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https://doi.org/10.2139/ssrn.4641471

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Arylthiolation of Arylamine Derivatives with (Arylthio)‐ pyrrolidine‐2,5‐diones
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Synthesis of Unsymmetrical Diorganyl Chalcogenides under Greener Conditions: Use of an Iodine/DMSO System, Solvent‐ and Metal‐Free Approach
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Odorless, Regioselective Synthesis of Diaryl Sulfides and α‐Thioaryl Carbonyls from Sodium Arylsulfinates via a Metal‐ Free Radical Strategy in Water
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Disulfide‐Directed C–H Hydroxylation for Synthesis of Sulfonyl Diphenyl Sulfides and 2‐(Phenylthio)phenols with Oxygen as Oxidant
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Copper‐Silver Dual Catalyzed Decyanative C–Se Cross‐Coupling
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Electrochemical Thiolation and Borylation of Arylazo Sulfones with Thiols and B 2 pin 2
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KIO 3 ‐Catalyzed C(sp 2 )‐H Bond Selenylation/Sulfenylation of (Hetero)arenes: Synthesis of Chalcogenated (Hetero)arenes and their Evaluation for Anti‐Alzheimer Activity
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Cobalt‐Catalyzed C−H Thiolation through Dehydrogenative Cross‐Coupling
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Synthesis of Tetrathiophosphates from White Phosphorus
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Palladium(II)/Copper(II)‐Catalyzed C–H Sulfidation or Selenation of Arenes Leading to Unsymmetrical Sulfides and Selenides
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Synthesis and evaluation of diaryl sulfides and diaryl selenide compounds for antitubulin and cytotoxic activity
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Visible-Light-Driven Halogen-Bond-Assisted Direct Synthesis of Heteroaryl Thioethers Using Transition-Metal-Free One-Pot C–I Bond Formation/C–S Cross-Coupling Reaction
inferredcites →https://doi.org/10.1021/acs.joc.6b00162openalex-extracted
Assembly of 3-Sulfenylbenzofurans and 3-Sulfenylindoles by Palladium-Catalyzed Cascade Annulation/Arylthiolation Reaction
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Palladium-Catalyzed Oxidative Sulfenylation of Indoles and Related Electron-Rich Heteroarenes with Aryl Boronic Acids and Elemental Sulfur
inferredcites →https://doi.org/10.1021/acs.joc.7b00767openalex-extracted
Transition-Metal-Free and Oxidant-Free Cross-Coupling of Arylhydrazines with Disulfides: Base-Promoted Synthesis of Unsymmetrical Aryl Sulfides
inferredcites →https://doi.org/10.1021/acs.joc.9b00075openalex-extracted
Achieving Nickel Catalyzed C–S Cross-Coupling under Mild Conditions Using Metal–Ligand Cooperativity
inferredcites →https://doi.org/10.1021/acs.orglett.0c02418openalex-extracted
A Robust Pd-Catalyzed C–S Cross-Coupling Process Enabled by Ball-Milling
inferredcites →https://doi.org/10.1021/acs.orglett.1c03232openalex-extracted
Pd-Catalyzed Double-Decarbonylative Aryl Sulfide Synthesis through Aryl Exchange between Amides and Thioesters
inferredcites →https://doi.org/10.1021/acs.orglett.5b01889openalex-extracted
Synthesis of Aryl Sulfides: Metal-Free C–H Sulfenylation of Electron-Rich Arenes
inferredcites →https://doi.org/10.1021/acs.orglett.7b03560openalex-extracted
Nickel Phosphite/Phosphine-Catalyzed C–S Cross-Coupling of Aryl Chlorides and Thiols
inferredcites →https://doi.org/10.1021/acs.orglett.8b03319openalex-extracted
Synthesis of Functionalized Diaryl Sulfides by Cobalt-Catalyzed Coupling between Arylzinc Pivalates and Diaryl Disulfides
inferredcites →https://doi.org/10.1021/acs.orglett.9b03192openalex-extracted
Switchable Synthesis of Aryl Sulfones and Sulfoxides through Solvent-Promoted Oxidation of Sulfides with O 2 /Air
inferredcites →https://doi.org/10.1021/acscatal.1c04895openalex-extracted
Acetate Facilitated Nickel Catalyzed Coupling of Aryl Chlorides and Alkyl Thiols
inferredcites →https://doi.org/10.1021/acscatal.5b01815openalex-extracted
Pd-NHC Catalytic System for the Efficient Atom-Economic Synthesis of Vinyl Sulfides from Tertiary, Secondary, or Primary Thiols
inferredcites →https://doi.org/10.1021/acscatal.9b02982openalex-extracted
RhCl3·3H2O-Catalyzed Ligand-Enabled Highly Regioselective Thiolation of Acrylic Acids
inferredcites →https://doi.org/10.1021/ja3092278openalex-extracted
Copper-Promoted Sulfenylation of sp 2 C–H Bonds
inferredcites →https://doi.org/10.1021/jacs.1c04215openalex-extracted
Ni-Catalyzed Aryl Sulfide Synthesis through an Aryl Exchange Reaction
inferredcites →https://doi.org/10.1021/jacs.7b07390openalex-extracted
Visible-Light-Promoted C–S Cross-Coupling via Intermolecular Charge Transfer
inferredcites →https://doi.org/10.1021/jm401375qopenalex-extracted
Data-Mining for Sulfur and Fluorine: An Evaluation of Pharmaceuticals To Reveal Opportunities for Drug Design and Discovery
inferredcites →https://doi.org/10.1021/jm501853mopenalex-extracted
A Survey of the Role of Noncovalent Sulfur Interactions in Drug Design
inferredcites →https://doi.org/10.1021/jo302480jopenalex-extracted
Transition-Metal-Free Synthesis of Unsymmetrical Diaryl Chalcogenides from Arenes and Diaryl Dichalcogenides
inferredcites →https://doi.org/10.1021/ma961740oopenalex-extracted
Selective and Efficient Synthesis of Cyclic Hexakis(thio-1,4-phenylene) through Oxidative Polymerization of Diphenyl Disulfide
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Enantioselective Diels–Alder Reactions of Enals and Alkylidene Diketones Catalyzed by N-Heterocyclic Carbenes
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Copper-Catalyzed Double C–S Bonds Formation via Different Paths: Synthesis of Benzothiazoles from N-Benzyl-2-iodoaniline and Potassium Sulfide
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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/ol901084kopenalex-extracted
Reductive Addition of the Benzenethiyl Radical to Alkynes by Amine-Mediated Single Electron Transfer Reaction to Diphenyl Disulfide
inferredcites →https://doi.org/10.1039/c1gc15725fopenalex-extracted
Synthesis of diaryl selenides using electrophilic selenium species and nucleophilic boron reagents in ionic liquids
inferredcites →https://doi.org/10.1039/c4cc03600jopenalex-extracted
Iron or boron-catalyzed C–H arylthiation of substituted phenols at room temperature
inferredcites →https://doi.org/10.1039/c4gc02047bopenalex-extracted
The copper–nicotinamide complex: sustainable applications in coupling and cycloaddition reactions
inferredcites →https://doi.org/10.1039/c5cc06250kopenalex-extracted
Copper-mediated stereospecific C–H oxidative sulfenylation of terminal alkenes with disulfides
inferredcites →https://doi.org/10.1039/c5gc00403aopenalex-extracted
Iodine catalyzed cross-dehydrogenative C–S coupling by C(sp 2 )–H bond activation: direct access to aryl sulfides from aryl thiols
inferredcites →https://doi.org/10.2174/1568026615666150915111741openalex-extracted
Sulfur Containing Scaffolds in Drugs: Synthesis and Application in Medicinal Chemistry
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