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Transition-Metal-Free Synthesis of Unsymmetrical Diaryl Chalcogenides from Arenes and Diaryl Dichalcogenides

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

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A Highly Efficient Palladium‐Catalyzed One‐Pot Synthesis of Unsymmetrical Aryl Alkyl Thioethers under Mild Conditions in Water

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Fast Synthesis of Benzofluorenes by Selenium‐Mediated Carbocyclizations

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Efficient and Economical Access to Substituted Benzothiazoles: Copper‐Catalyzed Coupling of 2‐Haloanilides with Metal Sulfides and Subsequent Condensation

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Assembly of Substituted Phenothiazines by a Sequentially Controlled CuI/ L ‐Proline‐Catalyzed Cascade CS and CN Bond Formation

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Domino Condensation/S‐Arylation/Heterocyclization Reactions: Copper‐Catalyzed Three‐Component Synthesis of 2‐N‐Substituted Benzothiazoles

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Oxidative Carbonylation Reactions: Organometallic Compounds (RM) or Hydrocarbons (RH) as Nucleophiles

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Pd‐Catalyzed Synthesis of ArSCF 3 Compounds under Mild Conditions

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Highly Efficient and Functional‐Group‐Tolerant Catalysts for the Palladium‐Catalyzed Coupling of Aryl Chlorides with Thiols

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A Simple and Efficient Catalytic System for N‐Arylation of Imidazoles in Water

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One‐Pot Synthesis of Unsymmetrical Diaryl Thioethers by Palladium‐Catalyzed Coupling of Two Aryl Bromides and a Thiol Surrogate

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Carbon–Sulfur Bond Formation of Challenging Substrates at Low Temperature by Using Pd‐PEPPSI‐IPent

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Cu‐Catalyzed Three‐Component Synthesis of Substituted Benzothiazoles in Water

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Synthesis, Structural Characterization and Fluorescence Properties of Organoselenium Compounds Bearing a Ligand Containing Both Bulky and Nonbonding Groups − The First Observation of Both Intramolecular Se···N and Se···O Interactions in a Diselenide Structure

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Copper‐Catalyzed Formation of Sulfur–Nitrogen Bonds by Dehydrocoupling of Thiols with Amines

inferredcites →https://doi.org/10.1016/j.tet.2011.09.141openalex-snapshot

Copper catalyzed/mediated synthetic methodology for ebselen and related isoselenazolones

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Copper-catalyzed direct thiolation of benzoxazole with diaryl disulfides and aryl thiols

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Potassium selenocyanate as an efficient selenium source in C–Se cross-coupling catalyzed by copper iodide in water

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An efficient copper mediated synthetic methodology for benzo[d]isothiazol-3(2H)-ones and related sulfur–nitrogen heterocycles

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Unexpectedly ligand-free copper-catalyzed C–S cross-coupling of benzothiazole with aryl iodides in aqueous solution

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Electrophilic 2-Thienylselenenylation of Thiophene. Preparation of Oligo(seleno-2,5-thienylenes)

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A general palladium-catalysed synthesis of aromatic and heteroaromatic thioethers

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Selenium catalyzed conversion of vinyl halides into α-alkoxy acetals

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Acetoxy lactonization of alkenyl acetic acids promoted by ammonium persulfate and trifluoromethanesulfonic acid in acetic acid

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Phenylseleno-lactonization of olefinic nitriles promoted byperoxydisulphate ion oxidation of diphenyl diselenide

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Electrophilic phenylselenenylation of thiophenes. Synthesis of poly(phenylseleno)thiophenes.

inferredcites →https://doi.org/10.1016/s0040-4039(00)72287-8openalex-snapshot

Iron-catalyzed aromatic sulfuration with sulfenyl chlorides

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The reaction of diphenyl diselenide with peroxydisulphate ions in methanol a convenient procedure to effect the methoxyselenenylation of alkenes

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Reaction of tryptophan derivatives with phenylsulphenyl chloride and phenylselenenyl bromide

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Heteroatom-Directed Aromatic Lithiation: A Versatile Route to the Synthesis of Organochalcogen (Se, Te) Compounds

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Carbon−Heteroatom Bond-Forming Reductive Eliminations of Amines, Ethers, and Sulfides

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Transition-Metal-Catalyzed C−S, C−Se, and C−Te Bond Formation via Cross-Coupling and Atom-Economic Addition Reactions

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Bond Formations between Two Nucleophiles: Transition Metal Catalyzed Oxidative Cross-Coupling Reactions

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Organoselenium Chemistry: Role of Intramolecular Interactions

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Thiol peroxidase activity of diaryl ditellurides as determined by a proton NMR method

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Cu(II)-Catalyzed Functionalizations of Aryl C−H Bonds Using O 2 as an Oxidant

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Facile Synthesis of 2-(Phenylthio)phenols by Copper(I)-Catalyzed Tandem Transformation of C−S Coupling/C−H Functionalization

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Nickel-Catalyzed Synthesis of Aryl Trifluoromethyl Sulfides at Room Temperature

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Biomimetic Seleninates and Selenonates

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Palladium-Catalyzed C−H Bond Functionalization with Arylsulfonyl Chlorides

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Mechanistic Course of the Asymmetric Methoxyselenenylation Reaction

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Investigations on the 4-Quinolone-3-carboxylic Acid Motif. 1. Synthesis and Structure−Activity Relationship of a Class of Human Immunodeficiency Virus type 1 Integrase Inhibitors

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Design, Synthesis, Biological Evaluation, and NMR Studies of a New Series of Arylsulfones As Selective and Potent Matrix Metalloproteinase-12 Inhibitors

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Selenium-mediated conversion of alkynes into .alpha.-dicarbonyl compounds

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Selenium-promoted conversion of .beta.-diketones and .beta.-keto esters into .alpha.,.alpha.-dimethoxy .beta.-diketones and .alpha.,.alpha.-dimethoxy .beta.-keto esters

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Arylthio amidation, etherification and lactonization of alkenes promoted by oxidation of bis(4-methoxyphenyl) disulfide with ammonium peroxydisulfate

inferredcites →https://doi.org/10.1021/jo00073a021openalex-snapshot

Free-radical homolytic substitution at selenium: an efficient method for the preparation of selenophenes

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Catalytic Antioxidant Activity of Diaryl Tellurides in a Two-Phase Lipid Peroxidation Model

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Novel and Direct Nucleophilic Sulfenylation and Thiocyanation of Phenol Ethers Using a Hypervalent Iodine(III) Reagent

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Arylation of dialkyl sulfides and of aryl alkyl sulfides to provide sulfonium salts

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Ring-closure reactions initiated by the peroxydisulfate ion oxidation of diphenyl diselenide

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Selenium-catalyzed conversion of methyl ketones into .alpha.-keto acetals

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Highly Active, Air-Stable Versatile Palladium Catalysts for the C−C, C−N, and C−S Bond Formations via Cross-Coupling Reactions of Aryl Chlorides

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Highly Active, Air-Stable Palladium Catalysts for the C−C and C−S Bond-Forming Reactions of Vinyl and Aryl Chlorides: Use of Commercially Available [(t-Bu)2P(OH)]2PdCl2, [(t-Bu)2P(OH)PdCl2]2, and [[(t-Bu)2PO···H···OP(t-Bu)2]PdCl]2 as Catalysts

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Magnesium-Induced Copper-Catalyzed Synthesis of Unsymmetrical Diaryl Chalcogenide Compounds from Aryl Iodide via Cleavage of the Se−Se or S−S Bond

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Alkyl- or Arylthiolation of Aryl Iodide via Cleavage of the S−S Bond of Disulfide Compound by Nickel Catalyst and Zinc

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Microwave-Assisted Copper-Catalyzed Preparation of Diaryl Chalcogenides

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Long-Lasting Antioxidant Protection: A Regenerable BHA Analogue

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Copper-Catalyzed Thiolation of the Di- or Trimethoxybenzene Arene C−H Bond with Disulfides

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Formation of Carbon–Sulfur and Carbon–Selenium Bonds by Palladium-Catalyzed Decarboxylative Cross-Couplings of Hindered 2,6-Dialkoxybenzoic Acids

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Synthesis of 2-Thio-Substituted Benzothiazoles via a Domino Condensation/S-Arylation/Heterocyclization Process

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Chan–Lam-Type S-Arylation of Thiols with Boronic Acids at Room Temperature

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A General Palladium-Catalyzed Coupling of Aryl Bromides/Triflates and Thiols

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Catalytic Use of Selenium Electrophiles in Cyclizations

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Selenium-Mediated Synthesis of Biaryls through Rearrangement

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Cu(II)-Mediated Methylthiolation of Aryl C−H Bonds with DMSO

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Organochalcogen Substituents in Phenolic Antioxidants

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Electrophilic Aromatic Selenylation: New OPRT Inhibitors

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Cu-Catalyzed Efficient Synthetic Methodology for Ebselen and Related Se−N Heterocycles

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An Efficient Copper-Catalyzed Carbon−Sulfur Bond Formation Protocol in Water

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Palladium-Catalyzed Cross-Coupling of Benzyl Thioacetates and Aryl Halides

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Selenium-Catalyzed Regioselective Cyclization of Unsaturated Carboxylic Acids Using Hypervalent Iodine Oxidants

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KOtBu Mediated Synthesis of Phenanthridinones and Dibenzoazepinones

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A Novel Practical Synthesis of Benzothiazoles via Pd-Catalyzed Thiol Cross-Coupling

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Catalytic Chain-Breaking Pyridinol Antioxidants

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Palladium-Catalyzed Synthesis of 2-Substituted Benzothiazoles via a C−H Functionalization/Intramolecular C−S Bond Formation Process

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Pyridine N-Oxides as Ligands in Cu-Catalyzed N-Arylation of Imidazoles in Water

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Chelate Ring Size Effect on the Reactivity of [2-(2-Phenyl-5,6-dihydro-4H-1,3-oxazinyl)]lithium and Se···N Interactions in Low-Valent Organoselenium Compounds: Facile Isolation of Diorganotriselenide

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Protection against Peroxynitrite-Mediated Nitration Reaction by Intramolecularly Coordinated Diorganoselenides

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Reactions of Di-o-tolyl Telluride and Selenide with Palladium Acetate: Isolation of a Novel Palladium Complex of a Tellurenic Acid Anhydride and Related Trinuclear and Tetranuclear Palladium Complexes

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Synthetic organoselenium compounds as antioxidants: glutathione peroxidase activity

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Relations between 77Se NMR chemical shifts of (phenylseleno)benzenes and their molecular structures derived from nine X-ray crystal structures

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Synthesis of organochalcogens stabilized by intramolecular non-bonded interactions of sterically unhindered 2-phenyl-2-oxazolineElectronic supplementary information (ESI) available: 77Se NMR spectrum of 14, molecular structure of 16 and packing diagram of 15. See…

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Copper(ii) complexes of thioether-substituted salcyen and salcyan derivatives and their silver(i) adducts

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Palladium-catalysed direct synthesis of benzo[b]thiophenes from thioenols

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Lithium pipecolinate as a facile and efficient ligand for copper-catalyzed hydroxylation of aryl halides in water

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Novel C–H functionalization of arenes: palladium-catalyzed synthesis of diaryl sulfides

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Transition-metal catalyzed oxidative cross-coupling reactions to form C–C bonds involving organometallic reagents as nucleophiles

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Fe-catalysed oxidative C–H functionalization/C–S bond formation

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Cu(ii)-catalyzed C–H (SP3) oxidation and C–N cleavage: base-switched methylenation and formylation using tetramethylethylenediamine as a carbon source

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Highly regioselective synthesis of aryl chalcogenides through C–H functionalization of arenes

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Catalytic conversion of (β,γ-unsaturated esters, amides and nitriles into γ-alkoxy or γ-hydroxy α,β-unsaturated derivatives induced by persulfate anion oxidation of diphenyl diselenide

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A Highly Efficient Copper-Catalyzed Method for the Synthesis of 2-Hydroxybenzamides in Water

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An Efficient Synthesis of Naphthyl Alkyl and Aryl Sulfides by the Reaction of Naphthols with Alkane- and Arenethiols

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Selenium Catalysed Conversion of β,γ-Unsaturated Acids into Butenolides

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Selenium Promoted Conversion of α-Substituted β,γ-Unsaturated Ketones into 2,3,5-Trisubstituted Furans

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Cross Coupling of Arylboronic Acids with Imidazoles by Sulfonatocopper(II)(salen) Complex in Water

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FeCl3-mediated Direct Chalcogenation of Phenols

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Magnetically Separable CuFe2O4 Nanoparticle Catalyzed C–Se Cross Coupling in Reusable PEG Medium

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The use of selenium containing intermediates to mediate or catalyze new organic reactions

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Preparation and Interconversion of Phenylselenenylated and Alkylselenenylated Aromatic Compounds

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.201500625openalex-snapshot

Direct Synthesis of 4‐Organylselanylpyrazoles by Copper‐ Catalyzed One‐Pot Cyclocondensation and CH Bond Selenylation Reactions

inferred← citeshttps://doi.org/10.1002/adsc.201500943openalex-snapshot

Iodine‐Mediated Synthesis of Aromatic Thioethers with Aromatic Amines and Sulfonyl Hydrazides in High Regioselectivity via C(sp2)H Bond Functionalization

inferred← citeshttps://doi.org/10.1002/adsc.201600429openalex-snapshot

Copper(I) Bromide‐Dimethyl Sulfide‐Catalyzed Direct Sulfanylation of 4‐Hydroxycoumarins and 4‐Hydroxyquinolinones with Arylsulfonylhydrazides and Selective Fluorescence Switch‐ On Sensing of Cadmium(II) Ion in Water

inferred← citeshttps://doi.org/10.1002/adsc.201600933openalex-snapshot

Copper‐Silver Dual Catalyzed Decyanative C–Se Cross‐Coupling

inferred← citeshttps://doi.org/10.1002/adsc.201701147openalex-snapshot

Ruthenium(II)‐Catalyzed C−H Chalcogenation of Anilides

inferred← citeshttps://doi.org/10.1002/adsc.201801510openalex-snapshot

Iodine(III) Enabled Dehydrogenative Aryl C−S Coupling by in situ Generated Sulfenium Ion

inferred← citeshttps://doi.org/10.1002/adsc.201901536openalex-snapshot

Rongalite‐Promoted on Water Synthesis of Functionalised Tellurides and Ditellurides

inferred← citeshttps://doi.org/10.1002/adsc.202001426openalex-snapshot

[Bis(trifluoroacetoxy)iodo]benzene Mediated C‐3 Selenylation of Pyrido[1,2‐a]Pyrimidin‐4‐Ones Under Ambient Conditions

inferred← citeshttps://doi.org/10.1002/adsc.202100371openalex-snapshot

Trichloroisocyanuric Acid‐Promoted Synthesis of Arylselenides and Aryltellurides from Diorganyl Dichalcogenides and Arylboronic Acids at Ambient Temperature

inferred← citeshttps://doi.org/10.1002/ajoc.201402289openalex-snapshot

Copper‐Catalyzed Regioselective C5 Sulfenylation of Imidazo[2,1‐b]thiazoles with Thiols

inferred← citeshttps://doi.org/10.1002/ajoc.201800332openalex-snapshot

Catalyst and Sensitizer‐Free Visible‐Light‐Induced C(sp 2 )−H Chalcogenation of Arenes/ Heteroarenes with Dichalcogenides

inferred← citeshttps://doi.org/10.1002/ajoc.201800346openalex-snapshot

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

inferred← citeshttps://doi.org/10.1002/ajoc.202200014openalex-snapshot

Tf 2 O‐Mediated Regioselective C(sp 2 )−H Sulfenylation of Enaminones Using Methyl Sulfoxides as Sulfur Sources

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

inferred← citeshttps://doi.org/10.1002/ajoc.202500508openalex-snapshot

K 2 S 2 O 8 ‐Promoted Direct Chalcogenation and Nitrosation at C‐3 Position of Imidazo[1,2‐ a ]pyridines Under Mild Conditions

inferred← citeshttps://doi.org/10.1002/ange.201411997openalex-snapshot

Heterogen katalysierte direkte C‐H‐Thiolierung von Heteroarenen

inferred← citeshttps://doi.org/10.1002/ange.202216296openalex-snapshot

Transition‐Metal‐Free Difunctionalization of Sulfur Nucleophiles**

inferred← citeshttps://doi.org/10.1002/anie.201411997openalex-snapshot

Heterogeneously Catalyzed Direct CH Thiolation of Heteroarenes

inferred← citeshttps://doi.org/10.1002/anie.202216296openalex-snapshot

Transition‐Metal‐Free Difunctionalization of Sulfur Nucleophiles**

inferred← citeshttps://doi.org/10.1002/aoc.4921openalex-snapshot

An environmentally benign and efficient synthesis of 4‐Selanylpyrazoles catalyzed by haloid salts in water

inferred← citeshttps://doi.org/10.1002/aoc.6482openalex-snapshot

A review on the latest progress of C‐S cross‐coupling in diaryl sulfide synthesis: Update from 2012 to 2021

inferred← citeshttps://doi.org/10.1002/asia.201601376openalex-snapshot

Synthesis of Thioethers and Thioesters with Alkyl Arylsulfinates as the Sulfenylation Agent under Metal‐Free Conditions

inferred← citeshttps://doi.org/10.1002/asia.202100139openalex-snapshot

Radical Chain Breaking Bis(ortho‐organoselenium) Substituted Phenolic Antioxidants

inferred← citeshttps://doi.org/10.1002/asia.202300993openalex-snapshot

Synthesis of Diaryl Tellurides with Sodium Aryltellurites under Mild Conditions

inferred← citeshttps://doi.org/10.1002/asia.202500817openalex-snapshot

Electrochemistry‐Driven Seleno‐Functionalization of Diverse Organic Scaffolds: A Recent Update

inferred← citeshttps://doi.org/10.1002/cctc.201402867openalex-snapshot

Copper Nanoparticles Catalyzed Se(Te)Se(Te) Bond Activation: A Straightforward Route Towards Unsymmetrical Organochalcogenides from Boronic Acids

inferred← citeshttps://doi.org/10.1002/chem.201304717openalex-snapshot

Palladium‐Catalyzed Direct Thiolation of Aryl CH Bonds with Disulfides

inferred← citeshttps://doi.org/10.1002/chem.201405895openalex-snapshot

Regenerable Antioxidants—Introduction of Chalcogen Substituents into Tocopherols

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/chem.202303883openalex-snapshot

Electrochemical Diselenation of BODIPY Fluorophores for Bioimaging Applications and Sensitization of 1O2

inferred← citeshttps://doi.org/10.1002/chin.201328173openalex-snapshot

ChemInform Abstract: Transition‐Metal‐Free Synthesis of Unsymmetrical Diaryl Chalcogenides from Arenes and Diaryl Dichalcogenides.

inferred← citeshttps://doi.org/10.1002/ejoc.201403169openalex-snapshot

Efficient Synthesis of 5‐Chalcogenyl‐1,3‐oxazin‐2‐ones by Chalcogen‐Mediated Yne–Carbamate Cyclisation: An Experimental and Theoretical Study

inferred← citeshttps://doi.org/10.1002/ejoc.201601562openalex-snapshot

Towards the Iodine‐Catalyzed Regioselective Sulfenylation of Unsymmetrical Ketones

inferred← citeshttps://doi.org/10.1002/ejoc.201700338openalex-snapshot

Sodium Persulfate Mediated Selenylation of Arenofurans

inferred← citeshttps://doi.org/10.1002/ejoc.201700744openalex-snapshot

Solvent‐ and Metal‐Free Chalcogenation of Bicyclic Arenes Using I2/DMSO as Non‐Metallic Catalytic System

inferred← citeshttps://doi.org/10.1002/ejoc.201801532openalex-snapshot

Ruthenium‐Catalyzed C–H Selenylations of Benzamides

inferred← citeshttps://doi.org/10.1002/ejoc.201900050openalex-snapshot

Ligand‐Free Palladium(II)‐Catalyzed ortho ‐C–H Chalcogenations of N ‐Arylsulfonamide via Weak Coordination

inferred← citeshttps://doi.org/10.1002/ejoc.201900544openalex-snapshot

Stereoselective Synthesis of Z‐Vinyl Selenides Through the Reaction of Sodium Selenide with Organic Halides and Alkynes

inferred← citeshttps://doi.org/10.1002/ejoc.201901548openalex-snapshot

Selenocystine Peptides Performance in 5‐endo‐dig Reactions

inferred← citeshttps://doi.org/10.1002/ejoc.202000216openalex-snapshot

Electrochemical Selenation/Cyclization of Quinones: A Rapid, Green and Efficient Access to Functionalized Trypanocidal and Antitumor Compounds

inferred← citeshttps://doi.org/10.1002/ejoc.202101394openalex-snapshot

XtalFluor‐E Enabled Regioselective Synthesis of Di‐Indole Sulfides by C3−H Sulfenylation of Indoles

inferred← citeshttps://doi.org/10.1002/ejoc.202300702openalex-snapshot

Synthesis of Benzyl Thioethers by C−S Coupling of Benzylic Trimethylammonium Salts and Sulfonyl Chlorides

inferred← citeshttps://doi.org/10.1002/slct.201601549openalex-snapshot

Piperidine Promoted Direct Sulfenylation of 2‐Naphthol with Aryl Thiols under Aqueous Conditions

inferred← citeshttps://doi.org/10.1002/slct.201702066openalex-snapshot

Synthesis of Thio and Selenoethers of Cyclic β‐Hydroxy Carbonyls and Amino Uracils: A Metal‐Free Regioselective I 2 /DMSO Mediated Reaction

inferred← citeshttps://doi.org/10.1002/slct.201801119openalex-snapshot

Iodine‐Catalyzed One‐Pot Decarboxylative Sulfenylation of Electron‐Rich Arenes and Indoles

inferred← citeshttps://doi.org/10.1002/slct.202104072openalex-snapshot

Oxyselenocyclization of 2‐Allylphenols for the Synthesis of 2,3‐Dihydrobenzofuran Selenides

inferred← citeshttps://doi.org/10.1002/slct.202304815openalex-snapshot

Oxone® Mediated Regioselective C(sp 2 )−H Selenylation and Thiocyanation of Pyrazolo[1,5‐ a ]pyrimidines at Room Temperature

inferred← citeshttps://doi.org/10.1002/slct.202305025openalex-snapshot

Synthesis of bis ‐Naphthol based Organoselenium Antioxidants as Efficient Inhibitors against Biofilms

inferred← citeshttps://doi.org/10.1002/slct.202502623openalex-snapshot

tert ‐Butyl Nitrite‐Mediated Deaminative Chalcogenation of Substituted 5‐Aminopyrazoles via Diaryl Dichalcogenides

inferred← citeshttps://doi.org/10.1002/tcr.202100133openalex-snapshot

Carbon‐Sulfur Bond Constructions: From Transition‐Metal Catalysis to Sustainable Catalysis

inferred← citeshttps://doi.org/10.1007/s00214-026-03276-yopenalex-snapshot

Theoretical insights into the interaction of [Au(XCH₃)₂]⁻ (X = S, Se, Te) complexes with Au(111) surface cluster: a density functional study

inferred← citeshttps://doi.org/10.1007/s10593-025-03407-6openalex-snapshot

Diselenides in heterocyclic chemistry: recent methodological breakthrough

inferred← citeshttps://doi.org/10.1007/s40010-016-0301-1openalex-snapshot

Structural and Reactivity Aspects of Organoselenium and Tellurium Cations

inferred← citeshttps://doi.org/10.1007/s40010-016-0306-9openalex-snapshot

Cinchona-Alkaloids Based Isoselenazolones: Synthesis and Their Catalytic Reactivity in Asymmetric Bromolactonization of Alkenoic Acid

inferred← citeshttps://doi.org/10.1007/s41061-018-0203-6openalex-snapshot

Engineered C–S Bond Construction

inferred← citeshttps://doi.org/10.1016/bs.aihch.2024.10.004openalex-snapshot

77Se NMR spectroscopy of selenium adducts of N-heterocyclic carbenes

inferred← citeshttps://doi.org/10.1016/j.ccr.2018.05.015openalex-snapshot

Rise of diselenides: Recent advances in the synthesis of heteroarylselenides

inferred← citeshttps://doi.org/10.1016/j.chempr.2024.05.025openalex-snapshot

B(C6F5)3-catalyzed selective C–H chalcogenation of arenes and heteroarenes

inferred← citeshttps://doi.org/10.1016/j.jphotochem.2025.116503openalex-snapshot

Thioethers synthesized via visible-light-mediated sulfonylation of enaminones with sulfur powder

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.2019.126908openalex-snapshot

Complexation of selenomethionine and its derivatives with some dimeric rhodium(II) tetracarboxylates: 1H and 13C nuclear magnetic resonance spectroscopy

inferred← citeshttps://doi.org/10.1016/j.molstruc.2020.127817openalex-snapshot

Ground and excited-state properties of 1,3-benzoselenazole derivatives: A combined theoretical and experimental photophysical investigation

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.2014.01.030openalex-snapshot

A convenient and efficient copper-catalyzed synthesis of unsymmetrical and symmetrical diaryl chalcogenides from arylboronic acids in ethanol at room temperature

inferred← citeshttps://doi.org/10.1016/j.tet.2015.06.077openalex-snapshot

Pd(II)-catalyzed selective sulfenylation of arene C–H bonds using N-arylthiobenzamides as thiolation reagent and oxidant

inferred← citeshttps://doi.org/10.1016/j.tet.2015.09.022openalex-snapshot

RETRACTED: Reusable biomacromolecule-Pd complex catalyzed C–C cross-coupling reactions via C–S cleavage of disulfides

inferred← citeshttps://doi.org/10.1016/j.tet.2017.02.046openalex-snapshot

Metal- and solvent-free, iodine-catalyzed cyclocondensation and C H bond sulphenylation: A facile access to C-4 sulfenylated pyrazoles via a domino multicomponent reaction

inferred← citeshttps://doi.org/10.1016/j.tet.2017.07.061openalex-snapshot

An easy one-step procedure for the synthesis of novel β-functionalised tellurides

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/10.1016/j.tetlet.2014.08.042openalex-snapshot

Iodine-promoted efficient synthesis of diheteroaryl thioethers via the integration of iodination/condensation/cyclization/dehydration sequences

inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.12.055openalex-snapshot

Solvent selective phenyl selenylation and phenyl tellurylation of aryl boronic acids catalyzed by Cu(II) grafted functionalized polystyrene

inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.06.006openalex-snapshot

Visible-light-promoted synthesis of diaryl sulfides under air

inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.151393openalex-snapshot

Facile preparation of 2-arylbenzoselenazoles from three components reactions: 2-Chloronitrobenzene, Se, and arylacetic acids

inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.152141openalex-snapshot

Flavin/I2 catalyzed aerobic oxidative C H sulfenylation of anilines

inferred← citeshttps://doi.org/10.1021/acs.inorgchem.3c02719openalex-snapshot

A Synthetic, Structural, Spectroscopic, and Computational Study of Alkali Metal–Thioether, −Selenoether, and −Telluroether Interactions

inferred← citeshttps://doi.org/10.1021/acs.inorgchem.4c00658openalex-snapshot

Synthesis and Conformational Dynamics of Selenanthrene (Oxides): Establishing an Energetic Flexibility Index for Scaffolds

inferred← citeshttps://doi.org/10.1021/acs.joc.0c00792openalex-snapshot

Metal-Free Synthesis of Phenol-Aryl Selenides via Dehydrogenative C–Se Coupling of Aryl Selenoxides with Phenols

inferred← citeshttps://doi.org/10.1021/acs.joc.0c00921openalex-snapshot

Silver-Catalyzed Remote C5–H Selenylation of Indoles

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.1c00478openalex-snapshot

Transition-Metal-Free HFIP-Mediated Organo Chalcogenylation of Arenes/Indoles with Thio-/Selenocyanates

inferred← citeshttps://doi.org/10.1021/acs.joc.3c00566openalex-snapshot

AcBr/DMSO Mediated Sulfenylation of Pyrrolo[2,1-a]isoquinolines

inferred← citeshttps://doi.org/10.1021/acs.joc.3c00788openalex-snapshot

Oxidative Three-Component Selenofunctionalization of Alkenes: Convenient Access to Vicinally Functionalized Selenides

inferred← citeshttps://doi.org/10.1021/acs.joc.4c01462openalex-snapshot

CuI-Catalyzed Selenylation of Pyrrolo[2,1-a]isoquinolines and Other Electron-Rich Heteroarenes

inferred← citeshttps://doi.org/10.1021/acs.joc.4c01732openalex-snapshot

Anionic N-Heterocyclic Carbenes from Mesoionic Imidazolium-4-pyrrolides: The Influence of Substituents, Solvents, and Charge on their 77Se NMR Chemical Shifts

inferred← citeshttps://doi.org/10.1021/acs.joc.4c02581openalex-snapshot

Studies on the Effect of Positive and Negative Charges on the 77Se NMR Shifts of Selenones and Selenenyls of N-heterocyclic Carbenes of Imidazolium-4,5-dicarboxylates

inferred← citeshttps://doi.org/10.1021/acs.joc.5b00247openalex-snapshot

Silver-Catalyzed Direct Thiolation of Quinones by Activation of Aryl Disulfides to Synthesize Quinonyl Aryl Thioethers

inferred← citeshttps://doi.org/10.1021/acs.joc.5b00540openalex-snapshot

Metal-Free Iodine-Catalyzed Direct Arylthiation of Substituted Anilines with Thiols

inferred← citeshttps://doi.org/10.1021/acs.joc.6c00137openalex-snapshot

Electrochemical Oxidative Nucleophilic Disulfenylation of Anilines

inferred← citeshttps://doi.org/10.1021/acs.joc.7b00050openalex-snapshot

Sequential Carbon–Carbon/Carbon–Selenium Bond Formation Mediated by Iron(III) Chloride and Diorganyl Diselenides: Synthesis and Reactivity of 2-Organoselenyl-Naphthalenes

inferred← citeshttps://doi.org/10.1021/acs.joc.7b01320openalex-snapshot

Making Flavone Thioethers Using Halides and Powdered Sulfur or Na2S2O3

inferred← citeshttps://doi.org/10.1021/acs.joc.7b02384openalex-snapshot

Transition-Metal-Free C–S Bond Formation: Synthesis of Polysubstituted Diaryl Sulfides and α-Thioarylcarbonyl Compounds

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.joc.8b00974openalex-snapshot

Copper-Catalyzed 8-Aminoquinoline Assisted Aryl Chalcogenation of Ferroceneamide with Aryl Disulfides, Diselenides, and Ditellurides

inferred← citeshttps://doi.org/10.1021/acs.joc.9b02199openalex-snapshot

Iodine-Catalyzed Selenylation of 2H-Indazole

inferred← citeshttps://doi.org/10.1021/acs.joc.9b02963openalex-snapshot

Sequential Regioselective Diorganochalcogenations of Imidazo[1,2-a]pyrimidines Using I2/H3PO4 in Dimethylsulfoxide

inferred← citeshttps://doi.org/10.1021/acs.oprd.9b00548openalex-snapshot

Multistep Synthesis of Organic Selenides under Visible Light Irradiation: A Continuous-Flow Approach

inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02012openalex-snapshot

Copper-Mediated Regioselective C–H Sulfenylation and Selenation of Phenols with Phenanthroline Bidentate Auxiliary

inferred← citeshttps://doi.org/10.1021/acs.orglett.1c03090openalex-snapshot

Direct C–H Thiolation for Selective Cross-Coupling of Arenes with Thiophenols via Aerobic Visible-Light Catalysis

inferred← citeshttps://doi.org/10.1021/acs.orglett.2c00607openalex-snapshot

Electrochemical Mn-Promoted Radical Selenylation of Boronic Acids with Diselenide Reagents

inferred← citeshttps://doi.org/10.1021/acs.orglett.5b01889openalex-snapshot

Synthesis of Aryl Sulfides: Metal-Free C–H Sulfenylation of Electron-Rich Arenes

inferred← citeshttps://doi.org/10.1021/acs.orglett.6b02059openalex-snapshot

Alkyldisulfanium Salts: Isolable, Electrophilic Sulfur Reagents Competent for Polyene Cyclizations

inferred← citeshttps://doi.org/10.1021/acs.orglett.6b02142openalex-snapshot

Selective Oxidative Decarbonylative Cleavage of Unstrained C( sp 3)–C( sp 2) Bond: Synthesis of Substituted Benzoxazinones

inferred← citeshttps://doi.org/10.1021/acs.orglett.6b02939openalex-snapshot

N-Heterocyclic Carbene Catalyzed Sulfenylation of α,β-Unsaturated Aldehydes

inferred← citeshttps://doi.org/10.1021/acs.orglett.6b03735openalex-snapshot

Transition-Metal-Free Selective Oxidative C(sp 3 )–S/Se Coupling of Oxindoles, Tetralone, and Arylacetamides: Synthesis of Unsymmetrical Organochalcogenides

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/10.1021/acs.orglett.8b02756openalex-snapshot

An Organodiselenide with Dual Mimic Function of Sulfhydryl Oxidases and Glutathione Peroxidases: Aerial Oxidation of Organothiols to Organodisulfides

inferred← citeshttps://doi.org/10.1021/acs.orglett.8b02889openalex-snapshot

Site-Specific Oxidative C–H Chalcogenation of (Hetero)Aryl-Fused Cyclic Amines Enabled by Nanocobalt Oxides

inferred← citeshttps://doi.org/10.1021/acscatal.4c01660openalex-snapshot

Cyclopropenium Sulfide as Lewis Base Catalyst for Chemoselective and Regioselective Electrophilic Selenylation of Phenols

inferred← citeshttps://doi.org/10.1021/jacs.2c02126openalex-snapshot

Dual Ligand Enabled Nondirected C–H Chalcogenation of Arenes and Heteroarenes

inferred← citeshttps://doi.org/10.1021/jo402071bopenalex-snapshot

Reaction under Ball-Milling: Solvent-, Ligand-, and Metal-Free Synthesis of Unsymmetrical Diaryl Chalcogenides

inferred← citeshttps://doi.org/10.1021/jo501793qopenalex-snapshot

Regioselective Thiolation of Arenes and Heteroarenes: C–H Functionalization Strategy for C–S Bond Formation

inferred← citeshttps://doi.org/10.1021/ol4036209openalex-snapshot

Palladium Catalyzed Aryl(alkyl)thiolation of Unactivated Arenes

inferred← citeshttps://doi.org/10.1021/ol502470eopenalex-snapshot

Palladium-Catalyzed Debenzylative Cross-Coupling of Aryl Benzyl Sulfides with Aryl Bromides: Synthesis of Diaryl Sulfides

inferred← citeshttps://doi.org/10.1038/s41467-018-06763-4openalex-snapshot

A selenium-catalysed para-amination of phenols

inferred← citeshttps://doi.org/10.1039/c3gc41671bopenalex-snapshot

Iodine-catalyzed efficient 2-arylsulfanylphenol formation from thiols and cyclohexanones

inferred← citeshttps://doi.org/10.1039/c3ob41083hopenalex-snapshot

KOtBu-mediated stereoselective addition of quinazolines to alkynes under mild conditions

inferred← citeshttps://doi.org/10.1039/c3ob41601aopenalex-snapshot

Metal free sulfenylation and bis-sulfenylation of indoles: persulfate mediated synthesis

inferred← citeshttps://doi.org/10.1039/c4cc04503copenalex-snapshot

Metal-free sp 3 C–H functionalization: a novel approach for the syntheses of selenide ethers and thioesters from methyl arenes

inferred← citeshttps://doi.org/10.1039/c4cs00239copenalex-snapshot

Recent advances in C–S bond formation via C–H bond functionalization and decarboxylation

inferred← citeshttps://doi.org/10.1039/c4ra08014aopenalex-snapshot

Iodine-promoted 2-arylsulfanylphenol formation using cyclohexanones as phenol source

inferred← citeshttps://doi.org/10.1039/c4ra17237jopenalex-snapshot

Iodine–triphenylphosphine mediated sulfenylation of imidazoheterocycles with sodium sulfinates

inferred← citeshttps://doi.org/10.1039/c5cc10245fopenalex-snapshot

Organoselenium and DMAP co-catalysis: regioselective synthesis of medium-sized halolactones and bromooxepanes from unactivated alkenes

inferred← citeshttps://doi.org/10.1039/c5cy01503kopenalex-snapshot

DMSO/iodine-catalyzed oxidative C–Se/C–S bond formation: a regioselective synthesis of unsymmetrical chalcogenides with nitrogen- or oxygen-containing arenes

inferred← citeshttps://doi.org/10.1039/c5gc02292dopenalex-snapshot

Chemoselective cross-coupling reaction of sodium sulfinates with phenols under aqueous conditions

inferred← citeshttps://doi.org/10.1039/c5nj02945gopenalex-snapshot

Synthesis of enantiomerically pure bis(2,2-dimethyl-1,3-dioxolanylmethyl)chalcogenides and dichalcogenides

inferred← citeshttps://doi.org/10.1039/c5ob00149hopenalex-snapshot

Nickel-catalyzed synthesis of diarylsulfides and sulfones via C–H bond functionalization of arylamides

inferred← citeshttps://doi.org/10.1039/c5ob02193fopenalex-snapshot

Iodine-catalyzed thiolation of electron-rich aromatics using sulfonyl hydrazides as sulfenylation reagents

inferred← citeshttps://doi.org/10.1039/c5ob02619aopenalex-snapshot

Sulfuration of the C(sp 2 )–H bond of enaminones: a protocol for the synthesis of thioether using elemental sulfur as a sulfurating reagent

inferred← citeshttps://doi.org/10.1039/c5qo00311copenalex-snapshot

Copper-catalyzed domino synthesis of benzo[b]thiophene/imidazo[1,2-a]pyridines by sequential Ullmann-type coupling and intramolecular C(sp 2 )–H thiolation

inferred← citeshttps://doi.org/10.1039/c5ra06773aopenalex-snapshot

Unexpected CN bond formation via NaI-catalyzed oxidative de-tetra-hydrogenative cross-couplings between N,N-dimethyl aniline and sulfamides

inferred← citeshttps://doi.org/10.1039/c5ra07204bopenalex-snapshot

K 2 S 2 O 8 /I 2 promoted syntheses of α-thio-β-dicarbonyl compounds via oxidative C–S coupling reactions under transition metal-free and solvent-free conditions

inferred← citeshttps://doi.org/10.1039/c5ra16729aopenalex-snapshot

Catalyst-free selenylation of imidazoheterocycles

inferred← citeshttps://doi.org/10.1039/c5ra21964gopenalex-snapshot

Theoretical exploration of seleno and tellurophenols as promising alternatives to sulfur ligands for anchoring to gold (111) materials

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/c6dt02167kopenalex-snapshot

Palladium-catalysed direct thiolation and selenation of aryl C–H bonds assisted by directing groups

inferred← citeshttps://doi.org/10.1039/c6ob01856dopenalex-snapshot

Regioselective transition metal- and halogen-free direct dithiolation at C(sp 3 )–H of nitrotoluenes with diaryl disulfides

inferred← citeshttps://doi.org/10.1039/c6qo00407eopenalex-snapshot

Metal-free iodine-catalyzed direct cross-dehydrogenative coupling (CDC) between pyrazoles and thiols

inferred← citeshttps://doi.org/10.1039/c6ra18997kopenalex-snapshot

Direct C–H heteroarylation of azoles with 1,2-di(pyrimidin-2-yl)disulfides through C–S cleavage of disulfides

inferred← citeshttps://doi.org/10.1039/c7ob02066jopenalex-snapshot

Copper-catalyzed ipso -selenation of aromatic carboxylic acids

inferred← citeshttps://doi.org/10.1039/c7ob02860aopenalex-snapshot

DABCO-catalyzed silver-promoted direct thiolation of pyrazolones with diaryl disulfides

inferred← citeshttps://doi.org/10.1039/c7qo00326aopenalex-snapshot

Iodine-catalyzed cascade annulation of alkynes with sodium arylsulfinates: assembly of 3-sulfenylcoumarin and 3-sulfenylquinolinone derivatives

inferred← citeshttps://doi.org/10.1039/c7ra04817copenalex-snapshot

Regio- and stereoselective syntheses of allylic thioethers under metal free conditions

inferred← citeshttps://doi.org/10.1039/c8cc04543gopenalex-snapshot

Convenient synthesis of selenyl-indoles via iodide ion-catalyzed electrochemical C–H selenation

inferred← citeshttps://doi.org/10.1039/c8nj01998copenalex-snapshot

Synthesis of symmetrical and unsymmetrical tellurides via silver catalysis

inferred← citeshttps://doi.org/10.1039/c8nj05554hopenalex-snapshot

T3P® mediated domino C(sp 2 )–H sulfenylation/annulation of enaminones and methylsulfinyls for the synthesis of chromone thioether derivatives

inferred← citeshttps://doi.org/10.1039/c8ob03209bopenalex-snapshot

Synthesis and nano-Pd catalyzed chemoselective oxidation of symmetrical and unsymmetrical sulfides

inferred← citeshttps://doi.org/10.1039/c8qo00909kopenalex-snapshot

Acid-catalyzed oxidative cleavage of S–S and Se–Se bonds with DEAD: efficient access to sulfides and selenides

inferred← citeshttps://doi.org/10.1039/c9cc03789fopenalex-snapshot

Transition-metal- and oxidant-free directed anodic C–H sulfonylation of N , N -disubstituted anilines with sulfinates

inferred← citeshttps://doi.org/10.1039/c9cc05099jopenalex-snapshot

Facile synthesis of 1,2-thiobenzonitriles via Cu-catalyzed denitrogenative radical coupling reaction

inferred← citeshttps://doi.org/10.1039/c9dt00473dopenalex-snapshot

Transition metal catalysed direct selanylation of arenes and heteroarenes

inferred← citeshttps://doi.org/10.1039/c9gc00007kopenalex-snapshot

Visible-light-induced metal and reagent-free oxidative coupling of sp 2 C–H bonds with organo-dichalcogenides: synthesis of 3-organochalcogenyl indoles

inferred← citeshttps://doi.org/10.1039/c9nj02682gopenalex-snapshot

Substrate-switched dual functionalization of alkenes: catalyst-free synthetic route for β-hydroxy and β-keto thioethers

inferred← citeshttps://doi.org/10.1039/c9ob01061kopenalex-snapshot

Metal-free regioselective direct thiolation of 2-pyridones

inferred← citeshttps://doi.org/10.1039/c9qo00350aopenalex-snapshot

Metal- and phosphine-free electrophilic vicinal chloro-alkylthiolation and trifluoromethylthiolation of indoles using sodium sulfinate in the presence of triphosgene

inferred← citeshttps://doi.org/10.1039/c9qo01497gopenalex-snapshot

Chelation-assisted transition metal-catalysed C–H chalcogenylations

inferred← citeshttps://doi.org/10.1039/d0ob01073aopenalex-snapshot

Arylseleninic acid as a green, bench-stable selenylating agent: synthesis of selanylanilines and 3-selanylindoles

inferred← citeshttps://doi.org/10.1039/d0ra10629aopenalex-snapshot

Synthetic strategies for aryl/heterocyclic selenides and tellurides under transition-metal-catalyst free conditions

inferred← citeshttps://doi.org/10.1039/d1na00822fopenalex-snapshot

Magnetic mesocellular foams with nickel complexes: as efficient and reusable nanocatalysts for the synthesis of symmetrical and asymmetrical diaryl chalcogenides

inferred← citeshttps://doi.org/10.1039/d1ob02108gopenalex-snapshot

Electrochemical regioselective C–H selenylation of 2 H -indazole derivatives

inferred← citeshttps://doi.org/10.1039/d2cc02181aopenalex-snapshot

A base-free copper-assisted synthesis of C 2 -symmetric spirotelluranes and biaryls based on divergent stoichiometry of Na 2 Te

inferred← citeshttps://doi.org/10.1039/d2nj04068aopenalex-snapshot

Solvent free synthesis of organoselenides under green conditions

inferred← citeshttps://doi.org/10.1039/d2ob00022aopenalex-snapshot

Synthesis of phenoxathiins using an iron-catalysed C–H thioarylation

inferred← citeshttps://doi.org/10.1039/d2qo00148aopenalex-snapshot

The electrochemically selective C3-thiolation of quinolines

inferred← citeshttps://doi.org/10.1039/d3gc00664fopenalex-snapshot

Electrochemical single-step N -acylation and S -cyclization synthesis of thiazolimide via radical process

inferred← citeshttps://doi.org/10.1039/d3ob00150dopenalex-snapshot

Regioselective C–H chalcogenylation and halogenation of arenes and alkenes under metal-free conditions

inferred← citeshttps://doi.org/10.1039/d3ob01847dopenalex-snapshot

Recent advances in selective mono-/dichalcogenation and exclusive dichalcogenation of C(sp 2 )–H and C(sp 3 )–H bonds

inferred← citeshttps://doi.org/10.1039/d3qo01844jopenalex-snapshot

Electrochemical difunctionalization of alkenes and alkynes for the synthesis of organochalcogens involving C–S/Se bond formation

inferred← citeshttps://doi.org/10.1039/d4ob01382dopenalex-snapshot

Fe( iii )-catalyzed p -selective C–H bond chalcogenation of phenols

inferred← citeshttps://doi.org/10.1039/d4ob01929fopenalex-snapshot

FeCl 3 -catalyzed oxidative diselenylation of pyrrole-tethered indoles

inferred← citeshttps://doi.org/10.1039/d6ma00112bopenalex-snapshot

Copper immobilized on a layered magnetite-based nanocatalyst for sustainable Ullmann cross-coupling reaction

inferred← citeshttps://doi.org/10.1039/d6qo01013jopenalex-snapshot

Calcium( ii )-catalyzed selective C–H selenylation of arenes with selenium–nitrogen exchange (SeNEx) reagents

inferred← citeshttps://doi.org/10.1055/a-1592-6394openalex-snapshot

Tetrabutylammonium Iodide Mediated Sulfenylation of Polysubstituted 1H-Pyrazol-5-amines with Arylsulfonyl Hydrazides

inferred← citeshttps://doi.org/10.1055/a-2112-2353openalex-snapshot

Visible-Light-Induced Metal-Free Selenation of Tryptamines/3-Substituted Indoles

inferred← citeshttps://doi.org/10.1055/s-0037-1609835openalex-snapshot

Latent Radical Cleavage of α-Allenylic C–O Bonds: Potassium Persulfate Mediated Thiolation of Allenylphosphine Oxides

inferred← citeshttps://doi.org/10.1055/s-0037-1610852openalex-snapshot

Recent Developments in Palladium-Catalysed Non-Directed C–H Bond Activation in Arenes

inferred← citeshttps://doi.org/10.1080/10426507.2015.1073278openalex-snapshot

Iodine-promoted direct sulfenylation of 2,3-dihydroimidazo[2,1-b]thiazoles with disulfides

inferred← citeshttps://doi.org/10.1246/cl.200015openalex-snapshot

Organoseleniums: Generated and Exploited in Oxidative Reactions

inferred← citeshttps://doi.org/10.14233/ajomc.2019.ajomc-p189openalex-snapshot

Synthesis, Characterization, Crystal and Molecular Structure Analysis of 1-(2-Chlorophenyl)-3-methyl-4-(p-tolylthio)-1H-pyrazol-5-ol

inferred← citeshttps://doi.org/10.2174/1385272824999200528130131openalex-snapshot

Recent Developments and Perspectives in the C-Se Cross Coupling Reactions

inferred← citeshttps://doi.org/10.26479/2019.0502.72openalex-snapshot

Synthesis and Crystallographic Analysis of 1-(2-chlorophenyl)-3-methyl-4-(p-tolylthio)-1h-pyrazol-5-ol

inferred← citeshttps://doi.org/10.3390/nano10061237openalex-snapshot

Exploration of the Interaction Strength at the Interface of Anionic Chalcogen Anchors and Gold (111)-Based Nanomaterials

inferred← citeshttps://doi.org/10.3762/bjoc.13.199openalex-snapshot

Transition-metal-free synthesis of 3-sulfenylated chromones via KIO3-catalyzed radical C(sp2)–H sulfenylation

inferred← citeshttps://doi.org/10.3762/bjoc.9.127openalex-snapshot

Photoinduced synthesis of unsymmetrical diaryl selenides from triarylbismuthines and diaryl diselenides

inferred← citeshttps://doi.org/10.3998/ark.5550190.p009.238openalex-snapshot

Transition metal- and solvent-free synthesis of unsymmetrical diaryl sulfides and selenides under ball-milling

inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.76.11openalex-snapshot

Direct Thiolation and Selenation of Aryl C-H Bonds Catalyzed by Palladium or Nickel

inferred← citeshttps://doi.org/10.6023/cjoc202407024openalex-snapshot

Efficient Synthesis of Diaryl Sulfides via Three Component Cross Coupling

inferred← citeshttps://doi.org/10.7287/peerj.4706v0.1/reviews/1openalex-snapshot

Peer Review #1 of "Ultrasound-promoted synthesis of 2-organoselanyl-naphthalenes using Oxone® in aqueous medium as an oxidizing agent (v0.1)"

inferred← citeshttps://doi.org/10.7287/peerj.4706v0.1/reviews/2openalex-snapshot

Peer Review #2 of "Ultrasound-promoted synthesis of 2-organoselanyl-naphthalenes using Oxone® in aqueous medium as an oxidizing agent (v0.1)"

inferred← citeshttps://doi.org/10.7287/peerj.4706v0.1/reviews/3openalex-snapshot

Peer Review #3 of "Ultrasound-promoted synthesis of 2-organoselanyl-naphthalenes using Oxone® in aqueous medium as an oxidizing agent (v0.1)"

inferred← citeshttps://doi.org/10.7717/peerj.4706openalex-snapshot

Ultrasound-promoted synthesis of 2-organoselanyl-naphthalenes using Oxone ® in aqueous medium as an oxidizing agent

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.