On the public citation graph
Superelectrophilic Chemistry of Imidazoles
0 signed · 69 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known work and none has been retracted — and get a dated CiteStamped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/chem.200701470openalex-snapshot
Superelectrophiles: Charge–Charge Repulsive Effects
inferredcites →https://doi.org/10.1016/j.bmcl.2008.06.094openalex-snapshot
Synthesis of 6- or 4-functionalized indoles via a reductive cyclization approach and evaluation as aromatase inhibitors
inferredcites →https://doi.org/10.1016/j.bmcl.2008.09.036openalex-snapshot
2,4(5)-Diarylimidazoles: Synthesis and biological evaluation of a new class of sodium channel blockers against hNav1.2
inferredcites →https://doi.org/10.1016/s0928-0987(00)00074-9openalex-snapshot
Synthesis of new potent and selective aromatase inhibitors based on long-chained diarylalkylimidazole and diarylalkyltriazole molecule skeletons
inferredcites →https://doi.org/10.1021/ja00004a044openalex-snapshot
Friedel-Crafts-type reactions involving di- and tricationic species. Onium-allyl dications and O,O-diprotonated aci-nitro species bearing a protonated carbonyl group
inferredcites →https://doi.org/10.1021/ja00083a023openalex-snapshot
High-Resolution Electron Energy-Loss Studies of Hydrocarbon Formation from Methane Decomposition on Ru(0001) and Ru(11.hivin.20) Catalysts
inferredcites →https://doi.org/10.1021/ja00843a067openalex-snapshot
Electrophilic reactions at single bonds. XVIII. Indication of protosolvated de facto substituting agents in the reactions of alkanes with acetylium and nitronium ions in superacidic media
inferredcites →https://doi.org/10.1021/ja0520161openalex-snapshot
Catalytic Conjugate Additions of Carbonyl Anions under Neutral Aqueous Conditions
inferredcites →https://doi.org/10.1021/ja8062953openalex-snapshot
N-Heterocyclic Superelectrophiles and Evidence for Single Electron Transfer Chemistry
inferredcites →https://doi.org/10.1021/jm00041a011openalex-snapshot
A Structure-Activity Relationship Study of Benzylic Modifications of 4-[1-(1-Naphthyl)ethyl]-1H-imidazoles on .alpha.1- and .alpha.2-Adrenergic Receptors
inferredcites →https://doi.org/10.1021/jm030502yopenalex-snapshot
Potent and Selective Farnesyl Transferase Inhibitors
inferredcites →https://doi.org/10.1021/jm0511435openalex-snapshot
Imidazole−Dioxolane Compounds as Isozyme-Selective Heme Oxygenase Inhibitors
inferredcites →https://doi.org/10.1021/jm0607247openalex-snapshot
NO-Donor COX-2 Inhibitors. New Nitrooxy-Substituted 1,5-Diarylimidazoles Endowed with COX-2 Inhibitory and Vasodilator Properties
inferredcites →https://doi.org/10.1021/jm061429popenalex-snapshot
Design and Synthesis of Potent Antimalarial Agents Based on Clotrimazole Scaffold: Exploring an Innovative Pharmacophore
inferredcites →https://doi.org/10.1021/jm800505mopenalex-snapshot
X-ray Crystal Structure of Human Heme Oxygenase-1 in Complex with 1-(Adamantan-1-yl)-2-(1H-imidazol-1-yl)ethanone: A Common Binding Mode for Imidazole-Based Heme Oxygenase-1 Inhibitors
inferredcites →https://doi.org/10.1021/jm800512zopenalex-snapshot
Structure Based Development of Phenylimidazole-Derived Inhibitors of Indoleamine 2,3-Dioxygenase
inferredcites →https://doi.org/10.1021/jo030024zopenalex-snapshot
Dicationic Electrophiles from Olefinic Amines in Superacid
inferredcites →https://doi.org/10.1021/jo030327topenalex-snapshot
Superacid-Catalyzed Reactions of Cinnamic Acids and the Role of Superelectrophiles1
inferredcites →https://doi.org/10.1021/jo040218uopenalex-snapshot
Reactive Dications: The Superacid-Catalyzed Reactions of Alkynes Bearing Adjacent N-Heterocycles or Amine Groups
inferredcites →https://doi.org/10.1021/jo8003474openalex-snapshot
Preparation of Aza-Polycyclic Aromatic Compounds via Superelectrophilic Cyclizations
inferredcites →https://doi.org/10.1021/ol049512zopenalex-snapshot
Dicationic Intermediates Involving Protonated Amides: Dual Modes of Reactivity Including the Acylation of Arenes
inferredcites →https://doi.org/10.1021/ol060125uopenalex-snapshot
Charge Migration in Dicationic Electrophiles and Its Application to the Synthesis of Aza-polycyclic Aromatic Compounds
inferredcites →https://doi.org/10.1070/rc2008v077n06abeh003777openalex-snapshot
Superelectrophiles in the synthesis of condensation monomers and polymers
inferredcites →https://doi.org/10.1163/156856789x00104openalex-snapshot
Protonated (protosolvated) onium ions (onlum dications)
inferredcites →https://doi.org/10.1246/bcsj.53.1638openalex-snapshot
N-Acylimidazoles–Trifluoroacetic Acid System as the Acylating Agent for Aromatic Hydrocarbons
inferredcites →https://doi.org/10.1560/c64h-mnq6-58ma-ffq2openalex-snapshot
Dynamic equilibrium of self‐assembled cyclic trimer and tetramer of 1‐methyl‐5‐imidazolylcobalt(III)porphyrin
inferredcites →https://doi.org/10.3987/com-08-s(n)90openalex-snapshot
Facile Synthesis of Diarylmethylpyridines/Diarylmethylquinolines through Superelectrophilic Activation of Pyridinecarboxaldehydes/Quinolinecarboxaldehydes with Boron Trifluoride Monohydrate
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.4578065openalex-extracted
Superelectrophiles Reactions Assisted by Hydrogen Bonds Synthesis of Multi-Diazafluorenes Units (Mdafs)
inferred← citeshttps://doi.org/10.1002/9781119972471.ch6openalex-snapshot
Electrophilic Aromatic Substitution
inferred← citeshttps://doi.org/10.1002/ajoc.202100287openalex-snapshot
Selective Synthesis of Trisubstituted Imidazoles by Iodine‐Catalyzed [3+2] Cycloadditions
inferred← citeshttps://doi.org/10.1002/chin.200931113openalex-snapshot
ChemInform Abstract: Superelectrophilic Chemistry of Imidazoles.
inferred← citeshttps://doi.org/10.1002/ejoc.201100595openalex-snapshot
The N ‐Alkylation of Substituted 4‐Tetrazolo[1,5‐ a ]pyridines: Easy Access to a New Series of Electrophiles
inferred← citeshttps://doi.org/10.1007/s10593-020-02759-5openalex-snapshot
Reactions of quinoline-2(6,8)-carbaldehydes with arenes by the action of various Brønsted or Lewis acids: synthesis of diarylmethylquinolines
inferred← citeshttps://doi.org/10.1016/b978-0-08-096807-0.00008-7openalex-snapshot
Five-Membered Ring Systems: With More than One N Atom
inferred← citeshttps://doi.org/10.1016/b978-0-08-099406-2.00009-1openalex-snapshot
Five-Membered Ring Systems
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.103024openalex-snapshot
Synthesis, in vitro urease inhibitory potential and molecular docking study of Benzimidazole analogues
inferred← citeshttps://doi.org/10.1016/j.cdc.2023.100996openalex-snapshot
Synthesis, in vitro β-glucuronidase inhibitory potential and molecular docking study of benzimidazole analogues
inferred← citeshttps://doi.org/10.1016/j.ejmech.2018.03.011openalex-snapshot
2-Aryl benzimidazoles: Synthesis, In vitro α-amylase inhibitory activity, and molecular docking study
inferred← citeshttps://doi.org/10.1016/j.ejmech.2023.115230openalex-snapshot
Design, synthesis, spectroscopic characterization, single crystal X-ray analysis, in vitro α-amylase inhibition assay, DPPH free radical evaluation and computational studies of naphtho[2,3-d]imidazole-4,9-dione appended 1,2,3-triazoles
inferred← citeshttps://doi.org/10.1016/j.jechem.2024.07.017openalex-snapshot
High-performance imidazole-containing polymers for applications in high temperature polymer electrolyte membrane fuel cells
inferred← citeshttps://doi.org/10.1016/j.memsci.2025.125120openalex-snapshot
Rational design of pendant thiazole functionalized polyarylenes and their applications in high temperature proton exchange membrane fuel cells
inferred← citeshttps://doi.org/10.1016/j.molstruc.2019.06.091openalex-snapshot
The N-alkylation of 4-nitrobenzochalcogenadiazoles: Synthesis and theoretical approach
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.07.067openalex-snapshot
Condensations of aryl trifluoromethyl ketones with arenes in acidic media
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.01.049openalex-snapshot
Utilization of the hydroxyalkylation reaction to prepare bis(benzocrown ethers)
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.01.085openalex-snapshot
On the power of super acid—iodination of aromatic ring in the presence of imidazole moiety of the potent gamma secretase modulators (GSM) en route to tritium labeling
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.06.100openalex-snapshot
Superacid-promoted synthesis of polychlorinated dibenzofurans
inferred← citeshttps://doi.org/10.1016/j.tetlet.2023.154816openalex-snapshot
Superelectrophilic-initiated Friedel–Crafts reaction of diazafluorenols: Synthesis of multi-diazafluorene units (MDAFs)
inferred← citeshttps://doi.org/10.1016/s0959-6380(11)22008-7openalex-snapshot
Five Membered Ring Systems
inferred← citeshttps://doi.org/10.1021/acs.joc.7b01781openalex-snapshot
Substrate-Controlled Selectivity Switch in a Three-Component Reaction: A Ag-Catalyzed Strategy for the Synthesis of Functionalized Imidazoles
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b02595openalex-snapshot
Carbon Cationic Relay via Superelectrophiles: Synthesis of Spiro-diazafluorenes
inferred← citeshttps://doi.org/10.1021/acssuschemeng.5c06214openalex-snapshot
High-Performance Ether-Free Poly(terphenyl-co-9,9-dimethylfluorene-ethylimidazole) Membranes for High Temperature Proton Exchange Membrane Fuel Cells
inferred← citeshttps://doi.org/10.1021/cr4001385openalex-snapshot
Contemporary Carbocation Chemistry: Applications in Organic Synthesis
inferred← citeshttps://doi.org/10.1021/jo5007416openalex-snapshot
Cyclodehydrations Leading to Indene Products Having N-Heterocyclic Substituents
inferred← citeshttps://doi.org/10.1039/b910172aopenalex-snapshot
Iodine-mediated cyclization of N-thioacyl-1-(2-pyridyl)-1,2-aminoalcohols and their subsequent condensation leading to the formation of novel bis(1-imidazo[1,5-a]pyridyl)arylmethanes
inferred← citeshttps://doi.org/10.1039/c2py20877fopenalex-snapshot
Synthesis of hyperbranched polymers with controlled structure
inferred← citeshttps://doi.org/10.1039/c7ob01242jopenalex-snapshot
Silver-catalyzed [3 + 2] domino reaction: an efficient strategy to synthesize imidazole-5-carbaldehydes
inferred← citeshttps://doi.org/10.1039/d0ta12100bopenalex-snapshot
Alkaline polymers of intrinsic microporosity: high-conduction and low-loss anhydrous proton exchange membranes for energy conversion
inferred← citeshttps://doi.org/10.1039/d4ob02069copenalex-snapshot
Generation of C(sp 3 )–C Ar bonds in the synthesis of triarylmethanes (TRAMs): comprehensive progress since 2009
inferred← citeshttps://doi.org/10.1039/d6cc01260dopenalex-snapshot
Advances in basic-group-containing polyaromatic membranes via superacid-catalyzed polyhydroxyalkylation for high temperature proton exchange membrane fuel cells
inferred← citeshttps://doi.org/10.1039/d6ra06580eopenalex-snapshot
Rational design of naphtho[2,3- d ]imidazole-4,9-dione-linked 1,3,4-oxadiazoles as α-amylase inhibitors supported by QSAR, docking, molecular dynamics, and ADME approaches
inferred← citeshttps://doi.org/10.1211/jpp.62.04.0012openalex-snapshot
Imidazole inhibits B16 melanoma cell migration via degradation of β-catenin
inferred← citeshttps://doi.org/10.3762/bjoc.12.202openalex-snapshot
Superelectrophilic activation of 5-hydroxymethylfurfural and 2,5-diformylfuran: organic synthesis based on biomass-derived products
inferred← citeshttps://doi.org/10.3762/bjoc.12.93openalex-snapshot
Reactions of N,3-diarylpropiolamides with arenes under superelectrophilic activation: synthesis of 4,4-diaryl-3,4-dihydroquinolin-2(1H)-ones and their derivatives
inferred← citeshttps://doi.org/10.3762/bjoc.15.191openalex-snapshot
Reactions of 2-carbonyl- and 2-hydroxy(or methoxy)alkyl-substituted benzimidazoles with arenes in the superacid CF 3 SO 3 H. NMR and DFT studies of dicationic electrophilic species
inferred← citeshttps://doi.org/10.70675/258cc130z0b87z46f2za0f8zd79d12ad741bopenalex-snapshot
Activation superélectrophile de composés organophosphorés insaturés et de composés azotés insaturés en milieu superacide
inferred← citeshttps://doi.org/10.70675/da6f7988z3ecbz4452z9553z6525cc2eaf90openalex-snapshot
Synthèse et réactivité de dérivés benzochalcogénadiazoliques : Approche expérimentale et théorique
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.