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Electrochemical Direct Synthesis of N-Sulfenylimines from Amines in the Presence of Thiophenols
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/anie.202016310openalex-snapshot
Nickel‐Catalyzed N ‐Arylation of NH ‐Sulfoximines with Aryl Halides via Paired Electrolysis
inferredcites →https://doi.org/10.1002/ejoc.201800838openalex-snapshot
Oxidative Coupling with S–N Bond Formation
inferredcites →https://doi.org/10.1002/tcr.202100064openalex-snapshot
Recent Advances in the Electrochemical Synthesis of Organosulfur Compounds
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/j.scib.2021.07.011openalex-snapshot
Recent advances in organic electrosynthesis employing transition metal complexes as electrocatalysts
inferredcites →https://doi.org/10.1016/j.tet.2007.01.051openalex-snapshot
The use of N-sulfenylimines in the β-lactam synthon method: Staudinger reaction, oxidation of the cycloadducts and ring opening of β-lactams
inferredcites →https://doi.org/10.1016/s0040-4020(01)01154-1openalex-snapshot
The reaction of oximes with tributylphosphine–phenyldisulfide: mechanistic insight and new synthetic possibilities
inferredcites →https://doi.org/10.1021/acs.joc.2c00415openalex-snapshot
Synthesis of N-Sulfenylimines from Disulfides and Primary Methanamines
inferredcites →https://doi.org/10.1021/ar020066uopenalex-snapshot
N-tert-Butanesulfinyl Imines: Versatile Intermediates for the Asymmetric Synthesis of Amines
inferredcites →https://doi.org/10.1021/jacs.1c00288openalex-snapshot
Electrochemical Oxidation Enables Regioselective and Scalable α-C(sp3)-H Acyloxylation of Sulfides
inferredcites →https://doi.org/10.1021/jacs.9b02266openalex-snapshot
Sulfonamide Synthesis through Electrochemical Oxidative Coupling of Amines and Thiols
inferredcites →https://doi.org/10.1021/jo00956a016openalex-snapshot
Chemistry of the sulfur-nitrogen bond. VI. Convenient one-step synthesis of sulfenimines (S-aryl thiooximes)
inferredcites →https://doi.org/10.1021/jo061027popenalex-snapshot
Adventures in Sulfur−Nitrogen Chemistry
inferredcites →https://doi.org/10.1021/ma501044bopenalex-snapshot
Functionalization of Methacrylate Polymers with Thiooximes: A Robust Postpolymerization Modification Reaction and a Method for the Preparation of H2S-Releasing Polymers
inferredcites →https://doi.org/10.1021/ol500385aopenalex-snapshot
S-Aroylthiooximes: A Facile Route to Hydrogen Sulfide Releasing Compounds with Structure-Dependent Release Kinetics
inferredcites →https://doi.org/10.1021/ol503760bopenalex-snapshot
Copper-Catalyzed Oxidative N–S Bond Formation for the Synthesis of N-Sulfenylimines
inferredcites →https://doi.org/10.1021/ol702212nopenalex-snapshot
Efficient Preparation of N-Phenylsulfenyl Ketimines from Oximes or Nitro Compounds without Racemization of α-Stereocenters
inferredcites →https://doi.org/10.1039/c39720000634openalex-snapshot
Sulphenimines: a new synthesis and barriers of stereomutation
inferredcites →https://doi.org/10.1039/c6ra01971dopenalex-snapshot
Direct synthesis of N-sulfenylimines through oxidative coupling of amines with disulfides/thiols over copper based metal–organic frameworks
inferredcites →https://doi.org/10.1039/c8ob00063hopenalex-snapshot
Recent advances in iodine mediated electrochemical oxidative cross-coupling
inferredcites →https://doi.org/10.1039/c8ob03211dopenalex-snapshot
Scalable electrochemical oxidant-and metal-free dehydrogenative coupling of S–H/N–H
inferredcites →https://doi.org/10.1080/17415990600733112openalex-snapshot
Recent advances in thionating reagents for the synthesis of organosulfur compounds
inferredcites →https://doi.org/10.6023/a23030075openalex-snapshot
Research on Selective Dehalogenation of α,α,α-Trihalogen (Chloro, Bromo) methyl Ketones Under Electrochemical Conditions
inferredcites →https://doi.org/10.6023/cjoc202101017openalex-snapshot
Electrochemically Mediated S—N Bond Formation: Synthesis of Sulfenamides
inferredcites →https://doi.org/10.6023/cjoc202205026openalex-snapshot
Electrochemical Synthesis of N-Acyl/Sulfonylsulfenamides Using Potassium Iodide as Mediator
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/ajoc.202500324openalex-snapshot
Electrochemical Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/ajoc.70534openalex-snapshot
Synthetic Strategies of Heterocycle‐Linked Sulfonamide Hybrids as Emerging Anticancer Agents: An Update
inferred← citeshttps://doi.org/10.1002/cjoc.70708openalex-snapshot
Photoinduced‐Atom Transfer Radical Cyclization of 1,5‐Enenitriles with Thiosulfonates for the Synthesis of γ‐Lactams Bearing Sulfonyl and N‐ Sulfenyliminyl Groups
inferred← citeshttps://doi.org/10.1016/b978-0-443-31482-7.00048-5openalex-snapshot
Imines and Their N-Substituted Derivatives: Oximes and Their O-R Substituted Analogs
inferred← citeshttps://doi.org/10.1016/j.rser.2026.117038openalex-snapshot
Advances in anodic electrocatalysts enabling coupled organonitrogen electrosynthesis and hydrogen production
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/10.1021/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.6c00221openalex-snapshot
Electrochemical Sulfenamide Synthesis Bypassing Gaseous Amines with Formamide Surrogates
inferred← citeshttps://doi.org/10.1063/5.0261967openalex-snapshot
UV-photoelectron spectroscopy and MS-CASPT2/CASSCF study of the thermolysis of azidoethyl-methyl sulfide: Characterization and mechanism of the formation of S-methyl-N-sulfenylethanimine
inferred← citeshttps://doi.org/10.1515/9783111850825-006openalex-snapshot
2235 Electrochemical-induced cross-coupling reaction for organic synthesis
inferred← citeshttps://doi.org/10.6023/a24040119openalex-snapshot
Synthesis of N-Benzylidene Benzylamine from Dibenzylamine and Derivatization under Electrochemical Conditions
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