On the public citation graph
Copper-Catalyzed Oxidative N–S Bond Formation for the Synthesis of N-Sulfenylimines
0 signed · 89 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/adsc.201100100openalex-snapshot
Copper‐Catalyzed Aerobic Oxidation of Amines to Imines under Neat Conditions with Low Catalyst Loading
inferredcites →https://doi.org/10.1002/adsc.201300453openalex-snapshot
Copper Nanoparticles from Copper Aluminum Hydrotalcite: An Efficient Catalyst for Acceptor‐ and Oxidant‐Free Dehydrogenation of Amines and Alcohols
inferredcites →https://doi.org/10.1002/adsc.201400116openalex-snapshot
Copper(I)‐Induced Sulfenylation of H‐Phosphonates, H‐Phosphonites and Phosphine Oxides with Aryl/alkylsulfonylhydrazides as a Thiol Surrogate
inferredcites →https://doi.org/10.1002/anie.201007056openalex-snapshot
Selective Formation of Imines by Aerobic Photocatalytic Oxidation of Amines on TiO2
inferredcites →https://doi.org/10.1002/anie.201103945openalex-snapshot
Copper‐Catalyzed Aerobic Oxidative CH Functionalizations: Trends and Mechanistic Insights
inferredcites →https://doi.org/10.1002/anie.201209975openalex-snapshot
Copper‐Catalyzed Oxidative Cross‐Coupling of Sulfoximines and Alkynes
inferredcites →https://doi.org/10.1002/chem.200401082openalex-snapshot
Efficient Ruthenium‐Catalyzed Aerobic Oxidation of Amines by Using a Biomimetic Coupled Catalytic System
inferredcites →https://doi.org/10.1002/chem.201304717openalex-snapshot
Palladium‐Catalyzed Direct Thiolation of Aryl CH Bonds with Disulfides
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.201403311openalex-snapshot
Copper‐Catalyzed Cross‐Coupling of Thiols, Alcohols, and Oxygen for the Synthesis of Esters
inferredcites →https://doi.org/10.1002/hlca.201200175openalex-snapshot
Metal‐Free 2,2,6,6‐Tetramethylpiperidin‐1‐yloxy Radical (TEMPO) Catalyzed Aerobic Oxidation of Hydroxylamines and Alkoxyamines to Oximes and Oxime Ethers
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/j.tetlet.2006.06.019openalex-snapshot
Synthesis and reactivity of 4″-phenylsulfinimine-avermectin B1 and 4′-phenylsulfinimine-avermectin B1 monosaccharide derivative
inferredcites →https://doi.org/10.1016/j.tetlet.2007.04.012openalex-snapshot
Stereoselective synthesis of trans-disubstituted-β-lactams from N-phenylsulfenylimines
inferredcites →https://doi.org/10.1016/j.tetlet.2009.02.214openalex-snapshot
Copper-catalyzed direct thiolation of benzoxazole with diaryl disulfides and aryl thiols
inferredcites →https://doi.org/10.1016/j.tetlet.2010.07.056openalex-snapshot
Direct conversion of thiols and disulfides into sulfonamides
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/ja061715qopenalex-snapshot
Cu(II)-Catalyzed Functionalizations of Aryl C−H Bonds Using O 2 as an Oxidant
inferredcites →https://doi.org/10.1021/ja077406xopenalex-snapshot
Copper-Catalyzed Aerobic Oxidative Amidation of Terminal Alkynes: Efficient Synthesis of Ynamides
inferredcites →https://doi.org/10.1021/ja102175wopenalex-snapshot
Copper-Mediated Aerobic Oxidative Trifluoromethylation of Terminal Alkynes with Me3SiCF3
inferredcites →https://doi.org/10.1021/ja9023397openalex-snapshot
Copper-Catalyzed Aerobic Oxidative Coupling of Terminal Alkynes with H -Phosphonates Leading to Alkynylphosphonates
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/jo1014849openalex-snapshot
Copper-Catalyzed Thiolation of the Di- or Trimethoxybenzene Arene C−H Bond with Disulfides
inferredcites →https://doi.org/10.1021/jo501378vopenalex-snapshot
Thiol as a Synthon for Preparing Thiocarbonyl: Aerobic Oxidation of Thiols for the Synthesis of Thioamides
inferredcites →https://doi.org/10.1021/jo502274topenalex-snapshot
Palladium-Catalyzed peri-Selective Chalcogenation of Naphthylamines with Diaryl Disulfides and Diselenides via C–H Bond Cleavage
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/ol1030298openalex-snapshot
Copper-Catalyzed Oxidative Amination of Benzoxazoles via C−H and C−N Bond Activation: A New Strategy for Using Tertiary Amines as Nitrogen Group Sources
inferredcites →https://doi.org/10.1021/ol4010118openalex-snapshot
Iron-Catalyzed Direct Synthesis of Imines from Amines or Alcohols and Amines via Aerobic Oxidative Reactions under Air
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/ol702212nopenalex-snapshot
Efficient Preparation of N-Phenylsulfenyl Ketimines from Oximes or Nitro Compounds without Racemization of α-Stereocenters
inferredcites →https://doi.org/10.1039/a827013zopenalex-snapshot
Asymmetric synthesis of amino acids using sulfinimines (thiooxime S-oxides)
inferredcites →https://doi.org/10.1039/b403953jopenalex-snapshot
Aerial oxidation of primary alcohols and amines catalyzed by Cu( ii ) complexes of 2,2′-selenobis(4,6-di-tert-butylphenol) providing [O,Se,O]-donor atoms
inferredcites →https://doi.org/10.1039/c0cs00125bopenalex-snapshot
Transition-metal catalyzed oxidative cross-coupling reactions to form C–C bonds involving organometallic reagents as nucleophiles
inferredcites →https://doi.org/10.1039/c2cc31159copenalex-snapshot
Heterogeneously catalyzed selective aerobic oxidative cross-coupling of terminal alkynes and amides with simple copper(ii) hydroxide
inferredcites →https://doi.org/10.1039/c2cc34659aopenalex-snapshot
Copper-mediated oxidative direct C–C (hetero)aromatic cross-coupling
inferredcites →https://doi.org/10.1039/c2cs15323hopenalex-snapshot
Recent advances in copper-catalyzed dehydrogenative functionalization via a single electron transfer (SET) process
inferredcites →https://doi.org/10.1039/c2ob06670jopenalex-snapshot
Simple copper/TEMPO catalyzed aerobic dehydrogenation of benzylic amines and anilines
inferredcites →https://doi.org/10.1039/c39720000634openalex-snapshot
Sulphenimines: a new synthesis and barriers of stereomutation
inferredcites →https://doi.org/10.1039/c39940000085openalex-snapshot
Synthesis of a biologically active analogue of antibiotic A-32390A
inferredcites →https://doi.org/10.1039/c3cc41249kopenalex-snapshot
Copper-catalyzed sulfonamides formation from sodium sulfinates and amines
inferredcites →https://doi.org/10.1039/c3cc45680copenalex-snapshot
Phosphoramidate synthesis via copper-catalysed aerobic oxidative coupling of amines and H-phosphonates
inferredcites →https://doi.org/10.1039/c4cc01353kopenalex-snapshot
Copper-mediated S–N formation via an oxygen-activated radical process: a new synthesis method for sulfonamides
inferredcites →https://doi.org/10.1039/cc9960000041openalex-snapshot
The total synthesis of (±)-trichoviridin
inferredcites →https://doi.org/10.1039/jr9500000132openalex-snapshot
28. Complexes between metal salts and long-chain aliphatic amines. Part III. The oxidation of copper(I) complexes to copper(II) complexes
inferredcites →https://doi.org/10.1039/p19860002243openalex-snapshot
Reduction of oximes and aliphatic nitro compounds to imines for further in situ reactions: a novel synthesis of pyrroles and pyrrolin-2-ones
inferredcites →https://doi.org/10.1055/s-0030-1261232openalex-snapshot
Convenient One-Pot Synthesis of Sulfonamides and Sulfonyl Azides from Thiols Using N-Chlorosuccinimide
inferredcites →https://doi.org/10.1055/s-1989-20334openalex-snapshot
The Total Synthesis of (±)-lsonitrin B (Deoxytrichoviridin)
inferredcites →https://doi.org/10.1080/00397911.2010.515361openalex-snapshot
One-Pot Oxidation of Alanine and Its Ethyl Ester with a Mild Oxidant 4′-Methylazobenzene-2-sulfenyl Bromide
inferredcites →https://doi.org/10.1246/bcsj.76.2399openalex-snapshot
Copper-Catalyzed Oxidation of Amines with Molecular Oxygen
inferredcites →https://doi.org/10.5012/bkcs.2012.33.2.383openalex-snapshot
Convenient One-Pot Synthesis of Sulfonamides from Thiols and Disulfides Using 1,3-Dichloro-5,5-dimethylhydantoin (DCH)
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/adsc.201500785openalex-snapshot
Copper‐Catalyzed Aerobic Formation of Unstable Sulfinyl Radicals for the Synthesis of Sulfinates and Thiosulfonates
inferred← citeshttps://doi.org/10.1002/ajoc.201600588openalex-snapshot
TEMPO‐Catalyzed Aerobic Oxidative Coupling of Thiols for Metal‐Free Formation of S−N/S−S Bonds
inferred← citeshttps://doi.org/10.1002/chin.201528118openalex-snapshot
ChemInform Abstract: Copper‐Catalyzed Oxidative N—S Bond Formation for the Synthesis of N‐Sulfenylimines.
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/10.1002/ejoc.201500857openalex-snapshot
Copper‐Catalyzed Synthesis of N‐Formyl/Acylsulfenamides and ‐thiosulfonamides
inferred← citeshttps://doi.org/10.1002/ejoc.201700148openalex-snapshot
Palladium‐Catalyzed 3‐Aryl‐5‐acyl‐1,2,4‐thiadiazole Formation from Ketones, Amidines, and Sulfur Powder
inferred← citeshttps://doi.org/10.1002/ejoc.201800670openalex-snapshot
One‐Pot Synthesis of 3‐Aryl‐5‐amino‐1,2,4‐thiadiazoles from Imidates and Thioureas by I2‐Mediated Oxidative Construction of the N–S Bond
inferred← citeshttps://doi.org/10.1002/ejoc.201800838openalex-snapshot
Oxidative Coupling with S–N Bond Formation
inferred← citeshttps://doi.org/10.1002/ejoc.202000541openalex-snapshot
Recent Advances in Sulfur‐Centered S–X (X = N, P, O) Bond Formation Catalyzed by Transition Metals
inferred← citeshttps://doi.org/10.1002/ejoc.202100440openalex-snapshot
Aerobic Visible‐Light Induced Intermolecular S−N Bond Construction: Synthesis of 1,2,4‐Thiadiazoles from Thioamides under Photosensitizer‐Free Conditions
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.tet.2018.02.049openalex-snapshot
Synthesis of novel dithiocarbamates and xanthates using dialkyl azodicarboxylates: S N bond formation
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.2c00415openalex-snapshot
Synthesis of N-Sulfenylimines from Disulfides and Primary Methanamines
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.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.6b03016openalex-snapshot
Synthesis of Sulfones and Sulfonamides via Sulfinate Anions: Revisiting the Utility of Thiosulfonates
inferred← citeshttps://doi.org/10.1021/acs.joc.7b00814openalex-snapshot
Synthesis of 5-Amino and 3,5-Diamino Substituted 1,2,4-Thiadiazoles by I 2 -Mediated Oxidative N–S Bond Formation
inferred← citeshttps://doi.org/10.1021/acs.joc.8b01223openalex-snapshot
Synthesis of C-Unsubstituted 1,2-Diazetidines and Their Ring-Opening Reactions via Selective N–N Bond Cleavage
inferred← citeshttps://doi.org/10.1021/acs.joc.8b01292openalex-snapshot
Copper-Catalyzed Aerobic Oxidative [3+2] Annulation for the Synthesis of 5-Amino/Imino-Substituted 1,2,4-Thiadiazoles through C–N/N–S Bond Formation
inferred← citeshttps://doi.org/10.1021/acs.joc.8b02151openalex-snapshot
Hydrolytic Decomposition of S-Aroylthiooximes: Effect of pH and N-Arylidene Substitution on Reaction Rate
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c00110openalex-snapshot
Exploiting N-Centered Umpolung Reactivity of α-Iminomalonates for the Synthesis of N-Sulfenylimines and Sulfonamides
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02545openalex-snapshot
Iodine/Manganese Dual Catalysis for Oxidative Dehydrogenation Coupling of Amines with Thiols
inferred← citeshttps://doi.org/10.1021/acsomega.0c04162openalex-snapshot
Copper-Catalyzed Oxidative Cleavage of the C–C Bonds of β-Alkoxy Alcohols and β-1 Compounds
inferred← citeshttps://doi.org/10.1039/c5ob01790dopenalex-snapshot
One pot oxidative N–S bond formation to access 2-sulfenylimine chromenes
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1039/c7ob01887hopenalex-snapshot
One-pot synthesis of 3,5-disubstituted 1,2,4-thiadiazoles from nitriles and thioamides via I 2 -mediated oxidative formation of an N–S bond
inferred← citeshttps://doi.org/10.1039/c7qo00766copenalex-snapshot
Synthesis of N -sulfenyl-sulfoximines and -sulfenamides through a metal-free N–H/S–H dehydrocoupling reaction
inferred← citeshttps://doi.org/10.1039/c8ra00356dopenalex-snapshot
Recent advances in sulfur–nitrogen bond formation via cross-dehydrogenative coupling reactions
inferred← citeshttps://doi.org/10.1039/c9nj01419eopenalex-snapshot
Transition-metal-free S–N bond formation: synthesis of 5-amino-1,2,4-thiadiazoles from isothiocyanates and amidines
inferred← citeshttps://doi.org/10.1039/d1ob00285fopenalex-snapshot
5-(Diarylimino)- and 5-(sulfoximido)dibenzothiophenium triflates: syntheses and applications as electrophilic aminating reagents
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/d3gc04329kopenalex-snapshot
Heterogeneous photocatalytic synthesis of sulfenamides with carbon doped potassium poly(heptazine imide) through effective electron delocalization
inferred← citeshttps://doi.org/10.1055/sos-sd-240-00191openalex-snapshot
18 Heteroatom—Heteroatom Bond Formation through Cross-Dehydrogenative Coupling
inferred← citeshttps://doi.org/10.31635/ccschem.021.202101350openalex-snapshot
Radical–Radical Cross-Coupling Assisted N–S Bond Formation Using Alternating Current Protocol
inferred← citeshttps://doi.org/10.6023/cjoc202101017openalex-snapshot
Electrochemically Mediated S—N Bond Formation: Synthesis of Sulfenamides
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.