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Acetate Facilitated Nickel Catalyzed Coupling of Aryl Chlorides and Alkyl Thiols

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

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The First Phosphine Oxide Ligand Precursors for Transition Metal Catalyzed Cross-Coupling Reactions: C−C, C−N, and C−S Bond Formation on Unactivated Aryl Chlorides
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Preparation of Arylphosphonates by Palladium(0)‐Catalyzed Cross‐Coupling in the Presence of Acetate Additives: Synthetic and Mechanistic Studies
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Well‐Defined Allylnickel Chloride/N‐Heterocyclic Carbene [(NHC)Ni(allyl)Cl] Complexes as Highly Active Precatalysts for CN and CS Cross‐Coupling Reactions
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Palladium‐Catalyzed Selective Dehydrogenative Cross‐Couplings of Heteroarenes
inferredcites →https://doi.org/10.1002/anie.201806036openalex-snapshot
Site‐Selective C−S Bond Formation at C−Br over C−OTf and C−Cl Enabled by an Air‐Stable, Easily Recoverable, and Recyclable Palladium(I) Catalyst
inferredcites →https://doi.org/10.1002/anie.201808386openalex-snapshot
Modular Functionalization of Arenes in a Triply Selective Sequence: Rapid C(sp2) and C(sp3) Coupling of C−Br, C−OTf, and C−Cl Bonds Enabled by a Single Palladium(I) Dimer
inferredcites →https://doi.org/10.1002/anie.201900956openalex-snapshot
Nickel‐Catalyzed Thiolation of Aryl Halides and Heteroaryl Halides through Electrochemistry
inferredcites →https://doi.org/10.1002/anie.201910436openalex-snapshot
Nickel‐Catalyzed Inter‐ and Intramolecular Aryl Thioether Metathesis by Reversible Arylation
inferredcites →https://doi.org/10.1002/anie.202013017openalex-snapshot
Safe, Scalable, Inexpensive, and Mild Nickel‐Catalyzed Migita‐Like C−S Cross‐Couplings in Recyclable Water
inferredcites →https://doi.org/10.1002/chem.201801887openalex-snapshot
Nickel‐Catalyzed Coupling of Arylzinc Halides with Thioesters
inferredcites →https://doi.org/10.1002/chem.202004437openalex-snapshot
Chemodivergence between Electrophiles in Cross‐Coupling Reactions
inferredcites →https://doi.org/10.1002/chem.202101906openalex-snapshot
Ni(II) Precatalysts Enable Thioetherification of (Hetero)Aryl Halides and Tosylates and Tandem C−S/C−N Couplings
inferredcites →https://doi.org/10.1002/ejoc.201402022openalex-snapshot
Efficient C–N and C–S Bond Formation Using the Highly Active [Ni(allyl)Cl(IPr* OMe )] Precatalyst
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Properties, environmental stability, and molding characteristics of polyphenylene sulfide
inferredcites →https://doi.org/10.1002/wcms.1327openalex-snapshot
Software update: the ORCA program system, version 4.0
inferredcites →https://doi.org/10.1007/s41061-018-0184-5openalex-snapshot
Analysis of US FDA-Approved Drugs Containing Sulfur Atoms
inferredcites →https://doi.org/10.1016/j.catcom.2017.02.007openalex-snapshot
C-S cross-coupling of aryl halides with alkyl thiols catalyzed by in-situ generated nickel(II) N-heterocyclic carbene complexes
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C S cross-coupling catalyzed by a series of easily accessible, well defined Ni(II) complexes of the type [(NHC)Ni(Cp)(Br)]
inferredcites →https://doi.org/10.1016/j.tet.2004.05.044openalex-snapshot
A general and efficient method for the palladium-catalyzed cross-coupling of thiols and secondary phosphines
inferredcites →https://doi.org/10.1016/j.tetlet.2012.08.055openalex-snapshot
Efficient nickel/N-heterocyclic carbene catalyzed C–S cross-coupling
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Mechanisms of Nickel-Catalyzed Cross-Coupling Reactions
inferredcites →https://doi.org/10.1021/acs.organomet.0c00732openalex-snapshot
Mono- and Dinuclear α-Diimine Nickel(II) and Palladium(II) Complexes in C–S Cross-Coupling
inferredcites →https://doi.org/10.1021/acs.organomet.7b00208openalex-snapshot
Oxidative Addition of Aryl Electrophiles to a Prototypical Nickel(0) Complex: Mechanism and Structure/Reactivity Relationships
inferredcites →https://doi.org/10.1021/acs.organomet.8b00438openalex-snapshot
Comprehensive Study of the Reactions Between Chelating Phosphines and Ni(cod)2
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Dual Nickel-/Palladium-Catalyzed Reductive Cross-Coupling Reactions between Two Phenol Derivatives
inferredcites →https://doi.org/10.1021/acs.orglett.6b00208openalex-snapshot
Thioetherification via Photoredox/Nickel Dual Catalysis
inferredcites →https://doi.org/10.1021/acs.orglett.7b03560openalex-snapshot
Nickel Phosphite/Phosphine-Catalyzed C–S Cross-Coupling of Aryl Chlorides and Thiols
inferredcites →https://doi.org/10.1021/acs.orglett.8b03476openalex-snapshot
Cross-Coupling of Chloro(hetero)arenes with Thiolates Employing a Ni(0)-Precatalyst
inferredcites →https://doi.org/10.1021/acs.orglett.9b01957openalex-snapshot
Semiheterogeneous Dual Nickel/Photocatalytic (Thio)etherification Using Carbon Nitrides
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Unexpected Nickel Complex Speciation Unlocks Alternative Pathways for the Reactions of Alkyl Halides with dppf-Nickel(0)
inferredcites →https://doi.org/10.1021/acscatal.1c03010openalex-snapshot
CgPhen-DalPhos Enables the Nickel-Catalyzed O-Arylation of Tertiary Alcohols with (Hetero)Aryl Electrophiles
inferredcites →https://doi.org/10.1021/acscatal.5b00072openalex-snapshot
Nickel: The “Spirited Horse” of Transition Metal Catalysis
inferredcites →https://doi.org/10.1021/acscatal.6b03344openalex-snapshot
When Weaker Can Be Tougher: The Role of Oxidation State (I) in P- vs N-Ligand-Derived Ni-Catalyzed Trifluoromethylthiolation of Aryl Halides
inferredcites →https://doi.org/10.1021/acscatal.9b03715openalex-snapshot
Nickel-Catalyzed C–N Cross-Coupling of Ammonia, (Hetero)anilines, and Indoles with Activated (Hetero)aryl Chlorides Enabled by Ligand Design
inferredcites →https://doi.org/10.1021/cr00002a004openalex-snapshot
A survey of Hammett substituent constants and resonance and field parameters
inferredcites →https://doi.org/10.1021/cs500874zopenalex-snapshot
Catalytic C–S Cross-Coupling Reactions Employing Ni Complexes of Pyrrole-Based Pincer Ligands
inferredcites →https://doi.org/10.1021/ic50170a033openalex-snapshot
Bonding of aromatic hydrocarbons to nickel(0). Structure of bis(tricyclohexylphosphine)(1,2-.eta.2-anthracene)nickel(0)-toluene
inferredcites →https://doi.org/10.1021/j100096a001openalex-snapshot
Ab Initio Calculation of Vibrational Absorption and Circular Dichroism Spectra Using Density Functional Force Fields
inferredcites →https://doi.org/10.1021/ja01280a022openalex-snapshot
The Effect of Structure upon the Reactions of Organic Compounds. Benzene Derivatives
inferredcites →https://doi.org/10.1021/ja0580340openalex-snapshot
A General and Long-Lived Catalyst for the Palladium-Catalyzed Coupling of Aryl Halides with Thiols
inferredcites →https://doi.org/10.1021/ja205294yopenalex-snapshot
Theoretical Analysis of the Mechanism of Palladium(II) Acetate-Catalyzed Oxidative Heck Coupling of Electron-Deficient Arenes with Alkenes: Effects of the Pyridine-Type Ancillary Ligand and Origins of the meta-Regioselectivity
inferredcites →https://doi.org/10.1021/ja802533uopenalex-snapshot
Analysis of the Concerted Metalation-Deprotonation Mechanism in Palladium-Catalyzed Direct Arylation Across a Broad Range of Aromatic Substrates
inferredcites →https://doi.org/10.1021/ja810157eopenalex-snapshot
Mechanism of Ni-Catalyzed Selective C−O Bond Activation in Cross-Coupling of Aryl Esters
inferredcites →https://doi.org/10.1021/jacs.0c06995openalex-snapshot
Small Phosphine Ligands Enable Selective Oxidative Addition of Ar–O over Ar–Cl Bonds at Nickel(0)
inferredcites →https://doi.org/10.1021/jacs.1c04215openalex-snapshot
Ni-Catalyzed Aryl Sulfide Synthesis through an Aryl Exchange Reaction
inferredcites →https://doi.org/10.1021/jacs.5b00538openalex-snapshot
Fundamental Studies and Development of Nickel-Catalyzed Trifluoromethylthiolation of Aryl Chlorides: Active Catalytic Species and Key Roles of Ligand and Traceless MeCN Additive Revealed
inferredcites →https://doi.org/10.1021/jacs.5b11244openalex-snapshot
Photoredox Mediated Nickel Catalyzed Cross-Coupling of Thiols With Aryl and Heteroaryl Iodides via Thiyl Radicals
inferredcites →https://doi.org/10.1021/jf60194a021openalex-snapshot
Absorption, translocation, and metabolism of metribuzin (BAY-94337) in sugarcane
inferredcites →https://doi.org/10.1021/jp810292nopenalex-snapshot
Universal Solvation Model Based on Solute Electron Density and on a Continuum Model of the Solvent Defined by the Bulk Dielectric Constant and Atomic Surface Tensions
inferredcites →https://doi.org/10.1021/ol071248xopenalex-snapshot
The First N-Heterocyclic Carbene-Based Nickel Catalyst for C−S Coupling
inferredcites →https://doi.org/10.1021/ol303366uopenalex-snapshot
Nickel-Mediated Inter- and Intramolecular C–S Coupling of Thiols and Thioacetates with Aryl Iodides at Room Temperature
inferredcites →https://doi.org/10.1021/om050715gopenalex-snapshot
New Insights into Xantphos/Pd-Catalyzed C−N Bond Forming Reactions: A Structural and Kinetic Study
inferredcites →https://doi.org/10.1021/om500156qopenalex-snapshot
A Broadly Applicable Strategy for Entry into Homogeneous Nickel(0) Catalysts from Air-Stable Nickel(II) Complexes
inferredcites →https://doi.org/10.1021/op400088kopenalex-snapshot
Development of an Efficient Pd-Catalyzed Coupling Process for Axitinib
inferredcites →https://doi.org/10.1021/op500412aopenalex-snapshot
Development of the Commercial Route for the Manufacture of a 5-Lipoxygenase Inhibitor PF-04191834
inferredcites →https://doi.org/10.1038/nature13274openalex-snapshot
Recent advances in homogeneous nickel catalysis
inferredcites →https://doi.org/10.1039/b508541aopenalex-snapshot
Balanced basis sets of split valence, triple zeta valence and quadruple zeta valence quality for H to Rn: Design and assessment of accuracy
inferredcites →https://doi.org/10.1039/c7ob00892aopenalex-snapshot
A room temperature cyanation of (hetero)aromatic chlorides by an air stable nickel( ii ) XantPhos precatalyst and Zn(CN) 2
inferredcites →https://doi.org/10.1055/a-1503-6330openalex-snapshot
C–O-Selective Cross-Coupling of Chlorinated Phenol Derivatives
inferredcites →https://doi.org/10.1055/s-1981-29636openalex-snapshot
Synthesis of Diaryl Sulfides by Nickel(II)-Catalyzed Arylation of Arenethiolates
inferredcites →https://doi.org/10.1063/1.2370993openalex-snapshot
A new local density functional for main-group thermochemistry, transition metal bonding, thermochemical kinetics, and noncovalent interactions
inferredcites →https://doi.org/10.1063/1.3382344openalex-snapshot
A consistent and accurate ab initio parametrization of density functional dispersion correction (DFT-D) for the 94 elements H-Pu
inferredcites →https://doi.org/10.1063/1.464913openalex-snapshot
Density-functional thermochemistry. III. The role of exact exchange
inferredcites →https://doi.org/10.1126/science.1141956openalex-snapshot
The Catalytic Cross-Coupling of Unactivated Arenes
inferredcites →https://doi.org/10.1246/bcsj.53.1385openalex-snapshot
The Palladium Catalyzed Nucleophilic Substitution of Aryl Halides by Thiolate Anions
inferredcites →https://doi.org/10.1246/cl.1987.2221openalex-snapshot
Nickel(0)-catalyzed Synthesis of Diaryl Sulfides from Aryl Halides and Aromatic Thiols

What points at this work

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

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Multicomponent Selective Thioetherification of KSAc: Easy Access to Symmetrical/Unsymmetrical 4‐Alkylthio‐3‐halo‐2(5H)‐furanones
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Advancement in the Synthetic Methodologies for C─O and C─S Cross‐Coupling Reactions via Homogeneous Catalysis: A Decade of Progress
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Nickel‐Catalyzed Chemoselective Arylation of Amino Alcohols
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Manganese‐Catalyzed Redox‐Neutral Thiolation of Alkyl Halides with Thioformates
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C─S Bond Formation of Aryl Germanes
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Nickel‐Catalyzed Chemoselective Arylation of Amino Alcohols
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Manganese‐Catalyzed Redox‐Neutral Thiolation of Alkyl Halides with Thioformates
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C─S Bond Formation of Aryl Germanes
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Mechanistic insights for nickel catalyzed light‐assisted carbon–sulfur cross‐coupling reaction
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Ni‐Catalyzed Thioetherification of Alkyl and Aryl Thiols With Aryl Bromides Under Base‐Free Condition
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Taming the Lewis Superacid Al(ORF)3 (RF=C(CF3)3): DFT Guided Identification of the “Stable yet Reactive” Adduct SiPr2→Al(ORF)3; Its Use as ORF‐ Abstractor from a “Ni‐ORF” complex
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Neutral Chalcogen Bonding Enabled Photoinduced Cross‐Electrophile C—S/Se Coupling of Aryl Iodides via S RN 1 Process
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C−S Cross‐Coupling Reactions Catalyzed by Well‐Defined Copper and Nickel Complexes
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Modular Synthesis of ortho‐Thiolated Aryl Esters Enabled with Thiocarbonate through Catellani Strategy
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Transition Metal Catalysed C‐S Cross‐Coupling Reactions at Room Temperature.
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Thioesterification and Hydrothiolation of α, β‐ Unsaturated Esters with Aliphatic Thiols under Mild Conditions
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Emerging Trends in Advanced Materials for C─S Coupling Reactions: Design Strategies and Future Perspectives
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Developing Ni and Pd precatalysts for demanding cross-coupling reactions
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Ruthenium-Catalyzed 1,6-Hydroalkylation of para-Quinone Methides with Ketones via the in Situ Activation of C(sp3)–H Bonds
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Nucleophilic Aromatic Substitution of Heteroaryl Halides with Thiols
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Mechanochemical Electron Donor–Acceptor (EDA)-Complex-Mediated Thioetherification Reaction via Site-Selective C–H Functionalization Using Aryl (DMIX)iodonium Salt
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Recent Advances in Nonprecious Metal Catalysis
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Photochemical Organocatalytic Synthesis of Thioethers from Aryl Chlorides and Alcohols
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Advances in accessing rare oxidation states of nickel for catalytic innovation
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Low-coordinate bis-phosphine and monophosphine Ni(0) complexes: synthesis and reactivity in C–S cross-coupling
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Visible-light-driven catalyst-free C–S cross-coupling of thiol derivatives and aryl halides
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Nickel catalyzed C–S cross coupling of sterically hindered substrates enabled by flexible bidentate phosphines
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Data-driven discovery of active phosphine ligand space for cross-coupling reactions
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Metal-catalyzed methylthiolation of chloroarenes and diverse aryl electrophiles
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Recent Metal-Catalyzed Methods for Thioether Synthesis
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82325 Forging carbon–chalcogen bonds via transition metal catalysis: C–S and C–Se cross-coupling strategies
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Nickel Catalyzed C–S Cross Coupling of Sterically Hindered Aryl Triflates with Alkyl Thiols
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Recent Advances in Electrochemical Formation of C—S Bond and Construction of Organosulfur Compounds
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New Catalytic Process for C-Heteroatom Bond Formation
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