On the public citation graph

Metal‐ and Chemical‐Oxidant‐Free CH/CH Cross‐Coupling of Aromatic Compounds: The Use of Radical‐Cation Pools

0 signed · 273 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.
Claim with ORCID
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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

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

inferredcites →https://doi.org/10.1002/1521-3765(20020617)8:12<2650::aid-chem2650>3.0.co;2-sopenalex-snapshot
Basic Concepts of “Cation Pool” and “Cation Flow” Methods and Their Applications in Conventional and Combinatorial Organic Synthesis
inferredcites →https://doi.org/10.1002/ange.19780900425openalex-snapshot
Hexafluorophosphat des Bis(naphthalin)-Radikalkations
inferredcites →https://doi.org/10.1002/ange.19800921119openalex-snapshot
Radikalkationensalze einfacher Arene – eine neue Familie „organischer Metalle”
inferredcites →https://doi.org/10.1002/ange.19810931107openalex-snapshot
CC‐Verknüpfungen an Anode und Kathode
inferredcites →https://doi.org/10.1002/ange.200353597openalex-snapshot
Hochmodularer Aufbau unterschiedlich substituierter Dihydrodibenzo[a,c]cycloheptene: ein schneller und effizienter Zugang zu Derivaten des 2,2′‐Cyclo‐7,8′‐neolignans
inferredcites →https://doi.org/10.1002/ange.200704092openalex-snapshot
Multiple CH Activations To Construct Biologically Active Molecules in a Process Completely Free of Organohalogen and Organometallic Components
inferredcites →https://doi.org/10.1002/ange.200704495openalex-snapshot
Oxidative Cross‐Coupling of Arenes Induced by Single‐Electron Transfer Leading to Biaryls by Use of Organoiodine(III) Oxidants
inferredcites →https://doi.org/10.1002/ange.200904763openalex-snapshot
Anodische Phenol‐Aren‐Kreuzkupplung an bordotierten Diamantelektroden
inferredcites →https://doi.org/10.1002/ange.201006208openalex-snapshot
Palladium‐katalysierte dehydrierende Kreuzkupplungen von Benzazolen mit Azolen
inferredcites →https://doi.org/10.1002/ange.201101416openalex-snapshot
Palladium‐Catalyzed Oxidative CH/CH Cross‐Coupling of Indoles and Pyrroles with Heteroarenes
inferredcites →https://doi.org/10.1002/ange.201101597openalex-snapshot
Organokatalyse und C‐H‐Aktivierung treffen auf Radikal‐ und Elektronentransferreaktionen
inferredcites →https://doi.org/10.1002/anie.197802751openalex-snapshot
Hexafluorophosphate of the Bis(naphthalene) Radical Cation
inferredcites →https://doi.org/10.1002/anie.198009121openalex-snapshot
Radical Cation Salts of Simple Arenes—A New Family of “Organic Metals”
inferredcites →https://doi.org/10.1002/anie.198109111openalex-snapshot
Anodic and Cathodic CC‐Bond Formation
inferredcites →https://doi.org/10.1002/anie.200353597openalex-snapshot
Highly Modular Construction of Differently Substituted Dihydrodibenzo[a,c]cycloheptenes: Fast and Efficient Access to Derivatives of 2,2′‐Cyclo‐7,8′‐neolignans
inferredcites →https://doi.org/10.1002/anie.200704092openalex-snapshot
Multiple CH Activations To Construct Biologically Active Molecules in a Process Completely Free of Organohalogen and Organometallic Components
inferredcites →https://doi.org/10.1002/anie.200704495openalex-snapshot
Oxidative Cross‐Coupling of Arenes Induced by Single‐Electron Transfer Leading to Biaryls by Use of Organoiodine(III) Oxidants
inferredcites →https://doi.org/10.1002/anie.200904763openalex-snapshot
Anodic Phenol–Arene Cross‐Coupling Reaction on Boron‐Doped Diamond Electrodes
inferredcites →https://doi.org/10.1002/anie.201006208openalex-snapshot
Palladium‐Catalyzed Dehydrogenative Cross‐Couplings of Benzazoles with Azoles
inferredcites →https://doi.org/10.1002/anie.201101416openalex-snapshot
Palladium‐Catalyzed Oxidative CH/CH Cross‐Coupling of Indoles and Pyrroles with Heteroarenes
inferredcites →https://doi.org/10.1002/anie.201101597openalex-snapshot
Organocatalysis and CH Activation Meet Radical‐ and Electron‐Transfer Reactions
inferredcites →https://doi.org/10.1002/cber.19811141117openalex-snapshot
Elektrochemische Synthesen, XVIII: Reaktionen des Naphthalinradikalkations mit Nucleophilen
inferredcites →https://doi.org/10.1002/chin.200316116openalex-snapshot
Electroauxiliary‐Assisted Sequential Introduction of Two Carbon Nucleophiles on the Same α‐Carbon of Nitrogen: Application to the Synthesis of Spiro Compounds.
inferredcites →https://doi.org/10.1007/978-3-642-69493-6openalex-snapshot
Electroorganic Chemistry as a New Tool in Organic Synthesis
inferredcites →https://doi.org/10.1016/b978-0-444-72007-8.x5000-9openalex-snapshot
Electrochemical Reactions and Mechanisms in Organic Chemistry
inferredcites →https://doi.org/10.1016/j.tet.2011.04.065openalex-snapshot
Electrochemical synthesis of dendritic diarylcarbenium ion pools
inferredcites →https://doi.org/10.1016/j.tetlet.2010.05.140openalex-snapshot
A new highly sterically demanding silyl (TEDAMS) group. Synthesis by multiple substitution of tris(diphenylmethyl)silane with diarylcarbenium ions
inferredcites →https://doi.org/10.1016/s0040-4020(00)00840-1openalex-snapshot
Synthetic Applications of Anodic Electrochemistry
inferredcites →https://doi.org/10.1016/s0040-4020(01)91472-3openalex-snapshot
Electroorganic chemistry in organic synthesis
inferredcites →https://doi.org/10.1016/s0040-4039(00)01801-3openalex-snapshot
Synthesis of dibromotetraalkoxybiphenyls using ferric chloride
inferredcites →https://doi.org/10.1021/ar700155popenalex-snapshot
Function-Oriented Synthesis, Step Economy, and Drug Design
inferredcites →https://doi.org/10.1021/ar800164nopenalex-snapshot
Cross-Dehydrogenative Coupling (CDC): Exploring C−C Bond Formations beyond Functional Group Transformations
inferredcites →https://doi.org/10.1021/cr0680843openalex-snapshot
Modern Strategies in Electroorganic Synthesis
inferredcites →https://doi.org/10.1021/cr100280dopenalex-snapshot
Catalytic Dehydrogenative Cross-Coupling: Forming Carbon−Carbon Bonds by Oxidizing Two Carbon−Hydrogen Bonds
inferredcites →https://doi.org/10.1021/ja002123popenalex-snapshot
Electrooxidative Generation and Accumulation of Alkoxycarbenium Ions and Their Reactions with Carbon Nucleophiles
inferredcites →https://doi.org/10.1021/ja015823iopenalex-snapshot
“Cation Flow” Method: A New Approach to Conventional and Combinatorial Organic Syntheses Using Electrochemical Microflow Systems
inferredcites →https://doi.org/10.1021/ja028663zopenalex-snapshot
Electroauxiliary-Assisted Sequential Introduction of Two Carbon Nucleophiles on the Same α-Carbon of Nitrogen: Application to the Synthesis of Spiro Compounds
inferredcites →https://doi.org/10.1021/ja050414yopenalex-snapshot
“Cation Pool” Method Based on C−C Bond Dissociation. Effective Generation of Monocations and Dications
inferredcites →https://doi.org/10.1021/ja0625778openalex-snapshot
Indirect Cation Pool Method. Rapid Generation of Alkoxycarbenium Ion Pools from Thioacetals
inferredcites →https://doi.org/10.1021/ja068589aopenalex-snapshot
Reactions of a N-Acyliminium Ion Pool with Benzylsilanes. Implication of a Radical/Cation/Radical Cation Chain Mechanism Involving Oxidative C−Si Bond Cleavage
inferredcites →https://doi.org/10.1021/ja074395zopenalex-snapshot
Catalytic and Highly Regioselective Cross-Coupling of Aromatic C−H Substrates
inferredcites →https://doi.org/10.1021/ja0745862openalex-snapshot
Elements of Regiocontrol in Palladium-Catalyzed Oxidative Arene Cross-Coupling
inferredcites →https://doi.org/10.1021/ja100783copenalex-snapshot
Palladium-Catalyzed Ortho-Arylation of O-Phenylcarbamates with Simple Arenes and Sodium Persulfate
inferredcites →https://doi.org/10.1021/ja106046popenalex-snapshot
Pd-Catalyzed Oxidative Cross-Coupling of Perfluoroarenes with Aromatic Heterocycles
inferredcites →https://doi.org/10.1021/ja111401hopenalex-snapshot
Copper-Mediated Intermolecular Direct Biaryl Coupling
inferredcites →https://doi.org/10.1021/ja211005gopenalex-snapshot
Efficient Anodic and Direct Phenol-Arene C,C Cross-Coupling: The Benign Role of Water or Methanol
inferredcites →https://doi.org/10.1021/ja8026295openalex-snapshot
Palladium-Catalyzed C−H Functionalization of Pyridine N -Oxides: Highly Selective Alkenylation and Direct Arylation with Unactivated Arenes
inferredcites →https://doi.org/10.1021/ja803487qopenalex-snapshot
Iterative Molecular Assembly Based on the Cation-Pool Method. Convergent Synthesis of Dendritic Molecules
inferredcites →https://doi.org/10.1021/ja808940nopenalex-snapshot
Metal-Free Oxidative Cross-Coupling of Unfunctionalized Aromatic Compounds
inferredcites →https://doi.org/10.1021/ja909807fopenalex-snapshot
Palladium(II)-Catalyzed Oxidative C−H/C−H Cross-Coupling of Heteroarenes
inferredcites →https://doi.org/10.1021/ja9920112openalex-snapshot
Direct Oxidative Carbon−Carbon Bond Formation Using the “Cation Pool” Method. 1. Generation of Iminium Cation Pools and Their Reaction with Carbon Nucleophiles
inferredcites →https://doi.org/10.1021/jo1006812openalex-snapshot
Aiming for the Ideal Synthesis
inferredcites →https://doi.org/10.1021/jo950814bopenalex-snapshot
Synthesis of Binaphthyl Derivatives through Radical Cation Formation
inferredcites →https://doi.org/10.1021/ol071308zopenalex-snapshot
C−C Bond Formation via Double C−H Functionalization: Aerobic Oxidative Coupling as a Method for Synthesizing Heterocoupled Biaryls
inferredcites →https://doi.org/10.1021/ol101498ropenalex-snapshot
Metal-Free Regioselective Oxidative Biaryl Coupling Leading to Head-to-Tail Bithiophenes: Reactivity Switching, a Concept Based on the Iodonium(III) Intermediate
inferredcites →https://doi.org/10.1021/ol201030gopenalex-snapshot
Anodic Coupling of Guaiacol Derivatives on Boron-Doped Diamond Electrodes
inferredcites →https://doi.org/10.1021/ol800619copenalex-snapshot
Twofold C−H Functionalization: Palladium-Catalyzed Ortho Arylation of Anilides
inferredcites →https://doi.org/10.1038/nchem.143openalex-snapshot
Synthesizing our future
inferredcites →https://doi.org/10.1039/b202841gopenalex-snapshot
Dehydrodimerization of iodobenzenes to iodinated biaryls
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/c1cc10923eopenalex-snapshot
Direct dendronization of polystyrenes using dendritic diarylcarbenium ion pools
inferredcites →https://doi.org/10.1039/cs9972600157openalex-snapshot
Trends in organic electrosynthesis
inferredcites →https://doi.org/10.1055/s-2002-22696openalex-snapshot
Anodic Oxidation of Phenols Towards the Synthesis of Bioactive Natural Products
inferredcites →https://doi.org/10.1126/science.1141956openalex-snapshot
The Catalytic Cross-Coupling of Unactivated Arenes
inferredcites →https://doi.org/10.1126/science.1962206openalex-snapshot
The Atom Economy—A Search for Synthetic Efficiency
inferredcites →https://doi.org/10.1149/1.1462037openalex-snapshot
A Century of Organic Electrochemistry
inferredcites →https://doi.org/10.3891/acta.chem.scand.25-3770openalex-snapshot
Electrolysis in Non-nucleophilic Media. Part IV. Anodic Mixed Coupling. Synthesis of 1-Mesitylnaphthalene.
inferredcites →https://doi.org/10.3891/acta.chem.scand.27-0503openalex-snapshot
Electrolysis in Non-nucleophilic Media. Part V. Formation of Mixed Biaryls in the Anodic Oxidation of Naphthalene in the Presence of Alkylbenzenes.

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.4642807openalex-extracted
Photoformation of Epfrs During Phototransformation of Polycyclic Aromatic Hydrocarbons (Pahs) on Particles in an Aqueous Solution: The Hydrogenation of Pahs and Effect of Co-Existing Water Matrix Factors
inferred← citeshttps://doi.org/10.1002/9781119092490.ch13openalex-snapshot
Oxidative Cross‐Coupling of Aryl sp 2 C─H Bond with Inert C─H Bond
inferred← citeshttps://doi.org/10.1002/9781119304197.ch15openalex-snapshot
The Recent Developments of Electrochemical Oxidation
inferred← citeshttps://doi.org/10.1002/9783527822508.ch79openalex-snapshot
Electrons, Electrodes, and the Transformation of Organic Molecules
inferred← citeshttps://doi.org/10.1002/9783527834242.chf0066openalex-snapshot
(Hetero)Aryl CH Amination via Organic Electrochemistry
inferred← citeshttps://doi.org/10.1002/9783527834242.chf0224openalex-snapshot
Electrochemical Oxidative CH Functionalization: A Metal‐Free Approach
inferred← citeshttps://doi.org/10.1002/adsc.201300111openalex-snapshot
Direct C‐2 Alkylation of Quinoline N ‐Oxides with Ethers via Palladium‐Catalyzed Dehydrogenative Cross‐Coupling Reaction
inferred← citeshttps://doi.org/10.1002/adsc.201300502openalex-snapshot
Efficient Indirect Electrochemical Synthesis of 2‐Substituted Benzoxazoles using Sodium Iodide as Mediator
inferred← citeshttps://doi.org/10.1002/adsc.201601331openalex-snapshot
Efficient Oxidative Coupling of Arenes via Electrochemical Regeneration of 2,3‐Dichloro‐5,6‐dicyano‐1,4‐benzoquinone (DDQ) under Mild Reaction Conditions
inferred← citeshttps://doi.org/10.1002/adsc.201900156openalex-snapshot
Electrochemical ipso‐Thiocyanation of Arylboron Compounds
inferred← citeshttps://doi.org/10.1002/adsc.202000267openalex-snapshot
Electrochemical Nonacidic N‐Nitrosation/N‐Nitration of Secondary Amines through a Biradical Coupling Reaction
inferred← citeshttps://doi.org/10.1002/adsc.70420openalex-snapshot
O 2 ‐Mediated Cu‐Catalyzed Dehydrogenative Sulfilimination of Tyrosines and Bioactive Phenols
inferred← citeshttps://doi.org/10.1002/ajoc.201700242openalex-snapshot
Visible‐Light‐Mediated Dehydrogenative Cross‐Coupling: Synthesis of Nonsymmetrical Atropisomeric Biaryls
inferred← citeshttps://doi.org/10.1002/ajoc.202200553openalex-snapshot
Photo‐induced Cobalt‐catalyzed Aerobic N−N Coupling of Diarylamines at Room Temperature
inferred← citeshttps://doi.org/10.1002/ajoc.202400268openalex-snapshot
Palladium(0)‐Catalyzed Synthesis of Indoles and Carbazoles from o‐ Alkenyl (Alkyl) Anilines via C−H Amination Cyclization
inferred← citeshttps://doi.org/10.1002/ange.201208851openalex-snapshot
Metal‐Free Cross‐Dehydrogenative Coupling of Heterocycles with Aldehydes
inferred← citeshttps://doi.org/10.1002/ange.201210238openalex-snapshot
Oxidative aromatische Kupplung und Scholl‐Reaktion im Vergleich
inferred← citeshttps://doi.org/10.1002/ange.201306920openalex-snapshot
A Visible‐Light‐Mediated Synthesis of Carbazoles
inferred← citeshttps://doi.org/10.1002/ange.201400627openalex-snapshot
Metall‐ und reagensfreie hochselektive anodische Kreuzkupplung von Phenolen
inferred← citeshttps://doi.org/10.1002/ange.201402925openalex-snapshot
Intramolecular Metal‐Free Oxidative Aryl–Aryl Coupling: An Unusual Hypervalent‐Iodine‐Mediated Rearrangement of 2‐Substituted N‐Phenylbenzamides
inferred← citeshttps://doi.org/10.1002/ange.201405082openalex-snapshot
Renaissance elektrochemischer Methoden zum Aufbau komplexer Moleküle
inferred← citeshttps://doi.org/10.1002/ange.201508035openalex-snapshot
Überoxidation als Schlüsselschritt im Mechanismus der MoCl 5 ‐ vermittelten dehydrierenden Arenkupplung
inferred← citeshttps://doi.org/10.1002/ange.201600400openalex-snapshot
Heterogeneous Rhodium‐Catalyzed Aerobic Oxidative Dehydrogenative Cross‐Coupling: Nonsymmetrical Biaryl Amines
inferred← citeshttps://doi.org/10.1002/ange.201604321openalex-snapshot
Selektive Synthese teilgeschützter unsymmetrischer Biphenole durch reagens‐ und metallfreie anodische Kreuzkupplung
inferred← citeshttps://doi.org/10.1002/ange.201605865openalex-snapshot
Synthese von meta‐Terphenyl‐2,2′′‐diolen durch anodische C‐C‐Kreuzkupplungen
inferred← citeshttps://doi.org/10.1002/ange.201612311openalex-snapshot
Transition‐Metal‐Free C3 Arylation of Indoles with Aryl Halides
inferred← citeshttps://doi.org/10.1002/ange.201612613openalex-snapshot
Reagens‐ und metallfreie anodische C‐C‐Kreuzkupplung von Anilinderivaten
inferred← citeshttps://doi.org/10.1002/ange.201700012openalex-snapshot
Electrocatalytic Oxidant‐Free Dehydrogenative C−H/S−H Cross‐Coupling
inferred← citeshttps://doi.org/10.1002/ange.201707906openalex-snapshot
Electrochemically Enabled, Nickel‐Catalyzed Amination
inferred← citeshttps://doi.org/10.1002/ange.201708946openalex-snapshot
Einfache und doppelte metall‐ und reagensfreie anodische C‐C‐Kreuzkupplung von Phenolen mit Thiophenen
inferred← citeshttps://doi.org/10.1002/ange.201711060openalex-snapshot
Elektrifizierung der organischen Synthese
inferred← citeshttps://doi.org/10.1002/ange.201712732openalex-snapshot
Moderne Aspekte der Elektrochemie zur Synthese hochwertiger organischer Produkte
inferred← citeshttps://doi.org/10.1002/ange.201800240openalex-snapshot
Electrochemical Oxidative C−H Amination of Phenols: Access to Triarylamine Derivatives
inferred← citeshttps://doi.org/10.1002/ange.201801372openalex-snapshot
Electrochemical Hydroxylation of Arenes Catalyzed by a Keggin Polyoxometalate with a Cobalt(IV) Heteroatom
inferred← citeshttps://doi.org/10.1002/ange.201807592openalex-snapshot
Metal‐ and Oxidant‐Free Alkenyl C−H/Aromatic C−H Cross‐Coupling Using Electrochemically Generated Iodosulfonium Ions
inferred← citeshttps://doi.org/10.1002/ange.202003656openalex-snapshot
Electrochemical Oxidative [4+2] Annulation for the π‐Extension of Unfunctionalized Heterobiaryl Compounds
inferred← citeshttps://doi.org/10.1002/ange.202201142openalex-snapshot
Direkter Dehydrierender Zugang zu unsymmetrischen Phenonen
inferred← citeshttps://doi.org/10.1002/ange.202206064openalex-snapshot
Oxidation Potential Gap (ΔEox): The Hidden Parameter in Redox Chemistry
inferred← citeshttps://doi.org/10.1002/anie.201208851openalex-snapshot
Metal‐Free Cross‐Dehydrogenative Coupling of Heterocycles with Aldehydes
inferred← citeshttps://doi.org/10.1002/anie.201210238openalex-snapshot
Comparison of Oxidative Aromatic Coupling and the Scholl Reaction
inferred← citeshttps://doi.org/10.1002/anie.201306920openalex-snapshot
A Visible‐Light‐Mediated Synthesis of Carbazoles
inferred← citeshttps://doi.org/10.1002/anie.201400627openalex-snapshot
Metal‐ and Reagent‐Free Highly Selective Anodic Cross‐Coupling Reaction of Phenols
inferred← citeshttps://doi.org/10.1002/anie.201402925openalex-snapshot
Intramolecular Metal‐Free Oxidative Aryl–Aryl Coupling: An Unusual Hypervalent‐Iodine‐Mediated Rearrangement of 2‐Substituted N ‐Phenylbenzamides
inferred← citeshttps://doi.org/10.1002/anie.201405082openalex-snapshot
Renaissance of Electrosynthetic Methods for the Construction of Complex Molecules
inferred← citeshttps://doi.org/10.1002/anie.201508035openalex-snapshot
Over‐Oxidation as the Key Step in the Mechanism of the MoCl 5 ‐Mediated Dehydrogenative Coupling of Arenes
inferred← citeshttps://doi.org/10.1002/anie.201600400openalex-snapshot
Heterogeneous Rhodium‐Catalyzed Aerobic Oxidative Dehydrogenative Cross‐Coupling: Nonsymmetrical Biaryl Amines
inferred← citeshttps://doi.org/10.1002/anie.201604321openalex-snapshot
Selective Synthesis of Partially Protected Nonsymmetric Biphenols by Reagent‐ and Metal‐Free Anodic Cross‐Coupling Reaction
inferred← citeshttps://doi.org/10.1002/anie.201605865openalex-snapshot
Synthesis of meta‐Terphenyl‐2,2′′‐diols by Anodic C−C Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/anie.201612311openalex-snapshot
Transition‐Metal‐Free C3 Arylation of Indoles with Aryl Halides
inferred← citeshttps://doi.org/10.1002/anie.201612613openalex-snapshot
Reagent‐ and Metal‐Free Anodic C−C Cross‐Coupling of Aniline Derivatives
inferred← citeshttps://doi.org/10.1002/anie.201700012openalex-snapshot
Electrocatalytic Oxidant‐Free Dehydrogenative C−H/S−H Cross‐Coupling
inferred← citeshttps://doi.org/10.1002/anie.201707906openalex-snapshot
Electrochemically Enabled, Nickel‐Catalyzed Amination
inferred← citeshttps://doi.org/10.1002/anie.201708946openalex-snapshot
Single and Twofold Metal‐ and Reagent‐Free Anodic C−C Cross‐Coupling of Phenols with Thiophenes
inferred← citeshttps://doi.org/10.1002/anie.201711060openalex-snapshot
Electrifying Organic Synthesis
inferred← citeshttps://doi.org/10.1002/anie.201712732openalex-snapshot
Modern Electrochemical Aspects for the Synthesis of Value‐Added Organic Products
inferred← citeshttps://doi.org/10.1002/anie.201800240openalex-snapshot
Electrochemical Oxidative C−H Amination of Phenols: Access to Triarylamine Derivatives
inferred← citeshttps://doi.org/10.1002/anie.201801372openalex-snapshot
Electrochemical Hydroxylation of Arenes Catalyzed by a Keggin Polyoxometalate with a Cobalt(IV) Heteroatom
inferred← citeshttps://doi.org/10.1002/anie.201807592openalex-snapshot
Metal‐ and Oxidant‐Free Alkenyl C−H/Aromatic C−H Cross‐Coupling Using Electrochemically Generated Iodosulfonium Ions
inferred← citeshttps://doi.org/10.1002/anie.202003656openalex-snapshot
Electrochemical Oxidative [4+2] Annulation for the π‐Extension of Unfunctionalized Heterobiaryl Compounds
inferred← citeshttps://doi.org/10.1002/anie.202201142openalex-snapshot
Direct Dehydrogenative Access to Unsymmetrical Phenones
inferred← citeshttps://doi.org/10.1002/anie.202206064openalex-snapshot
Oxidation Potential Gap (ΔEox): The Hidden Parameter in Redox Chemistry
inferred← citeshttps://doi.org/10.1002/asia.201800584openalex-snapshot
Radical Cation Salt‐initiated Aerobic C−H Phosphorylation of N‐Benzylanilines: Synthesis of α‐Aminophosphonates
inferred← citeshttps://doi.org/10.1002/cctc.201402366openalex-snapshot
Carbon–Carbon Bond Formation via Electron Transfer: Anodic Coupling
inferred← citeshttps://doi.org/10.1002/celc.201800422openalex-snapshot
Direct Anodic Dehydrogenative Cross‐ and Homo‐Coupling of Formanilides
inferred← citeshttps://doi.org/10.1002/celc.201900753openalex-snapshot
Hexafluoro‐2‐Propanol‐Promoted Electro‐Oxidative [3+2] Annulation of 1,3‐Dicarbonyl Compounds and Alkenes
inferred← citeshttps://doi.org/10.1002/chem.201301028openalex-snapshot
Metal‐Free Oxidative para Cross‐Coupling of Phenols
inferred← citeshttps://doi.org/10.1002/chem.201406398openalex-snapshot
Electrochemical Intramolecular CH Amination: Synthesis of Benzoxazoles and Benzothiazoles
inferred← citeshttps://doi.org/10.1002/chem.201602454openalex-snapshot
Electrochemical Oxidative C−H/N−H Coupling between γ‐Lactams and Anilines
inferred← citeshttps://doi.org/10.1002/chem.201702497openalex-snapshot
A Consecutive C−H Functionalization Triggered by Oxidation of Active sp3 C−H Bonds: Construction of 3,4‐Dihydroquinoline‐3‐one Derivatives
inferred← citeshttps://doi.org/10.1002/chem.201904750openalex-snapshot
Electrochemical Cross‐Dehydrogenative Coupling between Phenols and β‐Dicarbonyl Compounds: Facile Construction of Benzofurans
inferred← citeshttps://doi.org/10.1002/chem.201905224openalex-snapshot
Catalyst‐Free Decarboxylation of Carboxylic Acids and Deoxygenation of Alcohols by Electro‐Induced Radical Formation
inferred← citeshttps://doi.org/10.1002/chem.201905774openalex-snapshot
Electrophotocatalytic Undirected C−H Trifluoromethylations of (Het)Arenes
inferred← citeshttps://doi.org/10.1002/chem.202005158openalex-snapshot
Electro‐Oxidative Selective Esterification of Methylarenes and Benzaldehydes
inferred← citeshttps://doi.org/10.1002/chem.202202135openalex-snapshot
Electrochemical Dehydrogenative C−H Aminomethylation of Imidazopyridines and Related Heterocycles
inferred← citeshttps://doi.org/10.1002/chem.202401353openalex-snapshot
peri‐Benzo‐Diindenotetracenyl: Helically π‐Extended Allyl Radical with Robust Stability
inferred← citeshttps://doi.org/10.1002/chem.202503607openalex-snapshot
Magnesium‐Promoted Benzidine‐Type Rearrangement for Regioselective Construction of Polyfunctionalized Biaryls
inferred← citeshttps://doi.org/10.1002/chin.201252021openalex-snapshot
ChemInform Abstract: Metal‐ and Chemical‐Oxidant‐Free C—H/C—H Cross‐Coupling of Aromatic Compounds: The Use of Radical‐Cation Pools.
inferred← citeshttps://doi.org/10.1002/cjoc.201800031openalex-snapshot
Electrochemical Intramolecular C—H/O—H Cross‐Coupling of 2‐Arylbenzoic Acids
inferred← citeshttps://doi.org/10.1002/cjoc.201800560openalex-snapshot
Electrocatalytic Synthesis of Non‐Symmetric Biphenols Mediated by Tri(p‐bromophenyl)amine: Selective Oxidative Cross‐Coupling of Different Phenols and Naphthols
inferred← citeshttps://doi.org/10.1002/cjoc.202000304openalex-snapshot
Dual Palladium/Scandium Catalysis toward Rotationally Hindered C3‐Naphthylated Indoles from β‐Alkynyl Ketones and o‐Alkynyl Anilines
inferred← citeshttps://doi.org/10.1002/cptc.202200130openalex-snapshot
Cross Dehydrogenative Coupling of Chloro‐ and Fluoroalkanes with Methylarenes
inferred← citeshttps://doi.org/10.1002/cssc.70801openalex-snapshot
Mechanochemical Dehydrogenative Phenochalcogenazination: A Pronounced Water Effect
inferred← citeshttps://doi.org/10.1002/ejoc.201700269openalex-snapshot
Electrooxidative Metal‐Free Dehydrogenative α‐Sulfonylation of 1H‐Indole with Sodium Sulfinates
inferred← citeshttps://doi.org/10.1002/ejoc.202000785openalex-snapshot
Recent Developments in Transition Metal‐Free Cross‐Dehydrogenative Coupling Reactions for C–C Bond Formation
inferred← citeshttps://doi.org/10.1002/elan.70216openalex-snapshot
Carbon‐Based Electrodes in Electro‐Organic Synthesis: Materials, Applications, and Perspectives
inferred← citeshttps://doi.org/10.1002/open.201900246openalex-snapshot
Efficient Protocol for Synthesis of β‐Hydroxy(alkoxy)selenides via Electrochemical Iodide‐Catalyzed Oxyselenation of Styrene Derivatives with Dialkyl(aryl)diselenides
inferred← citeshttps://doi.org/10.1002/qua.25003openalex-snapshot
Origins of regioselectivity in radical arylation of aniline: A computational study
inferred← citeshttps://doi.org/10.1002/tcr.201500020openalex-snapshot
Pioneering Metal‐Free Oxidative Coupling Strategy of Aromatic Compounds Using Hypervalent Iodine Reagents
inferred← citeshttps://doi.org/10.1002/tcr.202100016openalex-snapshot
Electrosynthesis in Laminar Flow Using a Flow Microreactor
inferred← citeshttps://doi.org/10.1007/978-981-10-3421-3_2openalex-snapshot
Metal Catalyzed Synthetic Reactions via Aerobic Oxidation as a Key Step
inferred← citeshttps://doi.org/10.1007/978-981-33-6897-2_11openalex-snapshot
Green Chemistry on C–H Activation
inferred← citeshttps://doi.org/10.1007/s11426-016-0435-5openalex-snapshot
Recent advances in direct dehydrogenative biphenyl couplings
inferred← citeshttps://doi.org/10.1007/s11426-025-3190-6openalex-snapshot
Photoredox-catalyzed site-selective dearomative cross-coupling of electron-deficient indoles and naphthalenes with electron-rich (hetero)arenes
inferred← citeshttps://doi.org/10.1016/b978-0-08-099406-2.00007-8openalex-snapshot
Five-Membered Ring Systems
inferred← citeshttps://doi.org/10.1016/b978-0-443-15742-4.00108-3openalex-snapshot
Tools of Green Synthesis: Electrochemistry
inferred← citeshttps://doi.org/10.1016/b978-0-443-18939-5.00006-8openalex-snapshot
Five-membered ring systems: pyrroles and benzo analogs
inferred← citeshttps://doi.org/10.1016/b978-0-443-33399-6.00029-8openalex-snapshot
Electrochemistry of hydrocarbons
inferred← citeshttps://doi.org/10.1016/bs.aihch.2019.11.002openalex-snapshot
Application of electrochemical oxidative methods in the C(sp2) H functionalization of heterocyclic compounds
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.coelec.2017.10.026openalex-snapshot
Combinatorial electrochemistry for organic synthesis
inferred← citeshttps://doi.org/10.1016/j.coelec.2022.101054openalex-snapshot
Recent advances in electroanalytical methods for electroorganic synthesis
inferred← citeshttps://doi.org/10.1016/j.crgsc.2024.100406openalex-snapshot
C–C and C–N bond formation in electro-oxidation reactions of aromatic compounds
inferred← citeshttps://doi.org/10.1016/j.isci.2025.113325openalex-snapshot
Metal-free molecular editing of indole via tandem reaction: Access to 2-aryl-3-aryldiazenylindole for theranostic applications
inferred← citeshttps://doi.org/10.1016/j.jelechem.2017.05.034openalex-snapshot
Electrochemically promoted arylation of iodoaromatics
inferred← citeshttps://doi.org/10.1016/j.trechm.2021.12.008openalex-snapshot
Single-electron transfer oxidation-induced C–H bond functionalization via photo-/electrochemistry
inferred← citeshttps://doi.org/10.1021/acs.analchem.1c04467openalex-snapshot
Revisiting Thin-Layer Electrochemistry in a Chip-Type Cell for the Study of Electro-organic Reactions
inferred← citeshttps://doi.org/10.1021/acs.cgd.5c00966openalex-snapshot
Flow Electrochemical Synthesis and Packing Structure-Dependent Photophysical Properties of Sulfur-Containing Polycyclic Aromatic Hydrocarbons
inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00567openalex-snapshot
Oxidative C–H/C–H Coupling Reactions between Two (Hetero)arenes
inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00620openalex-snapshot
Recent Advances in Radical C–H Activation/Radical Cross-Coupling
inferred← citeshttps://doi.org/10.1021/acs.chemrev.7b00397openalex-snapshot
Synthetic Organic Electrochemical Methods Since 2000: On the Verge of a Renaissance
inferred← citeshttps://doi.org/10.1021/acs.chemrev.7b00475openalex-snapshot
Electrogenerated Cationic Reactive Intermediates: The Pool Method and Further Advances
inferred← citeshttps://doi.org/10.1021/acs.chemrev.7b00532openalex-snapshot
Miniaturization and Combinatorial Approach in Organic Electrochemistry
inferred← citeshttps://doi.org/10.1021/acs.chemrev.8b00233openalex-snapshot
Electrochemical Arylation Reaction
inferred← citeshttps://doi.org/10.1021/acs.chemrev.9b00045openalex-snapshot
Recent Advances in Oxidative R1-H/R2-H Cross-Coupling with Hydrogen Evolution via Photo-/Electrochemistry
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02188openalex-snapshot
Synthesis of Tetrahydroindolizino[8,7-b]indole Derivatives in the Presence of Fe(OTf)3 or CF3SO3H through Intramolecular Dearomatization of Indole
inferred← citeshttps://doi.org/10.1021/acs.joc.1c02827openalex-snapshot
O2-Mediated Dehydrogenative Phenoxazination of Phenols
inferred← citeshttps://doi.org/10.1021/acs.joc.2c01311openalex-snapshot
One-Step Regio- and Stereoselective Electrochemical Synthesis of Orexin Receptor Antagonist Oxidative Metabolites
inferred← citeshttps://doi.org/10.1021/acs.joc.4c02590openalex-snapshot
O2-Mediated Cu-Catalyzed Dehydrogenative Phenothiazination
inferred← citeshttps://doi.org/10.1021/acs.joc.6c00418openalex-snapshot
N–N–N–N–O Benzotriazole Carbamates by Hypervalent Iodane Mediated Cross-Dehydrogenative N–N Coupling
inferred← citeshttps://doi.org/10.1021/acs.joc.9b01704openalex-snapshot
En Route to Intermolecular Cross-Dehydrogenative Coupling Reactions
inferred← citeshttps://doi.org/10.1021/acs.jpcc.5c04347openalex-snapshot
ECE vs DISP Mechanisms in Anodic Electrolysis of Benzyl Alcohols: Computational Prediction of Microscopic Rate Constants
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c01082openalex-snapshot
Electrochemical Total Synthesis of Pyrrolophenanthridone Alkaloids: Controlling the Anodically Initiated Electron Transfer Process
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c01244openalex-snapshot
Benzo- and Thieno-Annulated Tetracenes: A One-Pot Synthesis via Cross-Dehydrogenative Annulation
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c00573openalex-snapshot
Dehydrogenative C–H Phenochalcogenazination
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c01034openalex-snapshot
Cross-Dehydrogenative N–N Coupling of Aromatic and Aliphatic Methoxyamides with Benzotriazoles
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c02921openalex-snapshot
Domino Cross-Scholl Reaction of Tetracene with Molecular Benzene: Synthesis, Structure, and Mechanism
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c00125openalex-snapshot
Te(II)-Catalyzed Cross-Dehydrogenative Phenothiazination of Anilines
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c00445openalex-snapshot
Electrochemical Continuous-Flow Scholl Reaction toward Polycyclic Aromatic Hydrocarbons
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b03152openalex-snapshot
Synthesis of 4H-1,3-Benzoxazines via Metal- and Oxidizing Reagent-Free Aromatic C–H Oxygenation
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b01536openalex-snapshot
Thermoinduced Free-Radical C–H Acyloxylation of Tertiary Enaminones: Catalyst-Free Synthesis of Acyloxyl Chromones and Enaminones
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b03191openalex-snapshot
Electrochemical Sulfonylation/Heteroarylation of Alkenes via Distal Heteroaryl ipso-Migration
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b03306openalex-snapshot
Synthesis of Isoxazolines and Oxazines by Electrochemical Intermolecular [2 + 1 + n] Annulation: Diazo Compounds Act as Radical Acceptors
inferred← citeshttps://doi.org/10.1021/acsaenm.6c00453openalex-snapshot
Cathodic-Dehalogenation-Polymerized Membranes for Efficient Oil–Water Separation
inferred← citeshttps://doi.org/10.1021/acscatal.1c01674openalex-snapshot
Electrocatalytic Oxyesterification of Hydrocarbons by Tetravalent Lead
inferred← citeshttps://doi.org/10.1021/acscatal.7b03551openalex-snapshot
Electro-oxidative C(sp3)–H Amination of Azoles via Intermolecular Oxidative C(sp3)–H/N–H Cross-Coupling
inferred← citeshttps://doi.org/10.1021/acscatal.8b01682openalex-snapshot
Electrocatalytic C–H Activation
inferred← citeshttps://doi.org/10.1021/acscatal.8b01697openalex-snapshot
Recent Advances in C–H Functionalization Using Electrochemical Transition Metal Catalysis
inferred← citeshttps://doi.org/10.1021/acsomega.1c05479openalex-snapshot
An Air-Stable Alkene-Derived Organic Radical Cation
inferred← citeshttps://doi.org/10.1021/cr500431sopenalex-snapshot
Oxidative Coupling between Two Hydrocarbons: An Update of Recent C–H Functionalizations
inferred← citeshttps://doi.org/10.1021/ja402083eopenalex-snapshot
Electrochemical C–H Amination: Synthesis of Aromatic Primary Amines via N -Arylpyridinium Ions
inferred← citeshttps://doi.org/10.1021/ja407944popenalex-snapshot
Organocatalytic C–H/C–H′ Cross-Biaryl Coupling: C-Selective Arylation of Sulfonanilides with Aromatic Hydrocarbons
inferred← citeshttps://doi.org/10.1021/ja4092648openalex-snapshot
Halogen and Chalcogen Cation Pools Stabilized by DMSO. Versatile Reagents for Alkene Difunctionalization
inferred← citeshttps://doi.org/10.1021/ja501093mopenalex-snapshot
Direct C–N Coupling of Imidazoles with Aromatic and Benzylic Compounds via Electrooxidative C–H Functionalization
inferred← citeshttps://doi.org/10.1021/jacs.5b06526openalex-snapshot
Heterocyclization Approach for Electrooxidative Coupling of Functional Primary Alkylamines with Aromatics
inferred← citeshttps://doi.org/10.1021/jacs.6b05273openalex-snapshot
The Stabilized Cation Pool Method: Metal- and Oxidant-Free Benzylic C–H/Aromatic C–H Cross-Coupling
inferred← citeshttps://doi.org/10.1021/jacs.6b10278openalex-snapshot
Metal-Free Approach to Biaryls from Phenols and Aryl Sulfoxides by Temporarily Sulfur-Tethered Regioselective C–H/C–H Coupling
inferred← citeshttps://doi.org/10.1021/jacs.8b02535openalex-snapshot
Asymmetric Synthesis of Gonytolide A: Strategic Use of an Aryl Halide Blocking Group for Oxidative Coupling
inferred← citeshttps://doi.org/10.1021/jacs.8b07327openalex-snapshot
Oxidative R1–H/R2–H Cross-Coupling with Hydrogen Evolution
inferred← citeshttps://doi.org/10.1021/jacs.9b13920openalex-snapshot
Dehydrogenative Coupling of Benzylic and Aldehydic C–H Bonds
inferred← citeshttps://doi.org/10.1021/jacsau.2c00193openalex-snapshot
O2-Mediated Te(II)-Redox Catalysis for the Cross-Dehydrogenative Coupling of Indoles
inferred← citeshttps://doi.org/10.1021/jacsau.5c00653openalex-snapshot
Benzo-Extended [ n ]Phenacenes: e-Flow Synthesis and Length-Dependent Properties
inferred← citeshttps://doi.org/10.1021/jo501736wopenalex-snapshot
Electrochemically Initiated Oxidative Amination of Benzoxazoles Using Tetraalkylammonium Halides As Redox Catalysts
inferred← citeshttps://doi.org/10.1021/jo5022184openalex-snapshot
Electrochemically Induced Ring-Opening/Friedel–Crafts Arylation of Chalcone Epoxides Catalyzed by a Triarylimidazole Redox Mediator
inferred← citeshttps://doi.org/10.1021/om500957aopenalex-snapshot
Palladium-Catalyzed Regioselective Homocoupling of Arenes Using Anodic Oxidation: Formal Electrolysis of Aromatic Carbon–Hydrogen Bonds
inferred← citeshttps://doi.org/10.1038/s41428-024-00958-xopenalex-snapshot
Post-functionalization of alternating π-conjugated copolymers containing fluorene moieties via anodic chlorination using AlCl3
inferred← citeshttps://doi.org/10.1038/s41467-017-00873-1openalex-snapshot
External oxidant-free electrooxidative [3 + 2] annulation between phenol and indole derivatives
inferred← citeshttps://doi.org/10.1038/s41467-024-46890-9openalex-snapshot
RETRACTED ARTICLE: Metal free cross-dehydrogenative N-N coupling of primary amides with Lewis basic amines
inferred← citeshttps://doi.org/10.1039/c2cc33925kopenalex-snapshot
Oxidative transformation of aryls using molybdenum pentachloride
inferred← citeshttps://doi.org/10.1039/c3ob40315gopenalex-snapshot
Integration of electrooxidative cyclization and chemical oxidation via alkoxysulfonium ions. Synthesis of exocyclic ketones from alkenes with cyclization
inferred← citeshttps://doi.org/10.1039/c3ra40813bopenalex-snapshot
Recent advances in transition-metal-free direct C–C and C–heteroatom bond forming reactions
inferred← citeshttps://doi.org/10.1039/c4fd00049hopenalex-snapshot
Synthesis of iodobiaryls and dibenzofurans by direct coupling at BDD anodes
inferred← citeshttps://doi.org/10.1039/c4ob00002aopenalex-snapshot
KOAc-promoted alkynylation of α-C–H bonds of ethers with alkynyl bromides under transition-metal-free conditions
inferred← citeshttps://doi.org/10.1039/c4ob00475bopenalex-snapshot
Synthesis of 1,4-dihydroquinoline derivatives under transition-metal-free conditions and their diverse applications
inferred← citeshttps://doi.org/10.1039/c5cc01253hopenalex-snapshot
An anodic aromatic C,C cross-coupling reaction using parallel laminar flow mode in a flow microreactor
inferred← citeshttps://doi.org/10.1039/c5ob01215eopenalex-snapshot
Putting corannulene in its place. Reactivity studies comparing corannulene with other aromatic hydrocarbons
inferred← citeshttps://doi.org/10.1039/c6gc00666copenalex-snapshot
Electrochemical C–H functionalization and subsequent C–S and C–N bond formation: paired electrosynthesis of 3-amino-2-thiocyanato-α,β-unsaturated carbonyl derivatives mediated by bromide ions
inferred← citeshttps://doi.org/10.1039/c6ra26278copenalex-snapshot
Transition metal-free cross-dehydrogenative coupling acylation of coumarins by the K 2 S 2 O 8 /Aliquat 336 catalytic system: a versatile strategy towards 4-aroylcoumarin derivatives
inferred← citeshttps://doi.org/10.1039/c7cc00410aopenalex-snapshot
Electrocatalytic intramolecular oxidative annulation of N-aryl enamines into substituted indoles mediated by iodides
inferred← citeshttps://doi.org/10.1039/c7cs00619eopenalex-snapshot
Electrochemical strategies for C–H functionalization and C–N bond formation
inferred← citeshttps://doi.org/10.1039/c7gc00468kopenalex-snapshot
Electrochemical intramolecular dehydrogenative C–S bond formation for the synthesis of benzothiazoles
inferred← citeshttps://doi.org/10.1039/c7gc02775copenalex-snapshot
Highly selective sp 3 C–N bond activation of tertiary anilines modulated by steric and thermodynamic factors
inferred← citeshttps://doi.org/10.1039/c7gc03563bopenalex-snapshot
An electrochemical oxidative homo-coupling reaction of imidazopyridine heterocycles to biheteroaryls
inferred← citeshttps://doi.org/10.1039/c7sc04634kopenalex-snapshot
Photoinduced oxidative activation of electron-rich arenes: alkenylation with H 2 evolution under external oxidant-free conditions
inferred← citeshttps://doi.org/10.1039/c8gc01337copenalex-snapshot
Electrochemical oxidative radical oxysulfuration of styrene derivatives with thiols and nucleophilic oxygen sources
inferred← citeshttps://doi.org/10.1039/c8gc03413copenalex-snapshot
A micellar catalysis strategy applied to the Pd-catalyzed C–H arylation of indoles in water
inferred← citeshttps://doi.org/10.1039/c8gc03622eopenalex-snapshot
Electrochemically initiated intermolecular C–N formation/cyclization of ketones with 2-aminopyridines: an efficient method for the synthesis of imidazo[1,2- a ]pyridines
inferred← citeshttps://doi.org/10.1039/c8ob00063hopenalex-snapshot
Recent advances in iodine mediated electrochemical oxidative cross-coupling
inferred← citeshttps://doi.org/10.1039/c8qo00798eopenalex-snapshot
A metal-free biaryl coupling reaction activated by a sulfonium salt
inferred← citeshttps://doi.org/10.1039/d0cc05830kopenalex-snapshot
Arylation of aryllithiums with S -arylphenothiazinium ions for biaryl synthesis
inferred← citeshttps://doi.org/10.1039/d0ob00441copenalex-snapshot
Recent progress in (hetero)arene cation radical-based heteroarene modification
inferred← citeshttps://doi.org/10.1039/d0ob00917bopenalex-snapshot
FeCl 2 catalyzed direct modification of dihydropyrrolo[2,1- a ]isoquinolines with phenols
inferred← citeshttps://doi.org/10.1039/d1sc03851fopenalex-snapshot
Cross-dehydrogenative N–N couplings
inferred← citeshttps://doi.org/10.1039/d1sc06157gopenalex-snapshot
Ortho -selective C–H arylation of phenols with N -carboxyindoles under Brønsted acid- or Cu( i )-catalysis
inferred← citeshttps://doi.org/10.1039/d3qo00307hopenalex-snapshot
Electro-catalytic multicomponent reaction toward asymmetrical biaryls through heteroarylation of in situ generated fused polycyclic heteroaromatics
inferred← citeshttps://doi.org/10.1039/d5ob01863copenalex-snapshot
Electrochemical synthesis of 2-substituted quinazolinones from primary benzylic C(sp 3 )–H bonds and 2-aminobenzamides
inferred← citeshttps://doi.org/10.1055/a-2034-9821openalex-snapshot
Electrochemical Cross-Coupling Reactions between Arylboronic Esters and Aryllithiums Using NaBr as a Halogen Mediator
inferred← citeshttps://doi.org/10.1055/s-0037-1610303openalex-snapshot
Solvent Control in Electro-Organic Synthesis
inferred← citeshttps://doi.org/10.1073/pnas.2005122117openalex-snapshot
Cathodic electroorganic reaction on silicon oxide dielectric electrode
inferred← citeshttps://doi.org/10.1126/sciadv.adz5235openalex-snapshot
Cross-dehydrogenative coupling via C(sp 2 )─H bond activation by PSP-pincer rhodium photocatalysis
inferred← citeshttps://doi.org/10.1246/bcsj.20150100openalex-snapshot
Reaction Integration Using Electrogenerated Cationic Intermediates
inferred← citeshttps://doi.org/10.1246/cl.130947openalex-snapshot
Addition of N-Acyliminium Ion Pools to Alkenes Having a Nucleophilic Moiety: Integration of Intermolecular and Intramolecular Reactions
inferred← citeshttps://doi.org/10.1556/jfc-d-12-00019openalex-snapshot
Continuous In Situ Electrogeneration of o-Benzoquinone in Microreactor: Application to High Yield Reaction with Benzenethiols
inferred← citeshttps://doi.org/10.20517/cs.2024.177openalex-snapshot
Electrosynthesis reactions with divided cells: unlocking potentials in organic synthesis
inferred← citeshttps://doi.org/10.21203/rs.3.rs-3819561/v1openalex-snapshot
Photoformation of EPFRs during phototransformation of polycyclic aromatic hydrocarbons (PAHs) on particles in an aqueous solution: The hydrogenation of PAHs and effect of co-existing water matrix factors
inferred← citeshttps://doi.org/10.26434/chemrxiv-2021-kpk93openalex-snapshot
Thin-Layer Electroanalysis Microchip Reveals More about Electrochemical Reactions of Organic Compounds
inferred← citeshttps://doi.org/10.3389/fchem.2022.956502openalex-snapshot
Electrochemical organic reactions: A tutorial review
inferred← citeshttps://doi.org/10.3390/chemistry5040175openalex-snapshot
Recent Advances in C–H Functionalization of Pyrenes
inferred← citeshttps://doi.org/10.3390/toxics12110796openalex-snapshot
Photoformation of Environmentally Persistent Free Radicals During Phototransformation of Poly-Cyclic Aromatic Hydrocarbons (PAHs) on Particles in an Aqueous Solution: The Hydrogenation of PAHs and Effect of Co-Existing Water Matrix Factors
inferred← citeshttps://doi.org/10.3762/bjoc.11.18openalex-snapshot
Electrochemical selenium- and iodonium-initiated cyclisation of hydroxy-functionalised 1,4-dienes
inferred← citeshttps://doi.org/10.3762/bjoc.11.53openalex-snapshot
Highly selective generation of vanillin by anodic degradation of lignin: a combined approach of electrochemistry and product isolation by adsorption
showing the first 200 of 205 · page through all 205
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.