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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

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What this work says

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

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Preparation of n‐Butyl 4‐Chlorophenyl Sulfide

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Topics in Current Chemistry

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A general rhodium-catalyzed cross-coupling reaction of thiols with aryl iodides

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Palladium - catalyzed reactions of trialkylstannyl phenyl sulfides with alkenyl bromides. A new diastereoselective synthesis of (E)-1-alkenyl phenyl sulfides

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Phosphazene bases for the preparation of biaryl thioethers from aryl iodides and arenethiols

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

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Ligand-Free Copper-Catalyzed C−S Coupling of Aryl Iodides and Thiols

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Palladium-Catalyzed Carbon−Sulfur Cross-Coupling Reactions with Indium Tri(organothiolate) and Its Application to Sequential One-Pot Processes

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Zinc-Mediated Palladium-Catalyzed Formation of Carbon−Sulfur Bonds

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Copper-Mediated Cross-Coupling of Aryl Boronic Acids and Alkyl Thiols

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PREPARATION OF n-BUTYL 4-CHLOROPHENYL SULFIDE

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

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Aqueous Compatible Protocol to Both Alkyl and Aryl Thioamide Synthesis

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inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02161openalex-snapshot

A Novel Fluorescent Skeleton from Disubstituted Thiochromenones via Nickel-Catalyzed Cycloaddition of Sulfobenzoic Anhydrides with Alkynes

inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02584openalex-snapshot

Transition-Metal-Free Aryl–Heteroatom Bond Formation via C–S Bond Cleavage

inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02784openalex-snapshot

Thiocarbonyl Surrogate via Combination of Potassium Sulfide and Chloroform for Dithiocarbamate Construction

inferred← citeshttps://doi.org/10.1021/acscatal.4c04604openalex-snapshot

Selective Syntheses of Unsymmetrical Diaryl Sulfides Enabled by a Sulfur Dioxide Surrogate as a Divalent Sulfur Source and an Activating Agent

inferred← citeshttps://doi.org/10.1021/acscatal.7b02735openalex-snapshot

Controllable Sulfoxidation and Sulfenylation with Organic Thiosulfate Salts via Dual Electron- and Energy-Transfer Photocatalysis

inferred← citeshttps://doi.org/10.1021/acscatal.9b01913openalex-snapshot

Monophosphine Ligands Promote Pd-Catalyzed C–S Cross-Coupling Reactions at Room Temperature with Soluble Bases

inferred← citeshttps://doi.org/10.1021/jacs.0c11937openalex-snapshot

Photoredox Nickel-Catalyzed C–S Cross-Coupling: Mechanism, Kinetics, and Generalization

inferred← citeshttps://doi.org/10.1021/jacs.3c13900openalex-snapshot

Photochemical Organocatalytic Synthesis of Thioethers from Aryl Chlorides and Alcohols

inferred← citeshttps://doi.org/10.1021/jacs.6b01707openalex-snapshot

Utility of Ligand Effect in Homogenous Gold Catalysis: Enabling Regiodivergent π-Bond-Activated Cyclization

inferred← citeshttps://doi.org/10.1021/jacs.6b02495openalex-snapshot

Cleavage of the C(O)–S Bond of Thioesters by Palladium/Norbornene/Copper Cooperative Catalysis: An Efficient Synthesis of 2-(Arylthio)aryl Ketones

inferred← citeshttps://doi.org/10.1021/ol5009747openalex-snapshot

A Highly Efficient Cu-Catalyzed S-Transfer Reaction: From Amine to Sulfide

inferred← citeshttps://doi.org/10.1021/ol5011449openalex-snapshot

Syntheses of Sulfides and Selenides through Direct Oxidative Functionalization of C(sp3)–H Bond

inferred← citeshttps://doi.org/10.1021/ol502381eopenalex-snapshot

Direct Synthesis of Diverse 2-Aminobenzo[b]thiophenes via Palladium-Catalyzed Carbon–Sulfur Bond Formation Using Na2S2O3as the Sulfur Source

inferred← citeshttps://doi.org/10.1021/ol5025162openalex-snapshot

Sulfur Incorporation: Copper-Catalyzed Cascade Cyclization of 1,7-Enynes with Metal Sulfides toward Thieno[3,4-c]quinolin-4(5H)-ones

inferred← citeshttps://doi.org/10.1039/c4cc04148hopenalex-snapshot

Stereoselective construction of a key hydroindole precursor of epidithiodiketopiperazine (ETP) natural products

inferred← citeshttps://doi.org/10.1039/c4cc08367aopenalex-snapshot

Sulfide synthesis through copper-catalyzed C–S bond formation under biomolecule-compatible conditions

inferred← citeshttps://doi.org/10.1039/c4cc08370aopenalex-snapshot

Palladium-catalyzed benzothieno[2,3-b]indole formation via dehydrative–dehydrogenative double C–H sulfuration using sulfur powder, indoles and cyclohexanones

inferred← citeshttps://doi.org/10.1039/c4cc09633aopenalex-snapshot

Transition-metal-free persulfuration to construct unsymmetrical disulfides and mechanistic study of the sulfur redox process

inferred← citeshttps://doi.org/10.1039/c4ob01992jopenalex-snapshot

Efficient silver-catalyzed direct sulfenylation and selenylation of rich arenes

inferred← citeshttps://doi.org/10.1039/c4ra11490fopenalex-snapshot

An odorless, one-pot synthesis of nitroaryl thioethers via S N Ar reactions through the in situ generation of S-alkylisothiouronium salts

inferred← citeshttps://doi.org/10.1039/c5cc03038bopenalex-snapshot

CO 2 -promoted oxidative cross-coupling reaction for C–S bond formation via masked strategy in an odourless way

inferred← citeshttps://doi.org/10.1039/c5ob00769kopenalex-snapshot

Catalyst-free direct decarboxylative coupling of α-keto acids with thiols: a facile access to thioesters

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/c5qo00276aopenalex-snapshot

2′-Cyanoethyl thioglycosides: effective nucleophiles for synthesis of (hetero)aryl thioglycosides under the catalysis of Cu

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/c5ra01381jopenalex-snapshot

An odorless thia-Michael addition using Bunte salts as thiol surrogates

inferred← citeshttps://doi.org/10.1039/c5ra05244kopenalex-snapshot

Ligand-free Cu-catalyzed odorless synthesis of unsymmetrical sulfides through cross-coupling reaction of aryl/benzyl/alkyl halides with an aryl boronic acid/S 8 system as a thiolating agent in PEG

inferred← citeshttps://doi.org/10.1039/c5ra16879aopenalex-snapshot

The direct synthesis of symmetrical disulfides and diselenides by metal–organic framework MOF-199 as an efficient heterogenous catalyst

inferred← citeshttps://doi.org/10.1039/c6cc09201bopenalex-snapshot

Cu( ii )-catalyzed sulfide construction: both aryl groups utilization of intermolecular and intramolecular diaryliodonium salt

inferred← citeshttps://doi.org/10.1039/c6ob02833kopenalex-snapshot

Recent developments in sulfur–carbon bond formation reaction involving thiosulfates

inferred← citeshttps://doi.org/10.1039/c6ra27201kopenalex-snapshot

CuI promoted sulfenylation of organozinc reagents with arylsulfonyl chlorides

inferred← citeshttps://doi.org/10.1039/c6sc04504aopenalex-snapshot

Metal-free O–H/C–H difunctionalization of phenols by o-hydroxyarylsulfonium salts in water

inferred← citeshttps://doi.org/10.1039/c7qo00724hopenalex-snapshot

A thiol-free synthesis of alkynyl chalcogenides by the copper-catalyzed C–X (X = S, Se) cross-coupling of alkynyl carboxylic acids with Bunte salts

inferred← citeshttps://doi.org/10.1039/c7qo01114hopenalex-snapshot

Elemental sulfur accelerated the reactivity of the 3-position of indole for the construction of chromeno[2,3- b ]indoles

inferred← citeshttps://doi.org/10.1039/c8cc07599aopenalex-snapshot

NaHS· n H 2 O-induced umpolung: the synthesis of 2-acyl-3-aminoindoles from aryl methyl ketones and 2-aminobenzonitriles

inferred← citeshttps://doi.org/10.1039/c8ob01758aopenalex-snapshot

Cesium carbonate-promoted synthesis of aryl methyl sulfides using S -methylisothiourea sulfate under transition-metal-free conditions

inferred← citeshttps://doi.org/10.1039/c8ob02680gopenalex-snapshot

Direct halosulfenylation of benzo[ b ]furans: a metal-free synthesis of 3-halo-2-thiobenzo[ b ]furans

inferred← citeshttps://doi.org/10.1039/c8qo00435hopenalex-snapshot

One pot preparation of α-dithioacetal/α-diselenoacetal amides via a dual-C–S/C–Se bond formation and C–C bond cleavage cascade of 3-oxo-butanamides

inferred← citeshttps://doi.org/10.1039/c8qo00481aopenalex-snapshot

Green carbon disulfide surrogate via a combination of potassium sulfide and chloroform for benzothiazine-thione and benzothiazole-thione construction

inferred← citeshttps://doi.org/10.1039/c9gc01718fopenalex-snapshot

A palladium-catalyzed three-component cascade S-transfer reaction in ionic liquids

inferred← citeshttps://doi.org/10.1039/c9nj03024gopenalex-snapshot

Environmentally friendly synthesis of unsymmetrical dialkyl disulfides by reacting organic halides with thiourea and sodium thiosulfate in an aqueous medium

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

Chelation-assisted transition metal-catalysed C–H chalcogenylations

inferred← citeshttps://doi.org/10.1039/d0ob00828aopenalex-snapshot

Palladium-catalyzed three-component cascade arylthiolation with aryldiazonium salts as S -arylation sources

inferred← citeshttps://doi.org/10.1039/d0ob02320eopenalex-snapshot

Metal-catalyzed C–S bond formation using sulfur surrogates

inferred← citeshttps://doi.org/10.1039/d0qo00377hopenalex-snapshot

Recent developments in palladium-catalyzed C–S bond formation

inferred← citeshttps://doi.org/10.1039/d0qo00609bopenalex-snapshot

Recent advances in metal catalyzed or mediated cyclization/functionalization of alkynes to construct isoxazoles

inferred← citeshttps://doi.org/10.1039/d0qo01226bopenalex-snapshot

Synthetic developments on the preparation of sulfides from thiol-free reagents

inferred← citeshttps://doi.org/10.1039/d0ra00719fopenalex-snapshot

Palladium nanoparticles immobilized on a nano-silica triazine dendritic polymer: a recyclable and sustainable nanoreactor for C–S cross-coupling

inferred← citeshttps://doi.org/10.1039/d0sc01060jopenalex-snapshot

Steric and stereoscopic disulfide construction for cross-linkage via N -dithiophthalimides

inferred← citeshttps://doi.org/10.1039/d1nj04662dopenalex-snapshot

The journey of C–S bond formation from metal catalysis to electrocatalysis

inferred← citeshttps://doi.org/10.1039/d1qo00001bopenalex-snapshot

Phthalimide-based-SSCF 3 reagent for enantioselective dithiotrifluoromethylation

inferred← citeshttps://doi.org/10.1039/d1ra05773aopenalex-snapshot

Palladium-catalyzed bisthiolation of terminal alkynes for the assembly of diverse ( Z )-1,2-bis(arylthio)alkene derivatives

inferred← citeshttps://doi.org/10.1039/d2nj03164gopenalex-snapshot

Copper catalyzed reaction of alcohols, alkyl halides and Na 2 S 2 O 3 : an odorless and ligand-free route to unsymmetrical thioether synthesis

inferred← citeshttps://doi.org/10.1039/d2nj05472hopenalex-snapshot

Silver( i ) complexes containing heteroleptic diorganochalcogen( ii ) ligands

inferred← citeshttps://doi.org/10.1039/d2nj06287aopenalex-snapshot

ADDP facilitates C–S bond formation from sulfonyl chlorides with alcohols

inferred← citeshttps://doi.org/10.1039/d2ob01679fopenalex-snapshot

A copper-catalyzed three-component reaction of dithioacetals with diazo ketones and ketimines

inferred← citeshttps://doi.org/10.1039/d3ob00220aopenalex-snapshot

One-pot synthesis of 11-sulfenyl dibenzodiazepines via tandem sulfenylation/cyclization of o -isocyanodiaryl amines and diaryl disulfides

inferred← citeshttps://doi.org/10.1039/d3ob00279aopenalex-snapshot

Base-mediated chalcogenoaminative annulation of 2-alkynylanilines for direct access to 3-sulfenyl/selenyl-1 H -indoles

inferred← citeshttps://doi.org/10.1039/d4ra00057aopenalex-snapshot

C(sp 2 )–H selenylation of substituted benzo[4,5]imidazo[2,1- b ]thiazoles using phenyliodine( iii )bis(trifluoroacetate) as a mediator

inferred← citeshttps://doi.org/10.1039/d5cc07298kopenalex-snapshot

Stereoselective thiosulfonylation of alkynes using sodium thiosulfate as a sulfur transfer agent to access bis -( Z )-vinyl sulfones

inferred← citeshttps://doi.org/10.1080/10426507.2019.1603231openalex-snapshot

Construction of thiocarbonyl (C = S) with inorganic sulfur

inferred← citeshttps://doi.org/10.1080/10426507.2026.2613657openalex-snapshot

Bunte salts-promoted transition-metal-free sulfenylation of 1,3-diketones: Design, synthesis and in silico evaluation of 3-(organylthio)-4-hydroxyalken-2-ones

inferred← citeshttps://doi.org/10.2139/ssrn.6411845openalex-snapshot

Synthesis of Pyrrolo[2,1-a]isoquinoline-Derived Diheteroaryl Sulfides through Na2S2O3/DMSO/HI-Based Sulfenylation

inferred← citeshttps://doi.org/10.2174/1385272824999201111204317openalex-snapshot

An Updated Coverage on the Synthesis of Benzo[b]thiophenes via Transition-metalcatalyzed Reactions: A Review

inferred← citeshttps://doi.org/10.2174/1568026615666150915111741openalex-snapshot

Sulfur Containing Scaffolds in Drugs: Synthesis and Application in Medicinal Chemistry

inferred← citeshttps://doi.org/10.2174/1570179419666220412084111openalex-snapshot

Coupling of Thiols and Aryl Halides Mediated by Dicyclohexano-18- crown-6 and Potassium Carbonate

inferred← citeshttps://doi.org/10.3184/174751915x14323930440061openalex-snapshot

Deep Eutectic Mixture Catalysed the Synthesis of Disulfides Using Bunte Salts as Thiol Surrogates

inferred← citeshttps://doi.org/10.3390/ijms232315360openalex-snapshot

Efficient Construction of Symmetrical Diaryl Sulfides via a Supported Pd Nanocatalyst-Catalyzed C-S Coupling Reaction

inferred← citeshttps://doi.org/10.3390/molecules29112485openalex-snapshot

Expedient Synthesis of Alkyl and Aryl Thioethers Using Xanthates as Thiol-Free Reagents

inferred← citeshttps://doi.org/10.3762/bjoc.17.24openalex-snapshot

Selective synthesis of α-organylthio esters and α-organylthio ketones from β-keto esters and sodiumS-organyl sulfurothioates under basic conditions

inferred← citeshttps://doi.org/10.59761/rcr5141openalex-snapshot

Methods for functionalization of anthraquinones

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