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Arylthiolation of Arylamine Derivatives with (Arylthio)‐ pyrrolidine‐2,5‐diones

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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/adsc.200505207openalex-snapshot
Alkyl‐ and Arylthiolation of Aryl Halides Catalyzed by Fluorinated Bis‐Imino‐Nickel NNN Pincer Complexes [NiCl2{C5H3N‐2,6‐(CHNArf)2}]
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Moderne Synthesemethoden: Kupfer‐vermittelte C(Aryl)‐O‐, C(Aryl)‐N‐ und C(Aryl)‐S‐Verknüpfungen
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Synthese funktionalisierter Benzylmagnesiumreagentien unter Verwendung einer S/Mg‐Austauschreaktion
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Iron‐Catalyzed S‐Arylation of Thiols with Aryl Iodides
inferredcites →https://doi.org/10.1002/anie.200300594openalex-snapshot
Modern Synthetic Methods for Copper‐Mediated C(aryl)O, C(aryl)N, and C(aryl)S Bond Formation
inferredcites →https://doi.org/10.1002/anie.200490023openalex-snapshot
Modern Synthetic Methods for Copper‐Mediated C(aryl)O, C(aryl)N, and C(aryl)S Bond Formation
inferredcites →https://doi.org/10.1002/anie.200501882openalex-snapshot
Functionalized Benzylic Magnesium Reagents through a Sulfur–Magnesium Exchange
inferredcites →https://doi.org/10.1002/anie.200705668openalex-snapshot
Iron‐Catalyzed S‐Arylation of Thiols with Aryl Iodides
inferredcites →https://doi.org/10.1002/asia.201300636openalex-snapshot
Transfer of Sulfur: From Simple to Diverse
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.201102158openalex-snapshot
Carbon–Sulfur Bond Formation of Challenging Substrates at Low Temperature by Using Pd‐PEPPSI‐IPent
inferredcites →https://doi.org/10.1002/ejoc.200700119openalex-snapshot
Unusual Influence of the Structures of Transition Metal Complexes on Catalytic C–S and C–Se Bond Formation Under Homogeneous and Heterogeneous Conditions
inferredcites →https://doi.org/10.1016/c2009-0-21293-1openalex-snapshot
Sulfur Reagents in Organic Synthesis
inferredcites →https://doi.org/10.1016/j.bmcl.2010.09.097openalex-snapshot
The synthesis and SAR of novel diarylsulfone 11β-HSD1 inhibitors
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.2007.12.118openalex-snapshot
Efficient ligand-free nickel-catalyzed C–S cross-coupling of thiols with aryl iodides
inferredcites →https://doi.org/10.1016/j.tetlet.2009.02.214openalex-snapshot
Copper-catalyzed direct thiolation of benzoxazole with diaryl disulfides and aryl thiols
inferredcites →https://doi.org/10.1016/j.tetlet.2009.11.025openalex-snapshot
Gold-catalyzed C–S bond formation from thiols
inferredcites →https://doi.org/10.1016/j.tetlet.2010.02.038openalex-snapshot
The use of anhydrous CeCl3 as a catalyst for the synthesis of 3-sulfenyl indoles
inferredcites →https://doi.org/10.1016/j.tetlet.2012.09.127openalex-snapshot
Silver catalyzed C–C and C–S coupling of aryl halides and thiols with boronic acids
inferredcites →https://doi.org/10.1021/cr100347kopenalex-snapshot
Transition-Metal-Catalyzed C−S, C−Se, and C−Te Bond Formation via Cross-Coupling and Atom-Economic Addition Reactions
inferredcites →https://doi.org/10.1021/cr9902749openalex-snapshot
Metal-Catalyzed Carbon−Sulfur Bond Formation
inferredcites →https://doi.org/10.1021/ja061715qopenalex-snapshot
Cu(II)-Catalyzed Functionalizations of Aryl C−H Bonds Using O 2 as an Oxidant
inferredcites →https://doi.org/10.1021/ja404050fopenalex-snapshot
A New Family of Nucleophiles for Photoinduced, Copper-Catalyzed Cross-Couplings via Single-Electron Transfer: Reactions of Thiols with Aryl Halides Under Mild Conditions (O °C)
inferredcites →https://doi.org/10.1021/ja8049996openalex-snapshot
Rhodium-Catalyzed Substitution Reaction of Aryl Fluorides with Disulfides: p-Orientation in the Polyarylthiolation of Polyfluorobenzenes
inferredcites →https://doi.org/10.1021/jm049360dopenalex-snapshot
Arylthioindoles, Potent Inhibitors of Tubulin Polymerization
inferredcites →https://doi.org/10.1021/jm2014748openalex-snapshot
Potent Inhibitors of LpxC for the Treatment of Gram-Negative Infections
inferredcites →https://doi.org/10.1021/jo00255a030openalex-snapshot
Conformational effects in the alkali-metal reduction of diaryl sulfides. 2. Evidence for episulfide intermediates
inferredcites →https://doi.org/10.1021/jo049758hopenalex-snapshot
A Facile One-Pot Synthesis of Alkyl Aryl Sulfides from Aryl Bromides
inferredcites →https://doi.org/10.1021/jo062131+openalex-snapshot
Convenient Synthesis of Unsymmetrical Organochalcogenides Using Organoboronic Acids with Dichalcogenides via Cleavage of the S−S, Se−Se, or Te−Te Bond by a Copper Catalyst
inferredcites →https://doi.org/10.1021/jo1014849openalex-snapshot
Copper-Catalyzed Thiolation of the Di- or Trimethoxybenzene Arene C−H Bond with Disulfides
inferredcites →https://doi.org/10.1021/jo2017444openalex-snapshot
Copper-Mediated C–H Activation/C–S Cross-Coupling of Heterocycles with Thiols
inferredcites →https://doi.org/10.1021/jo300100xopenalex-snapshot
Chan–Lam-Type S-Arylation of Thiols with Boronic Acids at Room Temperature
inferredcites →https://doi.org/10.1021/jo302088topenalex-snapshot
Synthesis of Aryl Thioethers through the N-Chlorosuccinimide-Promoted Cross-Coupling Reaction of Thiols with Grignard Reagents
inferredcites →https://doi.org/10.1021/jo800491kopenalex-snapshot
Ligand-Free Copper-Catalyzed C−S Coupling of Aryl Iodides and Thiols
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/ol0266673openalex-snapshot
A General, Efficient, and Inexpensive Catalyst System for the Coupling of Aryl Iodides and Thiols
inferredcites →https://doi.org/10.1021/ol0477935openalex-snapshot
Copper-Catalyzed Synthesis of Vinyl Sulfides
inferredcites →https://doi.org/10.1021/ol051588nopenalex-snapshot
Rhodium-Catalyzed Reductive Coupling of Disulfides and Diselenides with Alkyl Halides, Using Hydrogen as a Reducing Agent
inferredcites →https://doi.org/10.1021/ol052615copenalex-snapshot
Development of a Novel, Highly Efficient Halide-Catalyzed Sulfenylation of Indoles
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/ol100449copenalex-snapshot
Cu(II)-Mediated Methylthiolation of Aryl C−H Bonds with DMSO
inferredcites →https://doi.org/10.1021/ol201970mopenalex-snapshot
A Practical, One-Pot Synthesis of Highly Substituted Thiophenes and Benzo[b]thiophenes from Bromoenynes and o-Alkynylbromobenzenes
inferredcites →https://doi.org/10.1021/ol2020863openalex-snapshot
Efficient Copper-Catalyzed S-Vinylation of Thiols with Vinyl Halides
inferredcites →https://doi.org/10.1021/ol4036209openalex-snapshot
Palladium Catalyzed Aryl(alkyl)thiolation of Unactivated Arenes
inferredcites →https://doi.org/10.1021/ol802033popenalex-snapshot
Palladium-Catalyzed Synthesis of 2-Substituted Benzothiazoles via a C−H Functionalization/Intramolecular C−S Bond Formation Process
inferredcites →https://doi.org/10.1021/ol900009aopenalex-snapshot
Nano Indium Oxide as a Recyclable Catalyst for C−S Cross-Coupling of Thiols with Aryl Halides under Ligand Free conditions
inferredcites →https://doi.org/10.1021/ol900958zopenalex-snapshot
Heterocycle Formation via Palladium-Catalyzed Intramolecular Oxidative C−H Bond Functionalization: An Efficient Strategy for the Synthesis of 2-Aminobenzothiazoles
inferredcites →https://doi.org/10.1039/b002081hopenalex-snapshot
The synthesis of thiols, selenols, sulfides, selenides, sulfoxides, selenoxides, sulfones and selenones
inferredcites →https://doi.org/10.1039/b811362aopenalex-snapshot
Palladium-catalysed direct synthesis of benzo[b]thiophenes from thioenols
inferredcites →https://doi.org/10.1039/b907362kopenalex-snapshot
Iron-catalyzed thioetherification of thiols with aryl iodides
inferredcites →https://doi.org/10.1039/b918117bopenalex-snapshot
Synthesis of CuO on mesoporous silica and its applications for coupling reactions of thiols with aryl iodides
inferredcites →https://doi.org/10.1039/c0cc04405aopenalex-snapshot
Novel C–H functionalization of arenes: palladium-catalyzed synthesis of diaryl sulfides
inferredcites →https://doi.org/10.1039/c2cc33950aopenalex-snapshot
Highly regioselective synthesis of aryl chalcogenides through C–H functionalization of arenes
inferredcites →https://doi.org/10.1039/c2cc36711dopenalex-snapshot
Transition metal-free direct C–H bond thiolation of 1,3,4-oxadiazoles and related heteroarenes
inferredcites →https://doi.org/10.1039/c4cc03600jopenalex-snapshot
Iron or boron-catalyzed C–H arylthiation of substituted phenols at room temperature
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/bcsj.58.3657openalex-snapshot
Palladium-catalyzed Reaction of Stannyl Sulfide with Aryl Bromide. Preparation of Aryl Sulfide
inferredcites →https://doi.org/10.1248/cpb.47.980openalex-snapshot
AlCl3-Mediated Aromatic Phenylthiation with N-Phenylthiophthalimide.
inferredcites →https://doi.org/10.3390/molecules16010590openalex-snapshot
Transition Metal Catalyzed Synthesis of Aryl Sulfides

What points at this work

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

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Graphical Abstract: Adv. Synth. Catal. 2‐3/2015
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Iron‐Catalyzed Azidoalkylthiation of Alkenes with Trimethylsilyl Azide and 1‐(Alkylthio)pyrrolidine‐2,5‐diones
inferred← citeshttps://doi.org/10.1002/adsc.201900301openalex-snapshot
Thioesters as Bifunctional Reagents for 2‐Naphthylamine Sulfuracylation
inferred← citeshttps://doi.org/10.1002/adsc.202000948openalex-snapshot
Palladium‐Catalyzed Distal C−H Selenylation of 2‐Aryl Acetamides with Diselenides and Selenyl Chlorides
inferred← citeshttps://doi.org/10.1002/asia.201701163openalex-snapshot
Sodium Iodide (NaI)‐Catalyzed Cross‐Coupling for C−S Bond Formation via Oxidative Dehydrogenation: Cheap, Direct Access to Unsymmetrical Aryl Sulfides
inferred← citeshttps://doi.org/10.1002/chem.202301751openalex-snapshot
Silver‐Catalyzed para‐Selective Sulfenyl Group Transfer Reactions of N‐Sulfenylanilides
inferred← citeshttps://doi.org/10.1002/chin.201526107openalex-snapshot
ChemInform Abstract: Arylthiolation of Arylamine Derivatives with (Arylthio)‐ pyrrolidine‐2,5‐diones.
inferred← citeshttps://doi.org/10.1002/ejoc.201700017openalex-snapshot
An Efficient Coupling of p‐Quinone Mono‐Imine Ketals and Aryl/Alkyl Thiols: Rapid Synthesis of Biaryl/Aryl–Alkyl Sulfides
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AlCl3‐Catalyzed Intermolecular Annulation of Thiol Derivatives and Alkynes by 1,2‐Sulfur Migration: Construction of 6‐Substituted Benzo[b]thiophenes
inferred← citeshttps://doi.org/10.1002/ejoc.201801532openalex-snapshot
Ruthenium‐Catalyzed C–H Selenylations of Benzamides
inferred← citeshttps://doi.org/10.1002/ejoc.202201458openalex-snapshot
Hemin‐Promoted Direct C−H Thiolation in the Synthesis of Diaryl Sulfides
inferred← citeshttps://doi.org/10.1002/slct.202102042openalex-snapshot
Transition Metal‐Free Sulfenylation of C−H Bonds for C−S Bond Formation in Recent Years: Mechanistic Approach and Promising Future
inferred← citeshttps://doi.org/10.1016/j.bioorg.2026.109987openalex-snapshot
Green synthesis and biological evaluation of novel thio−/seleno-imidazo[1,2-a]pyridine derivatives as novel and potent colchicine-site tubulin inhibitors
inferred← citeshttps://doi.org/10.1016/j.mcat.2022.112485openalex-snapshot
C4-Sulfenylation of 4-iodine-1H-pyrazole-5-amine with arylsulfonyl hydrazide in water
inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.136165openalex-snapshot
Highly selective C3-sulfenylation and C3-selenylation of 3-iodo-5-arylpyrazolo[1,5-a]pyrimidin-7-amine in water
inferred← citeshttps://doi.org/10.1016/j.tet.2020.131646openalex-snapshot
TBAI-mediated sulfenylation of arenes with arylsulfonyl hydrazides in DPDME
inferred← citeshttps://doi.org/10.1016/j.tet.2024.133941openalex-snapshot
Iodine-promoted metal-free synthesis of mono- / di- and tri-substituted aryl sulfides / selenides in aqueous medium
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02078openalex-snapshot
Iodine/DMSO-Promoted Selective Direct Arylthiation of Anilines with Thiols under Metal-Free Conditions
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00448openalex-snapshot
Regioselective C–H Thioarylation of Electron-Rich Arenes by Iron(III) Triflimide Catalysis
inferred← citeshttps://doi.org/10.1021/acs.joc.5c00250openalex-snapshot
Iron-Catalyzed Thioarylation of Arenes Using Saccharin-Derived Reagents
inferred← citeshttps://doi.org/10.1021/acs.joc.6c00744openalex-snapshot
Accelerated Thioarylation of Arenes Using Lewis Acid and Lewis Base Dual Catalysis
inferred← citeshttps://doi.org/10.1021/acs.joc.8b00435openalex-snapshot
Phenyliodine(III) Bis(trifluoroacetate) (PIFA)-Mediated Synthesis of Aryl Sulfides in Water
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c04261openalex-snapshot
Copper-Catalyzed Regioselective Remote C–H Bond Chalcogenation of Aromatic Amine Derivatives without Using Any Large Template
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b02147openalex-snapshot
Regioselective C–H Sulfanylation of Aryl Sulfoxides by Means of Pummerer-Type Activation
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b01281openalex-snapshot
Lewis Acid/Brønsted Acid Controlled Pd(II)-Catalyzed Chemodivergent Functionalization of C(sp2)–H Bonds with N-(Arylthio)i(a)mides
inferred← citeshttps://doi.org/10.1039/c5ob00252dopenalex-snapshot
Metal-free oxysulfenylation of alkenes with 1-(arylthio)pyrrolidine-2,5-diones and alcohols
inferred← citeshttps://doi.org/10.1039/c5ob01679gopenalex-snapshot
Highly regioselective para-methylthiolation/bridging methylenation of arylamines promoted by NH 4 I
inferred← citeshttps://doi.org/10.1039/c5ra27324bopenalex-snapshot
DFT studies on the mechanism of palladium catalyzed arylthiolation of unactive arene to diaryl sulfide
inferred← citeshttps://doi.org/10.1039/c6cc07627kopenalex-snapshot
Metal-free C–H thioarylation of arenes using sulfoxides: a direct, general diaryl sulfide synthesis
inferred← citeshttps://doi.org/10.1039/c6cc09998jopenalex-snapshot
A conjugate Lewis base-Brønsted acid catalyst for the sulfenylation of nitrogen containing heterocycles under mild conditions
inferred← citeshttps://doi.org/10.1039/c8ob02800aopenalex-snapshot
KIO 3 -catalyzed cross dehydrogenative coupling reaction: sulfenylation of phenol and arylamine derivatives in water at room temperature
inferred← citeshttps://doi.org/10.1039/c9cc05099jopenalex-snapshot
Facile synthesis of 1,2-thiobenzonitriles via Cu-catalyzed denitrogenative radical coupling reaction
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Aryldithiocarbamates as thiol alternatives in Cu-catalyzed C(aryl)–S coupling reactions using aryldiazonium tetrafluoroborate salts
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Synthetic developments on the preparation of sulfides from thiol-free reagents
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Thioarylation of anilines using dual catalysis: two-step synthesis of phenothiazines
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Recent advances in selective mono-/dichalcogenation and exclusive dichalcogenation of C(sp 2 )–H and C(sp 3 )–H bonds
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Transition metal-free synthesis of polyfluoroaryl sulfides via S -transfer reaction
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Tetrabutylammonium Iodide Mediated Sulfenylation of Polysubstituted 1H-Pyrazol-5-amines with Arylsulfonyl Hydrazides
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A New Method for Synthesis of Thioethers from Phenyl N-Sulfonamide
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A New Method for Synthesis of Thioethers from Phenyl N-Sulfonamide
inferred← citeshttps://doi.org/10.3390/chemistry5030100openalex-snapshot
Metal-Free Eliminative C-H Arylthiolation of 2H-Imidazole N-Oxides with Thiophenols
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N -Sulfenylsuccinimide/phthalimide: an alternative sulfenylating reagent in organic transformations
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