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Role of the Base and Control of Selectivity in the Suzuki–Miyaura Cross‐Coupling Reaction

https://doi.org/10.1002/cctc.201301080
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/9783527619535openalex-snapshot
Metal‐Catalyzed Cross‐Coupling Reactions
inferredcites →https://doi.org/10.1002/9783527639328openalex-snapshot
Boronic Acids
inferredcites →https://doi.org/10.1002/ange.200300638openalex-snapshot
Die Mechanismen der Stille‐Reaktion
inferredcites →https://doi.org/10.1002/ange.201101379openalex-snapshot
Kreuzkupplungen von Organoboranen: ein einfacher Weg zum Aufbau von C‐C‐Bindungen (Nobel‐Aufsatz)
inferredcites →https://doi.org/10.1002/ange.201301737openalex-snapshot
Transmetallierung in der Suzuki‐Miyaura‐Kupplung: Gabelung des Reaktionsverlaufs
inferredcites →https://doi.org/10.1002/anie.200300638openalex-snapshot
The Mechanisms of the Stille Reaction
inferredcites →https://doi.org/10.1002/anie.201101379openalex-snapshot
Cross‐Coupling Reactions Of Organoboranes: An Easy Way To Construct CC Bonds (Nobel Lecture)
inferredcites →https://doi.org/10.1002/anie.201301737openalex-snapshot
Transmetalation in the Suzuki–Miyaura Coupling: The Fork in the Trail
inferredcites →https://doi.org/10.1002/chem.201001911openalex-snapshot
Kinetic Data for the Transmetalation/Reductive Elimination in Palladium‐Catalyzed Suzuki–Miyaura Reactions: Unexpected Triple Role of Hydroxide Ions Used as Base
inferredcites →https://doi.org/10.1002/chem.201300177openalex-snapshot
Mechanism of Palladium‐Catalyzed Suzuki–Miyaura Reactions: Multiple and Antagonistic Roles of Anionic “Bases” and Their Countercations
inferredcites →https://doi.org/10.1007/3-540-45313-x_1openalex-snapshot
Introduction to Cross-Coupling Reactions
inferredcites →https://doi.org/10.1007/3-540-45313-x_2openalex-snapshot
Organoboron Compounds
inferredcites →https://doi.org/10.1007/978-1-4684-3393-7openalex-snapshot
Aspects of Mechanism and Organometallic Chemistry
inferredcites →https://doi.org/10.1016/j.jct.2007.08.008openalex-snapshot
Standard molar enthalpies of formation and of sublimation of the terphenyl isomers
inferredcites →https://doi.org/10.1016/j.tet.2004.08.051openalex-snapshot
The relationship among pKa, pH, and binding constants in the interactions between boronic acids and diols—it is not as simple as it appears
inferredcites →https://doi.org/10.1016/j.tet.2010.11.081openalex-snapshot
Exploring the selectivity of the Suzuki–Miyaura cross-coupling reaction in the synthesis of arylnaphthalenes
inferredcites →https://doi.org/10.1016/j.tetlet.2005.09.101openalex-snapshot
Deprotection of pinacolyl boronate esters via hydrolysis of intermediate potassium trifluoroborates
inferredcites →https://doi.org/10.1016/s0022-328x(00)82013-6openalex-snapshot
Mercury in organic chemistry
inferredcites →https://doi.org/10.1016/s0022-328x(02)01264-0openalex-snapshot
Cross-coupling reaction of organoboron compounds via base-assisted transmetalation to palladium(II) complexes
inferredcites →https://doi.org/10.1016/s0040-4039(01)95429-2openalex-snapshot
A new stereospecific cross-coupling by the palladium-catalyzed reaction of 1-alkenylboranes with 1-alkenyl or 1-alkynyl halides
inferredcites →https://doi.org/10.1021/cr00039a007openalex-snapshot
Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds
inferredcites →https://doi.org/10.1021/ja00094a083openalex-snapshot
Observation of Catalytic Intermediates in the Suzuki Reaction by Electrospray Mass Spectrometry
inferredcites →https://doi.org/10.1021/ja00290a037openalex-snapshot
Novel and convenient method for the stereo- and regiospecific synthesis of conjugated alkadienes and alkenynes via the palladium-catalyzed cross-coupling reaction of 1-alkenylboranes with bromoalkenes and bromoalkynes
inferredcites →https://doi.org/10.1021/ja01465a063openalex-snapshot
THE REACTION OF TRIETHYLBORANE WITH OXIDES OF SILVER, GOLD AND PLATINUM—A NEW CONVENIENT ROUTE TO NOBLE METAL ALKYLS AND TO FREE RADICAL CHEMISTRY
inferredcites →https://doi.org/10.1021/ja01465a064openalex-snapshot
THE REACTION OF TRIALKYLBORANES WITH ALKALINE SILVER NITRATE—A NEW GENERAL COUPLING REACTION
inferredcites →https://doi.org/10.1021/ja050583iopenalex-snapshot
Computational Characterization of the Role of the Base in the Suzuki−Miyaura Cross-Coupling Reaction
inferredcites →https://doi.org/10.1021/ja0569959openalex-snapshot
Mechanism of the Palladium-Catalyzed Homocoupling of Arylboronic Acids: Key Involvement of a Palladium Peroxo Complex
inferredcites →https://doi.org/10.1021/ja1108326openalex-snapshot
Distinguishing Between Pathways for Transmetalation in Suzuki−Miyaura Reactions
inferredcites →https://doi.org/10.1021/ja992130hopenalex-snapshot
Highly Active Palladium Catalysts for Suzuki Coupling Reactions
inferredcites →https://doi.org/10.1021/jo00096a056openalex-snapshot
Highly Efficient and Accelerated Suzuki Aryl Couplings Mediated by Phosphine-Free Palladium Sources
inferredcites →https://doi.org/10.1021/jo050105qopenalex-snapshot
Single and Double Suzuki−Miyaura Couplings with Symmetric Dihalobenzenes
inferredcites →https://doi.org/10.1021/jo050724zopenalex-snapshot
Phosphine-Free Palladium Acetate Catalyzed Suzuki Reaction in Water
inferredcites →https://doi.org/10.1021/jo060122vopenalex-snapshot
Synthesis of Biaryls and Polyaryls by Ligand-Free Suzuki Reaction in Aqueous Phase
inferredcites →https://doi.org/10.1021/jo971681sopenalex-snapshot
Alkylboranes in the Suzuki−Miyaura Coupling: Stereochemical and Mechanistic Studies
inferredcites →https://doi.org/10.1021/jp053658dopenalex-snapshot
Coordinate Covalent C → B Bonding in Phenylborates and Latent Formation of Phenyl Anions from Phenylboronic Acid
inferredcites →https://doi.org/10.1021/jp207593sopenalex-snapshot
Structural and Thermodynamic Characterization of Polyphenylbenzenes
inferredcites →https://doi.org/10.1021/om060206uopenalex-snapshot
Chemical Properties of Mononuclear and Dinuclear Phenylplatinum(II) Hydroxo Complexes with Cod Ligands. Transmetalation of Arylboronic Acids, Coupling of the Phenyl Ligands, and Carbonylation
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
inferredcites →https://doi.org/10.1039/b507375hopenalex-snapshot
Carbon–carbon bonding made easy
inferredcites →https://doi.org/10.1055/s-1992-21315openalex-snapshot
Synthesis of Sterically Hindered Biaryls via the Palladium-Catalyzed Cross-Coupling Reaction of Arylboronic Acids or their Esters with Haloarenes
inferredcites →https://doi.org/10.1063/1.1569242openalex-snapshot
Improved second-order Møller–Plesset perturbation theory by separate scaling of parallel- and antiparallel-spin pair correlation energies
inferredcites →https://doi.org/10.1080/00397918108063618openalex-snapshot
The Palladium-Catalyzed Cross-Coupling Reaction of Phenylboronic Acid with Haloarenes in the Presence of Bases
inferredcites →https://doi.org/10.1590/s0103-50532007000700021openalex-snapshot
Pd-catalyzed Suzuki cross-Coupling reaction of bromostilbene: insights on the nature of the boron Species
inferredcites →https://doi.org/10.5860/choice.43-3398openalex-snapshot
Modern physical organic chemistry

What points at this work

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

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A Study of Heterogeneous Catalysis by Nanoparticle‐Embedded Paper‐Spray Ionization Mass Spectrometry
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Room Temperature Anhydrous Suzuki–Miyaura Polymerization Enabled by C−S Bond Activation
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A Bio‐Inspired Magnetically Recoverable Palladium Nanocatalyst for the Ullmann Coupling reaction of Aryl halides and Arylboronic acids In Aqueous Media
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CeO2/Pd Nanoparticles Incorporated Fly Ash Zeolite: An Efficient and Recyclable Catalyst for Csp2‐Csp2Bond Formation Reactions
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Nickel‐Catalyzed Efficient, Regioselective One‐Pot Synthesis of 1‐Methyleneindenes via Tandem C–C Bond Formation: Computational Mechanistic Insights and Docking Studies
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The Transmetalation Process in Suzuki–Miyaura Reactions: Calculations Indicate Lower Barrier via Boronate Intermediate
inferred← citeshttps://doi.org/10.1002/cctc.202401825openalex-snapshot
Pd/CeO2 Single‐Atom Catalyst Forms Atypical C4 Product in a Suzuki Reaction with 2,4‐Dibromopyridine
inferred← citeshttps://doi.org/10.1002/chem.201800024openalex-snapshot
Mechanistic Exploration of the Transmetalation and Reductive Elimination Events Involving PdIV–Abnormal NHC Complexes in Suzuki–Miyaura Coupling Reactions: A DFT Study
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Mechanistic Aspects of the Palladium‐Catalyzed Suzuki‐Miyaura Cross‐Coupling Reaction
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Triple Regioselective Functionalization of Cationic [4]Helicenes via Iridium‐Catalyzed Borylation and Suzuki Cross‐Coupling Reactivity
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Reduced Tiara‐like Palladium Complex for Suzuki Cross‐Coupling Reactions
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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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Suzuki‐Miyaura Cross‐Couplings: Juxtaposing the Transmetalation of Arylboronic Acids and Alkylboranes
inferred← citeshttps://doi.org/10.1002/chem.202501539openalex-snapshot
One‐Pot Photoreactions: A Source for Metal‐Polymer Nanocomposites
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Reaction Optimization of a Suzuki‐Miyaura Cross‐Coupling Using Design of Experiments
inferred← citeshttps://doi.org/10.1002/ejic.202400068openalex-snapshot
Application of Biaryl Phosphacycles in Palladium‐Catalysed Suzuki‐Miyaura Cross‐Coupling Reactions of Aryl Chlorides
inferred← citeshttps://doi.org/10.1002/ejoc.201600095openalex-snapshot
Multicomponent Cascade Synthesis of Biaryl‐Based Chalcones in Pure Water and in an Aqueous Micellar Environment
inferred← citeshttps://doi.org/10.1002/ejoc.201701241openalex-snapshot
A Zwitterionic Palladium(II) Complex as a Precatalyst for Neat‐Water‐Mediated Cross‐Coupling Reactions of Heteroaryl, Benzyl, and Aryl Acid Chlorides with Organoboron Reagents
inferred← citeshttps://doi.org/10.1002/ejoc.201900410openalex-snapshot
Pseudo‐Solid‐State Suzuki–Miyaura Reaction and the Role of Water Formed by Dehydration of Arylboronic Acids
inferred← citeshttps://doi.org/10.1002/ijch.201900082openalex-snapshot
Solvent Effects on the Selectivity of Palladium‐Catalyzed Suzuki‐Miyaura Couplings
inferred← citeshttps://doi.org/10.1002/jccs.202000351openalex-snapshot
Importance of some factors on the Suzuki‐Miyaura cross‐coupling reaction
inferred← citeshttps://doi.org/10.1002/slct.202101394openalex-snapshot
One‐Pot Synthesis of Xanthone by Carbonylative Suzuki Coupling Reaction
inferred← citeshttps://doi.org/10.1002/slct.202202370openalex-snapshot
Experimental Selection of Bases for Colloidal Gold‐Polymer Composite Catalyst in Homocoupling Reactions
inferred← citeshttps://doi.org/10.1007/s10562-026-05386-5openalex-snapshot
Poly(vinylimidazole)-Grafted Graphene Oxide Supported Palladium as a Dual-Function Pickering Emulsion Catalyst for Aqueous Suzuki Coupling
inferred← citeshttps://doi.org/10.1007/s11172-024-4469-2openalex-snapshot
Synthesis of new aryl derivatives of isobornylphenols by the Suzuki reaction
inferred← citeshttps://doi.org/10.1007/s11243-014-9847-4openalex-snapshot
Efficient PdCl2-catalyzed Suzuki reactions using simple dicationic imidazolium salts as ligands in aqueous DMF
inferred← citeshttps://doi.org/10.1007/s11426-025-2636-1openalex-snapshot
Asymmetric Suzuki-Miyaura coupling for the catalytic enantioselective synthesis of planar chiral pillar[5]arenes
inferred← citeshttps://doi.org/10.1007/s12274-020-2885-7openalex-snapshot
Single-atom Pd catalyst anchored on Zr-based metal-organic polyhedra for Suzuki-Miyaura cross coupling reactions in aqueous media
inferred← citeshttps://doi.org/10.1007/s13738-019-01625-2openalex-snapshot
Isinglass–palladium as collagen peptide–metal complex: a highly efficient heterogeneous biocatalyst for Suzuki cross-coupling reaction in water
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/b978-0-12-819539-0.00006-3openalex-snapshot
Biomass-derived aqueous extracts as green solvents for organic transformations
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Density Functional Theory for Transition Metal Catalysis
inferred← citeshttps://doi.org/10.1016/j.catcom.2018.08.023openalex-snapshot
Oxygen-promoted Suzuki–Miyaura reaction of aryl fluorosulfates and potassium aryltrifluoroborates: Mild and efficient access to biaryls and terphenyls
inferred← citeshttps://doi.org/10.1016/j.cej.2024.153906openalex-snapshot
Synthesis of spiroindoline derivatives and biphenyl compounds in green solvent via a “capture–release” mechanism using modified polyacrylonitrile fiber as a catalyst
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Push button, automated flow synthesis of biaryls and stilbenes using palladium-catalysed cross-coupling reactions
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.colsurfa.2023.132304openalex-snapshot
Oyster shell powder-gold nanoparticle composites as a reactive, recyclable, and green catalyst
inferred← citeshttps://doi.org/10.1016/j.eurpolymj.2023.111867openalex-snapshot
Intramolecular catalyst transfer on N-acyl dithieno[3,2-b:2′,3′-d]pyrroles in nonstoichiometric Suzuki-Miyaura polycondensation toward high molecular weight conjugated copolymers at room temperature
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Towards control in Suzuki-Miyaura CTCP – the synergy between water and RuPhos
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Facile and economical Miyaura borylation and one-pot Suzuki–Miyaura cross-coupling reaction
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Utilization of supercritical carbon dioxide as green solvent for the Suzuki-Miyaura reaction
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La-Metal-Organic Framework incorporating Fe3O4 nanoparticles, post-synthetically modified with Schiff base and Pd. A highly active, magnetically recoverable, recyclable catalyst for C C cross-couplings at low Pd loadings
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A novel zinc-catalyzed Suzuki-type cross-coupling reaction of aryl boronic acids with alkynyl bromides
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[Pd(4-RSi-IPr)(allyl)Cl]/KCO/EtOH: A highly effective catalytic system for the Suzuki-Miyaura cross-coupling reaction
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Recent advances on Pd schiff base catalysts in suzuki-miyaura cross-coupling reaction: A review
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Enhancing catalytic activity of Pd/g-C3N4/CeO2 by heterojunctions and zirconium doping for Suzuki coupling reactions
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Assessment of a Pd–Fe3O4-biochar nanocomposite as a heterogeneous catalyst for the solvent-free Suzuki-Miyaura reaction
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Bimetallic Cu/Pd(ppm)-catalyzed Suzuki-Miyaura couplings: DFT studies on mechanism, roles of Pd(ppm) and ligands
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Nematic stability of 2,2′,4-trifluoro-4″-alkyl-[1,1′:4′,1″]terphenyls and its deuterated isotopologue
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[ZrFe2O4@SiO2–N–(TMSP)–ASP–Pd(0)] Complex: Synthesis, characterizations, and its application as a nanomagnetic catalyst in cross-coupling and click reactions
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Recent developments on carbon-carbon cross-coupling reactions using rare-earth metals-derived coordination polymers as efficient and selective Pd catalytic systems
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Sustainable nano fibrillated cellulose supported in situ biogenic Pd nanoparticles as heterogeneous catalyst for C–C cross coupling reactions
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Aqueous extracts of biomass ash as an alternative class of Green Solvents for organic transformations: A review update
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Palladium catalysed sequential imine arylation/Suzuki–Miyaura coupling: synthesis of α-(biarylyl)benzylamines
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Simple and efficient microwave-assisted synthesis of new N-biphenyl cinnamamides/3-arylpropanamides and C6-substituted phenanthridines
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Synthesis and Functionalization of Challenging meso-Substituted Aryl Bis-pocket Porphyrins Accessed via Suzuki–Miyaura Cross-Coupling
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Synthesis and Evaluation of Diguanosine Cap Analogs Modified at the C8-Position by Suzuki–Miyaura Cross-Coupling: Discovery of 7-Methylguanosine-Based Molecular Rotors
inferred← citeshttps://doi.org/10.1021/acs.joc.5b00793openalex-snapshot
Ohmic Heating-Assisted Synthesis of 3-Arylquinolin-4(1H)-ones by a Reusable and Ligand-Free Suzuki–Miyaura Reaction in Water
inferred← citeshttps://doi.org/10.1021/acs.joc.5b00981openalex-snapshot
Organotrifluoroborates: Another Branch of the Mighty Oak
inferred← citeshttps://doi.org/10.1021/acs.joc.5b02255openalex-snapshot
Palladium-Catalyzed Double-Suzuki–Miyaura Reactions Using Cyclic Dibenziodoniums: Synthesis of o -Tetraaryls
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Rh(I)-Catalyzed 1,4-Conjugate Addition of Alkenylboronic Acids to a Cyclopentenone Useful for the Synthesis of Prostaglandins
inferred← citeshttps://doi.org/10.1021/acs.oprd.9b00255openalex-snapshot
Overcoming Halide Inhibition of Suzuki–Miyaura Couplings with Biaryl Monophosphine-Based Catalysts
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Nuances in Fundamental Suzuki–Miyaura Cross-Couplings Employing [Pd(PPh3)4]: Poor Reactivity of Aryl Iodides at Lower Temperatures
inferred← citeshttps://doi.org/10.1021/acs.organomet.8b00705openalex-snapshot
Real-Time Mass Spectrometric Investigations into the Mechanism of the Suzuki–Miyaura Reaction
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02250openalex-snapshot
Decarbonylative Suzuki–Miyaura Cross-Coupling of Aroyl Chlorides
inferred← citeshttps://doi.org/10.1021/acsanm.2c04378openalex-snapshot
Micelle-Derived Palladium Nanoparticles for Suzuki–Miyaura Coupling Reactions in Water at Room Temperature
inferred← citeshttps://doi.org/10.1021/acscatal.4c05053openalex-snapshot
Suzuki–Miyaura Cross-Couplings of Alkylboranes: Transmetalation Studies and Synthesis of Model Organopalladium Pretransmetalation Species
inferred← citeshttps://doi.org/10.1021/acscatal.6b03490openalex-snapshot
Mechanism of a Suzuki-Type Homocoupling Reaction Catalyzed by Palladium Nanocubes
inferred← citeshttps://doi.org/10.1021/acscatal.6c01768openalex-snapshot
Nonthermal Charge Carriers Control Selectivity in Plasmon-Induced Suzuki–Miyaura Cross-Coupling Reaction on Spiked Au/Pd Nanowires
inferred← citeshttps://doi.org/10.1021/acsmacrolett.7b00696openalex-snapshot
Impact of Precatalyst Activation on Suzuki-Miyaura Catalyst-Transfer Polymerizations: New Mechanistic Scenarios for Pre-transmetalation Events
inferred← citeshttps://doi.org/10.1021/acsomega.0c03415openalex-snapshot
Ligand Steric Effects of α-Diimine Nickel(II) and Palladium(II) Complexes in the Suzuki–Miyaura Cross-Coupling Reaction
inferred← citeshttps://doi.org/10.1021/acssuschemeng.0c08315openalex-snapshot
Pd Nanoparticles-Loaded Honeycomb-Structured Bio-nanocellulose as a Heterogeneous Catalyst for Heteroaryl Cross-Coupling Reaction
inferred← citeshttps://doi.org/10.1021/jacs.1c08283openalex-snapshot
Potassium Trimethylsilanolate-Promoted, Anhydrous Suzuki–Miyaura Cross-Coupling Reaction Proceeds via the “Boronate Mechanism”: Evidence for the Alternative Fork in the Trail
inferred← citeshttps://doi.org/10.1021/jacs.7b04279openalex-snapshot
Combined Theoretical and Experimental Studies of Nickel-Catalyzed Cross-Coupling of Methoxyarenes with Arylboronic Esters via C–O Bond Cleavage
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/10.1039/c5ra10744jopenalex-snapshot
A novel route for the synthesis of alkanes from glycerol in a two step process using a Pd/SBA-15 catalyst
inferred← citeshttps://doi.org/10.1039/c7nj03567eopenalex-snapshot
Pd-Catalyzed Suzuki coupling reactions of aryl halides containing basic nitrogen centers with arylboronic acids in water in the absence of added base
inferred← citeshttps://doi.org/10.1039/c8qo01100aopenalex-snapshot
Synergistic effect of the Pd–Ni bimetal/carbon nanofiber composite catalyst in Suzuki coupling reaction
inferred← citeshttps://doi.org/10.1039/c9gc00617fopenalex-snapshot
Solvent effects in palladium catalysed cross-coupling reactions
inferred← citeshttps://doi.org/10.1039/c9ra04511bopenalex-snapshot
Palladium decorated on a new dendritic complex with nitrogen ligation grafted to graphene oxide: fabrication, characterization, and catalytic application
inferred← citeshttps://doi.org/10.1039/d0dt00770fopenalex-snapshot
Striking dual functionality of a novel Pd@Eu-MOF nanocatalyst in C(sp 2 )–C(sp 2 ) bond-forming and CO 2 fixation reactions
inferred← citeshttps://doi.org/10.1039/d0nj03651jopenalex-snapshot
Monolith catalyst design via 3D printing: a reusable support for modern palladium-catalyzed cross-coupling reactions
inferred← citeshttps://doi.org/10.1039/d1ra07231eopenalex-snapshot
C(acyl)–C(sp 2 ) and C(sp 2 )–C(sp 2 ) Suzuki–Miyaura cross-coupling reactions using nitrile-functionalized NHC palladium complexes
inferred← citeshttps://doi.org/10.1039/d2ob00371fopenalex-snapshot
A detailed theoretical investigation to unravel the molecular mechanism of the ligand-free copper-catalyzed Suzuki cross-coupling reaction
inferred← citeshttps://doi.org/10.1039/d3an01266bopenalex-snapshot
A photoluminescent and electrochemiluminescent probe based on an iridium( iii ) complex with a boronic acid-functionalised ancillary ligand for the selective detection of mercury( ii ) ions
inferred← citeshttps://doi.org/10.1039/d3en00123gopenalex-snapshot
SERS-based detection of an organochlorine pesticide through surface plasmon-induced C–C coupling
inferred← citeshttps://doi.org/10.1039/d4nj05058dopenalex-snapshot
Ionic liquid-mediated Pd-free biaryl synthesis catalysed by in situ generated nickel nanoparticles
inferred← citeshttps://doi.org/10.1039/d5qo00230copenalex-snapshot
Direct Suzuki–Miyaura cross-coupling of C(sp 2 )–B(dan) bonds: designed in pursuit of usability
inferred← citeshttps://doi.org/10.1039/d6mr00081aopenalex-snapshot
β-Citronellol as a sustainable additive for mechanochemical Suzuki–Miyaura cross-coupling reactions
inferred← citeshttps://doi.org/10.1080/10426507.2025.2605091openalex-snapshot
Optimized synthesis of novel C2-substituted benzo[b]thiophene derivatives via Suzuki–Miyaura cross-coupling and investigation of their biological activities
inferred← citeshttps://doi.org/10.1134/s0023158416030095openalex-snapshot
Role of the base and endogenous anions in “ligand-free” catalytic systems for the Suzuki–Miyaura reaction
inferred← citeshttps://doi.org/10.11606/t.46.2023.tde-22112023-152907openalex-snapshot
Investigação da atividade catalítica de nanocatalisadores plasmônicos bifuncionais via monitoramento SERS >i /i<
inferred← citeshttps://doi.org/10.17586/2226-1494-2020-20-6-863-870openalex-snapshot
Prediction of reaction conditions by deep learning techniques
inferred← citeshttps://doi.org/10.2174/138527282613221027161544openalex-snapshot
Current Opinion on Base Influenced Organic Transformations
inferred← citeshttps://doi.org/10.2174/1570193x16666190617160339openalex-snapshot
An Overview of Solid Supported Palladium and Nickel Catalysts for C-C Cross Coupling Reactions
inferred← citeshttps://doi.org/10.2174/2211544711666220629110020openalex-snapshot
Recent Advances in Palladium-catalyzed Borylation
inferred← citeshttps://doi.org/10.3384/9789179291341openalex-snapshot
Synthetic Functionalities for Ion and Electron Conductive Polymers : Applications in Organic Electronics and Biological Interfaces
inferred← citeshttps://doi.org/10.3390/catal11050582openalex-snapshot
Hollow-Shell-Structured Mesoporous Silica-Supported Palladium Catalyst for an Efficient Suzuki-Miyaura Cross-Coupling Reaction
inferred← citeshttps://doi.org/10.3390/catal12080828openalex-snapshot
A Facile One-Pot Synthesis of New Poly Functionalized Pyrrolotriazoles via a Regioselective Multicomponent Cyclisation and Suzuki–Miyaura Coupling Reactions
inferred← citeshttps://doi.org/10.3390/catal13060928openalex-snapshot
Highlights on the General Preference for Multi-Over Mono-Coupling in the Suzuki–Miyaura Reaction
inferred← citeshttps://doi.org/10.3390/inorganics11080326openalex-snapshot
PEPPSI-Type Pd(II)—NHC Complexes on the Base of p-tert-Butylthiacalix[4]arene: Synthesis and Catalytic Activities
inferred← citeshttps://doi.org/10.3390/knowledge3010001openalex-snapshot
Catalyst Recycling in the Suzuki Coupling Reaction: Toward a Greener Synthesis in the Pharmaceutical Industry
inferred← citeshttps://doi.org/10.3390/molecules23102435openalex-snapshot
Efficient Suzuki–Miyaura C-C Cross-Couplings Induced by Novel Heterodinuclear Pd-bpydc-Ln Scaffolds
inferred← citeshttps://doi.org/10.3390/molecules28207208openalex-snapshot
Synthesis and Antiproliferative Activity of 2,6-Disubstituted Imidazo[4,5-b]pyridines Prepared by Suzuki Cross Coupling
inferred← citeshttps://doi.org/10.3390/pr8121653openalex-snapshot
Study of Deactivation in Suzuki Reaction of Polymer-Stabilized Pd Nanocatalysts
inferred← citeshttps://doi.org/10.3762/bjoc.15.258openalex-snapshot
Acid-catalyzed rearrangements in arenes: interconversions in the quaterphenyl series
inferred← citeshttps://doi.org/10.69997/sct.101097openalex-snapshot
Foundation Model-Guided Optimization of Chemical Reaction Spaces for Autonomous Experimentation
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