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Odorless, Regioselective Synthesis of Diaryl Sulfides and α‐Thioaryl Carbonyls from Sodium Arylsulfinates via a Metal‐ Free Radical Strategy in Water
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Thienoacene‐Based Organic Semiconductors
inferredcites →https://doi.org/10.1002/adsc.200505122openalex-snapshot
Ionic Liquid as Catalyst and Reaction Medium: A Simple, Convenient and Green Procedure for the Synthesis of Thioethers, Thioesters and Dithianes using an Inexpensive Ionic Liquid, [pmIm]Br
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Palladium on Charcoal as a Recyclable Catalyst for CS Cross‐Coupling of Thiols with Aryl Halides under Ligand‐Free Conditions
inferredcites →https://doi.org/10.1002/adsc.201201059openalex-snapshot
An Odorless, One‐Pot Synthesis of Thioesters from Organic Halides, Thiourea and Benzoyl Chlorides in Water
inferredcites →https://doi.org/10.1002/adsc.201300493openalex-snapshot
Iodine‐Catalyzed Selective Synthesis of 2‐Sulfanylphenols via Oxidative Aromatization of Cyclohexanones and Disulfides
inferredcites →https://doi.org/10.1002/adsc.201300773openalex-snapshot
Iodine‐Catalyzed Regioselective Sulfenylation of Indoles with Sodium Sulfinates
inferredcites →https://doi.org/10.1002/ange.201505090openalex-snapshot
Katalyse von Radikalreaktionen: Konzepte aus Sicht der Radikalchemie
inferredcites →https://doi.org/10.1002/anie.201505090openalex-snapshot
Catalysis of Radical Reactions: A Radical Chemistry Perspective
inferredcites →https://doi.org/10.1016/j.tet.2015.04.117openalex-snapshot
Recent advances in sulfur- and phosphorous-centered radical reactions for the formation of S–C and P–C bonds
inferredcites →https://doi.org/10.1016/j.tetlet.2004.09.021openalex-snapshot
Direct, organocatalytic α-sulfenylation of aldehydes and ketones
inferredcites →https://doi.org/10.1016/j.tetlet.2008.02.136openalex-snapshot
N-Chlorosuccinimide as a versatile reagent for the sulfenylation of ketones: a facile synthesis of α-ketothioethers
inferredcites →https://doi.org/10.1016/s0040-4039(00)87382-7openalex-snapshot
Regiospecific synthesis of α-(phenylthio)ketones via rhodium(II) acetate catalysed addition of thiophenol to α-diazoketones
inferredcites →https://doi.org/10.1016/s0040-4039(01)86424-8openalex-snapshot
Aldehyde enolates III direct sulfenylation and iodination of aldehyde anions.
inferredcites →https://doi.org/10.1016/s0040-4039(99)01843-2openalex-snapshot
InCl3: A new Lewis acid catalyst for reactions with α-diazocarbonyl compounds
inferredcites →https://doi.org/10.1021/acs.joc.5b00540openalex-snapshot
Metal-Free Iodine-Catalyzed Direct Arylthiation of Substituted Anilines with Thiols
inferredcites →https://doi.org/10.1021/acs.joc.5b02322openalex-snapshot
Cyclization of N ‑Arylacrylamides via Radical Arylsulfenylation of Carbon–Carbon Double Bonds with Sulfonyl Hydrazides
inferredcites →https://doi.org/10.1021/acs.orglett.5b01488openalex-snapshot
Odorless, One-Pot Regio- and Stereoselective Iodothiolation of Alkynes with Sodium Arenesulfinates under Metal-Free Conditions in Water
inferredcites →https://doi.org/10.1021/acs.orglett.5b01889openalex-snapshot
Synthesis of Aryl Sulfides: Metal-Free C–H Sulfenylation of Electron-Rich Arenes
inferredcites →https://doi.org/10.1021/acs.orglett.5b02752openalex-snapshot
NaI-Mediated Acetamidosulphenylation of Alkenes with Nitriles as the Nucleophiles: A Direct Access to Acetamidosulfides
inferredcites →https://doi.org/10.1021/acs.orglett.5b03654openalex-snapshot
A Route to α-Fluoroalkyl Sulfides from α-Fluorodiaroylmethanes
inferredcites →https://doi.org/10.1021/acs.orglett.6b00764openalex-snapshot
Radical–Radical Cross-Coupling for C–S Bond Formation
inferredcites →https://doi.org/10.1021/acssuschemeng.5b01784openalex-snapshot
Facile Sulfa-Michael Reactions with Sodium Arylsulfinates in Water: The Promotion of Water on the Reaction
inferredcites →https://doi.org/10.1021/ar50132a004openalex-snapshot
Some aspects of organosulfur-mediated synthetic methods
inferredcites →https://doi.org/10.1021/ar8000298openalex-snapshot
Copper/Amino Acid Catalyzed Cross-Couplings of Aryl and Vinyl Halides with Nucleophiles
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/cr400441mopenalex-snapshot
Thiyl Radicals in Organic Synthesis
inferredcites →https://doi.org/10.1021/cr60314a002openalex-snapshot
.alpha.-Sulfenylated carbonyl compounds in organic synthesis
inferredcites →https://doi.org/10.1021/cr9902749openalex-snapshot
Metal-Catalyzed Carbon−Sulfur Bond Formation
inferredcites →https://doi.org/10.1021/ja00432a034openalex-snapshot
New synthetic reactions. Sulfenylations and dehydrosulfenylations of esters and ketones
inferredcites →https://doi.org/10.1021/ja075045fopenalex-snapshot
Single Microwire Transistors of Oligoarenes by Direct Solution Process
inferredcites →https://doi.org/10.1021/ja406257uopenalex-snapshot
Consecutive Thiophene-Annulation Approach to π-Extended Thienoacene-Based Organic Semiconductors with [1]Benzothieno[3,2- b ][1]benzothiophene (BTBT) Substructure
inferredcites →https://doi.org/10.1021/jm070165jopenalex-snapshot
Design and Synthesis of Classical and Nonclassical 6-Arylthio-2,4-diamino-5-ethylpyrrolo[2,3- d ]pyrimidines as Antifolates
inferredcites →https://doi.org/10.1021/jo0493727openalex-snapshot
Indium(I) Iodide-Promoted Cleavage of Diaryl Diselenides and Disulfides and Subsequent Condensation with Alkyl or Acyl Halides. One-Pot Efficient Synthesis of Diorganyl Selenides, Sulfides, Selenoesters, and Thioesters
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/jo402586vopenalex-snapshot
Diaryl and Heteroaryl Sulfides: Synthesis via Sulfenyl Chlorides and Evaluation as Selective Anti-Breast-Cancer Agents
inferredcites →https://doi.org/10.1021/ol051049iopenalex-snapshot
Allyl Sulfones as Precursors to Allylzincs in the Palladium-Catalyzed Zinc-ene Cyclization: Highly Efficient Synthesis of Enantiopure (−)-Erythrodiene
inferredcites →https://doi.org/10.1021/ol500067fopenalex-snapshot
The Reaction of Grignard Reagents with Bunte Salts: A Thiol-Free Synthesis of Sulfides
inferredcites →https://doi.org/10.1021/ol9024088openalex-snapshot
Copper-Catalyzed Domino Intra- and Intermolecular C−S Cross-Coupling Reactions: Synthesis of 2-(Arylthio)arylcyanamides
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/c1cc13633jopenalex-snapshot
Synthesis of di(hetero)aryl sulfides by directly using arylsulfonyl chlorides as a sulfur source
inferredcites →https://doi.org/10.1039/c3gc41671bopenalex-snapshot
Iodine-catalyzed efficient 2-arylsulfanylphenol formation from thiols and cyclohexanones
inferredcites →https://doi.org/10.1039/c4ra02607aopenalex-snapshot
Iodine–PPh3-mediated C3-sulfenylation of indoles with sodium sulfinates
inferredcites →https://doi.org/10.1039/c4ra08014aopenalex-snapshot
Iodine-promoted 2-arylsulfanylphenol formation using cyclohexanones as phenol source
inferredcites →https://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
inferredcites →https://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
inferredcites →https://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
inferredcites →https://doi.org/10.1039/c5gc02292dopenalex-snapshot
Chemoselective cross-coupling reaction of sodium sulfinates with phenols under aqueous conditions
inferredcites →https://doi.org/10.1039/c5ob02193fopenalex-snapshot
Iodine-catalyzed thiolation of electron-rich aromatics using sulfonyl hydrazides as sulfenylation reagents
inferredcites →https://doi.org/10.1039/c5qo00102aopenalex-snapshot
Autoinductive thiolation/oxygenation of alkenes at room temperature
inferredcites →https://doi.org/10.1039/c5ra17913kopenalex-snapshot
Disulfide-based metal-free α-sulfanylation of ketones
inferredcites →https://doi.org/10.1039/c5ra24351copenalex-snapshot
Iodine-mediated thiolation of phenol/phenylamine derivatives and sodium arylsulfinates in neat water
inferredcites →https://doi.org/10.1139/v09-043openalex-snapshot
On the reactivity of indium(III) benzenechalcogenolates (chalcogen = sulfur and selenium) towards organyl halides for the synthesis of organyl phenyl chalcogenides
inferredcites →https://doi.org/10.1246/bcsj.56.3791openalex-snapshot
Stereoselective Epoxidation of Allylic Alcohols and Dehydrogenative Oxidation of Secondary Alcohols by Means of t-Butyl Hydroperoxide and Aluminium Reagents
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/9783527834242.chf0172openalex-snapshot
Regioselective C(sp 2 )H Functionalization of Anilines
inferred← citeshttps://doi.org/10.1002/adsc.201701190openalex-snapshot
Metal‐Free Thiolation of Imidazopyridines with Functionalized Haloalkanes Using Elemental Sulfur
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Aniline ortho C−H Sulfuration/Cyclization with Elemental Sulfur for Efficient Synthesis of 2‐Substituted Benzothiazoles under Metal‐Free Conditions
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External Oxidant‐Free Oxidative Tandem Cyclization: NaI‐Catalyzed Thiolation for the Synthesis of 3‐Thiosubstituted Pyrroles
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DABCO‐promoted Diaryl Thioether Formation by Metal‐catalyzed Coupling of Sodium Sulfinates and Aryl Iodides
inferred← citeshttps://doi.org/10.1002/adsc.70321openalex-snapshot
Substrate‐Guided Divergent Synthesis of Thiochromanes and Allyl Sulfides via a Mannich‐Type Reaction
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Transition‐Metal‐Free C2‐H Sulfonylation of Quinoline N‐Oxides via Insertion of Sulfur Dioxide
inferred← citeshttps://doi.org/10.1002/ajoc.202000400openalex-snapshot
Transition‐Metal‐Free Csp2−H Regioselective Thiocyanation of Free Anilines
inferred← citeshttps://doi.org/10.1002/ajoc.202300499openalex-snapshot
I2/PPh3‐Mediated Cyclization of Enaminones with Sodium Sulfinates: A Protocol for the Synthesis of 3‐Thiolated Chromones
inferred← citeshttps://doi.org/10.1002/ajoc.202500203openalex-snapshot
Deallyloxylative C─H Sulfenylation of (Hetero)arenes by Allyl Sulfoxides in Water
inferred← citeshttps://doi.org/10.1002/ange.201914333openalex-snapshot
1,1‐Diphenylvinylsulfide as a Functional AIEgen Derived from the Aggregation‐Caused‐Quenching Molecule 1,1‐Diphenylethene through Simple Thioetherification
inferred← citeshttps://doi.org/10.1002/anie.201914333openalex-snapshot
1,1‐Diphenylvinylsulfide as a Functional AIEgen Derived from the Aggregation‐Caused‐Quenching Molecule 1,1‐Diphenylethene through Simple Thioetherification
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/cctc.201801548openalex-snapshot
NIS/TBHP Induced Regioselective Selenation of (Hetero)Arenes via Direct C−H Functionalization
inferred← citeshttps://doi.org/10.1002/ejoc.201701293openalex-snapshot
Iodine‐Catalyzed Mono‐ and Disulfenylation of Indoles in PEG400 through a Facile Microwave‐Assisted Process
inferred← citeshttps://doi.org/10.1002/ejoc.201801601openalex-snapshot
A Micellar Catalysis Strategy for Amidation of Alkynyl Bromides: Synthesis of Ynamides in Water
inferred← citeshttps://doi.org/10.1002/ejoc.202000508openalex-snapshot
Flavin/I 2 ‐Catalyzed Aerobic Oxidative C–H Sulfenylation of Aryl‐Fused Cyclic Amines
inferred← citeshttps://doi.org/10.1002/ejoc.202201156openalex-snapshot
Iodine and Iodide in Reductive Transformations
inferred← citeshttps://doi.org/10.1002/slct.201903251openalex-snapshot
Base‐Promoted Direct Chalcogenylation of 2‐Naphthols
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Recent Advances of C−S Coupling Reaction of (Hetero)Arenes by C−H Functionalization
inferred← citeshttps://doi.org/10.1016/j.cclet.2025.111006openalex-snapshot
The sulfenylation of enamine esters with heterocyclic thiols or disulfides in water and application to DNA-compatible chemistry
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Highly selective C3-sulfenylation and C3-selenylation of 3-iodo-5-arylpyrazolo[1,5-a]pyrimidin-7-amine in water
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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.2018.10.032openalex-snapshot
Fe-based metal-organic frameworks for the synthesis of N-arylsulfonamides via the reactions of sodium arylsulfinates or arylsulfonyl chlorides with nitroarenes in water
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Transition-metal- and phosphorus-free electrophilic trifluoromethylthiolation of indoles with sodium trifluoromethanesulfinates in ionic liquids
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.2c01803openalex-snapshot
Nonyl Acridine Orange as a Prospective Photocatalyst in Chalcogenylation of Coumarins and Quinolinones
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inferred← citeshttps://doi.org/10.1021/acs.joc.5c00586openalex-snapshot
CCl 4 -Induced Synthesis of Phosphonothioates, Sulfoxides, and Sulfones from Sodium Sulfinates
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02459openalex-snapshot
Acid/Phosphide-Induced Radical Route to Alkyl and Alkenyl Sulfides and Phosphonothioates from Sodium Arylsulfinates in Water
inferred← citeshttps://doi.org/10.1021/acs.joc.7b01320openalex-snapshot
Making Flavone Thioethers Using Halides and Powdered Sulfur or Na2S2O3
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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.8b02619openalex-snapshot
Iron-Promoted Three-Component 2-Substituted Benzothiazole Formation via Nitroarene ortho-C–H Sulfuration with Elemental Sulfur
inferred← citeshttps://doi.org/10.1021/acs.joc.8b02844openalex-snapshot
Metal-Free Catalytic Synthesis of Thiocarbamates Using Sodium Sulfinates as the Sulfur Source
inferred← citeshttps://doi.org/10.1021/acs.joc.9b00178openalex-snapshot
Iodine-Catalyzed Odorless Synthesis of S-Thiocarbamates with Sulfonyl Chlorides as a Sulfur Source
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inferred← citeshttps://doi.org/10.1039/c7qo00634aopenalex-snapshot
Synthesis of thiophosphates through a three-component reaction by using sulfur dioxide as the sulfur source
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inferred← citeshttps://doi.org/10.1039/c8qo00840jopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c8qo01355aopenalex-snapshot
Copper-catalyzed direct and odorless selenylation with a sodium selenite-based reagent
inferred← citeshttps://doi.org/10.1039/c9cc05652aopenalex-snapshot
Switchable regioselection of C–H thiolation of indoles using different TMS counterions
inferred← citeshttps://doi.org/10.1039/c9gc03384jopenalex-snapshot
Metal- and solvent-free direct C–H thiolation of aromatic compounds with sulfonyl chlorides
inferred← citeshttps://doi.org/10.1039/c9ob02235jopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d0cc00043dopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d0ra09759dopenalex-snapshot
Synthesis and applications of sodium sulfinates (RSO 2 Na): a powerful building block for the synthesis of organosulfur compounds
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/d2ra04872hopenalex-snapshot
One-pot thiol-free synthetic approach to sulfides, and sulfoxides selectively
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/d3qo01312jopenalex-snapshot
Reductive thiolation and oxidative dehydroaromatization of cyclohexanones with primary amines and sodium sulfinates to access o -sulfanylanilines
inferred← citeshttps://doi.org/10.1039/d3qo01492dopenalex-snapshot
Directing-group-free strategy for the iodine-mediated regioselective dichalcogenation of indolines: understanding the full catalytic cycles
inferred← citeshttps://doi.org/10.1055/s-0039-1690015openalex-snapshot
Synthesis of Thioethers from Sulfonyl Chlorides, Sodium Sulfinates, and Sulfonyl Hydrazides
inferred← citeshttps://doi.org/10.1080/10426507.2018.1513518openalex-snapshot
Metal-free synthesis of (E)-vinyl sulfones via denitrative coupling reactions of β-nitrostyrenes with sodium sulfinates
inferred← citeshttps://doi.org/10.1080/17415993.2017.1408809openalex-snapshot
An efficient and recyclable catalytic system for carbon–sulfur coupling reaction and synthesis of 5-substituted 1H-tetrazoles
inferred← citeshttps://doi.org/10.1080/17415993.2019.1683181openalex-snapshot
Aryl sulfonyl chlorides and sodium aryl sulfinates: non-volatile, non-stench, and non-toxic aryl thiol surrogates for direct aryl-sulfenylation of C–H bonds
inferred← citeshttps://doi.org/10.26434/chemrxiv.13010558openalex-snapshot
A New Method for Synthesis of Thioethers from Phenyl N-Sulfonamide
inferred← citeshttps://doi.org/10.26434/chemrxiv.13010558.v1openalex-snapshot
A New Method for Synthesis of Thioethers from Phenyl N-Sulfonamide
inferred← citeshttps://doi.org/10.3390/molecules29112411openalex-snapshot
Iodophor-Catalyzed Disulfenylation of Amino Naphthalenes with Aryl Sulfonyl Hydrazines
inferred← citeshttps://doi.org/10.6023/cjoc202206029openalex-snapshot
KI-Catalyzed Selective C(5)-Sulfenylation and C(5),C(7)-Disulfenylation of Unprotected 8-Aminoquinolines and the Indole C(2),C(3)-Disulfenylation
inferred← citeshttps://doi.org/10.6023/cjoc202302008openalex-snapshot
Fe-Catalyzed Synthesis of Sulfide-Based Aromatic Primary Amines in Water Promoted by Sodium-Ascorbate
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Activation de liaisons C-H asymétrique catalysée au cobalt basse-valence : application à la synthèse d’indoles atropoisomériques
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