On the public citation graph
Palladium‐Catalyzed Direct C−H Arylation of Arenes Promoted by Quaternary Ammonium Salt
0 signed · 87 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known work and none has been retracted — and get a dated CiteStamped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/(sici)1521-3757(20000103)112:1<170::aid-ange170>3.0.co;2-aopenalex-snapshot
Phosphanfreie Palladium-katalysierte Kupplungen: die entscheidende Rolle von Pd-Nanoteilchen
inferredcites →https://doi.org/10.1002/(sici)1521-3773(20000103)39:1<165::aid-anie165>3.0.co;2-bopenalex-snapshot
Phosphane-Free Palladium-Catalyzed Coupling Reactions: The Decisive Role of Pd Nanoparticles
inferredcites →https://doi.org/10.1002/1521-3757(20010601)113:11<2226::aid-ange2226>3.0.co;2-qopenalex-snapshot
Formation of Aryl- and Benzylboronate Esters by Rhodium-Catalyzed C−H Bond Functionalization with Pinacolborane
inferredcites →https://doi.org/10.1002/1521-3773(20010601)40:11<2168::aid-anie2168>3.0.co;2-0openalex-snapshot
Formation of Aryl- and Benzylboronate Esters by Rhodium-Catalyzed C−H Bond Functionalization with Pinacolborane
inferredcites →https://doi.org/10.1002/1615-4169(200210)344:9<996::aid-adsc996>3.0.co;2-jopenalex-snapshot
A Practical Recycle of a Ligand-Free Palladium Catalyst for Heck Reactions
inferredcites →https://doi.org/10.1002/adma.200400284openalex-snapshot
New Trends in the Use of Transition Metal–Ligand Complexes for Applications in Electroluminescent Devices
inferredcites →https://doi.org/10.1002/adsc.200404331openalex-snapshot
Heterogeneous or Homogeneous? A Case Study Involving Palladium‐Containing Perovskites in the Suzuki Reaction
inferredcites →https://doi.org/10.1002/adsc.200505229openalex-snapshot
Palladium Nanoclusters in Sonogashira Cross‐Coupling: A True Catalytic Species?
inferredcites →https://doi.org/10.1002/adsc.200505473openalex-snapshot
On the Nature of the Active Species in Palladium Catalyzed Mizoroki–Heck and Suzuki–Miyaura Couplings – Homogeneous or Heterogeneous Catalysis, A Critical Review
inferredcites →https://doi.org/10.1002/adsc.201400798openalex-snapshot
Rhodium(III)‐Catalyzed ortho‐Arylation of Anilides with Aryl Halides
inferredcites →https://doi.org/10.1002/adsc.201601121openalex-snapshot
Chelation‐Assisted Palladium‐Catalyzed γ‐Arylation of Aliphatic Carboxylic Acid Derivatives
inferredcites →https://doi.org/10.1002/adsc.201801378openalex-snapshot
Palladium Catalyzed Regioselective C4‐Arylation and Olefination of Indoles and Azaindoles
inferredcites →https://doi.org/10.1002/ange.200500766openalex-snapshot
Nanopartikel als regenerierbare Katalysatoren: an der Nahtstelle zwischen homogener und heterogener Katalyse
inferredcites →https://doi.org/10.1002/ange.200906870openalex-snapshot
Iron‐Catalyzed Direct Arylation of Unactivated Arenes with Aryl Halides
inferredcites →https://doi.org/10.1002/ange.201107334openalex-snapshot
Zur Interpretation des kinetischen Isotopeneffekts bei der Funktionalisierung von C‐H‐Bindungen durch Übergangsmetallkomplexe
inferredcites →https://doi.org/10.1002/ange.201201666openalex-snapshot
Funktionalisierung von C‐H‐Bindungen: neue Synthesemethoden für Naturstoffe und Pharmazeutika
inferredcites →https://doi.org/10.1002/ange.201203269openalex-snapshot
Ohne dirigierende Gruppen: übergangsmetallkatalysierte C‐H‐Aktivierung einfacher Arene
inferredcites →https://doi.org/10.1002/ange.201301451openalex-snapshot
Katalytische Funktionalisierung von C(sp2)‐H‐ und C(sp3)‐H‐Bindungen unter Verwendung von zweizähnigen dirigierenden Gruppen
inferredcites →https://doi.org/10.1002/ange.201703354openalex-snapshot
Rhodium(I)‐Catalyzed Tertiary Phosphine Directed C−H Arylation: Rapid Construction of Ligand Libraries
inferredcites →https://doi.org/10.1002/anie.200500766openalex-snapshot
Nanoparticles as Recyclable Catalysts: The Frontier between Homogeneous and Heterogeneous Catalysis
inferredcites →https://doi.org/10.1002/anie.200906870openalex-snapshot
Iron‐Catalyzed Direct Arylation of Unactivated Arenes with Aryl Halides
inferredcites →https://doi.org/10.1002/anie.201107334openalex-snapshot
On the Interpretation of Deuterium Kinetic Isotope Effects in CH Bond Functionalizations by Transition‐Metal Complexes
inferredcites →https://doi.org/10.1002/anie.201201666openalex-snapshot
CH Bond Functionalization: Emerging Synthetic Tools for Natural Products and Pharmaceuticals
inferredcites →https://doi.org/10.1002/anie.201203269openalex-snapshot
Beyond Directing Groups: Transition‐Metal‐Catalyzed CH Activation of Simple Arenes
inferredcites →https://doi.org/10.1002/anie.201301451openalex-snapshot
Catalytic Functionalization of C(sp 2 )H and C(sp 3 )H Bonds by Using Bidentate Directing Groups
inferredcites →https://doi.org/10.1002/anie.201703354openalex-snapshot
Rhodium(I)‐Catalyzed Tertiary Phosphine Directed C−H Arylation: Rapid Construction of Ligand Libraries
inferredcites →https://doi.org/10.1002/anie.201900479openalex-snapshot
Iterative Arylation of Amino Acids and Aliphatic Amines via δ‐C(sp3)−H Activation: Experimental and Computational Exploration
inferredcites →https://doi.org/10.1002/anie.201907262openalex-snapshot
Ligand‐Enabled PdII‐Catalyzed Iterative γ‐C(sp3)−H Arylation of Free Aliphatic Acid
inferredcites →https://doi.org/10.1002/asia.201403201openalex-snapshot
Mechanistic Studies of Magnetically Recyclable PdFe3O4 Heterodimeric Nanocrystal‐Catalyzed Organic Reactions
inferredcites →https://doi.org/10.1002/cctc.201300099openalex-snapshot
Synthesis of 2,5‐Diarylpyrroles by Ligand‐Free Palladium‐Catalyzed CH Activation of Pyrroles in Ionic Liquids
inferredcites →https://doi.org/10.1002/chem.201002290openalex-snapshot
Cobalt‐Catalyzed Direct Arylation of Unactivated Arenes with Aryl Halides
inferredcites →https://doi.org/10.1002/ejoc.201300704openalex-snapshot
Mild Palladium‐Catalyzed Regioselective Direct Arylation of Azoles Promoted by Tetrabutylammonium Acetate
inferredcites →https://doi.org/10.1002/ejoc.201300743openalex-snapshot
Iron‐Catalyzed Direct C–H Arylation of Heterocycles and Quinones with Arylboronic Acids
inferredcites →https://doi.org/10.1016/0040-4020(96)00547-9openalex-snapshot
On the efficiency of tetraalkylammonium salts in Heck type reactions
inferredcites →https://doi.org/10.1016/j.apcata.2013.06.046openalex-snapshot
[IL]2[PdCl4] complexes (IL = imidazolium cation) as efficient catalysts for Suzuki–Miyaura cross-coupling of aryl bromides and aryl chlorides
inferredcites →https://doi.org/10.1016/j.ccr.2017.06.018openalex-snapshot
Cobalt(II)-catalyzed C H functionalization using an N,N′-bidentate directing group
inferredcites →https://doi.org/10.1016/s0022-328x(00)00224-2openalex-snapshot
First intermolecular palladium catalyzed arylation of an unfunctionalized aromatic hydrocarbon
inferredcites →https://doi.org/10.1016/s0277-5387(99)00289-2openalex-snapshot
Synthesis and characterization of monomeric and dimeric palladium(II)–ammonium complexes: their use for the catalytic oxidation of alcohols
inferredcites →https://doi.org/10.1016/s1381-1169(02)00728-8openalex-snapshot
A review of the problem of distinguishing true homogeneous catalysis from soluble or other metal-particle heterogeneous catalysis under reducing conditions
inferredcites →https://doi.org/10.1021/acs.orglett.5b02458openalex-snapshot
Palladium-Catalyzed C–H Arylation of (Benzo)oxazoles or (Benzo)thiazoles with Aryltrimethylammonium Triflates
inferredcites →https://doi.org/10.1021/acscatal.6b03655openalex-snapshot
Cross-Coupling Catalysis by an Anionic Palladium Complex
inferredcites →https://doi.org/10.1021/acscatal.7b00397openalex-snapshot
Ligand-Promoted Direct C–H Arylation of Simple Arenes: Evidence for a Cooperative Bimetallic Mechanism
inferredcites →https://doi.org/10.1021/acscatal.8b03436openalex-snapshot
Nickel-Catalyzed Heteroarenes Cross Coupling via Tandem C–H/C–O Activation
inferredcites →https://doi.org/10.1021/acscentsci.6b00032openalex-snapshot
Undirected, Homogeneous C–H Bond Functionalization: Challenges and Opportunities
inferredcites →https://doi.org/10.1021/ar200185gopenalex-snapshot
Weak Coordination as a Powerful Means for Developing Broadly Useful C–H Functionalization Reactions
inferredcites →https://doi.org/10.1021/ar980063aopenalex-snapshot
Anionic Pd(0) and Pd(II) Intermediates in Palladium-Catalyzed Heck and Cross-Coupling Reactions
inferredcites →https://doi.org/10.1021/cr00039a007openalex-snapshot
Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds
inferredcites →https://doi.org/10.1021/cr000664ropenalex-snapshot
Aryl−Aryl Bond Formation One Century after the Discovery of the Ullmann Reaction
inferredcites →https://doi.org/10.1021/cr020033sopenalex-snapshot
The Combinatorial Synthesis of Bicyclic Privileged Structures or Privileged Substructures
inferredcites →https://doi.org/10.1021/cr0505268openalex-snapshot
Selected Patented Cross-Coupling Reaction Technologies
inferredcites →https://doi.org/10.1021/cr100412jopenalex-snapshot
Carboxylate-Assisted Transition-Metal-Catalyzed C−H Bond Functionalizations: Mechanism and Scope
inferredcites →https://doi.org/10.1021/cr2002905openalex-snapshot
Resolving Heterogeneity Problems and Impurity Artifacts in Operationally Homogeneous Transition Metal Catalysts
inferredcites →https://doi.org/10.1021/cr300153jopenalex-snapshot
Ruthenium(II)-Catalyzed C–H Bond Activation and Functionalization
inferredcites →https://doi.org/10.1021/cr900005nopenalex-snapshot
Rhodium-Catalyzed C−C Bond Formation via Heteroatom-Directed C−H Bond Activation
inferredcites →https://doi.org/10.1021/cr900184eopenalex-snapshot
Palladium-Catalyzed Ligand-Directed C−H Functionalization Reactions
inferredcites →https://doi.org/10.1021/ja016877vopenalex-snapshot
Are Heterogeneous Catalysts Precursors to Homogeneous Catalysts?
inferredcites →https://doi.org/10.1021/ja051834qopenalex-snapshot
Kinetics and Mechanistic Aspects of the Heck Reaction Promoted by a CN−Palladacycle
inferredcites →https://doi.org/10.1021/ja064500popenalex-snapshot
Direct C−H Arylation of (Hetero)arenes with Aryl Iodides via Rhodium Catalysis
inferredcites →https://doi.org/10.1021/ja067144jopenalex-snapshot
Palladium-Catalyzed Benzene Arylation: Incorporation of Catalytic Pivalic Acid as a Proton Shuttle and a Key Element in Catalyst Design
inferredcites →https://doi.org/10.1021/ja1113936openalex-snapshot
Assessment of the Intermediacy of Arylpalladium Carboxylate Complexes in the Direct Arylation of Benzene: Evidence for C−H Bond Cleavage by “Ligandless” Species
inferredcites →https://doi.org/10.1021/ja910687uopenalex-snapshot
Iron-Catalyzed Direct Arylation through an Aryl Radical Transfer Pathway
inferredcites →https://doi.org/10.1021/jacs.5b11569openalex-snapshot
Palladium-Catalyzed C–H Arylation of Indoles at the C7 Position
inferredcites →https://doi.org/10.1021/jo4000465openalex-snapshot
Rhodium- and Iridium-Catalyzed Dehydrogenative Cyclization through Double C–H Bond Cleavages To Produce Fluorene Derivatives
inferredcites →https://doi.org/10.1021/ol9001587openalex-snapshot
Nickel-Catalyzed Biaryl Coupling of Heteroarenes and Aryl Halides/Triflates
inferredcites →https://doi.org/10.1021/ol900778mopenalex-snapshot
Cp2Ni-KOt-Bu-BEt3 (or PPh3) Catalyst System for Direct C−H Arylation of Benzene, Naphthalene, and Pyridine
inferredcites →https://doi.org/10.1021/om060151wopenalex-snapshot
Palladium(II) Complexes of a Sterically Bulky, Benzannulated N-Heterocyclic Carbene with Unusual Intramolecular C−H···Pd and C c arbene ···Br Interactions and Their Catalytic Activities
inferredcites →https://doi.org/10.1021/om50001a013openalex-snapshot
Dibenzo[a,e]cyclooctatetraene in a proposed test for heterogeneity in catalysts formed from soluble platinum-group metal complexes
inferredcites →https://doi.org/10.1038/nchem.2904openalex-snapshot
Palladium-catalysed anti-Markovnikov selective oxidative amination
inferredcites →https://doi.org/10.1039/b506276bopenalex-snapshot
A unifying mechanism for all high-temperature Heck reactions. The role of palladium colloids and anionic species
inferredcites →https://doi.org/10.1039/b515481mopenalex-snapshot
Palladium-catalyzed direct arylation of simple arenes in synthesis of biaryl molecules
inferredcites →https://doi.org/10.1039/c5cc08367bopenalex-snapshot
Copper mediated decarboxylative direct C–H arylation of heteroarenes with benzoic acids
inferredcites →https://doi.org/10.1039/c5qo00004aopenalex-snapshot
Transition metal-catalyzed C–H bond functionalizations by the use of diverse directing groups
inferredcites →https://doi.org/10.1039/c7cc06226eopenalex-snapshot
Pd-Catalyzed C–H arylation of pyridazine-based fused 1,2,4-triazoles: overriding selectivity at the usual position by undermining of preferred chelate formation
inferredcites →https://doi.org/10.1039/c7sc01732dopenalex-snapshot
Pivalophenone imine as a benzonitrile surrogate for directed C–H bond functionalization
inferredcites →https://doi.org/10.1039/c8cs00201kopenalex-snapshot
A comprehensive overview of directing groups applied in metal-catalysed C–H functionalisation chemistry
inferredcites →https://doi.org/10.1039/d0cc01129kopenalex-snapshot
Pd-Catalyzed intermolecular C–H bond arylation reactions: effect of bulkiness of carboxylate ligands
inferredcites →https://doi.org/10.1246/cl.2010.1118openalex-snapshot
Overview of the Mechanistic Work on the Concerted Metallation–Deprotonation Pathway
inferredcites →https://doi.org/10.5860/choice.27-5777openalex-snapshot
Organic building blocks of the chemical industry
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.4111366openalex-extracted
Design and Synthesis of Functionalized4-Aryl-Catechol Derivatives as New Anti-Inflammatory Agents with In Vivo Efficacy PART I
inferred← citeshttps://doi.org/10.1002/ange.202201750openalex-snapshot
S,O‐Ligand Promoted meta‐C−H Arylation of Anisole Derivatives via Palladium/Norbornene Catalysis
inferred← citeshttps://doi.org/10.1002/ange.202400689openalex-snapshot
Non‐Directed C−H Arylation of Anisole Derivatives via Pd/S,O‐Ligand Catalysis
inferred← citeshttps://doi.org/10.1002/anie.202201750openalex-snapshot
S,O‐Ligand Promoted meta ‐C−H Arylation of Anisole Derivatives via Palladium/Norbornene Catalysis
inferred← citeshttps://doi.org/10.1002/anie.202400689openalex-snapshot
Non‐Directed C−H Arylation of Anisole Derivatives via Pd/S,O‐Ligand Catalysis
inferred← citeshttps://doi.org/10.1002/ejoc.202100866openalex-snapshot
Chroman‐4‐one‐Based Amino Bidentate Ligand: An Efficient Ligand for Suzuki‐Miyaura and Mizoroki‐Heck Coupling Reactions in Aqueous Medium
inferred← citeshttps://doi.org/10.1016/j.ejmech.2022.114788openalex-snapshot
Design and synthesis of functionalized 4-aryl-Catechol derivatives as new antiinflammtory agents with in vivo efficacy
inferred← citeshttps://doi.org/10.1039/d6qo00493hopenalex-snapshot
Thioxanthone-modified flavin for photo-decarboxylation of aromatic acids to enable C-2 arylation of nitrogen heterocycles
inferred← citeshttps://doi.org/10.3390/molecules26164931openalex-snapshot
Benzothiadiazole vs. iso-Benzothiadiazole: Synthesis, Electrochemical and Optical Properties of D–A–D Conjugated Molecules Based on Them
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.