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Palladium Catalyzed Aryl(alkyl)thiolation of Unactivated Arenes

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What this work says

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

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Palladium‐Catalyzed Direct Synthesis of Phosphole Derivatives from Triarylphosphines through Cleavage of Carbon–Hydrogen and Carbon–Phosphorus Bonds

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A general and efficient method for the palladium-catalyzed cross-coupling of thiols and secondary phosphines

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Functionalized Acenes and Heteroacenes for Organic Electronics

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A General and Long-Lived Catalyst for the Palladium-Catalyzed Coupling of Aryl Halides with Thiols

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Pd-Catalyzed Intermolecular C–H Amination with Alkylamines

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Consecutive Thiophene-Annulation Approach to π-Extended Thienoacene-Based Organic Semiconductors with [1]Benzothieno[3,2- b ][1]benzothiophene (BTBT) Substructure

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

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

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Rhodium Catalyzed Cyanation of Chelation Assisted C–H Bonds

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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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Heterogeneously Catalyzed Direct CH Thiolation of Heteroarenes

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Hemilabile and Redox‐Active Quinone Ligands Unlock sp 3 ‐Rich Couplings in Nickel‐Catalyzed Olefin Carbosulfenylation

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ChemInform Abstract: Palladium Catalyzed Aryl(alkyl)thiolation of Unactivated Arenes.

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Rhodium Catalyzed C2-Selective Cyanation of Indoles and Pyrroles

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

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

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Electrochemical Oxidative Nucleophilic Disulfenylation of Anilines

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Cobalt-Catalyzed Aerobic Cross-Dehydrogenative Coupling of C–H and Thiols in Water for C–S Formation

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Palladium-Catalyzed Oxidative Cross-Coupling of Arylhydrazines and Arenethiols with Molecular Oxygen as the Sole Oxidant

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

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Acid-Mediated Sulfonylthiolation of Arenes via Selective Activation of SS-Morpholino Dithiosulfonate

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Copper-Catalyzed Regioselective Remote C–H Bond Chalcogenation of Aromatic Amine Derivatives without Using Any Large Template

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Acid-Promoted Carbosulfenylation of 1,6-Dienes: Selective Synthesis of Dehydropiperidines Scaffolds

inferred← citeshttps://doi.org/10.1021/acs.orglett.3c03851openalex-snapshot

Synthesis of Thiazoloindole α-Amino Acids: Chromophores Amenable to One- and Two-Photon Induced Fluorescence

inferred← citeshttps://doi.org/10.1021/acs.orglett.5b00337openalex-snapshot

Direct ortho-Thiolation of Arenes and Alkenes by Nickel Catalysis

inferred← citeshttps://doi.org/10.1021/acs.orglett.5b00471openalex-snapshot

Nickel-Catalyzed Direct Thioetherification of β-C(sp3)–H Bonds of Aliphatic Amides

inferred← citeshttps://doi.org/10.1021/acs.orglett.5b01746openalex-snapshot

Rhodium-Catalyzed Cyanation of C(sp2)–H Bond of Alkenes

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.5c00198openalex-snapshot

Regioselective N-arylation of N-Acylsulfenamides Enabled by o-Quinone Diimides

inferred← citeshttps://doi.org/10.1021/acs.orglett.5c01557openalex-snapshot

A Unified Strategy for Transition-Metal-Free Synthesis of Benzothienopyridines, Benzoselenopyridines, and Benzotelluropyridines and Related Analogues

inferred← citeshttps://doi.org/10.1021/acs.orglett.5c05467openalex-snapshot

Access to Imidazolidin-2-ones via Azocarboxamide-Enabled Enantioselective 1,2-Diamination of Aldehyde

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.6c01427openalex-snapshot

Skeletal Editing of Isoquinolines Via CN/CC Atom-Pair Swap Enables the Synthesis of 3-Arylthio-2-O-acylated Naphthols and DFT Studies

inferred← citeshttps://doi.org/10.1021/acs.orglett.7b02599openalex-snapshot

Synthesis of Diverse o-Arylthio-Substituted Diaryl Ethers by Direct Oxythiolation of Arynes with Diaryl Sulfoxides Involving Migratory O-Arylation

inferred← citeshttps://doi.org/10.1021/acs.orglett.8b00065openalex-snapshot

Acid-Mediated Oxychalcogenation of o -Vinylanilides with N -(Arylthio/arylseleno)succinimides

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.8b02347openalex-snapshot

Cyclization of 2-Biphenylthiols to Dibenzothiophenes under PdCl2/DMSO Catalysis

inferred← citeshttps://doi.org/10.1021/acscatal.6b03236openalex-snapshot

Expedient C–H Chalcogenation of Indolines and Indoles by Positional-Selective Copper Catalysis

inferred← citeshttps://doi.org/10.1021/acscatal.8b03912openalex-snapshot

Palladium-Catalyzed Asymmetric C–H Arylation for the Synthesis of Planar Chiral Benzothiophene-Fused Ferrocenes

inferred← citeshttps://doi.org/10.1021/acscatal.9b04931openalex-snapshot

Dechalcogenization of Aryl Dichalcogenides to Synthesize Aryl Chalcogenides via Copper Catalysis

inferred← citeshttps://doi.org/10.1021/acscentsci.5c01231openalex-snapshot

Metal and Additive-Free Nondirected Meta-C–S Bond Formation on Anilines: Toward Biologically Relevant S -Aryl Dithiocarbamates

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/jo501778hopenalex-snapshot

Iodine-Mediated Thiolation of Substituted Naphthols/Naphthylamines and Arylsulfonyl Hydrazides via C(sp2)–H Bond Functionalization

inferred← citeshttps://doi.org/10.1021/ol500874popenalex-snapshot

Rhodium Catalyzed Direct Arylation of α-Diazoimines

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/s41467-019-11398-0openalex-snapshot

Sulfenamide-enabled ortho thiolation of aryl iodides via palladium/norbornene cooperative catalysis

inferred← citeshttps://doi.org/10.1039/c4cc02876gopenalex-snapshot

Palladium-catalyzed thiolation of alkanes and ethers with arylsulfonyl hydrazides

inferred← citeshttps://doi.org/10.1039/c4cc03600jopenalex-snapshot

Iron or boron-catalyzed C–H arylthiation of substituted phenols at room temperature

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/c4cc10446copenalex-snapshot

Nickel-catalyzed thiolation of unactivated aryl C–H bonds: efficient access to diverse aryl sulfides

inferred← citeshttps://doi.org/10.1039/c5cc01436kopenalex-snapshot

Nickel-catalyzed direct thiolation of unactivated C(sp 3 )–H bonds with disulfides

inferred← citeshttps://doi.org/10.1039/c5cc05421dopenalex-snapshot

TFA-promoted direct C–H sulfenylation at the C2 position of non-protected indoles

inferred← citeshttps://doi.org/10.1039/c5cc07463kopenalex-snapshot

A mild and facile synthesis of aryl and alkenyl sulfides via copper-catalyzed deborylthiolation of organoborons with thiosulfonates

inferred← citeshttps://doi.org/10.1039/c5gc00403aopenalex-snapshot

Iodine catalyzed cross-dehydrogenative C–S coupling by C(sp 2 )–H bond activation: direct access to aryl sulfides from aryl thiols

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/c5ob00252dopenalex-snapshot

Metal-free oxysulfenylation of alkenes with 1-(arylthio)pyrrolidine-2,5-diones and alcohols

inferred← citeshttps://doi.org/10.1039/c5ob01241dopenalex-snapshot

Regioselective functionalisation of dibenzothiophenes through gold-catalysed intermolecular alkyne oxyarylation

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/c5ra01342aopenalex-snapshot

Regioselective copper-catalyzed thiolation of imidazo[1,2-a]pyridines: an efficient C–H functionalization strategy for C–S bond formation

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/c5sc04890gopenalex-snapshot

Palladium( ii )-catalyzed synthesis of dibenzothiophene derivatives via the cleavage of carbon–sulfur and carbon–hydrogen bonds

inferred← citeshttps://doi.org/10.1039/c6cc04486gopenalex-snapshot

Aerobic copper-catalyzed decarboxylative thiolation

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/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/c6qo00477fopenalex-snapshot

Highly selective synthesis of 6-substituted benzothiophenes by Sc(OTf) 3 -catalyzed intermolecular cyclization and sulfur migration

inferred← citeshttps://doi.org/10.1039/c6qo00841kopenalex-snapshot

Thiolate–palladium( iv ) or sulfonium–palladate(0)? A theoretical study on the mechanism of palladium-catalyzed C–S bond formation reactions

inferred← citeshttps://doi.org/10.1039/c7ob01225jopenalex-snapshot

Intermolecular sulfenoamination of alkenes with sulfonamides and N-sulfanylsuccinimides to access β-sulfonylamino sulfides and dihydrobenzothiazines

inferred← citeshttps://doi.org/10.1039/c7qo00218aopenalex-snapshot

DMSO-promoted regioselective synthesis of sulfenylated pyrazoles via a radical pathway

inferred← citeshttps://doi.org/10.1039/c7qo00717eopenalex-snapshot

Highly mono-selective ortho -methylthiolation of benzamides via cobalt-catalyzed sp 2 C–H activation

inferred← citeshttps://doi.org/10.1039/c7ra02350bopenalex-snapshot

Regioselective thiolation of electron rich arenes and heterocycles in recyclable catalytic media

inferred← citeshttps://doi.org/10.1039/c8cc00271aopenalex-snapshot

Decarbonylative thioetherification by nickel catalysis using air- and moisture-stable nickel precatalysts

inferred← citeshttps://doi.org/10.1039/c8cc08328bopenalex-snapshot

Nitrosonium ion catalysis: aerobic, metal-free cross-dehydrogenative carbon–heteroatom bond formation

inferred← citeshttps://doi.org/10.1039/c8cc09821bopenalex-snapshot

Transition-metal-free regioselective cross-coupling of BODIPYs with thiols

inferred← citeshttps://doi.org/10.1039/c8ob00235eopenalex-snapshot

A Pd-catalyzed optional approach for the synthesis of dibenzothiophenes

inferred← citeshttps://doi.org/10.1039/c8ob00238jopenalex-snapshot

A visible-light photocatalytic thiolation of aryl, heteroaryl and vinyl iodides

inferred← citeshttps://doi.org/10.1039/c8ob01481gopenalex-snapshot

Nickel-catalyzed direct C–H bond sulfenylation of acylhydrazines

inferred← citeshttps://doi.org/10.1039/c8ob02111bopenalex-snapshot

Cp*Co( iii )-catalysed selective alkylation of C–H bonds of arenes and heteroarenes with α-diazocarbonyl compounds

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/c9ob01255aopenalex-snapshot

Copper-mediated direct thiolation of aryl C–H bonds with disulfides

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

Chelation-assisted transition metal-catalysed C–H chalcogenylations

inferred← citeshttps://doi.org/10.1039/d0nj05904hopenalex-snapshot

Metal-free efficient thiolation of C(sp 2 ) functionalization via in situ -generated NHTS for the synthesis of novel sulfenylated 2-aminothiazole and imidazothiazole

inferred← citeshttps://doi.org/10.1039/d0ob00244eopenalex-snapshot

Room temperature nickel-catalyzed cross-coupling of aryl-boronic acids with thiophenols: synthesis of diarylsulfides

inferred← citeshttps://doi.org/10.1039/d0ob02035dopenalex-snapshot

Advances in Cu and Ni-catalyzed Chan–Lam-type coupling: synthesis of diarylchalcogenides, Ar 2 –X (X = S, Se, Te)

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

Recent developments in palladium-catalyzed C–S bond formation

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/d0qo01576hopenalex-snapshot

General and practical intramolecular decarbonylative coupling of thioesters via palladium catalysis

inferred← citeshttps://doi.org/10.1039/d1cc03760aopenalex-snapshot

Cp*Co( iii )-catalyzed C2-thiolation and C2,C3-dithiolation of substituted indoles with N -(arylthio)succinimide

inferred← citeshttps://doi.org/10.1039/d1cc05835eopenalex-snapshot

Catalytic enantioselective oxysulfenylation of o -vinylanilides

inferred← citeshttps://doi.org/10.1039/d1nj04033bopenalex-snapshot

BF 3 ·Et 2 O catalyzed transannulation of pyridotriazoles with isothiocyanates: synthesis of thiazolo[3,4- a ]pyridin-3-imines

inferred← citeshttps://doi.org/10.1039/d1qo00824bopenalex-snapshot

Decarbonylative sulfide synthesis from carboxylic acids and thioesters via cross-over C–S activation and acyl capture

inferred← citeshttps://doi.org/10.1039/d1qo00972aopenalex-snapshot

NaI/TBHP-promoted reaction of indole-2-thiones with arylsulfonyl hydrazides: construction of achiral axial 3,3′-biindole-2,2′-dibenzenesulfonothioate derivatives

inferred← citeshttps://doi.org/10.1039/d2cc06706dopenalex-snapshot

Rapid access to polycyclic thiopyrylium compounds from unfunctionalized aromatics by thia-APEX reaction

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

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

inferred← citeshttps://doi.org/10.1039/d2ob00986bopenalex-snapshot

Transition metal catalysed direct sulfanylation of unreactive C–H bonds: an overview of the last two decades

inferred← citeshttps://doi.org/10.1039/d2ob01082hopenalex-snapshot

Thioarylation of anilines using dual catalysis: two-step synthesis of phenothiazines

inferred← citeshttps://doi.org/10.1039/d2ob01792jopenalex-snapshot

BiCl 3 catalyzed synthesis of 2-amino-1,4-naphthoquinones and 1,4-naphthoquinon-2-sulfides and one-pot sequential amine-arylation of 1,4-naphthoquinone

inferred← citeshttps://doi.org/10.1039/d2qo01317gopenalex-snapshot

“Thiol-free synthesized” and sustainable thiolating synthons for nickel-catalyzed reductive assembly of sulfides with high efficiency

inferred← citeshttps://doi.org/10.1039/d2qo01447eopenalex-snapshot

Recent advances in thiolation via sulfur electrophiles

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/d3qo00744hopenalex-snapshot

Predominant intermolecular decarbonylative thioetherification of carboxylic acids using nickel precatalysts

inferred← citeshttps://doi.org/10.1039/d4ob00524dopenalex-snapshot

Expedient, regioselective C–H chalcogenation of 3,4-dihydro-1,4-benzoxazines using a palladium–copper catalyst

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/d4qo00312hopenalex-snapshot

Vaska's complex–PMHS combination enabled mild and chemoselective reduction of sulfoxides to sulfides with low catalyst loading

inferred← citeshttps://doi.org/10.1039/d4qo01546kopenalex-snapshot

HSAB theory guiding electrophilic substitution reactions of o -carborane

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/d5cs00165jopenalex-snapshot

Metal-catalysed non-directed C(sp 2 )–H bond activation

inferred← citeshttps://doi.org/10.1039/d5qo01523eopenalex-snapshot

Samarium diiodide-mediated radical thioetherification of alkyl bromides with thiols by ruthenium catalysis

inferred← citeshttps://doi.org/10.1039/d6ob01085gopenalex-snapshot

Recent advances in the thioglycosylation of indoles and tryptophan: strategies and applications in natural product synthesis

inferred← citeshttps://doi.org/10.1055/a-2004-1006openalex-snapshot

Facile Synthesis of Diaryl Sulfones through Arylsulfonylation of Arynes and Thiosulfonates

inferred← citeshttps://doi.org/10.1055/a-2169-4078openalex-snapshot

Heteroatom-Embedding Annulative π-Extension (Hetero-APEX) Reactions: An Overview

inferred← citeshttps://doi.org/10.1055/a-2721-6900openalex-snapshot

Synthesis of Dibenzothiophenes via a Deglucosylative C−H Thiolation of Biarylthioglycosides

inferred← citeshttps://doi.org/10.1055/s-0036-1591505openalex-snapshot

Synthesis of 4-Aryl-3-arylthio-3,4-dihydroquinolin-2(1H)-ones via Cyclization of N-Arylcinnamamides with N-Thiosuccinimides

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/10.1080/00268976.2019.1576933openalex-snapshot

A DFT study on the mechanism of palladium-catalysed tandem reaction of ortho-electron-deficient alkynyl-substituted aryl aldehydes with indoles

inferred← citeshttps://doi.org/10.1080/00397911.2016.1181764openalex-snapshot

Transition-metal-free synthesis of thiocyanato- or nitro-arenes through diaryliodonium salts

inferred← citeshttps://doi.org/10.1080/10426507.2015.1012670openalex-snapshot

Mild synthesis of N-acylsulfenamides from arylamides and disulfides

inferred← citeshttps://doi.org/10.1134/s1023193520040138openalex-snapshot

Electrosynthesis of Mono- and Disulfides Based on C5–C8 Cycloalkanes, Hydrogen Sulfide, and Isomeric Dibutyl Disulfides

inferred← citeshttps://doi.org/10.1246/cl.151090openalex-snapshot

Synthesis of N-Acylsulfenamides through Aerobic Cross Dehydrogenative Coupling of Thiols and Amides by Supported Copper Hydroxide Catalyst

inferred← citeshttps://doi.org/10.1246/cl.180555openalex-snapshot

Generation of Arynes by Selective Cleavage of a Carbon–Phosphorus Bond of o-(Diarylphosphinyl)aryl Triflates Using a Grignard Reagent

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

Organoseleniums: Generated and Exploited in Oxidative Reactions

inferred← citeshttps://doi.org/10.1246/cl.200132openalex-snapshot

Synthesis of Phenoxathiins and Phenothiazines by Aryne Reactions with Thiosulfonates

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/10.16943/ptinsa/2016/48572openalex-snapshot

Palladium Catalyzed Aerobic Oxidative Cyclization of ortho-Vinylanilines with Isocyanides

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/10.2174/1570178615666180627111437openalex-snapshot

Cu(OAc)2-Promoted Thiolation and Selenylation of C(sp2)-H Bonds Using a 2-Amino Oxazole Directing Group

inferred← citeshttps://doi.org/10.26434/chemrxiv-2023-ft0bnopenalex-snapshot

Hemilabile Quinone Ligands Enable Nickel-Catalyzed C−S(Alkyl) Bond Formation in the Carbosulfenylation of Unactivated Alkenes

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/m2017openalex-snapshot

Novel Acid-Catalyzed Transformation of 1-Benzyl-3-Chloro-5-Hydroxy-4-[(4-Methylphenyl)Sulfanyl]-1,5-Dihydro-2H-Pyrrol-2-One

inferred← citeshttps://doi.org/10.3390/m985openalex-snapshot

Gold-Catalyzed Synthesis of 2-Sulfenylspiroindolenines via Spirocyclizations

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.19.106openalex-snapshot

N -Sulfenylsuccinimide/phthalimide: an alternative sulfenylating reagent in organic transformations

inferred← citeshttps://doi.org/10.3987/com-16-13531openalex-snapshot

Palladium Catalyzed Syntheses of Dibenzothiophenes by Ring-Closure of 2-Iodinated Diaryl Thioether

inferred← citeshttps://doi.org/10.3987/com-18-13974openalex-snapshot

HBr-Promoted Sulfenylation of Pyrazolones and 4-Hydroxycoumarins with N-(Organothio)succinimides

inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.76.1185openalex-snapshot

Catalytic Synthesis of Heterocycles via the Cleavage of Carbon-Heteroatom Bonds

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