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NiCl2(PCy3)2: A Simple and Efficient Catalyst Precursor for the Suzuki Cross-Coupling of Aryl Tosylates and Arylboronic Acids
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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/(sici)1521-3773(19981231)37:24<3387::aid-anie3387>3.0.co;2-popenalex-snapshot
A Convenient and General Method for Pd-Catalyzed Suzuki Cross-Couplings of Aryl Chlorides and Arylboronic Acids
inferredcites →https://doi.org/10.1016/s0022-328x(98)01055-9openalex-snapshot
Recent advances in the cross-coupling reactions of organoboron derivatives with organic electrophiles, 1995–1998
inferredcites →https://doi.org/10.1016/s0040-4039(97)00707-7openalex-snapshot
Suzuki-type coupling of chloroarenes with arylboronic acids catalysed by nickel complexes
inferredcites →https://doi.org/10.1021/ja0002058openalex-snapshot
Versatile Catalysts for the Suzuki Cross-Coupling of Arylboronic Acids with Aryl and Vinyl Halides and Triflates under Mild Conditions
inferredcites →https://doi.org/10.1021/ja992130hopenalex-snapshot
Highly Active Palladium Catalysts for Suzuki Coupling Reactions
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4847584openalex-extracted
Aryl/Hetero-Aryl Tosylates as Coupling Partners in Metal Mediated Suzuki and Hiyama Cross-Coupling Reactions in Ionic Liquids: Facile Synthesis of Biaryls/Heterobiaryls
inferred← citeshttps://doi.org/10.1002/047084289x.rd100.pub2openalex-snapshot
Dichlorobis(triphenylphosphine)nickel(II)
inferred← citeshttps://doi.org/10.1002/047084289x.rn00684.pub2openalex-snapshot
Tricyclohexylphosphine
inferred← citeshttps://doi.org/10.1002/047084289x.rn01201openalex-snapshot
Bis(tricyclohexylphosphine)dichloronickel
inferred← citeshttps://doi.org/10.1002/1521-3757(20020215)114:4<632::aid-ange632>3.0.co;2-mopenalex-snapshot
Eisenkatalysierte Kreuzkupplungen von Alkyl-Grignard-Verbindungen mit Arylchloriden, -tosylaten und -triflaten
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Iron-Catalyzed Cross-Coupling Reactions of Alkyl-Grignard Reagents with Aryl Chlorides, Tosylates, and Triflates
inferred← citeshttps://doi.org/10.1002/9780470503973.ch5openalex-snapshot
Preparation of Alkyls, Methylenes, and Aryls
inferred← citeshttps://doi.org/10.1002/9780471476665.ch5openalex-snapshot
Preparation of Alkyls, Methylenes and Aryls
inferred← citeshttps://doi.org/10.1002/9781118609811.ch3openalex-snapshot
Nanocatalysts for the Suzuki Coupling Reactions
inferred← citeshttps://doi.org/10.1002/9781118788981.ch5openalex-snapshot
Homogeneous Transition‐Metal‐Catalyzed C–O Bond Activation
inferred← citeshttps://doi.org/10.1002/9783527619405.ch2jopenalex-snapshot
Coupling of Aryl and Alkyl Halides with Organoboron Reagents (Suzuki Reaction)
inferred← citeshttps://doi.org/10.1002/9783527619467.ch10openalex-snapshot
Functional Organonickel Reagents
inferred← citeshttps://doi.org/10.1002/9783527619535.ch1openalex-snapshot
Mechanistic Aspects of Metal‐Catalyzed C,C‐ and C,X‐Bond‐Forming Reactions
inferred← citeshttps://doi.org/10.1002/9783527619986.ch3openalex-snapshot
Take the Right Catalyst: Palladium‐Catalyzed CC, CN and CO‐Bond Formation on Chloro‐Arenes
inferred← citeshttps://doi.org/10.1002/9783527620784.ch3dopenalex-snapshot
Take the Right Catalyst: Palladium‐Catalyzed CC, CN and CO‐Bond Formation on Chloro‐Arenes
inferred← citeshttps://doi.org/10.1002/9783527627325.ch2openalex-snapshot
Metal‐Catalyzed Coupling Reactions with Aryl Chlorides, Tosylates and Fluorides
inferred← citeshttps://doi.org/10.1002/9783527655588.ch1openalex-snapshot
Mechanistic Aspects of Metal‐Catalyzed C,C‐ and C,X‐Bond Forming Reactions
inferred← citeshttps://doi.org/10.1002/adsc.200303036openalex-snapshot
Suzuki–Miyaura Cross‐Coupling With Quasi‐Heterogeneous Palladium
inferred← citeshttps://doi.org/10.1002/adsc.200303045openalex-snapshot
Combinatorial Design of Copper‐Based Mixed Nanoclusters: New Catalysts for Suzuki Cross‐Coupling
inferred← citeshttps://doi.org/10.1002/adsc.200404187openalex-snapshot
Palladium‐Catalyzed Cross‐Coupling Reaction by Means of Organogermanium Trichlorides
inferred← citeshttps://doi.org/10.1002/adsc.200800414openalex-snapshot
Rhodium/N‐Heterocyclic Carbene‐Catalyzed Cross‐Couplings of Aryl Arenesulfonates with Arylboronic Acids
inferred← citeshttps://doi.org/10.1002/adsc.200800624openalex-snapshot
Iodine‐Catalyzed Suzuki–Miyaura Coupling Performed in Air
inferred← citeshttps://doi.org/10.1002/adsc.201000710openalex-snapshot
Highly Efficient Suzuki–Miyaura Coupling of Aryl Tosylates and Mesylates Catalyzed by Stable, Cost‐Effective [1,3‐Bis(diphenylphosphino)propane]nickel(II) Chloride [Ni(dppp)Cl2] with only 1 mol% Loading
inferred← citeshttps://doi.org/10.1002/adsc.201100101openalex-snapshot
A Highly Practical and Reliable Nickel Catalyst for Suzuki–Miyaura Coupling of Aryl Halides
inferred← citeshttps://doi.org/10.1002/adsc.201100141openalex-snapshot
A Mild Palladium‐Catalyzed Suzuki Coupling Reaction of Quinoline Carboxylates with Boronic Acids
inferred← citeshttps://doi.org/10.1002/adsc.201100151openalex-snapshot
Room Temperature Nickel(II) Complexes [(4‐MeOC6H4)Ni(PCy3)2OTs and Ni(PCy3)2X2]‐Catalyzed Cross‐Coupling Reactions of Aryl/Alkenyl Sulfonates with Arylboronic Acids
inferred← citeshttps://doi.org/10.1002/adsc.201600950openalex-snapshot
Synthesis of Trisubstituted Pyridines via Chemoselective Suzuki–Miyaura Coupling of 3,5‐ and 4,6‐Dibromo‐2‐tosyloxypyridines
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Palladium‐Catalyzed One‐Pot Synthesis of C2‐Quaternary Indolin‐3‐ones via 1H‐indole‐3‐sulfonates Generated in Situ from 2‐Alkynyl Arylazides and Sulfonic Acids
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Pd(0)/TPPMS‐Catalyzed Tsuji–Trost Type Cross‐Coupling of Allylic Alcohols with Organoboron Compounds in Water
inferred← citeshttps://doi.org/10.1002/ange.200803193openalex-snapshot
A General Palladium‐Catalyzed Suzuki–Miyaura Coupling of Aryl Mesylates
inferred← citeshttps://doi.org/10.1002/ange.200803814openalex-snapshot
Cross‐Coupling of Aryl/Alkenyl Pivalates with Organozinc Reagents through Nickel‐Catalyzed CO Bond Activation under Mild Reaction Conditions
inferred← citeshttps://doi.org/10.1002/ange.200900329openalex-snapshot
C(Aryl)‐O‐Aktivierung von Arylcarboxylaten in nickelkatalysierten Biarylsynthesen
inferred← citeshttps://doi.org/10.1002/ange.200904033openalex-snapshot
Palladium‐Catalyzed Cross‐Coupling of Aryl Halides Using Organotitanium Nucleophiles
inferred← citeshttps://doi.org/10.1002/ange.201101461openalex-snapshot
Mutual Activation: Suzuki–Miyaura Coupling through Direct Cleavage of the sp2 CO Bond of Naphtholate
inferred← citeshttps://doi.org/10.1002/ange.201103022openalex-snapshot
Praktische Eintopfsynthese von Magnesiumdi(hetero)aryl‐ und Magnesiumdialkenylboronaten für Suzuki‐Miyaura‐Kreuzkupplungen
inferred← citeshttps://doi.org/10.1002/ange.201810652openalex-snapshot
Nitromethane as a Carbanion Source for Domino Benzoannulation with Ynones: One‐Pot Synthesis of Polyfunctional Naphthalenes and a Total Synthesis of Macarpine
inferred← citeshttps://doi.org/10.1002/ange.2885584openalex-snapshot
Kinetic Analysis of Transmetalation at Prototypical Nickel (II) Catalyst Species: Rates, Mechanisms, and Implications for Catalysis
inferred← citeshttps://doi.org/10.1002/anie.200803193openalex-snapshot
A General Palladium‐Catalyzed Suzuki–Miyaura Coupling of Aryl Mesylates
inferred← citeshttps://doi.org/10.1002/anie.200803814openalex-snapshot
Cross‐Coupling of Aryl/Alkenyl Pivalates with Organozinc Reagents through Nickel‐Catalyzed CO Bond Activation under Mild Reaction Conditions
inferred← citeshttps://doi.org/10.1002/anie.200900329openalex-snapshot
C(aryl)O Activation of Aryl Carboxylates in Nickel‐Catalyzed Biaryl Syntheses
inferred← citeshttps://doi.org/10.1002/anie.200904033openalex-snapshot
Palladium‐Catalyzed Cross‐Coupling of Aryl Halides Using Organotitanium Nucleophiles
inferred← citeshttps://doi.org/10.1002/anie.201101461openalex-snapshot
Mutual Activation: Suzuki–Miyaura Coupling through Direct Cleavage of the sp2 CO Bond of Naphtholate
inferred← citeshttps://doi.org/10.1002/anie.201103022openalex-snapshot
Practical One‐Pot Preparation of Magnesium Di(hetero)aryl‐ and Magnesium Dialkenylboronates for Suzuki–Miyaura Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/anie.201810652openalex-snapshot
Nitromethane as a Carbanion Source for Domino Benzoannulation with Ynones: One‐Pot Synthesis of Polyfunctional Naphthalenes and a Total Synthesis of Macarpine
inferred← citeshttps://doi.org/10.1002/anie.2885584openalex-snapshot
Kinetic Analysis of Transmetalation at Prototypical Nickel (II) Catalyst Species: Rates, Mechanisms, and Implications for Catalysis
inferred← citeshttps://doi.org/10.1002/aoc.3000openalex-snapshot
Suzuki–Miyaura coupling reactions of aryl chlorides catalyzed by a new nickel(II) σ‐aryl complex
inferred← citeshttps://doi.org/10.1002/aoc.3289openalex-snapshot
Iron‐catalyzed cross‐coupling of heteroaromatic tosylates with alkyl and aryl Grignard reagents
inferred← citeshttps://doi.org/10.1002/aoc.5662openalex-snapshot
Air‐Stable Fe3O4@SiO2‐EDTA‐Ni(0) as an Efficient Recyclable Magnetic Nanocatalyst for Effective Suzuki‐Miyaura and Heck Cross‐Coupling via Aryl Sulfamates and Carbamates
inferred← citeshttps://doi.org/10.1002/aoc.5828openalex-snapshot
Immobilization of Au nanoparticles on poly(glycidyl methacrylate)‐functionalized magnetic nanoparticles for enhanced catalytic application in the reduction of nitroarenes and Suzuki reaction
inferred← citeshttps://doi.org/10.1002/aoc.6430openalex-snapshot
Advances in non‐palladium‐catalysed Stille couplings
inferred← citeshttps://doi.org/10.1002/cctc.201200417openalex-snapshot
Magnetic Fe–Ni Alloy Catalyzed Suzuki Cross‐Coupling Reactions of Aryl Halides with Phenylboronic Acid
inferred← citeshttps://doi.org/10.1002/cctc.201403057openalex-snapshot
Recent Applications of Magnetically Recoverable Nanocatalysts in CC and CX Coupling Reactions
inferred← citeshttps://doi.org/10.1002/ceur.202500213openalex-snapshot
Enabling Nickel‐Catalyzed Suzuki–Miyaura Cross‐Coupling of Carbamoyl Fluorides: Mechanism and Scope
inferred← citeshttps://doi.org/10.1002/chem.200600502openalex-snapshot
Nickel(II) Complexes of Bidentate N‐Heterocyclic Carbene/Phosphine Ligands: Efficient Catalysts for Suzuki Coupling of Aryl Chlorides
inferred← citeshttps://doi.org/10.1002/chem.200601142openalex-snapshot
9‐Fluorenylphosphines for the Pd‐Catalyzed Sonogashira, Suzuki, and Buchwald–Hartwig Coupling Reactions in Organic Solvents and Water
inferred← citeshttps://doi.org/10.1002/chem.200701418openalex-snapshot
Insights into Sonogashira Cross‐Coupling by High‐Throughput Kinetics and Descriptor Modeling
inferred← citeshttps://doi.org/10.1002/chem.200902132openalex-snapshot
Structure–Reactivity Relationships in Negishi Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/chem.201000420openalex-snapshot
Aryl Phosphoramides: Useful Electrophiles for Suzuki–Miyaura Coupling Catalyzed by a NiCl2/dppp System (dppp=1,3‐Bis(diphenylphosphino)propane)
inferred← citeshttps://doi.org/10.1002/chem.201002273openalex-snapshot
Activation of “Inert” Alkenyl/Aryl CO Bond and Its Application in Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/chem.201002354openalex-snapshot
Palladium‐Catalyzed Direct Arylation of Heteroarenes with Aryl Mesylates
inferred← citeshttps://doi.org/10.1002/chem.201003403openalex-snapshot
Nickel‐Catalyzed Cross‐Coupling of Phenols and Arylboronic Acids Through an In Situ Phenol Activation Mediated by PyBroP
inferred← citeshttps://doi.org/10.1002/chem.201103050openalex-snapshot
Biphenyl‐Based Diaminophosphine Oxides as Air‐Stable Preligands for the Nickel‐Catalyzed Kumada–Tamao–Corriu Coupling of Deactivated Aryl Chlorides, Fluorides, and Tosylates
inferred← citeshttps://doi.org/10.1002/chem.201503926openalex-snapshot
Direct Carboxylation of Aryl Tosylates by CO2 Catalyzed by In situ‐Generated Ni0
inferred← citeshttps://doi.org/10.1002/chem.201802635openalex-snapshot
N‐Boc‐Amides in Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/chem.202004132openalex-snapshot
Directing Group‐Promoted Inert C−O Bond Activation Using Versatile Boronic Acid as a Coupling Agent
inferred← citeshttps://doi.org/10.1002/chem.202402391openalex-snapshot
Mapping Electrophile Chemoselectivity in DalPhos/Nickel N‐Arylation Catalysis: The Unusual Influence of Remote Sterics
inferred← citeshttps://doi.org/10.1002/chin.200204125openalex-snapshot
ChemInform Abstract: NiCl2(PCy3)2: A Simple and Efficient Catalyst Precursor for the Suzuki Cross‐Coupling of Aryl Tosylates and Arylboronic Acids.
inferred← citeshttps://doi.org/10.1002/chin.200345079openalex-snapshot
Oxidative Addition of Aryl Tosylates to Palladium(0) and Coupling of Unactivated Aryl Tosylates at Room Temperature.
inferred← citeshttps://doi.org/10.1002/cplu.201402169openalex-snapshot
Poly(vinylpyridine)‐Grafted Silica Containing Palladium or Nickel Nanoparticles as Heterogeneous Catalysts for the Sonogashira Coupling Reaction
inferred← citeshttps://doi.org/10.1002/ejic.201601351openalex-snapshot
Catalytic Behaviour of Calixarenylphosphanes in Nickel‐Catalysed Suzuki–Miyaura Cross‐Coupling
inferred← citeshttps://doi.org/10.1002/ejic.201700057openalex-snapshot
Nickel(II) N‐Heterocyclic Carbene Complexes: Versatile Catalysts for C–C, C–S and C–N Coupling Reactions
inferred← citeshttps://doi.org/10.1002/ejoc.200500279openalex-snapshot
Solid‐Phase Synthesis of Biphenyls and Terphenyls by the Traceless Multifunctional Cleavage of Polymer‐Bound Arenesulfonates
inferred← citeshttps://doi.org/10.1002/ejoc.200600026openalex-snapshot
CuI/DABCO‐Catalyzed Cross‐Coupling Reactions of Aryl Halides with Arylboronic Acids
inferred← citeshttps://doi.org/10.1002/ejoc.200600469openalex-snapshot
RhCl(PPh3)3/DPPF: A Useful and Efficient Catalyst for Cross‐Coupling Reactions of Activated Alkenyl Tosylates with Arylboronic Acids
inferred← citeshttps://doi.org/10.1002/ejoc.200900067openalex-snapshot
N‐Heterocyclic Carbene Derived Nickel–Pincer Complexes: Efficient and Applicable Catalysts for Suzuki–Miyaura Coupling Reactions of Aryl/Alkenyl Tosylates and Mesylates
inferred← citeshttps://doi.org/10.1002/ejoc.201000147openalex-snapshot
NiII–(σ‐Aryl) Complex Catalyzed Suzuki Reaction of Aryl Tosylates with Arylboronic Acids
inferred← citeshttps://doi.org/10.1002/ejoc.201000251openalex-snapshot
Retraction: Suzuki–Miyaura Coupling of Aryl Tosylates and Mesylates in Water
inferred← citeshttps://doi.org/10.1002/ejoc.201001112openalex-snapshot
An Efficient Synthesis of Polysubstituted Naphthalene Derivatives by Gold‐Catalyzed Cyclization of 1‐Arylalka‐2,3‐dienyl Acetates
inferred← citeshttps://doi.org/10.1002/ejoc.201001519openalex-snapshot
Room‐Temperature Nickel‐Catalysed Suzuki–Miyaura Reactions of Aryl Sulfonates/Halides with Arylboronic Acids
inferred← citeshttps://doi.org/10.1002/ejoc.201200444openalex-snapshot
An Efficient Suzuki–Miyaura Coupling of Aryl Sulfamates and Boronic Acids Catalyzed by NiCl 2 (dppp)
inferred← citeshttps://doi.org/10.1002/ejoc.201200914openalex-snapshot
Recent Progress in Nickel‐Catalyzed Biaryl Coupling
inferred← citeshttps://doi.org/10.1002/ejoc.201300592openalex-snapshot
Palladium(II) Catalyzed Suzuki/Sonogashira Cross‐Coupling Reactions of Sulfonates: An Efficient Approach to C2‐Functionalized Pyrimidines and Pyridines
inferred← citeshttps://doi.org/10.1002/ejoc.201402919openalex-snapshot
Nickel‐Catalyzed Desulfitative Suzuki–Miyaura Cross‐Coupling of N,N‐Disulfonylmethylamines and Arylboronic Acids
inferred← citeshttps://doi.org/10.1002/ejoc.201500321openalex-snapshot
The Aza‐Achmatowicz Reaction: Facile Entry into Functionalized Piperidinones
inferred← citeshttps://doi.org/10.1002/ejoc.201500630openalex-snapshot
Nickel‐Catalyzed Decarbonylative Coupling of Aryl Esters and Arylboronic Acids
inferred← citeshttps://doi.org/10.1002/ejoc.202000417openalex-snapshot
Br vs. TsO Chemoselective Suzuki–Miyaura Cross‐Coupling Reaction on Nicotinaldehyde Moiety for the Preparation of 2,3,5‐Trisubstituted Pyridines
inferred← citeshttps://doi.org/10.1002/jhet.1712openalex-snapshot
An Innovative Protocol for the Synthesis of 3‐(Pyridin‐2‐yl)‐5‐sec‐aminobiphenyl‐4‐carbonitriles and 9,10‐Dihydro‐3‐(pyridine‐2‐yl)‐1‐sec‐aminophenanthrene‐2‐carbonitriles
inferred← citeshttps://doi.org/10.1002/marc.200350009openalex-snapshot
η3‐Benzyl‐Nickel‐Diimine Complex: Synthesis and Catalytic Properties in Ethylene Polymerization
inferred← citeshttps://doi.org/10.1002/mrc.3864openalex-snapshot
17O NMR studies of ortho‐substituent effects in substituted phenyl tosylates
inferred← citeshttps://doi.org/10.1002/slct.201803144openalex-snapshot
Ligand‐Free Cu‐Catalyzed Suzuki Coupling of Alkynyl Bromides with Boronic Acids in Ethanol Under Microwave Irradiation
inferred← citeshttps://doi.org/10.1002/slct.202403925openalex-snapshot
Aryl/Hetero‐Aryl Tosylates as Coupling Partners in Metal‐Mediated Suzuki and Hiyama Cross‐Coupling Reactions in Ionic Liquids: Ligand‐Free Facile Synthesis of Biaryls/Heterobiaryls
inferred← citeshttps://doi.org/10.1002/tcr.202100142openalex-snapshot
Synthetic Applications of Nickel‐Catalyzed Cross‐Coupling and Cyclisation Reactions
inferred← citeshttps://doi.org/10.1007/978-3-642-32368-3_2openalex-snapshot
Mechanisms and Fundamental Reactions
inferred← citeshttps://doi.org/10.1007/978-3-642-32368-3_7openalex-snapshot
Recent Advances in Cross-Coupling Reactions with Aryl Chlorides, Tosylates, and Mesylates
inferred← citeshttps://doi.org/10.1007/s10562-010-0385-1openalex-snapshot
Highly Efficient Pd-Catalyzed Cyanation of Aryl Chlorides and Arenesulfonates with Potassium Ferrocyanide in Aqueous Media
inferred← citeshttps://doi.org/10.1007/s10562-023-04513-wopenalex-snapshot
ZrO2 Supported Cu Nanoparticles for Sonogashira and Ullmann Coupling Reactions Under Palladium-Free Conditions
inferred← citeshttps://doi.org/10.1007/s10562-024-04815-7openalex-snapshot
Preparation and Application of WELAN to Pd(OAc)2-Catalyzed Suzuki–Miyaura Cross-Coupling Reaction
inferred← citeshttps://doi.org/10.1007/s11030-019-10001-4openalex-snapshot
Pd(NHC)(cinnamyl)Cl-catalyzed Suzuki cross-coupling reaction of aryl sulfonates with arylboronic acids
inferred← citeshttps://doi.org/10.1007/s11094-011-0605-zopenalex-snapshot
A new preparative method for the synthesis of 6-[3-(1-adamantyl)-4-methoxyphenyl]-2-naphthoic acid
inferred← citeshttps://doi.org/10.1007/s11144-009-0053-xopenalex-snapshot
Leaving group effect in the sulfonyl transfer reactions of aryl benzenesulfonates with Grignard reagents
inferred← citeshttps://doi.org/10.1007/s11172-007-0048-6openalex-snapshot
Trisodium heptaphosphide in reactions with alkyl and aryl tosylates
inferred← citeshttps://doi.org/10.1007/s11426-014-5138-3openalex-snapshot
Highly efficient nickel/phosphine catalyzed cross-couplings of diarylborinic acids with aryl tosylates and sulfamates
inferred← citeshttps://doi.org/10.1007/s12039-011-0092-5openalex-snapshot
Recyclable nickel catalysed Suzuki–Miyaura reaction in the presence of polyethyleneimine under phosphine-free conditions in ethylene glycol#
inferred← citeshttps://doi.org/10.1016/b0-08-043748-6/09089-7openalex-snapshot
Metal Complexes as Catalysts for CC Cross-coupling Reactions
inferred← citeshttps://doi.org/10.1016/b0-08-044655-8/00011-8openalex-snapshot
One or More CC Bond(s) Formed by Substitution or Addition
inferred← citeshttps://doi.org/10.1016/b0-08-045047-4/00143-6openalex-snapshot
C–C Bond Formation by Cross-coupling
inferred← citeshttps://doi.org/10.1016/b978-0-08-097774-4.00603-3openalex-snapshot
Cross-Coupling Reactions
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.03966-4openalex-snapshot
C–C Bond Formation by Cross-Coupling
inferred← citeshttps://doi.org/10.1016/b978-008044412-3/50006-3openalex-snapshot
The Suzuki-Miyaura reaction
inferred← citeshttps://doi.org/10.1016/bs.adomc.2024.04.002openalex-snapshot
A tale of two metals: The Mizoroki-Heck reaction as a guide to compare the chemical characters of nickel and palladium in catalysis
inferred← citeshttps://doi.org/10.1016/j.apcata.2012.09.048openalex-snapshot
Superb efficient and recycle polymer-anchored systems for palladium catalyzed Suzuki cross-coupling reactions in water
inferred← citeshttps://doi.org/10.1016/j.apcata.2014.05.020openalex-snapshot
Suzuki–Miyaura cross-coupling of aryl iodides and phenylboronic acid over palladium-free CeO2 catalysts
inferred← citeshttps://doi.org/10.1016/j.catcom.2009.09.024openalex-snapshot
Nickel(0) powder catalysis in Suzuki–Miyaura cross-coupling reaction
inferred← citeshttps://doi.org/10.1016/j.catcom.2014.08.010openalex-snapshot
Trans-chloro-(1-naphthyl)bis[tris-(4-methoxyphenyl)phosphane]-nickel(II) catalyzed Suzuki-Miyaura coupling of aryl chlorides with phenylboronic acid
inferred← citeshttps://doi.org/10.1016/j.ccr.2006.01.001openalex-snapshot
Metal complexes of chelating diarylamido phosphine ligands
inferred← citeshttps://doi.org/10.1016/j.inoche.2013.08.010openalex-snapshot
New dimeric phosphine ylide copper (I) complexes: Synthesis, coordination behavior, and application in Suzuki cross-coupling reactions
inferred← citeshttps://doi.org/10.1016/j.jcat.2012.11.020openalex-snapshot
Aerobic homocoupling of phenylboronic acid on Mg–Al mixed-oxides-supported Au nanoparticles
inferred← citeshttps://doi.org/10.1016/j.jcat.2017.04.034openalex-snapshot
Oriented Au nanoplatelets on graphene promote Suzuki-Miyaura coupling with higher efficiency and different reactivity pattern than supported palladium
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2009.09.044openalex-snapshot
Sulfonyl transfer mechanism in C–S coupling of phenylmagnesium bromide with phenyl arenesulfonates
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2011.01.003openalex-snapshot
Stoichiometric and catalytic C–Cl activation of Aryl Chlorides using an NHC-stabilized nickel(0) complex
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2015.12.032openalex-snapshot
Catalytic Suzuki couplings by an amido pincer complex of palladium
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2023.122954openalex-snapshot
CuNPs@Al2O3-cellulose composite for the ligand-free Suzuki cross-coupling reactions in batch and continuous flow process
inferred← citeshttps://doi.org/10.1016/j.mcat.2020.110845openalex-snapshot
A theoretical study of the influence of gold nanoplatelets sites in CC coupling reaction
inferred← citeshttps://doi.org/10.1016/j.molcata.2007.03.060openalex-snapshot
Layered double hydroxides supported rhodium(0): An efficient and reusable catalyst for Heck, Suzuki, and Stille reactions of haloarenes
inferred← citeshttps://doi.org/10.1016/j.molcata.2011.01.011openalex-snapshot
Palladium(0) nanoclusters stabilized by poly(4-styrenesulfonic acid-co-maleic acid) as an effective catalyst for Suzuki–Miyaura cross-coupling reactions in water
inferred← citeshttps://doi.org/10.1016/j.molcata.2014.10.031openalex-snapshot
Nickel(II) complex incorporating methylene bridged tetradentate dicarbene ligand as an efficient catalyst toward CC and CN bond formation reactions
inferred← citeshttps://doi.org/10.1016/j.molcata.2016.10.033openalex-snapshot
Suzuki-Miyaura coupling reactions using novel metal oxide supported ionic palladium catalysts
inferred← citeshttps://doi.org/10.1016/j.poly.2019.01.060openalex-snapshot
A green and cost-effective approach for the production of gold nanoparticles using corn silk extract: A recoverable catalyst for Suzuki–Miyaura reaction and adsorbent for removing of dye pollutants
inferred← citeshttps://doi.org/10.1016/j.tet.2004.03.072openalex-snapshot
Preparation of unsymmetrical terphenyls via the nickel-catalyzed cross-coupling of alkyl biphenylsulfonates with aryl Grignard reagents
inferred← citeshttps://doi.org/10.1016/j.tet.2007.10.091openalex-snapshot
Naphthidine di(radical cation)s-stabilized palladium nanoparticles for efficient catalytic Suzuki–Miyaura cross-coupling reactions
inferred← citeshttps://doi.org/10.1016/j.tet.2008.02.068openalex-snapshot
Highly efficient copper(0)-catalyzed Suzuki–Miyaura cross-coupling reactions in reusable PEG-400
inferred← citeshttps://doi.org/10.1016/j.tet.2011.03.066openalex-snapshot
Probing the electronic demands of transmetalation in the palladium-catalyzed cross-coupling of arylsilanolates
inferred← citeshttps://doi.org/10.1016/j.tet.2012.12.030openalex-snapshot
[Pd(PPh3)2(saccharinate)2]—general catalyst for Suzuki–Miyaura, Negishi cross-coupling and C–H bond functionalization of coumaryl and pyrone substrates
inferred← citeshttps://doi.org/10.1016/j.tet.2014.02.011openalex-snapshot
Calculated linear free energy relationships in the course of the Suzuki–Miyaura coupling reaction
inferred← citeshttps://doi.org/10.1016/j.tet.2014.04.059openalex-snapshot
A nickel precatalyst for efficient cross-coupling reactions of aryl tosylates with arylboronic acids: vital role of dppf
inferred← citeshttps://doi.org/10.1016/j.tet.2018.10.025openalex-snapshot
Ligation state of nickel during C O bond activation with monodentate phosphines
inferred← citeshttps://doi.org/10.1016/j.tet.2019.01.015openalex-snapshot
Practical and scalable preparation of Minodronic acid and Zolpidem from 2-chloroimidazole[1,2-a]pyridines
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.tetlet.2004.05.144openalex-snapshot
Iminophosphine–palladium(0) complexes as highly active catalysts in the Suzuki reaction. Synthesis of undecaaryl substituted corroles
inferred← citeshttps://doi.org/10.1016/j.tetlet.2004.09.020openalex-snapshot
Synthesis of diarylmethane derivatives from Pd-catalyzed cross-coupling reactions of benzylic halides with arylboronic acids
inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.10.018openalex-snapshot
A vicarious synthesis of unsymmetrical meta- and para- terphenyls from 2H-pyran-2-ones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.01.020openalex-snapshot
Palladium-catalyzed Suzuki–Miyaura couplings of potassium aryl trifluoroborates with 4-tosyloxycoumarins or 4-tosyloxyquinolin-2(1H)-one
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.01.145openalex-snapshot
Ferrocenylmethylphosphines as ligands for room temperature Ni(0)-catalyzed Suzuki–Miyaura cross-coupling reactions of aryl arenesulfonates and aryl chlorides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.07.085openalex-snapshot
Rh(I)-catalyzed cross-coupling reactions of alkenyl tosylates with potassium aryltrifluoroborates
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.08.085openalex-snapshot
Room temperature Ni-catalyzed reduction of aryl tosylates by borane hydrides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.01.175openalex-snapshot
Nickel(II)–aryl complexes as catalysts for the Suzuki cross-coupling reaction of chloroarenes and arylboronic acids
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.08.089openalex-snapshot
Ni-catalyzed cross-coupling reaction of aryl chlorides with arylboronic acids in IPA without using a reducing reagent
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.07.060openalex-snapshot
Palladium-free Suzuki–Miyaura cross-coupling at elevated pressures
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.10.096openalex-snapshot
An efficient route to 4-substituted coumarins, 2(5H)-furanones, and pyrones via palladium-catalyzed couplings of alkenyl tosylates with organoindium reagents
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.10.163openalex-snapshot
A new one-pot solvent-free synthesis of pyridinyl tosylates via diazotization of aminopyridines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.07.118openalex-snapshot
Cu(I) metal organic framework catalyzed C–C and C–N coupling reactions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.04.004openalex-snapshot
Copper-catalyzed site-selective S–S and C–C homocoupling of α-enolic dithioesters: straightforward and efficient access to 1,2-dithiols
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.10.009openalex-snapshot
Ni-catalyzed Suzuki–Miyaura coupling reactions of pyrimidin-2-yl phosphates, tosylates and pivalates with arylboronic acids
inferred← citeshttps://doi.org/10.1016/j.tetlet.2025.155723openalex-snapshot
[Ni(PnBu3)2Cl2] as an economical precatalyst for the Suzuki-Miyaura cross coupling reaction of aryl sulfonate esters and halides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2026.156149openalex-snapshot
Indium chloride catalysed annulation of arylmethyl carbonyls & arylalkynes for the synthesis of naphthalene derivatives
inferred← citeshttps://doi.org/10.1016/s0040-4020(02)01188-2openalex-snapshot
Recent applications of the Suzuki–Miyaura cross-coupling reaction in organic synthesis
inferred← citeshttps://doi.org/10.1016/s0040-4020(02)01351-0openalex-snapshot
Rapid analogue synthesis of C-5 substituted 1,2,3-triazolo[1,5-a]quinazolines
inferred← citeshttps://doi.org/10.1016/s0040-4039(02)00716-5openalex-snapshot
Suzuki cross-coupling of aryl halides with aryl boronic acids catalyzed by phosphine-free NiCl2·6H2O
inferred← citeshttps://doi.org/10.1016/s0040-4039(02)00718-9openalex-snapshot
Palladium-catalyzed cross-coupling reactions of 4-tosylcoumarin and arylboronic acids: synthesis of 4-arylcoumarin compounds
inferred← citeshttps://doi.org/10.1016/s0040-4039(02)00863-8openalex-snapshot
Platinum-catalyzed cross-couplings of organoboronic acids with aryl iodides
inferred← citeshttps://doi.org/10.1016/s1381-1169(03)00447-3openalex-snapshot
Novel palladium imidazole catalysts for Suzuki cross-coupling reactions
inferred← citeshttps://doi.org/10.1021/acs.joc.0c00793openalex-snapshot
Highly Selective Room-Temperature Suzuki–Miyaura Coupling of Bromo-2-sulfonyloxypyridines for Unsymmetrical Diarylpyridines
inferred← citeshttps://doi.org/10.1021/acs.joc.2c01964openalex-snapshot
Electrogenerated Nickel Catalyst for C–N Cross-Coupling
inferred← citeshttps://doi.org/10.1021/acs.joc.7b00081openalex-snapshot
Copper-Catalyzed Regioselective C-H Sulfonyloxylation of Electron-Rich Arenes with p-Toluenesulfonic Acid and Sulfonyloxylation of Aryl(mesityl)iodonium Sulfonates
inferred← citeshttps://doi.org/10.1021/acs.organomet.0c00485openalex-snapshot
Ni(4-tBustb)3: A Robust 16-Electron Ni(0) Olefin Complex for Catalysis
inferred← citeshttps://doi.org/10.1021/acs.organomet.5b00710openalex-snapshot
Aryl Ether Cleavage by Group 9 and 10 Transition Metals: Stoichiometric Studies of Selectivity and Mechanism
inferred← citeshttps://doi.org/10.1021/acs.organomet.6b00059openalex-snapshot
A Transmetalation Reaction Enables the Synthesis of [18F]5-Fluorouracil from [18F]Fluoride for Human PET Imaging
inferred← citeshttps://doi.org/10.1021/acs.organomet.7b00208openalex-snapshot
Oxidative Addition of Aryl Electrophiles to a Prototypical Nickel(0) Complex: Mechanism and Structure/Reactivity Relationships
inferred← citeshttps://doi.org/10.1021/acs.organomet.7b00446openalex-snapshot
Catalysis of Cross-Coupling and Homocoupling Reactions of Aryl Halides Utilizing Ni(0), Ni(I), and Ni(II) Precursors; Ni(0) Compounds as the Probable Catalytic Species but Ni(I) Compounds as Intermediates and Products
inferred← citeshttps://doi.org/10.1021/acs.organomet.8b00878openalex-snapshot
Nickel(II)- and Palladium(II)-NHC Complexes from Hydroxypyridine Functionalized C,O Chelate Type Ligands: Synthesis, Structure, and Catalytic Activity toward Kumada–Tamao–Corriu Reaction
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b00766openalex-snapshot
A Modular, Air-Stable Nickel Precatalyst
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02858openalex-snapshot
Transition-Metal-Catalyzed Transformation of Sulfonates via S–O Bond Cleavage: Synthesis of Alkyl Aryl Ether and Diaryl Ether
inferred← citeshttps://doi.org/10.1021/acscatal.0c03334openalex-snapshot
Activation of C–O and C–N Bonds Using Non-Precious-Metal Catalysis
inferred← citeshttps://doi.org/10.1021/acscatal.1c01201openalex-snapshot
The Emerging Applications of Sulfur(VI) Fluorides in Catalysis
inferred← citeshttps://doi.org/10.1021/acscatal.5b01021openalex-snapshot
Nickel- and Palladium-Catalyzed Coupling of Aryl Fluorosulfonates with Aryl Boronic Acids Enabled by Sulfuryl Fluoride
inferred← citeshttps://doi.org/10.1021/acscatal.8b00933openalex-snapshot
Taming Nickel-Catalyzed Suzuki-Miyaura Coupling: A Mechanistic Focus on Boron-to-Nickel Transmetalation
inferred← citeshttps://doi.org/10.1021/acscatal.9b00744openalex-snapshot
Nickel-Catalyzed Stille Cross Coupling of C–O Electrophiles
inferred← citeshttps://doi.org/10.1021/acsomega.7b01165openalex-snapshot
Palladium-Catalyzed Decarboxylative Coupling of Alkynyl Carboxylic Acids with Aryl Tosylates
inferred← citeshttps://doi.org/10.1021/ar100082dopenalex-snapshot
Exploration of New C−O Electrophiles in Cross-Coupling Reactions
inferred← citeshttps://doi.org/10.1021/cr1002276openalex-snapshot
Transmetalation of Unsaturated Carbon Nucleophiles from Boron-Containing Species to the Mid to Late d-Block Metals of Relevance to Catalytic C−X Coupling Reactions (X = C, F, N, O, Pb, S, Se, Te)
inferred← citeshttps://doi.org/10.1021/cr100259topenalex-snapshot
Nickel-Catalyzed Cross-Couplings Involving Carbon−Oxygen Bonds
inferred← citeshttps://doi.org/10.1021/cr100346gopenalex-snapshot
Large-Scale Applications of Transition Metal-Catalyzed Couplings for the Synthesis of Pharmaceuticals
inferred← citeshttps://doi.org/10.1021/ja027716+openalex-snapshot
Copper-Catalyzed Suzuki Cross-Coupling Using Mixed Nanocluster Catalysts
inferred← citeshttps://doi.org/10.1021/ja035835zopenalex-snapshot
Oxidative Addition of Aryl Tosylates to Palladium(0) and Coupling of Unactivated Aryl Tosylates at Room Temperature
inferred← citeshttps://doi.org/10.1021/ja038742qopenalex-snapshot
Ruthenium-Catalyzed Heck-Type Olefination and Suzuki Coupling Reactions: Studies on the Nature of Catalytic Species
inferred← citeshttps://doi.org/10.1021/ja070321bopenalex-snapshot
Studies on the Heck Reaction with Alkenyl Phosphates: Can the 1,2-Migration Be Controlled? Scope and Limitations
inferred← citeshttps://doi.org/10.1021/ja200398copenalex-snapshot
Suzuki−Miyaura Cross-Coupling of Aryl Carbamates and Sulfamates: Experimental and Computational Studies
inferred← citeshttps://doi.org/10.1021/ja207759eopenalex-snapshot
Nickel-Catalyzed Suzuki–Miyaura Reaction of Aryl Fluorides
inferred← citeshttps://doi.org/10.1021/ja300326topenalex-snapshot
Nickel-Mediated Hydrogenolysis of C–O Bonds of Aryl Ethers: What Is the Source of the Hydrogen?
inferred← citeshttps://doi.org/10.1021/ja804672mopenalex-snapshot
Palladium-Catalyzed Hiyama Cross-Couplings of Aryl Arenesulfonates with Arylsilanes
inferred← citeshttps://doi.org/10.1021/ja806244bopenalex-snapshot
Cross-Coupling Reactions of Aryl Pivalates with Boronic Acids
inferred← citeshttps://doi.org/10.1021/ja808935nopenalex-snapshot
Facile Synthesis of Highly Stable Gold Nanoparticles and Their Unexpected Excellent Catalytic Activity for Suzuki−Miyaura Cross-Coupling Reaction in Water
inferred← citeshttps://doi.org/10.1021/ja903091gopenalex-snapshot
Hydroxyphosphine Ligand for Nickel-Catalyzed Cross-Coupling through Nickel/Magnesium Bimetallic Cooperation
inferred← citeshttps://doi.org/10.1021/ja907700eopenalex-snapshot
N,N-DiethylO-Carbamate: Directed Metalation Group and Orthogonal Suzuki−Miyaura Cross-Coupling Partner
inferred← citeshttps://doi.org/10.1021/jacs.0c06995openalex-snapshot
Small Phosphine Ligands Enable Selective Oxidative Addition of Ar–O over Ar–Cl Bonds at Nickel(0)
inferred← citeshttps://doi.org/10.1021/jacs.1c08399openalex-snapshot
Stereoconvergent and -divergent Synthesis of Tetrasubstituted Alkenes by Nickel-Catalyzed Cross-Couplings
inferred← citeshttps://doi.org/10.1021/jacs.6b11412openalex-snapshot
Mechanistic Study of an Improved Ni Precatalyst for Suzuki–Miyaura Reactions of Aryl Sulfamates: Understanding the Role of Ni(I) Species
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