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A Robust Pd-Catalyzed C–S Cross-Coupling Process Enabled by Ball-Milling

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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/ange.200705668openalex-snapshot
Iron‐Catalyzed S‐Arylation of Thiols with Aryl Iodides
inferredcites →https://doi.org/10.1002/anie.201102543openalex-snapshot
Pd‐Catalyzed Synthesis of ArSCF 3 Compounds under Mild Conditions
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.201806480openalex-snapshot
Mechanochemical Activation of Zinc and Application to Negishi Cross‐Coupling
inferredcites →https://doi.org/10.1002/anie.201810141openalex-snapshot
Switching Chemoselectivity: Using Mechanochemistry to Alter Reaction Kinetics
inferredcites →https://doi.org/10.1002/anie.201914921openalex-snapshot
Direct Visualization of a Mechanochemically Induced Molecular Rearrangement
inferredcites →https://doi.org/10.1002/chem.200600251openalex-snapshot
Easily Prepared Air‐ and Moisture‐Stable Pd–NHC (NHC=N‐Heterocyclic Carbene) Complexes: A Reliable, User‐Friendly, Highly Active Palladium Precatalyst for the Suzuki–Miyaura Reaction
inferredcites →https://doi.org/10.1002/chem.200600949openalex-snapshot
Highly Efficient and Functional‐Group‐Tolerant Catalysts for the Palladium‐Catalyzed Coupling of Aryl Chlorides with Thiols
inferredcites →https://doi.org/10.1002/chem.200601737openalex-snapshot
Simple and Efficient Recyclable Catalytic System for Performing Copper‐Catalysed S‐Arylation Reactions in the Presence of Water
inferredcites →https://doi.org/10.1002/chem.201102158openalex-snapshot
Carbon–Sulfur Bond Formation of Challenging Substrates at Low Temperature by Using Pd‐PEPPSI‐IPent
inferredcites →https://doi.org/10.1002/chem.201303756openalex-snapshot
Potassium Isopropoxide: For Sulfination It is the Only Base You Need!
inferredcites →https://doi.org/10.1002/chem.201404705openalex-snapshot
[(IPent)PdCl2(morpholine)]: A Readily Activated Precatalyst for Room‐Temperature, Additive‐Free Carbon–Sulfur Coupling
inferredcites →https://doi.org/10.1002/cssc.201900886openalex-snapshot
A Ball‐Milling‐Enabled Reformatsky Reaction
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.2012.06.009openalex-snapshot
Conducting moisture sensitive reactions under mechanochemical conditions
inferredcites →https://doi.org/10.1016/j.tetlet.2018.04.078openalex-snapshot
Solvent-free mechanochemical Buchwald-Hartwig amination of aryl chlorides without inert gas protection
inferredcites →https://doi.org/10.1021/acs.joc.6b01938openalex-snapshot
Liquid-Assisted Grinding Accelerating: Suzuki–Miyaura Reaction of Aryl Chlorides under High-Speed Ball-Milling Conditions
inferredcites →https://doi.org/10.1021/acs.joc.6b02887openalex-snapshot
Altering Product Selectivity by Mechanochemistry
inferredcites →https://doi.org/10.1021/acs.joc.9b02876openalex-snapshot
A Mechanochemical Zinc-Mediated Barbier-Type Allylation Reaction under Ball-Milling Conditions
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.8b00931openalex-snapshot
Stainless Steel-Mediated Hydrogen Generation from Alkanes and Diethyl Ether and Its Application for Arene Reduction
inferredcites →https://doi.org/10.1021/acscatal.9b01913openalex-snapshot
Monophosphine Ligands Promote Pd-Catalyzed C–S Cross-Coupling Reactions at Room Temperature with Soluble Bases
inferredcites →https://doi.org/10.1021/acscentsci.6b00277openalex-snapshot
Mechanochemistry: A Force of Synthesis
inferredcites →https://doi.org/10.1021/acssuschemeng.7b03260openalex-snapshot
1,1′-Carbonyldiimidazole and Mechanochemistry: A Shining Green Combination
inferredcites →https://doi.org/10.1021/ic061926wopenalex-snapshot
Electronic Effects on Reductive Elimination To Form Carbon−Carbon and Carbon−Heteroatom Bonds from Palladium(II) Complexes
inferredcites →https://doi.org/10.1021/ja00151a033openalex-snapshot
Transmetalation, Involving Organotin Aryl, Thiolate, and Amide Compounds. An Unusual Type of Dissociative Ligand Substitution Reaction
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/ja901793wopenalex-snapshot
Resting State and Elementary Steps of the Coupling of Aryl Halides with Thiols Catalyzed by Alkylbisphosphine Complexes of Palladium
inferredcites →https://doi.org/10.1021/jacs.0c01739openalex-snapshot
Selective Mechanochemical Monoarylation of Unbiased Dibromoarenes by in Situ Crystallization
inferredcites →https://doi.org/10.1021/jo048552dopenalex-snapshot
Synthesis of meso-Arylsulfanyl- and Alkylsulfanyl-Substituted Porphyrins via Palladium-Mediated C−S Bond Formation
inferredcites →https://doi.org/10.1021/jo401492nopenalex-snapshot
Carbon–Sulfur Bond Formation Catalyzed by [Pd(IPr* OMe )(cin)Cl] (cin = cinnamyl)
inferredcites →https://doi.org/10.1021/jo801169hopenalex-snapshot
Palladium-Catalyzed Carbon−Sulfur Cross-Coupling Reactions with Indium Tri(organothiolate) and Its Application to Sequential One-Pot Processes
inferredcites →https://doi.org/10.1021/jo802594dopenalex-snapshot
A General, Efficient, and Functional-Group-Tolerant Catalyst System for the Palladium-Catalyzed Thioetherification of Aryl Bromides and Iodides
inferredcites →https://doi.org/10.1021/jo802731jopenalex-snapshot
Indium-Catalyzed C−S Cross-Coupling of Aryl Halides with Thiols
inferredcites →https://doi.org/10.1021/ol047996topenalex-snapshot
A General Palladium-Catalyzed Coupling of Aryl Bromides/Triflates and Thiols
inferredcites →https://doi.org/10.1021/ol062344lopenalex-snapshot
Cobalt-Catalyzed Aryl−Sulfur Bond Formation
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/ol500112yopenalex-snapshot
Direct Cross-Coupling Access to Diverse Aromatic Sulfide: Palladium-Catalyzed Double C–S Bond Construction Using Na 2 S 2 O 3 as a Sulfurating Reagent
inferredcites →https://doi.org/10.1021/ol502470eopenalex-snapshot
Palladium-Catalyzed Debenzylative Cross-Coupling of Aryl Benzyl Sulfides with Aryl Bromides: Synthesis of Diaryl Sulfides
inferredcites →https://doi.org/10.1021/op400278dopenalex-snapshot
Carbon–Heteroatom Coupling Using Pd-PEPPSI Complexes
inferredcites →https://doi.org/10.1039/c0cs00195copenalex-snapshot
Ball milling in organic synthesis: solutions and challenges
inferredcites →https://doi.org/10.1039/c1cs15171aopenalex-snapshot
Mechanochemistry: opportunities for new and cleaner synthesis
inferredcites →https://doi.org/10.1039/c7sc05371aopenalex-snapshot
Mechanochemistry as an emerging tool for molecular synthesis: what can it offer?
inferredcites →https://doi.org/10.1039/c8ob01781fopenalex-snapshot
Robust Buchwald–Hartwig amination enabled by ball-milling
inferredcites →https://doi.org/10.1039/c9cy02041aopenalex-snapshot
Preventing Pd–NHC bond cleavage and switching from nano-scale to molecular catalytic systems: amines and temperature as catalyst activators
inferredcites →https://doi.org/10.1039/c9sc02185jopenalex-snapshot
Solid-state Suzuki–Miyaura cross-coupling reactions: olefin-accelerated C–C coupling using mechanochemistry
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/cl.1978.13openalex-snapshot
REACTIONS OF ARYL HALIDES WITH THIOLATE ANIONS IN THE PRESENCE OF CATALYTIC AMOUNTS OF TETRAKIS(TRIPHENYLPHOSPHINE)PALLADIUM PREPARATION OF ARYL SULFIDES
inferredcites →https://doi.org/10.3762/bjoc.14.81openalex-snapshot
Mechanochemistry of nucleosides, nucleotides and related materials

What points at this work

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

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inferred← citeshttps://doi.org/10.1002/adsc.202300188openalex-snapshot
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Synergetic Bifunctional Effect of the Solvent Leading to External Base‐Free Neutral Construction of Unsymmetrical Thioethers From Thiols and Organohalides in N , N ‐Dimethylformamide
inferred← citeshttps://doi.org/10.1002/ajoc.202000724openalex-snapshot
Nickel(II)‐Mediated C−S Cross‐Coupling Between Thiols and ortho‐Substituted Arylboronic Acid
inferred← citeshttps://doi.org/10.1002/ajoc.202200211openalex-snapshot
Preparation of Benzothiazoles and Heterocyclic Spiro Compounds Through Cu‐catalyzed S−S Bond Cleavage and C−S Bond Formation
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Photocatalytic Reductive Borylation, Phosphonation, Sulfurization, and Selenization of Aryl Iodides to Access Aryl Borates, Aryl Phosphates, Aryl Sulfides, and Aryl Selenides
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DMF‐Promoted S─Si Bond Activation Leading to Efficient Activator‐ and Catalyst‐Free C‐S Couplings of Thiosilanes and Organohalides
inferred← citeshttps://doi.org/10.1002/ange.202013017openalex-snapshot
Safe, Scalable, Inexpensive, and Mild Nickel‐Catalyzed Migita‐Like C−S Cross‐Couplings in Recyclable Water
inferred← citeshttps://doi.org/10.1002/ange.202106412openalex-snapshot
Direct Amidation of Esters by Ball Milling**
inferred← citeshttps://doi.org/10.1002/ange.202108752openalex-snapshot
Ball‐Milling‐Enabled Reactivity of Manganese Metal**
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Allylation of C‐, N‐, and O‐Nucleophiles via a Mechanochemically‐Driven Tsuji–Trost Reaction Suitable for Late‐Stage Modification of Bioactive Molecules
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Selective Deuteration and Tritiation of Pharmaceutically Relevant Sulfoximines
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Mechanochemistry Meets Catalysis: Metal Complexes for Greener Organic Transformations
inferred← citeshttps://doi.org/10.1002/ange.3776319openalex-snapshot
C─S Bond Formation of Aryl Germanes
inferred← citeshttps://doi.org/10.1002/anie.202013017openalex-snapshot
Safe, Scalable, Inexpensive, and Mild Nickel‐Catalyzed Migita‐Like C−S Cross‐Couplings in Recyclable Water
inferred← citeshttps://doi.org/10.1002/anie.202106412openalex-snapshot
Direct Amidation of Esters by Ball Milling**
inferred← citeshttps://doi.org/10.1002/anie.202108752openalex-snapshot
Ball‐Milling‐Enabled Reactivity of Manganese Metal**
inferred← citeshttps://doi.org/10.1002/anie.202314637openalex-snapshot
Allylation of C ‐, N ‐, and O ‐Nucleophiles via a Mechanochemically‐Driven Tsuji–Trost Reaction Suitable for Late‐Stage Modification of Bioactive Molecules
inferred← citeshttps://doi.org/10.1002/anie.202417179openalex-snapshot
Selective Deuteration and Tritiation of Pharmaceutically Relevant Sulfoximines
inferred← citeshttps://doi.org/10.1002/anie.202600005openalex-snapshot
Mechanochemistry Meets Catalysis: Metal Complexes for Greener Organic Transformations
inferred← citeshttps://doi.org/10.1002/anie.3776319openalex-snapshot
C─S Bond Formation of Aryl Germanes
inferred← citeshttps://doi.org/10.1002/asia.70443openalex-snapshot
Ni‐Catalyzed Thioetherification of Alkyl and Aryl Thiols With Aryl Bromides Under Base‐Free Condition
inferred← citeshttps://doi.org/10.1002/cctc.202402021openalex-snapshot
Enantioselective Preparation of Chiral Succinimide Derivatives by Mechanochemical Catalytic Michael Addition
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Mechanically Driven Redox Catalysis: From Metal‐Catalyzed Coupling to Piezoelectric and Cooperative Systems
inferred← citeshttps://doi.org/10.1002/chem.202100348openalex-snapshot
Mechanoredox Chemistry as an Emerging Strategy in Synthesis
inferred← citeshttps://doi.org/10.1002/chem.202302119openalex-snapshot
Mechanochemical Nickel‐Catalyzed Carbon‐Sulfur Bond Formation between Aryl Iodides and Aromatic Sulfur Surrogates
inferred← citeshttps://doi.org/10.1002/chem.202402969openalex-snapshot
Overriding Cage Effect in Electron Donor‐Acceptor Photoactivation of Diaryliodonium Reagents: Synthesis of Chalcogenides
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Sustainability Assessment of Mechanochemistry by Using the Twelve Principles of Green Chemistry
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Mechanochemical Organocatalysis: Do High Enantioselectivities Contradict What We Might Expect?
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Metal‐Free C−X Functionalization in Solid‐State via Photochemistry in Ball Mills
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Facile Mechanochemical Reduction and Lithium‐Ion Doping of Transition‐Metal Oxides[]**
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Carbon−Sulfur Coupling Reactions Catalyzed by Nickel(II) N‐Heterocyclic Carbene Complexes
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Mechanochemical C−X/C−H Functionalization: An Alternative Strategic Access to Pharmaceuticals
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Solid‐State Direct Electrophilic Selenocyanation of (Hetero)Arenes using Mechanochemistry
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Transition Metal Catalysed C‐S Cross‐Coupling Reactions at Room Temperature.
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Mechanochemistry-Directed Ligand Design: Development of a High-Performance Phosphine Ligand for Palladium-Catalyzed Mechanochemical Organoboron Cross-Coupling
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C–S bond formation through nucleophilic substitution reaction of thiol derivatives with activated aryl halides
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Recent advances in mechanochemical metal-catalyzed cross-coupling reactions
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Ni-catalyzed C–S bond cleavage of aryl 2-pyridyl thioethers coupling with alkyl and aryl thiols
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Iodine-promoted metal-free synthesis of mono- / di- and tri-substituted aryl sulfides / selenides in aqueous medium
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Palladium- and nickel-catalyzed synthesis of thioethers via thioesters – Aryl halides coupling
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Rapid Photoracemization of Chiral Alkyl Aryl Sulfoxides
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inferred← citeshttps://doi.org/10.1039/d4gc01790kopenalex-snapshot
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A nickel-catalyzed carbon–sulfur cross-coupling reaction with disulfides enabled by mechanochemistry
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Nickel catalyzed C–S cross coupling of sterically hindered substrates enabled by flexible bidentate phosphines
inferred← citeshttps://doi.org/10.1039/d5cc04621aopenalex-snapshot
Aryl semicarbazides as aryl sources for mechanochemical oxidative Heck coupling by C–N bond activation
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Mechanochemical deutero-dehalogenation of aryl halides and fluorosulfates with activated aluminum
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Synthetic strategies employing dual metal catalysis and ball-milling for sustainable cross-coupling and C–H bond functionalization reactions
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Formation, functionalization and interconversion of sulfur containing functional groups in mechanochemical conditions
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Nickel Catalyzed C–S Cross Coupling of Sterically Hindered Aryl Triflates with Alkyl Thiols
inferred← citeshttps://doi.org/10.26434/chemrxiv.14770740openalex-snapshot
A Ball Milling Enabled Cross-Electrophile Coupling
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Transition-metal-catalyzed C-S bond formation: recent developments and pharmaceutical applications
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Palladium-catalyzed solid-state borylation of aryl halides using mechanochemistry
inferred← citeshttps://doi.org/10.6023/cjoc202310035openalex-snapshot
Sodium Halides-Promoted S—Si Bond Activation and Its Application in the Synthesis of Unsymmetrical Thioethers
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Mechanochemistry Enabled Friedel-Crafts Alkylation Reactions of Donor-Acceptor Cyclopropanes with 2-Indolymethanols
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