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Heck Reaction in Ionic Liquids and the in Situ Identification of N-Heterocyclic Carbene Complexes of Palladium
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/9783527612222openalex-snapshot
Metal‐Catalyzed Cross‐Coupling Reactions
inferredcites →https://doi.org/10.1002/anie.196801412openalex-snapshot
Direct Synthesis of a Mercury Salt‐Carbene Complex
inferredcites →https://doi.org/10.1002/anie.199523711openalex-snapshot
Metal Complexes of N‐Heterocyclic Carbenes—A New Structural Principle for Catalysts in Homogeneous Catalysis
inferredcites →https://doi.org/10.1002/cber.19961291213openalex-snapshot
Synthesis and Stereochemistry of the First Chiral (Imidazolinylidene)‐ and (Triazolinylidene)palladium(ii) Complexes
inferredcites →https://doi.org/10.1016/0022-328x(94)05177-dopenalex-snapshot
Homoleptic carbene complexes VI. Bis{1,1′-methylene-3,3′-dialkyl-diimidazolin-2,2′-diylidene}palladium chelate complexes by the free carbene route
inferredcites →https://doi.org/10.1016/0022-328x(96)06398-xopenalex-snapshot
First palladium-catalyzed Heck reactions with efficient colloidal catalyst systems
inferredcites →https://doi.org/10.1016/s0022-328x(00)88691-xopenalex-snapshot
1,3-Dimethyl-4-imidazolinyliden-(2)-pentacarbonylchrom ein neuer übergangsmetall-carben-komplex
inferredcites →https://doi.org/10.1016/s0022-328x(96)06892-1openalex-snapshot
N-heterocyclic carbene complexes of palladium and rhodium: cis/trans-isomers
inferredcites →https://doi.org/10.1016/s0022-328x(97)00464-6openalex-snapshot
Imidazoline-2-ylidene metal complexes with pendant ferrocenyl substituents
inferredcites →https://doi.org/10.1016/s0022-328x(98)00980-2openalex-snapshot
Homoleptic chelating N-heterocyclic carbene complexes of palladium and nickel
inferredcites →https://doi.org/10.1016/s0022-328x(98)01050-xopenalex-snapshot
Application of palladacycles in Heck type reactions
inferredcites →https://doi.org/10.1016/s0040-4039(00)98131-0openalex-snapshot
Highly stereospecific palladium-catalysed vinylation of vinylic halides under solid-liquid phase transfer conditions.
inferredcites →https://doi.org/10.1021/ic951325xopenalex-snapshot
Hydrophobic, Highly Conductive Ambient-Temperature Molten Salts
inferredcites →https://doi.org/10.1021/ja00022a026openalex-snapshot
Role and effects of halide ions on the rates and mechanisms of oxidative addition of iodobenzene to low-ligated zerovalent palladium complexes Pd0(PPh3)2
inferredcites →https://doi.org/10.1021/ol9907771openalex-snapshot
The Heck Reaction in Ionic Liquids: A Multiphasic Catalyst System
inferredcites →https://doi.org/10.1038/19887openalex-snapshot
Green processing using ionic liquids and CO2
inferredcites →https://doi.org/10.5860/choice.34-0938openalex-snapshot
Palladium reagents and catalysts: innovations in organic synthesis
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Theoretical and Experimental Insights into a New Derivative of Amimcl Ionic Liquid and its Comparison with Parent Compound
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Ionic Liquids in Metal Catalyzed Reactions
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Ionische Flüssigkeiten – neue „Lösungen“ für die Übergangsmetallkatalyse
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Enantioselective Hydrogenations of Arylalkenes Mediated by [Ir(cod)(JM-Phos)]+ Complexes
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Highly Active Palladium/Activated Carbon Catalysts for Heck Reactions: Correlation of Activity, Catalyst Properties, and Pd Leaching
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Ionic Liquids—New “Solutions” for Transition Metal Catalysis
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Microwave Preparation of Metal Fluorides and their Biological Application
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The Nature of N‐Heterocyclic Carbenes
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Group 10 Metal(II)‐NHC Complexes
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Ionic Liquids for Hydrogen Storage: Opportunities for Organometallic Chemistry
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Development of Methods: Section 3.1.1–3.1.2.2.4
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Homogeneous Catalysis ‐Quo vadis?
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Catalytic Hydrogenation using Ionic Liquids as Catalyst Phase
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Palladium‐Catalyzed Olefinations of Aryl Halides (Heck Reaction) and Related Transformations
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Transition Metal Catalysis using Ionic Liquids
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Recent Developments in Using Ionic Liquids as Solvents and Catalysts for Organic Synthesis
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Recent Developments in Using Ionic Liquids as Solvents and Catalysts for Organic Synthesis
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Transition Metal Catalysis in Ionic Liquids
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Heterogeneous Catalytic Sulfimidation using Immobilized Cu(acac)2
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On the Nature of the Active Species in Palladium Catalyzed Mizoroki–Heck and Suzuki–Miyaura Couplings – Homogeneous or Heterogeneous Catalysis, A Critical Review
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Palladium Nanoparticles in Suzuki Cross‐Couplings: Tapping into the Potential of Tris‐Imidazolium Salts for Nanoparticle Stabilization
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Oxidative Addition of Imidazolium Salts to Ni0 and Pd0: Synthesis and Structural Characterization of Unusually Stable Metal–Hydride Complexes
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Transition‐Metal‐Catalyzed Reactions Involving Imidazolium Salt/N‐Heterocyclic Carbene Couples as Substrates
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Nanopartikel als regenerierbare Katalysatoren: an der Nahtstelle zwischen homogener und heterogener Katalyse
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Aus der Sicht des Synthetikers: Palladiumkomplexe N‐heterocyclischer Carbene als Katalysatoren für Kreuzkupplungen
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Bis‐NHC‐Diarylethene Palladium Complexes: Dynamic Behavior and Self‐Tuning Photoswitching
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Oxidative Addition of Imidazolium Salts to Ni 0 and Pd 0 : Synthesis and Structural Characterization of Unusually Stable Metal–Hydride Complexes
inferred← citeshttps://doi.org/10.1002/anie.200454166openalex-snapshot
Transition‐Metal‐Catalyzed Reactions Involving Imidazolium Salt/N‐Heterocyclic Carbene Couples as Substrates
inferred← citeshttps://doi.org/10.1002/anie.200460431openalex-snapshot
On the Noninnocent Nature of 1,3‐Dialkylimidazolium Ionic Liquids
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Nanoparticles as Recyclable Catalysts: The Frontier between Homogeneous and Heterogeneous Catalysis
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Palladium Complexes of N‐Heterocyclic Carbenes as Catalysts for Cross‐Coupling Reactions—A Synthetic Chemist's Perspective
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Bis‐NHC‐Diarylethene Palladium Complexes: Dynamic Behavior and Self‐Tuning Photoswitching
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Reaction of the N‐heterocyclic carbene, 1,3‐dimesityl‐ imidazol‐2‐ylidene, with a uranyl triflate complex, UO2(OTf)2(thf)3
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Heck reactions in monoglyme and diglyme using BmimCl as pre‐ligand
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Exploration of amino‐functionalized ionic liquids as ligand and base for Heck reaction
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Accelerated Heck reaction using ortho‐palladated complex in a nonaqueous ionic liquid with controlled microwave heating
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Review: Synthesis of organometallics and catalytic hydrogenations in ionic liquids
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Palladium(II) Complexes with Small N‐Heterocyclic Carbene Ligands as Highly Active Catalysts for the Suzuki–Miyaura Cross‐Coupling Reaction
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Palladium‐Containing Ionic Liquid‐Based Ordered Mesoporous Organosilica: An Efficient and Reusable Catalyst for the Heck Reaction
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Electrochemical Stability of Ionic Liquids: General Influences and Degradation Mechanisms
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inferred← citeshttps://doi.org/10.1007/1-4020-3915-8_6openalex-snapshot
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Imidazolium Ionic Liquid-supported Diol: An Efficient and Recyclable Phosphine-free Ligand for Palladium Catalyzed Heck Reaction
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A Hybrid P,N-Ligand Functionalized Imidazolium Salt for Palladium-Catalyzed Heck Reactions in Ionic Liquid Solution
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The Ionic Palladium Porphyrin as a Highly Efficient and Recyclable Catalyst for Heck Reaction in Ionic Liquid Solution Under Aerobic Conditions
inferred← citeshttps://doi.org/10.1007/s10562-012-0919-9openalex-snapshot
Pd Nanoparticles in the Thermoregulated Ionic Liquid and Organic Biphasic System: An Efficient and Recyclable Catalyst for Heck Reaction
inferred← citeshttps://doi.org/10.1007/s10562-015-1609-1openalex-snapshot
Activity and Recyclability Improvement Through Adjusting the Tethering Strategy for Pd-Catalyzed Suzuki–Miyaura Coupling Reaction of Aryl Chlorides
inferred← citeshttps://doi.org/10.1007/s10562-026-05424-2openalex-snapshot
Palladium and Iron-Substituted Ceria as a Recyclable Bimetal Ionic Catalyst for the Ligand-Free Heck Coupling Reaction
inferred← citeshttps://doi.org/10.1007/s10563-024-09430-5openalex-snapshot
Role of Ionic Liquids as Solvent & Catalyst for Heck and Suzuki Reactions: A Comprehensive Review
inferred← citeshttps://doi.org/10.1007/s10812-017-0563-7openalex-snapshot
X-Ray Photoelectron Spectroscopy of Imidazolium Zwitterionic Salts: Comparison to Acetate Analogs and the Impact of the Alkyl Chain Length on the Charge Distribution
inferred← citeshttps://doi.org/10.1007/s11030-008-9103-yopenalex-snapshot
Fluorous Lewis acids and phase transfer catalysts
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Facile, efficient and one-pot access to diverse new functionalized aminoalkyl and amidoalkyl naphthol scaffolds via green multicomponent reaction using triethylammonium hydrogen sulfate ([Et3NH][HSO4]) as an acidic ionic liquid under solvent-free conditions
inferred← citeshttps://doi.org/10.1007/s11051-010-9950-1openalex-snapshot
Photoluminescent silicon nanocrystals stabilized by ionic liquid
inferred← citeshttps://doi.org/10.1007/s11164-022-04803-9openalex-snapshot
Green and one-pot synthesis of novel amidoalkyl naphthols using triethanolammonium acetate [(OHCH2CH2)3NH][OAc]) ionic liquid and their anti-H.pylori activity
inferred← citeshttps://doi.org/10.1007/s11172-013-0005-5openalex-snapshot
Activation of C-F bonds in ionic liquids catalyzed by nickel complex compounds
inferred← citeshttps://doi.org/10.1007/s12039-019-1594-9openalex-snapshot
Recyclable Pd ionic catalyst coated on cordierite monolith for high TOF Heck coupling reaction
inferred← citeshttps://doi.org/10.1016/b0-08-045047-4/00032-7openalex-snapshot
Organometallic Chemistry in Ionic Liquids
inferred← citeshttps://doi.org/10.1016/b0-08-045047-4/00102-3openalex-snapshot
Palladium Complexes with Carbonyl, Isocyanide, and Carbene Ligands
inferred← citeshttps://doi.org/10.1016/b0-08-045047-4/00182-5openalex-snapshot
Green Organometallic Chemistry
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00420-1openalex-snapshot
4.14 Vinyl Substitutions with Organopalladium Intermediates
inferred← citeshttps://doi.org/10.1016/b978-0-12-800171-4.00005-6openalex-snapshot
Bischler–Napieralski Reaction in the Syntheses of Isoquinolines∗
inferred← citeshttps://doi.org/10.1016/j.apcata.2003.11.008openalex-snapshot
Friedel–Crafts alkylation of 2-methylnaphthalene in room temperature ionic liquids
inferred← citeshttps://doi.org/10.1016/j.apcata.2005.05.023openalex-snapshot
Effects of kinds of ionic liquid catalysts on alkylations of 1-and 2-methylnaphthalene with alkenes
inferred← citeshttps://doi.org/10.1016/j.apcata.2007.09.040openalex-snapshot
Ionic liquid as an efficient promoting medium for synthesis of dimethyl carbonate by oxidative carbonylation of methanol
inferred← citeshttps://doi.org/10.1016/j.apcata.2009.05.020openalex-snapshot
Highly enantioselective Ru-catalyzed asymmetric hydrogenation of β-keto ester in ionic liquid/methanol mixtures
inferred← citeshttps://doi.org/10.1016/j.apcata.2011.09.038openalex-snapshot
Effect of chiral ionic liquids on palladium-catalyzed Heck arylation of 2,3-dihydrofuran
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.catcom.2006.05.002openalex-snapshot
Simple, efficient and recyclable palladium catalytic system for Heck reaction in functionalized ionic liquid network
inferred← citeshttps://doi.org/10.1016/j.catcom.2007.07.012openalex-snapshot
Selective hydrogenation of cinnamaldehyde catalyzed by palladium nanoparticles immobilized on ionic liquids modified-silica gel
inferred← citeshttps://doi.org/10.1016/j.catcom.2007.11.004openalex-snapshot
Efficient Heck reactions catalyzed by a palladium/diol–imidazolium salt in aerial atmosphere
inferred← citeshttps://doi.org/10.1016/j.catcom.2008.06.016openalex-snapshot
An efficient Heck reaction in water catalyzed by palladium nanoparticles immobilized on imidazolium–styrene copolymers
inferred← citeshttps://doi.org/10.1016/j.catcom.2011.01.008openalex-snapshot
Pd-TPPTS catalyzed Mizoroki–Heck coupling in halogen-free ionic liquids [Rmim][p-CH3C6H4SO3]
inferred← citeshttps://doi.org/10.1016/j.cattod.2014.03.029openalex-snapshot
Heterogeneous catalyst preparation in ionic liquids: Titania supported gold nanoparticles
inferred← citeshttps://doi.org/10.1016/j.ccr.2004.02.006openalex-snapshot
Redox processes involving hydrocarbylmetal (N-heterocyclic carbene) complexes and associated imidazolium salts: ramifications for catalysis
inferred← citeshttps://doi.org/10.1016/j.ccr.2004.05.013openalex-snapshot
Stability and reactivity of N-heterocyclic carbene complexes
inferred← citeshttps://doi.org/10.1016/j.ccr.2005.02.001openalex-snapshot
Structural and mechanistic studies of Pd-catalyzed CC bond formation: The case of carbonylation and Heck reaction
inferred← citeshttps://doi.org/10.1016/j.ccr.2008.05.018openalex-snapshot
Carbenes: Synthesis, properties, and organometallic chemistry
inferred← citeshttps://doi.org/10.1016/j.ccr.2011.03.005openalex-snapshot
Naked metal nanoparticles from metal carbonyls in ionic liquids: Easy synthesis and stabilization
inferred← citeshttps://doi.org/10.1016/j.ccr.2012.04.003openalex-snapshot
Stereochemical and structural characteristics of single- and double-site Pd(II)–N-heterocyclic carbene complexes: Promising catalysts in organic syntheses ranging from CC coupling to olefin polymerizations
inferred← citeshttps://doi.org/10.1016/j.ccr.2019.01.008openalex-snapshot
The role of palladium nanoparticles in catalytic C–C cross-coupling reactions
inferred← citeshttps://doi.org/10.1016/j.ccr.2021.213860openalex-snapshot
Formation and stabilization of nanosized Pd particles in catalytic systems: Ionic nitrogen compounds as catalytic promoters and stabilizers of nanoparticles
inferred← citeshttps://doi.org/10.1016/j.cej.2008.11.007openalex-snapshot
Reverse ATRP of ethyl acrylate with ionic liquids as reaction medium
inferred← citeshttps://doi.org/10.1016/j.cplett.2015.12.017openalex-snapshot
X-ray photoelectron spectroscopy as a probe of rhodium-ligand interaction in ionic liquids
inferred← citeshttps://doi.org/10.1016/j.cplett.2020.137857openalex-snapshot
Mechanism of promotion of SN2 fluorination by [Bmim]F in solvent-free environment: Quantum chemical analysis
inferred← citeshttps://doi.org/10.1016/j.crci.2010.07.001openalex-snapshot
Exceptional efficiency of palladium nanoparticle catalyzed Heck cross-coupling in binary task specific ionic liquids
inferred← citeshttps://doi.org/10.1016/j.electacta.2006.12.055openalex-snapshot
Spectroelectrochemical study of a soluble derivative of poly(aniline) in a room temperature ionic liquid
inferred← citeshttps://doi.org/10.1016/j.electacta.2007.04.064openalex-snapshot
Synthesis and characterization of two ionic liquids with emphasis on their chemical stability towards metallic lithium
inferred← citeshttps://doi.org/10.1016/j.ica.2004.11.053openalex-snapshot
The palladium complexes of a C3-bridged di(benzimidazol-2-ylidene) ligand via cleavage of a dibenzotetraazafulvalene
inferred← citeshttps://doi.org/10.1016/j.ica.2007.11.008openalex-snapshot
Two new N-heterocyclic carbene silver(I) complexes with the π–π stacking interactions
inferred← citeshttps://doi.org/10.1016/j.ica.2015.08.027openalex-snapshot
Synthesis, characterization, density function theory and catalytic performances of palladium(II)–N-heterocyclic carbene complexes derived from benzimidazol-2-ylidenes
inferred← citeshttps://doi.org/10.1016/j.ica.2024.122498openalex-snapshot
Palladium(II) coordination of N-heterocyclic carbene ligands with a triazole moiety in the nitrogen substituent
inferred← citeshttps://doi.org/10.1016/j.jcat.2008.07.009openalex-snapshot
Stabilization and recovery of gold catalysts in the cyclopropanation of alkenes within ionic liquids
inferred← citeshttps://doi.org/10.1016/j.jcat.2009.11.002openalex-snapshot
Pd catalysts immobilized onto gel-supported ionic liquid-like phases (g-SILLPs): A remarkable effect of the nature of the support
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2004.06.001openalex-snapshot
Fluorination of carbinols with 2,2-difluoro-1,3-dimethylimidazolidine in ionic liquid
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2007.11.006openalex-snapshot
Fluorination of activated aromatic systems with Selectfluor™ F-TEDA-BF4 in ionic liquids
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2003.07.028openalex-snapshot
Phospha-palladacycles and N-heterocyclic carbene palladium complexes: efficient catalysts for CC-coupling reactions
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2005.03.008openalex-snapshot
Highly regioselective Heck reactions of heteroaryl halides with electron-rich olefins in ionic liquid
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2005.05.031openalex-snapshot
Palladium-catalyzed hydroesterification of styrene derivatives in the presence of ionic liquids
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2005.07.097openalex-snapshot
Pd–benzothiazol-2-ylidene complex in ionic liquids: Efficient catalyst for carbon–carbon coupling reactions
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2005.07.115openalex-snapshot
Formation of chiral ionic liquids and imidazol-2-ylidene metal complexes from the proteinogenic aminoacid l-histidine
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2005.08.009openalex-snapshot
Organopalladium complex promoted asymmetric synthesis of a P-chiral phosphanorbornene in ionic liquids and in organic solvents
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2006.08.072openalex-snapshot
Atom transfer carbonylation using ionic liquids as reaction media
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2007.03.020openalex-snapshot
Preparation of NHC-substituted phosphitepalladacycles
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2007.04.037openalex-snapshot
Pd(II) complexes of a sterically bulky, benzannulated N-heterocyclic carbene and their catalytic activities in the Mizoroki–Heck reaction
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2007.05.005openalex-snapshot
New N-heterocyclic carbene silver(I) and mercury(II) 2-D supramolecular layers by the π–π stacking interactions
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2007.09.027openalex-snapshot
New mercury(II) and silver(I) complexes containing NHC metallacrown ethers with the π–π stacking interactions
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2008.04.017openalex-snapshot
Direct in situ synthesis of cationic N-heterocyclic carbene iridium and rhodium complexes from neat ionic liquid: Application in catalytic dehydrogenation of cyclooctadiene
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2010.05.007openalex-snapshot
Effect of ortho-substituents on the stereochemistry of 2-(o-substituted phenyl)-1H-imidazoline–palladium complexes
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2010.12.012openalex-snapshot
Effect of counterions and central cores of tripodal imidazolium salts on palladium-catalyzed Suzuki–Miyaura cross-coupling reactions
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2015.05.020openalex-snapshot
Catalytic application of zwitterionic palladium complexes in Mizoroki–Heck reactions using ionic liquid as solvent
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2019.05.019openalex-snapshot
New C-scorpionate nickel(II) catalyst for Heck C–C coupling under unconventional conditions
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2019.121093openalex-snapshot
A simple, efficient and green approach for the synthesis of palladium nanoparticles using Oxytocin: Application for ligand free Suzuki reaction and total synthesis of aspongpyrazine A
inferred← citeshttps://doi.org/10.1016/j.molcata.2003.09.032openalex-snapshot
Recyclable palladium(0)-catalysed silylstannation of terminal alkynes in ionic liquids
inferred← citeshttps://doi.org/10.1016/j.molcata.2003.11.007openalex-snapshot
Comparative studies on alkylation of phenol with tert-butyl alcohol in the presence of liquid or solid acid catalysts in ionic liquids
inferred← citeshttps://doi.org/10.1016/j.molcata.2003.11.033openalex-snapshot
Catalytic Pauson–Khand reaction in ionic liquids
inferred← citeshttps://doi.org/10.1016/j.molcata.2003.12.028openalex-snapshot
Regio- and stereo-selective carbon–carbon bond formation in ionic liquids
inferred← citeshttps://doi.org/10.1016/j.molcata.2004.08.008openalex-snapshot
Friedel–crafts alkylation of α-methylnaphthalene in the presence of ionic liquids
inferred← citeshttps://doi.org/10.1016/j.molcata.2004.12.022openalex-snapshot
Utilisation of ionic liquid solvents for the synthesis of Lily-of-the-Valley fragrance {β-Lilial®; 3-(4-t-butylphenyl)-2-methylpropanal}
inferred← citeshttps://doi.org/10.1016/j.molcata.2005.01.010openalex-snapshot
Alkylation of α-methylnaphthalene with long-chain alkenes catalyzed by butylpyridinium bromochloroaluminate ionic liquids
inferred← citeshttps://doi.org/10.1016/j.molcata.2005.03.013openalex-snapshot
The metal ion modified ionic liquids promoted free-solvent alkylations of α-methylnaphthalene with long-chain olefins
inferred← citeshttps://doi.org/10.1016/j.molcata.2005.12.016openalex-snapshot
Reactivity of chelating dicarbene metal complex catalysts, I: An investigation on the Heck reaction
inferred← citeshttps://doi.org/10.1016/j.molcata.2006.03.064openalex-snapshot
Base-free efficient palladium catalyst of Heck reaction in molten tetrabutylammonium bromide
inferred← citeshttps://doi.org/10.1016/j.molcata.2006.08.024openalex-snapshot
Palladium-catalyzed Heck arylation of 5-hexen-2-one in ionic liquid: A novel approach to arylated γ,δ-unsaturated ketones
inferred← citeshttps://doi.org/10.1016/j.molcata.2007.05.045openalex-snapshot
Photocatalytic selective aerobic oxidation of alcohols to aldehydes and ketones by HPW/MCM-41 in ionic liquids
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