer in the Reaction of C–C Coupling of Aromatic Halides and Boronic Acids

inferred← citeshttps://doi.org/10.1007/s11696-024-03520-4openalex-snapshot

Palladium-catalyzed C(sp3)-C(sp2) coupling: synthesis of C(3)-arylphthalides

inferred← citeshttps://doi.org/10.1007/s13738-022-02583-yopenalex-snapshot

Synthesis, spectral characterization, and theoretical investigation of Ni(II) and Pd(II) complexes incorporating symmetrical tetradentate Schiff base ligand: Suzuki-Miyaura cross-coupling reaction using PdLSym

inferred← citeshttps://doi.org/10.1007/s42250-024-01098-8openalex-snapshot

Sustainable Suzuki–Miyaura Cross Coupling Reaction Using Ag–Pd Alloy Nano-Particle Photo-Catalyst

inferred← citeshttps://doi.org/10.1016/b978-0-443-18939-5.00017-2openalex-snapshot

Eight-membered and larger rings

inferred← citeshttps://doi.org/10.1016/b978-0-443-27482-4.00005-8openalex-snapshot

Advances in ultrasound-enhanced green organic synthesis utilizing nanoparticles as highly efficient catalysts

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Two-group disconnections: bifunctional compounds containing two carbon–carbon multiple bonds (dienes, diynes, and enynes)

inferred← citeshttps://doi.org/10.1016/bs.adioch.2024.05.007openalex-snapshot

Comparative analysis of palladium, nickel and copper phosphane/carbene catalysts in Suzuki–Miyaura couplings: Mechanistic insights and reactivity trends

inferred← citeshttps://doi.org/10.1016/j.apcata.2025.120279openalex-snapshot

Influence of Pd speciation and support interactions for Suzuki reactions

inferred← citeshttps://doi.org/10.1016/j.apcatb.2025.125952openalex-snapshot

Metal-organic framework-supported palladium(II) single-site as a solid catalyst for the hydroformylation and hydroxycarbonylation of styrene with formic acid

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Nanocatalytic and antimicrobial potency of CQD@Pd nanoparticles: Experimental and theoretical approach

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Synergistic effect of multi-active site (Pd/PdO/Ni/NiO/Ni2O3) formed in situ on the surface of graphene oxide supported bi-Schiff-base hetero-organometallic Pd(II)/Ni(II) nano-sheet

inferred← citeshttps://doi.org/10.1016/j.arabjc.2022.104410openalex-snapshot

Hierarchical TiO2 microspheres supported ultrasmall palladium Nanocrystals: A highly efficient catalyst for Suzuki reaction

inferred← citeshttps://doi.org/10.1016/j.catcom.2024.106856openalex-snapshot

The role of immobilization supports for light-assisted Suzuki coupling reaction with low-loading Pd nanocatalyst

inferred← citeshttps://doi.org/10.1016/j.cclet.2022.03.008openalex-snapshot

A general strategy for in situ assembly of light-up fluorophores via bioorthogonal Suzuki-Miyaura cross-coupling

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Platinum group metal (PGM) complexes having acylthiourea ligand system as catalysts or anticancer agents

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Greener media for nano catalysts in Suzuki Miyaura reaction

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On the use of chemical bonding descriptors in machine learning

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Synthesis of spiroindoline derivatives and biphenyl compounds in green solvent via a “capture–release” mechanism using modified polyacrylonitrile fiber as a catalyst

inferred← citeshttps://doi.org/10.1016/j.cej.2025.167562openalex-snapshot

Agar-based Pickering emulsion: A platform for enzymatic and chemoenzymatic synthesis

inferred← citeshttps://doi.org/10.1016/j.cjche.2025.02.004openalex-snapshot

Configured droplet reactor by Pd/g-C3N4 for the Suzuki-Miyaura cross-coupling reaction under water condition

inferred← citeshttps://doi.org/10.1016/j.cjnm.2025.100013openalex-snapshot

Generation of halogenated angucyclinones with cytotoxicity activities against human cancer cell lines based on biosynthesis and chemical conversion

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Self-pillared hierarchical Silicalite-1 zeolites for enhanced Suzuki-Miyaura coupling reactions

inferred← citeshttps://doi.org/10.1016/j.crgsc.2022.100301openalex-snapshot

Biogenic palladium nanostructures for Suzuki-Miyaura and Sonogashira cross-coupling reaction under mild reaction conditions

inferred← citeshttps://doi.org/10.1016/j.eurpolymj.2025.113951openalex-snapshot

Towards control in Suzuki-Miyaura CTCP – the synergy between water and RuPhos

inferred← citeshttps://doi.org/10.1016/j.heliyon.2023.e17608openalex-snapshot

Palladium complexes containing NNN pincer type ligands and their activities in Suzuki-Miyaura cross coupling reaction

inferred← citeshttps://doi.org/10.1016/j.heliyon.2026.e45172openalex-snapshot

From scope to strategy: Recent advances in Suzuki cross-coupling for efficient total synthesis and molecule editing

inferred← citeshttps://doi.org/10.1016/j.ica.2022.121127openalex-snapshot

Utilization of supercritical carbon dioxide as green solvent for the Suzuki-Miyaura reaction

inferred← citeshttps://doi.org/10.1016/j.ica.2024.122249openalex-snapshot

Recent developments in nickel catalyzed Suzuki-Miyaura C–C cross-coupling reaction

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Group 10 metal complexes of the 3,4-bis(dicyclohexylphosphino)thiophene (dcypt) ligand: Synthesis, characterization and catalysis

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Palladium-catalyzed suzuki miyaura coupling reaction in aqueous ethanol

inferred← citeshttps://doi.org/10.1016/j.ica.2025.122848openalex-snapshot

Pd(II)-Schiff base complexes containing hydroxyl group for Suzuki-Miyaura and Mizoroki-Heck cross-coupling reactions in aqueous system

inferred← citeshttps://doi.org/10.1016/j.inoche.2024.112761openalex-snapshot

Palladium(II) complexes of amino acid derived ONO-tridentate enamine ligand for Suzuki-Miyaura cross-coupling reaction

inferred← citeshttps://doi.org/10.1016/j.inoche.2025.114911openalex-snapshot

In-situ formation of nanoparticles from a sulfur-ligated palladacycle: Catalytic performance in Suzuki-Miyaura and Sonogashira reactions

inferred← citeshttps://doi.org/10.1016/j.inoche.2025.115083openalex-snapshot

Palladium(0) complex of 1-(1H-benzo[d]imidazol-2-yl)guanidine on SBA-15 as an effective, selective, green, and robust catalyst for the Suzuki-Miyaura coupling reaction

inferred← citeshttps://doi.org/10.1016/j.jcat.2024.115399openalex-snapshot

Feasible preparation of preferentially oriented (111) Pd nanocrystals supported on cyano-COFs for ultrahigh activity in C-C cross-couplings

inferred← citeshttps://doi.org/10.1016/j.jcat.2024.115825openalex-snapshot

Detailed mechanistic studies on PNN-palladium pincer complex catalyzed Suzuki-Miyaura cross-coupling reaction proceeding through a PdII/PdIII/PdIV catalytic cycle

inferred← citeshttps://doi.org/10.1016/j.jcat.2025.116446openalex-snapshot

Cross-coupling catalysts for inactive substrates from a three-dimensional virtual screening

inferred← citeshttps://doi.org/10.1016/j.jcat.2026.116981openalex-snapshot

Mechanistic insights into the three-component aminative Suzuki-Miyaura coupling reaction: reaction sequence and chemoselectivity control

inferred← citeshttps://doi.org/10.1016/j.jece.2026.125070openalex-snapshot

Comprehensive review on recovery of platinum group metals from spent homogeneous catalysts: From deactivation pathways to recycling strategies

inferred← citeshttps://doi.org/10.1016/j.jorganchem.2022.122541openalex-snapshot

Magnetically separable mixed metal oxide nanocomposite (Pd/MnFe2O4) for Suzuki cross-coupling in aqueous medium

inferred← citeshttps://doi.org/10.1016/j.jorganchem.2023.122983openalex-snapshot

Palladium-catalyzed chemoselective Suzuki–Miyaura cross-coupling reaction of poly(pseudo)halogenated arenes

inferred← citeshttps://doi.org/10.1016/j.jorganchem.2024.123103openalex-snapshot

Evaluation of hemilabile Pd(II) NNS and NNSe non-symmetric pincers in Suzuki–Miyaura cross-coupling: Unexpected selective nitrile hydration of 4-bromonitrobenzene in mild conditions

inferred← citeshttps://doi.org/10.1016/j.jorganchem.2024.123444openalex-snapshot

Recent advances on Pd schiff base catalysts in suzuki-miyaura cross-coupling reaction: A review

inferred← citeshttps://doi.org/10.1016/j.jorganchem.2025.123569openalex-snapshot

Recent advances in palladium-catalyzed Suzuki-Miyaura cross-coupling reactions: Exploration of catalytic systems, reaction parameters, and ligand influences: A review

inferred← citeshttps://doi.org/10.1016/j.jorganchem.2025.123790openalex-snapshot

Design and fabrication of chitosan functionalized magnetic composite anchored Ru nanoparticles as a sustainable organometallic nanocatalyst for Suzuki-Miyaura coupling

inferred← citeshttps://doi.org/10.1016/j.jorganchem.2025.123837openalex-snapshot

Synergistic tuning of the phase structure of alumina in supported palladium catalyst for enhanced Suzuki-Miyaura coupling reaction

inferred← citeshttps://doi.org/10.1016/j.jorganchem.2025.123863openalex-snapshot

Design and supported gold nanoparticles over the modified magnetic iron oxide nanoparticles as an effective nanocatalyst for Suzuki-Miyaura reactions

inferred← citeshttps://doi.org/10.1016/j.jorganchem.2025.123960openalex-snapshot

Fabrication and characterization of APTMS-TCT-GO-Piperazine-Pd nanoparticle as a heterogeneous and reusable catalyst for Suzuki-Miyaura cross-coupling reaction under thermal and microwave conditions

inferred← citeshttps://doi.org/10.1016/j.jorganchem.2026.124134openalex-snapshot

Palladium(II) complexes with pyrimidine NHC (C*^Npyr) ligands in the Suzuki-Miyaura cross coupling reaction

inferred← citeshttps://doi.org/10.1016/j.jpcs.2023.111843openalex-snapshot

Decoration of MnFe2O4@cys with Pd as a highly efficient nanocatalyst in C-C coupling reaction at ambient temperature

inferred← citeshttps://doi.org/10.1016/j.mcat.2022.112232openalex-snapshot

Photoaccelerated Suzuki–Miyaura and Sonogashira coupling reactions catalyzed by an Ir-Pd binuclear complex

inferred← citeshttps://doi.org/10.1016/j.mcat.2022.112699openalex-snapshot

Polydentate P, N-based ligands for palladium-catalyzed cross-coupling reactions

inferred← citeshttps://doi.org/10.1016/j.mcat.2023.113747openalex-snapshot

Synthesis of biphenyl via sustainable Suzuki-Miyaura coupling reaction using mesoporous MCF-supported tin-palladium nanoparticles

inferred← citeshttps://doi.org/10.1016/j.mcat.2024.113843openalex-snapshot

Investigation on the synergistic effect in multiple active centers (Pd/Ni/PdO/NiO/Ni2O3) in situ formed on the surface of the self-assembly β-ketoimide Pd(II)/Ni(II) film anchored on graphene oxide for Suzuki-Miyaura cross-coupling reaction

inferred← citeshttps://doi.org/10.1016/j.mcat.2024.114061openalex-snapshot

Microgel stabilized palladium nanostructures for catalytic applications

inferred← citeshttps://doi.org/10.1016/j.mcat.2024.114103openalex-snapshot

Exploring the energetics of Suzuki cross-coupling reaction: A computational study of palladium and nickel catalysts

inferred← citeshttps://doi.org/10.1016/j.mcat.2024.114486openalex-snapshot

Catalytic property and synergistic effect of the multi-active sites Pd/PdO/Er2O3/Cu2O/PdCu3 formed in situ on the surface of the tri-organometallic Pd(II)/Er(III)/Cu(II) film

inferred← citeshttps://doi.org/10.1016/j.molliq.2026.129420openalex-snapshot

Design and synthesis of Fe₃O₄@Chitosan-Ru(II) complex for efficient Suzuki-Miyaura cross-coupling: Optimization, and reusability in green organic transformations

inferred← citeshttps://doi.org/10.1016/j.molstruc.2022.133839openalex-snapshot

Spectral, crystallographic, theoretical, and catalytic activity studies of the PdII complexes in different coordination modes of benzoylthiourea ligand

inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.135948openalex-snapshot

Efficient synthesis of nicotinaldehyde-based crystalline organic derivatives: Comparative analysis between experimental and DFT study

inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.139744openalex-snapshot

Facile synthesis, SC-XRD, spectroscopic characterization & key electronic properties of nicotinaldehyde based scaffolds

inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.140462openalex-snapshot

NNN type pincer Pd (II) complexes of pyridine-2,6-dicarboxamides: Catalytic activity and supramolecular formation

inferred← citeshttps://doi.org/10.1016/j.molstruc.2026.145702openalex-snapshot

Design, synthesis and biological evaluation of novel substituted pyrazole-hydrazine hybrids as potent and safe anti-leukemia agents

inferred← citeshttps://doi.org/10.1016/j.poly.2021.115622openalex-snapshot

Pd(II) and Ni(II) complexes containing ONNO tetradentate Schiff base ligand: Synthesis, crystal structure, spectral characterization, theoretical studies, and use of PdL as an efficient homogeneous catalyst for Suzuki–Miyaura cross-coupling reaction

inferred← citeshttps://doi.org/10.1016/j.poly.2025.117799openalex-snapshot

Pd@CuMoO₄ as a synergistic polyoxometalate catalyst for the suzuki-miyaura and sonogashira-hagihara coupling reactions

inferred← citeshttps://doi.org/10.1016/j.solener.2026.114782openalex-snapshot

Photothermal Suzuki coupling over palladium decorated copper oxide Mie resonator nanostructures

inferred← citeshttps://doi.org/10.1016/j.supflu.2024.106500openalex-snapshot

Supercritical CO2-assisted preparation of catalytically-active Pd/Ni nanoparticle-embedded carbon from a metal-organic framework

inferred← citeshttps://doi.org/10.1016/j.tet.2023.133468openalex-snapshot

Synthesis of 2,5-difunctionalized pyridines via sequential chemoselective amination and Suzuki–Miyaura reactions

inferred← citeshttps://doi.org/10.1016/j.tet.2025.134540openalex-snapshot

Sulfonyl-stabilized 4-alkylidene dihydropyridines as C-donor ligands in organotransition metal catalysis: Synthesis of palladium complexes

inferred← citeshttps://doi.org/10.1016/j.tet.2025.134682openalex-snapshot

Base-free palladium-catalyzed borylation of enol carboxylates and further reactivity toward deboronation and cross-coupling

inferred← citeshttps://doi.org/10.1016/j.tet.2026.135222openalex-snapshot

Backbone ester-functionalized imidazole-2-ylidene metal complexes: Synthesis, structure, and potential catalytic applications for fine chemicals

inferred← citeshttps://doi.org/10.1016/j.tet.2026.135434openalex-snapshot

Nickel-catalyzed cross-electrophilic coupling of aryl alkyl tellurides with aryl bromides

inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.154010openalex-snapshot

Novel synthesis of an [18F]aryl boronic acid ester as a reagent for 18F-labeling via Suzuki coupling

inferred← citeshttps://doi.org/10.1021/acs.chemmater.6c01303openalex-snapshot

Tuning Nanostructure of Flame-Made Palladium Deposited on Cerium Oxide: Unveiling Palladium Loading–Activity Relationships in Suzuki–Miyaura Cross-Coupling

inferred← citeshttps://doi.org/10.1021/acs.iecr.6c03586openalex-snapshot

Phosphine-Based Vinyl-Covalent Organic Frameworks for Integrated Palladium Recovery and Heterogeneous Catalysis

inferred← citeshttps://doi.org/10.1021/acs.inorgchem.3c03855openalex-snapshot

Unveiling Pre-Transmetalation Intermediates in Base-Free Suzuki–Miyaura Cross-Couplings: A Computational Study

inferred← citeshttps://doi.org/10.1021/acs.inorgchem.5c01666openalex-snapshot

Mechanism of Gold-Catalyzed Arylation-Lactonization: A Density Functional Theory Study on the Role of the (MIC^N)AuCl Complex in Au(I)/Au(III) Catalysis

inferred← citeshttps://doi.org/10.1021/acs.inorgchem.6c03053openalex-snapshot

Rigid vs Spacer Ligand Design: Modulating Cooperativity in Pd-NHC Catalysis

inferred← citeshttps://doi.org/10.1021/acs.jcim.2c00334openalex-snapshot

Calculating and Optimizing Physicochemical Property Distributions of Large Combinatorial Fragment Spaces

inferred← citeshttps://doi.org/10.1021/acs.jmedchem.2c01689openalex-snapshot

Dual-Bioorthogonal Catalysis by a Palladium Peptide Complex

inferred← citeshttps://doi.org/10.1021/acs.jmedchem.5c01220openalex-snapshot

Solvent Sustainability in Drug Discovery: Where Are We Now, and How Can We Improve?

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.3c00394openalex-snapshot

Discovery and Synthesis of a Naturally Derived Protein Kinase Inhibitor that Selectively Inhibits Distinct Classes of Serine/Threonine Kinases

inferred← citeshttps://doi.org/10.1021/acs.joc.3c00912openalex-snapshot

Suzuki–Miyaura Cross-Coupling of Amides by N–C Cleavage Mediated by Air-Stable, Well-Defined [Pd(NHC)(sulfide)Cl2] Catalysts: Reaction Development, Scope, and Mechanism

inferred← citeshttps://doi.org/10.1021/acs.joc.4c00103openalex-snapshot

[(NHC)Pd(OAc)2]: Highly Active Carboxylate Pd(II)–NHC (NHC = N-Heterocyclic Carbene) Precatalysts for Suzuki–Miyaura and Buchwald–Hartwig Cross-Coupling of Amides by N–C(O) Activation

inferred← citeshttps://doi.org/10.1021/acs.joc.4c00357openalex-snapshot

Pd-Catalyzed Miyaura Borylation and Telescopic Borylation/Suzuki–Miyaura Cross-Coupling Processes in Deep-Eutectic Solvents

inferred← citeshttps://doi.org/10.1021/acs.joc.4c00966openalex-snapshot

Pd(0)/Xantphos-Catalyzed Benzylic C(sp 3 )–O Arylation of Benzyl Heteroaryl Ethers: Reduction of Pd(II) to Pd(0) by Xantphos

inferred← citeshttps://doi.org/10.1021/acs.joc.4c01411openalex-snapshot

Using Common Alcohols to Transform N–H NHC-Palladium Complexes into Reactive Catalysts for the Suzuki–Miyaura Reaction with Aryl Chlorides

inferred← citeshttps://doi.org/10.1021/acs.joc.4c01519openalex-snapshot

Precision Propargylic Substitution Reaction: Pd-Catalyzed Suzuki–Miyaura Coupling of Nonactivated Propargylamines with Boronic Acids

inferred← citeshttps://doi.org/10.1021/acs.joc.5c00109openalex-snapshot

Solventless Catalytic C–H and C–X Functionalization without Ball Milling

inferred← citeshttps://doi.org/10.1021/acs.joc.5c01010openalex-snapshot

Microwave-Assisted Palladium-Catalyzed Domino Reaction: Concise Access to 5 H -Dibenzo[ a , c ][7]annulenes and Dihydrodibenzocycloheptacoumarins

inferred← citeshttps://doi.org/10.1021/acs.joc.5c01886openalex-snapshot

A Three-Component Path to Amino Thiadiazoles and Amino Oxadiazoles via a Nitrilium Ylide

inferred← citeshttps://doi.org/10.1021/acs.joc.5c02305openalex-snapshot

Palladium-Catalyzed Denitrogenative Suzuki Coupling of Benzothiatriazine Dioxides for Bi(hetero)aryl-2-sulfonamides

inferred← citeshttps://doi.org/10.1021/acs.jpcb.1c10834openalex-snapshot

R–D–A and R–D−π–A Structured AIEgens: Relationship between Electronic, Conformational Characteristics and Photophysical Properties

inferred← citeshttps://doi.org/10.1021/acs.jpcb.5c06092openalex-snapshot

Analyzing the Solvent Effects in Palladium/ N -Heterocyclic Carbene (Pd/NHC)-Catalyzed Suzuki–Miyaura Coupling of Aryl Chlorides: A Computational Study of the Oxidative Addition Step with Experimental Validation

inferred← citeshttps://doi.org/10.1021/acs.oprd.4c00242openalex-snapshot

Synthesis of Lenacapavir Sodium: Active Pharmaceutical Ingredient Process Development and Scale-up

inferred← citeshttps://doi.org/10.1021/acs.oprd.5c00351openalex-snapshot

Swiping Right on Palladium: Matching Precursors, Ligands, and Reaction Conditions

inferred← citeshttps://doi.org/10.1021/acs.organomet.3c00367openalex-snapshot

Comparative Study of Pd-Mediated Carbon–Carbon, Carbon–Heteroatom, and Heteroatom–Heteroatom Bond Formation/Breakage (C ═ Csp3, Csp2, Csp; X = B, N, O, Si, P, S, Se, Te)

inferred← citeshttps://doi.org/10.1021/acs.organomet.3c00537openalex-snapshot

Activation Strategies for Alkyl Precursors in Achieving C(sp3)–C(sp3) Cross-Coupling via Metallaphotoredox Catalysis

inferred← citeshttps://doi.org/10.1021/acs.organomet.4c00138openalex-snapshot

Bis(benzimidazolin-2-ylidenes): Exploring the Impact of Ligand Properties in the Nickel-Catalyzed Suzuki–Miyaura Coupling

inferred← citeshttps://doi.org/10.1021/acs.organomet.4c00204openalex-snapshot

Groups 9 and 10 Complexes of C–Donor Ligands Derived from Pyridinium-Stabilized Phosphorus Ylides

inferred← citeshttps://doi.org/10.1021/acs.organomet.5c00239openalex-snapshot

Flash Communication: Probing Fe Complex Assembly via Thermogravimetric Analysis

inferred← citeshttps://doi.org/10.1021/acs.organomet.5c00277openalex-snapshot

Synthesis of Type B Tetrazolylidene–Palladium Complexes and Comparative Analysis with a Type A Analog

inferred← citeshttps://doi.org/10.1021/acs.organomet.5c00333openalex-snapshot

Dinuclear Pd II Bis-MIC/PCy 3 Pre-Catalyst for Cooperative Catalysis: Suzuki–Miyaura Coupling of Aryl Chlorides and α-Arylation of Cyclic Amide

inferred← citeshttps://doi.org/10.1021/acs.organomet.5c00339openalex-snapshot

Enhanced Catalytic Activities of Palladium Complexes with Nitron-Based N -Heterocyclic Carbene Ligands

inferred← citeshttps://doi.org/10.1021/acs.orglett.6c01449openalex-snapshot

Electrochemical Steady-State Regulation of Pd 0 Enables a Switchable Suzuki–Miyaura Coupling Reaction

inferred← citeshttps://doi.org/10.1021/acs.orglett.6c02773openalex-snapshot

Construction of meta -Aryl Acetophenone Derivatives via Pd-Catalyzed Arylation/Dehydrogenative Aromatization

inferred← citeshttps://doi.org/10.1021/acsaenm.5c00568openalex-snapshot

Synergistic Tridoped Graphitic Carbon Nitride: A Multifunctional Photocatalyst for Suzuki Coupling and NADPH Regeneration

inferred← citeshttps://doi.org/10.1021/acsami.2c23010openalex-snapshot

2D-Self-Assembled Organic Materials in Undoped Hole Transport Bilayers for Efficient Inverted Perovskite Solar Cells

inferred← citeshttps://doi.org/10.1021/acscatal.3c00252openalex-snapshot

Fully Aqueous and Air-Compatible Cross-Coupling of Primary Alkyl Halides with Aryl Boronic Species: A Possible and Facile Method

inferred← citeshttps://doi.org/10.1021/acscatal.4c02407openalex-snapshot

Halide Salts Alleviate TMSOK Inhibition in Suzuki–Miyaura Cross-Couplings

inferred← citeshttps://doi.org/10.1021/acscatal.4c02624openalex-snapshot

Pd-Methylnaphthyl-tBuBrettPhos Complexes as Efficient and Selective Catalysts for the Monoarylation of Ammonia and Hydrazine

inferred← citeshttps://doi.org/10.1021/acscatal.4c07646openalex-snapshot

Enantioselective Synthesis of Pillar[5]arenes by Dynamic Kinetic Resolution via Pd-Catalyzed Suzuki Cross-Coupling

inferred← citeshttps://doi.org/10.1021/acscatal.5c03074openalex-snapshot

Initiation of Palladium Precatalysts: Efficiency and Product Selectivity as a Function of Ligand, Substrate, and Reaction Conditions

inferred← citeshttps://doi.org/10.1021/acscatal.6c00650openalex-snapshot

Monitoring Pd-Catalyst Speciation in Biphasic Suzuki Reactions: Insights from Flow-NMR and Online HPLC-MS

inferred← citeshttps://doi.org/10.1021/acsomega.1c05770openalex-snapshot

trans-Dichlorobis(XPhos)palladium(II) Precatalyst for Suzuki–Miyaura Cross-Coupling Reactions of Aryl/Vinyl Sulfonates/Halides: Scope, Mechanistic Study, and Synthetic Applications

inferred← citeshttps://doi.org/10.1021/acsomega.2c03603openalex-snapshot

Palladium-Supported Polydopamine-Coated NiFe 2 O 4 @TiO 2 : A Sole Photocatalyst for Suzuki and Sonogashira Coupling Reactions under Sunlight Irradiation

inferred← citeshttps://doi.org/10.1021/acspolymersau.5c00121openalex-snapshot

Global Analysis of Polyfluorene via AB-Type Suzuki–Miyaura Polymerization: Empirical and Mechanistic Rationalization of Structural and Reaction Parameters on Molar Mass, Dispersity, and Yield

inferred← citeshttps://doi.org/10.1021/jacs.4c10776openalex-snapshot

Selective Ni-Catalyzed Cross-Electrophile Coupling of Heteroaryl Chlorides and Aryl Bromides at 1:1 Substrate Ratio

inferred← citeshttps://doi.org/10.1021/jacs.5c13155openalex-snapshot

Deciphering the Synchronization of Alternating Current Frequency with the Nickel Catalytic Cycle in Selective C–N Cross-Coupling

inferred← citeshttps://doi.org/10.1021/jacs.5c15506openalex-snapshot

Decoding the Nested, Multicycle Mechanism of Ni-Catalyzed Redox-Neutral Cross-Coupling through Temperature Scanning Reaction Calorimetry

inferred← citeshttps://doi.org/10.1021/jacsau.3c00283openalex-snapshot

Distinguishing Competing Mechanistic Manifolds for C(acyl)–N Functionalization by a Ni/ N -Heterocyclic Carbene Catalyst System

inferred← citeshttps://doi.org/10.1038/s41467-024-49681-4openalex-snapshot

Phase transfer catalysts shift the pathway to transmetalation in biphasic Suzuki-Miyaura cross-couplings

inferred← citeshttps://doi.org/10.1038/s41598-025-27005-wopenalex-snapshot

Application of statistical design of experiment to identify key factors in cross coupling reactions

inferred← citeshttps://doi.org/10.1039/9781837070725-00193openalex-snapshot

Synthesis and catalytic applications of palladium pincer complexes of organoselenium ligands

inferred← citeshttps://doi.org/10.1039/9781837677191-00425openalex-snapshot

Magnetic Nanocomposites as Catalysts in Organic Reactions

inferred← citeshttps://doi.org/10.1039/9781837677191-00530openalex-snapshot

Nanocomposites as Catalysts in Organic Name Reactions

inferred← citeshttps://doi.org/10.1039/d1sc05862bopenalex-snapshot

Solvent coordination to palladium can invert the selectivity of oxidative addition

inferred← citeshttps://doi.org/10.1039/d2cc04228bopenalex-snapshot

A predictive journey towards trans -thioamides/amides

inferred← citeshttps://doi.org/10.1039/d2cs00139jopenalex-snapshot

Group 16 conjugated polymers based on furan, thiophene, selenophene, and tellurophene

inferred← citeshttps://doi.org/10.1039/d2dt01355jopenalex-snapshot

Ni( i )–TPA stabilization by hydrogen bond formation on the second coordination sphere: a DFT characterization

inferred← citeshttps://doi.org/10.1039/d2dt04139aopenalex-snapshot

Steric and electronic effects of arsa-Buchwald ligands on Suzuki–Miyaura coupling reaction

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