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Scalable electrochemical oxidant-and metal-free dehydrogenative coupling of S–H/N–H

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

inferredcites →https://doi.org/10.1002/14356007.o12_o06openalex-snapshot
Fungicides, Agricultural, 2. Individual Fungicides
inferredcites →https://doi.org/10.1002/adsc.201500165openalex-snapshot
Selective Oxidation of Amines to Aldehydes or Imines using Laccase‐Mediated Bio‐Oxidation
inferredcites →https://doi.org/10.1002/ajoc.201600588openalex-snapshot
TEMPO‐Catalyzed Aerobic Oxidative Coupling of Thiols for Metal‐Free Formation of S−N/S−S Bonds
inferredcites →https://doi.org/10.1002/anie.201503654openalex-snapshot
Catalytic Amine Oxidation under Ambient Aerobic Conditions: Mimicry of Monoamine Oxidase B
inferredcites →https://doi.org/10.1002/anie.201605463openalex-snapshot
Nickel‐Catalyzed Cross‐Coupling of Redox‐Active Esters with Boronic Acids
inferredcites →https://doi.org/10.1002/anie.201700012openalex-snapshot
Electrocatalytic Oxidant‐Free Dehydrogenative C−H/S−H Cross‐Coupling
inferredcites →https://doi.org/10.1002/anie.201712647openalex-snapshot
Electrochemical C−H/N−H Activation by Water‐Tolerant Cobalt Catalysis at Room Temperature
inferredcites →https://doi.org/10.1002/anie.201803342openalex-snapshot
Electrooxidative Rhodium‐Catalyzed C−H/C−H Activation: Electricity as Oxidant for Cross‐Dehydrogenative Alkenylation
inferredcites →https://doi.org/10.1002/anie.201803464openalex-snapshot
Electro‐Oxidative S−H/S−H Cross‐Coupling with Hydrogen Evolution: Facile Access to Unsymmetrical Disulfides
inferredcites →https://doi.org/10.1002/app.39699openalex-snapshot
A benzoxazole sulfenamide accelerator: Synthesis, structure, property, and implication in rubber vulcanization mechanism
inferredcites →https://doi.org/10.1002/app.44822openalex-snapshot
Influence of sulfenamide accelerators on cure kinetics and properties of natural rubber foam
inferredcites →https://doi.org/10.1002/ejoc.201000167openalex-snapshot
Copper‐Catalyzed Formation of Sulfur–Nitrogen Bonds by Dehydrocoupling of Thiols with Amines
inferredcites →https://doi.org/10.1002/ejoc.201402180openalex-snapshot
Hypervalent Iodine(III)‐Promoted Metal‐Free S–H Activation: An Approach for the Construction of S–S, S–N, and S–C Bonds
inferredcites →https://doi.org/10.1002/ejoc.201500857openalex-snapshot
Copper‐Catalyzed Synthesis of N‐Formyl/Acylsulfenamides and ‐thiosulfonamides
inferredcites →https://doi.org/10.1002/jhet.5570270417openalex-snapshot
Synthesis and In Vivo antitumor and antiviral activities of 2′‐deoxyribofuranosyl and arabinofuranosyl nucleosides of certain purine‐6‐sulfenamides, sulfinamides and sulfonamides
inferredcites →https://doi.org/10.1016/j.carres.2004.03.023openalex-snapshot
Novel approaches to the syntheses of N-substituted S-glycosyl-sulfenamides
inferredcites →https://doi.org/10.1016/j.chempr.2017.10.001openalex-snapshot
Electrochemical Oxidative Cross-coupling with Hydrogen Evolution: A Green and Sustainable Way for Bond Formation
inferredcites →https://doi.org/10.1016/s0040-4039(01)92729-7openalex-snapshot
Conversion of α-chlorosulfenyl chlorides to ketones via α-chlorosulfen-amides. Use of thionyl chloride for oxidation of active methylene compounds
inferredcites →https://doi.org/10.1021/acs.chemmater.7b02899openalex-snapshot
Interplay of Corrosion and Photocatalysis During Nonaqueous Benzylamine Oxidation on Cadmium Sulfide
inferredcites →https://doi.org/10.1021/acs.chemrev.7b00397openalex-snapshot
Synthetic Organic Electrochemical Methods Since 2000: On the Verge of a Renaissance
inferredcites →https://doi.org/10.1021/acs.joc.7b02718openalex-snapshot
Cobalt-Catalyzed Aerobic Cross-Dehydrogenative Coupling of C–H and Thiols in Water for C–S Formation
inferredcites →https://doi.org/10.1021/acs.orglett.8b01066openalex-snapshot
Lewis Base/Bronsted Acid Dual-Catalytic C–H Sulfenylation of Aromatics
inferredcites →https://doi.org/10.1021/cr0680843openalex-snapshot
Modern Strategies in Electroorganic Synthesis
inferredcites →https://doi.org/10.1021/cr60123a004openalex-snapshot
The Sulfenic Acids and their Derivatives.
inferredcites →https://doi.org/10.1021/jacs.7b13049openalex-snapshot
Cobalt(II)-Catalyzed Electrooxidative C–H Amination of Arenes with Alkylamines
inferredcites →https://doi.org/10.1021/jo00023a040openalex-snapshot
A one-pot synthesis of sulfenamides
inferredcites →https://doi.org/10.1021/jo00426a008openalex-snapshot
Chemistry of the sulfur-nitrogen bond. 12. Metal-assisted synthesis of sulfenamide derivatives from aliphatic and aromatic disulfides
inferredcites →https://doi.org/10.1021/ma300190bopenalex-snapshot
New Class of Biodegradable Polymers Formed from Reactions of an Inorganic Functional Group
inferredcites →https://doi.org/10.1021/ml2001483openalex-snapshot
Type 1 Phototherapeutic Agents, Part I: Preparation and Cancer Cell Viability Studies of Novel Photolabile Sulfenamides
inferredcites →https://doi.org/10.1038/nature17431openalex-snapshot
Scalable and sustainable electrochemical allylic C–H oxidation
inferredcites →https://doi.org/10.1038/nature18008openalex-snapshot
Cooperative electrocatalytic alcohol oxidation with electron-proton-transfer mediators
inferredcites →https://doi.org/10.1039/b512308aopenalex-snapshot
The application of cathodic reductions and anodic oxidations in the synthesis of complex molecules
inferredcites →https://doi.org/10.1039/c0cc02076aopenalex-snapshot
Disulfide formation via sulfenamides
inferredcites →https://doi.org/10.1039/c29710001625openalex-snapshot
A new one-step synthesis of sulphenamides from alkyl and aryl disulphides
inferredcites →https://doi.org/10.1039/c6cc01068gopenalex-snapshot
N-Tosyl-1,5,2,6-dithiadiazocane: a waste-free electrophilic sulfur reagent for the efficient synthesis of medium-ring S,N-heterocycles
inferredcites →https://doi.org/10.1039/c7cs00619eopenalex-snapshot
Electrochemical strategies for C–H functionalization and C–N bond formation
inferredcites →https://doi.org/10.1039/c7gc00401jopenalex-snapshot
Reusable cobalt-phthalocyanine in water: efficient catalytic aerobic oxidative coupling of thiols to construct S–N/S–S bonds
inferredcites →https://doi.org/10.1039/c7ob01540bopenalex-snapshot
Pd-Catalyzed double N-arylation of primary amines to synthesize phenoxazines and phenothiazines
inferredcites →https://doi.org/10.1039/c7qo00766copenalex-snapshot
Synthesis of N -sulfenyl-sulfoximines and -sulfenamides through a metal-free N–H/S–H dehydrocoupling reaction
inferredcites →https://doi.org/10.1055/s-1970-21640openalex-snapshot
One Hundred Years of Sulfenic Acid Chemistry I. Sulfenyl Halide Syntheses
inferredcites →https://doi.org/10.1055/s-1983-30481openalex-snapshot
A Facile Synthesis of N , N -Dialkylpropanesulfenamides and -benzenesulfenamides
inferredcites →https://doi.org/10.1055/s-2007-984539openalex-snapshot
Copper-Catalyzed Synthesis of Sulfenamides Utilizing Diaryl Disulfides with Alkyl Amines
inferredcites →https://doi.org/10.1126/science.aan6206openalex-snapshot
Metal-catalyzed electrochemical diazidation of alkenes
inferredcites →https://doi.org/10.3390/catal8020048openalex-snapshot
Highly Efficient Acetalization and Ketalization Catalyzed by Cobaloxime under Solvent-Free Condition

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4773913openalex-extracted
Synthesis of N-Sulfenylimines Via an Electrochemical Radical Coupling of Amines and Thiols Mediated by Bromide Ions
inferred← citeshttps://doi.org/10.2139/ssrn.4865942openalex-extracted
Synthesis of N-Sulfenylimines Via an Electrochemical Radical Coupling of Amines and Thiols Mediated by Bromide Ions
inferred← citeshttps://doi.org/10.1002/adma.202304716openalex-snapshot
Indirect Electrocatalysis S─N/S─S Bond Construction by Robust Polyoxometalate Based Foams
inferred← citeshttps://doi.org/10.1002/adma.74009openalex-snapshot
Heterogeneous Indirect Redox Electrocatalysis in Electrolyte
inferred← citeshttps://doi.org/10.1002/adsc.201901290openalex-snapshot
Electrochemical Synthesis of 1,2,4‐Thiadiazoles through Intermolecular Dehydrogenative S‐N Coupling
inferred← citeshttps://doi.org/10.1002/adsc.202300607openalex-snapshot
Convergent Paired Electrolysis for the Synthesis of Pyrazolyl‐Substituted Tetrahydroisoquinolines
inferred← citeshttps://doi.org/10.1002/adsc.70759openalex-snapshot
Electrosynthesis of 1,2,5‐Thiadiazines via Three‐Component Annulation of Isocyanides, Elemental Sulfur, and Diamines
inferred← citeshttps://doi.org/10.1002/ajoc.202000160openalex-snapshot
Efficient Synthesis of Sulfenamides through Mitsunobu‐type Coupling Reaction of Thiols with Amines using Dibenzyl Azodicarboxylate
inferred← citeshttps://doi.org/10.1002/ajoc.202400138openalex-snapshot
Synthesis of Sulfenamides from Benzoazole‐2‐thiones with Primary and Secondary Amines using Triphenylbismuth Dichloride‐Mediated S−N Bond Formation Reaction
inferred← citeshttps://doi.org/10.1002/ange.202413030openalex-snapshot
Solid‐Liquid‐Gas Three‐Phase Indirect Electrolysis Enabled by Affinity Auxiliary Imparted Covalent Organic Frameworks
inferred← citeshttps://doi.org/10.1002/anie.202413030openalex-snapshot
Solid‐Liquid‐Gas Three‐Phase Indirect Electrolysis Enabled by Affinity Auxiliary Imparted Covalent Organic Frameworks
inferred← citeshttps://doi.org/10.1002/ejoc.202100924openalex-snapshot
Electrochemical Direct Thiolation of Lactams with Mercaptans: An Efficient Access to N‐Acylsulfenamides
inferred← citeshttps://doi.org/10.1002/ejoc.202101165openalex-snapshot
Iodine‐Mediated Cross‐Dehydrogenative Coupling of Heterocyclic Thiols with Amines: An Easy and Practical Formation of S−N Bond
inferred← citeshttps://doi.org/10.1002/ejoc.202200419openalex-snapshot
An Efficient and Practical Construction of S−N Bond from Aryl Thioureas and Amines under Metal‐Free Conditions
inferred← citeshttps://doi.org/10.1002/ejoc.202500026openalex-snapshot
Advances in Sulfenamide Chemistry: Synthetic Strategies and Reactivity Profiles
inferred← citeshttps://doi.org/10.1007/s10311-022-01459-0openalex-snapshot
High-efficiency synthesis of sulfenamides and disulfides by electrochemical dehydrogenative coupling
inferred← citeshttps://doi.org/10.1016/b978-0-443-31482-7.00107-7openalex-snapshot
Vinyl- and Aryl Chalcogenides: Sulfur-, Selenium-, and Tellurium-Based Functional Groups
inferred← citeshttps://doi.org/10.1016/j.tet.2024.134133openalex-snapshot
Synthesis of N-sulfenylimines via an electrochemical radical coupling of amines and thiols mediated by bromide ions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.151631openalex-snapshot
Electrochemical synthesis of sulfinic esters from alcohols and thiophenols
inferred← citeshttps://doi.org/10.1021/acs.chemrev.1c00374openalex-snapshot
Photochemical and Electrochemical Applications of Proton-Coupled Electron Transfer in Organic Synthesis
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00317openalex-snapshot
Unified Approach to Benzo[ d ]thiazol-2-yl-Sulfonamides
inferred← citeshttps://doi.org/10.1021/acs.joc.3c02090openalex-snapshot
Electrochemical Direct Synthesis of N-Sulfenylimines from Amines in the Presence of Thiophenols
inferred← citeshttps://doi.org/10.1021/acs.joc.3c02444openalex-snapshot
Selective Synthesis of Sulfonamides and Sulfenamides from Sodium Sulfinates and Amines
inferred← citeshttps://doi.org/10.1021/acs.joc.4c00725openalex-snapshot
Selective Synthesis of Amides and α-Ketoamides via Electrochemical Decarboxylation and Dehydration
inferred← citeshttps://doi.org/10.1021/acs.joc.5c02958openalex-snapshot
Cu(I)-Catalyzed Synthesis of Sulfenamides via Coupling of Carbamothioate/Thiourea Derivatives with Sulfonyl Azides
inferred← citeshttps://doi.org/10.1021/acs.joc.9b03155openalex-snapshot
Electrochemical Oxidative Intramolecular N–S Bond Formation: Synthesis of 3-Substituted 5-Amino-1,2,4-Thiadiazoles
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c04454openalex-snapshot
Synthesis of Sulfenamides via Photoredox N–S Coupling of Dialkyl Azodicarboxylates and Thiols
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c00778openalex-snapshot
Visible Light-Induced Synthesis of Sulfenamides via Oxidative Coupling of Amines with Thiols
inferred← citeshttps://doi.org/10.1021/acscentsci.4c01733openalex-snapshot
Scaling Organic Electrosynthesis: The Crucial Interplay between Mechanism and Mass Transport
inferred← citeshttps://doi.org/10.1021/acssuschemeng.2c04720openalex-snapshot
Piezocatalyzed Decarboxylative Acylation of Quinoxalin-2(1 H )-ones Using Ball Milling
inferred← citeshttps://doi.org/10.1038/s41467-022-34223-7openalex-snapshot
Synthesis of N-acyl sulfenamides via copper catalysis and their use as S-sulfenylating reagents of thiols
inferred← citeshttps://doi.org/10.1039/c9gc02125fopenalex-snapshot
Metal- and oxidant-free electrochemical synthesis of sulfinic esters from thiols and alcohols
inferred← citeshttps://doi.org/10.1039/d1ob01368hopenalex-snapshot
Oxidative cross-coupling of thiols for S–X (X = S, N, O, P, and C) bond formation: mechanistic aspects
inferred← citeshttps://doi.org/10.1039/d1ra04368dopenalex-snapshot
Direct synthesis of sulfenamides, sulfinamides, and sulfonamides from thiols and amines
inferred← citeshttps://doi.org/10.1039/d3gc00175jopenalex-snapshot
Advances in S–N bond formation via electrochemistry: a green route utilizing diverse sulfur and nitrogen sources
inferred← citeshttps://doi.org/10.1039/d3ob01848bopenalex-snapshot
Thiosuccinimide enabled S–N bond formation to access N -sulfenylated sulfonamide derivatives with synthetic diversity
inferred← citeshttps://doi.org/10.1039/d4qo01962hopenalex-snapshot
Copper-catalyzed N–H bond chalcogenation of anilines
inferred← citeshttps://doi.org/10.1039/d5gc01831eopenalex-snapshot
Electrochemically driven tandem addition–cyclization: synthesis of thiadiazinanes and thiophosphonates
inferred← citeshttps://doi.org/10.1055/sos-sd-240-00191openalex-snapshot
18 Heteroatom—Heteroatom Bond Formation through Cross-Dehydrogenative Coupling
inferred← citeshttps://doi.org/10.1080/17415993.2020.1722818openalex-snapshot
Mixed bases mediated synthesis of thioamides in water
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1333688/v1openalex-snapshot
High-efficiency Electrochemical Dehydrogenative Coupling Synthesis of S-N/S-S Bonds
inferred← citeshttps://doi.org/10.6023/cjoc202101017openalex-snapshot
Electrochemically Mediated S—N Bond Formation: Synthesis of Sulfenamides
inferred← citeshttps://doi.org/10.6023/cjoc202205026openalex-snapshot
Electrochemical Synthesis of N-Acyl/Sulfonylsulfenamides Using Potassium Iodide as Mediator
inferred← citeshttps://doi.org/10.6023/cjoc202306014openalex-snapshot
N-Heterocyclic Carbene-Catalyzed Synthesis of Pentafluorophenyl Sulfides
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