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Phosphine Oxides as Preligands in Ruthenium-Catalyzed Arylations via C−H Bond Functionalization Using Aryl Chlorides
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Ruthenium‐Catalyzed Reactions via sp CH, sp 2 CH, sp 3 CH, and CHalogen Bond Activations
inferredcites →https://doi.org/10.1002/9783527619535openalex-snapshot
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inferredcites →https://doi.org/10.1002/anie.200460848openalex-snapshot
Enantioselective Catalysis with Chiral Phosphine Oxide Preligands
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3D‐Hybrid Networks with Controllable Electrical Conductivity from the Electrochemical Deposition of Terthiophene‐Functionalized Polyphenylene Dendrimers
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inferredcites →https://doi.org/10.1021/ja042510popenalex-snapshot
Site-Specific Phenylation of Pyridine Catalyzed by Phosphido-Bridged Ruthenium Dimer Complexes: A Prototype for C−H Arylation of Electron-Deficient Heteroarenes
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Organophosphorverbindungen mit tertiären Alkylsubstituenten. III*: Synthese und Reaktionen Di-1-adamantylsubstituierter Phosphorverbindungen; Kristallstruktur von Di-1-Adamantylphosphinsäurechlorid / Organophosphorus Compounds with Tertiary Alkyl Substituents. Ill: Synthesis and Reactions of…
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Formation of Alkanes and Arenes by Coupling Reactions
inferred← citeshttps://doi.org/10.1002/9781118788981.ch1openalex-snapshot
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Homogeneous Transition‐Metal‐Catalyzed C–H Bond Functionalization
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Nanodiamonds: Emergence of Functionalized Diamondoids and Their Unique Applications
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Oxidation of Aryl sp2C─H Bond Assisted by Directing Group
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Theoretical Study of R u‐Catalysis
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Arylation Reactions: A Historical Perspective
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Mechanistic Aspects of Transition Metal‐Catalyzed Direct Arylation Reactions
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Metal‐Catalyzed Direct Arylations (Excluding Palladium)
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Syntheses via C – H Bond Functionalizations
inferred← citeshttps://doi.org/10.1002/9783527648283.ch1openalex-snapshot
Palladium‐Catalyzed Cross‐Coupling Reactions – A General Introduction
inferred← citeshttps://doi.org/10.1002/9783527655588.ch17openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9783527672707.ch4openalex-snapshot
C–H Bond Activation for Arylations
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inferred← citeshttps://doi.org/10.1002/9783527834242.chf0032openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9783527834242.chf0034openalex-snapshot
Ru‐Catalyzed CC Bond Formation via CH Bond Cleavage
inferred← citeshttps://doi.org/10.1002/9783527834242.chf0039openalex-snapshot
Arene–Ruthenium(II) Complexes in CH Functionalization: Role of Ligands
inferred← citeshttps://doi.org/10.1002/9783527834242.chf0130openalex-snapshot
Ruthenium‐Catalyzed Asymmetric CH Functionalization
inferred← citeshttps://doi.org/10.1002/9783527834242.chf0158openalex-snapshot
Innate Directing Group‐Guided Transition Metal‐Catalyzed C(sp 2 )H Activation: Functionalization of Biosignificant Heterocyclic Scaffolds
inferred← citeshttps://doi.org/10.1002/adsc.200800016openalex-snapshot
Palladium‐Catalyzed Direct Arylations of 1,2,3‐Triazoles with Aryl Chlorides using Conventional Heating
inferred← citeshttps://doi.org/10.1002/adsc.200900350openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/adsc.201000049openalex-snapshot
(η6‐Arene)ruthenium(N‐heterocyclic carbene) Complexes for the Chelation‐Assisted Arylation and Deuteration of Arylpyridines: Catalytic Studies and Mechanistic Insights
inferred← citeshttps://doi.org/10.1002/adsc.201000975openalex-snapshot
The Pyridyldiisopropylsilyl Group: A Masked Functionality and Directing Group for Monoselective ortho‐Acyloxylation and ortho‐Halogenation Reactions of Arenes
inferred← citeshttps://doi.org/10.1002/adsc.201300999openalex-snapshot
A General Approach towards Catechol and Pyrogallol through Ruthenium‐ and Palladium‐Catalyzed CH Hydroxylation by Weak Coordination
inferred← citeshttps://doi.org/10.1002/adsc.201301156openalex-snapshot
Ferrocenylalkynes for Ruthenium‐Catalyzed Isohypsic CH/NO Bond Functionalizations
inferred← citeshttps://doi.org/10.1002/adsc.201400906openalex-snapshot
Ruthenium(II)‐Catalyzed CH Arylation of Anilides with Boronic Acids, Borinic Acids and Potassium Trifluoroborates
inferred← citeshttps://doi.org/10.1002/adsc.201600313openalex-snapshot
Ruthenium‐Mediated Dual Catalytic Reactions of Isoquinoline via C−H Activation and Dearomatization for Isoquinolone
inferred← citeshttps://doi.org/10.1002/adsc.201700663openalex-snapshot
Secondary Phosphine Oxide Preligands for Palladium‐Catalyzed C–H (Hetero)Arylations: Efficient Access to Pybox Ligands
inferred← citeshttps://doi.org/10.1002/adsc.201800216openalex-snapshot
Catalytic Cascade Access to Biaryl‐2‐Methyl Acetates from Pyruvate O‐Arylmethyl Ketoximes via the Palladium‐Catalyzed C(sp2)H Bond Arylation and C−O Bond Solvolysis
inferred← citeshttps://doi.org/10.1002/adsc.201800728openalex-snapshot
Diversity‐Oriented Synthesis of Functionalized Imidazopyridine Analogues with Anti‐Cancer Activity through a Transition‐Metal Free, One‐pot Cascade Reaction
inferred← citeshttps://doi.org/10.1002/ajoc.201200042openalex-snapshot
Iron‐Catalyzed ortho Monoarylation of Benzamide Derivatives
inferred← citeshttps://doi.org/10.1002/ange.200501860openalex-snapshot
Effiziente Aryl‐(Hetero‐)Aryl‐Kupplungen mittels Aktivierung von C‐Cl‐ und C‐F‐Bindungen durch den Einsatz von Nickelkomplexen luftstabiler Phosphanoxide
inferred← citeshttps://doi.org/10.1002/ange.200504450openalex-snapshot
Katalytische Arylierungen über C‐H‐Bindungsaktivierung mit Aryltosylaten
inferred← citeshttps://doi.org/10.1002/ange.200600111openalex-snapshot
Chemoselektive benzylische C‐H‐Aktivierungen für die Synthese kondensierter N‐Heterocyclen
inferred← citeshttps://doi.org/10.1002/ange.200602222openalex-snapshot
Ein Diaminochlorphosphan für die palladiumkatalysierte Arylierung von Aminen und Ketonen
inferred← citeshttps://doi.org/10.1002/ange.200603833openalex-snapshot
Domino‐N‐H/C‐H‐Bindungsaktivierung: palladiumkatalysierte Synthese von anellierten Heterocyclen mit Dichlor(hetero)arenen
inferred← citeshttps://doi.org/10.1002/ange.200604988openalex-snapshot
Ein effizienter Dirhodiumkatalysator für die nichtdirigierte Direktarylierung nichtaktivierter Arene
inferred← citeshttps://doi.org/10.1002/ange.200701727openalex-snapshot
Ruthenium(IV)‐Alkylidene als Katalysatorvorstufen für direkte Arylierungen von Alkenen mit Chlorarenen und eine Anwendung auf die sequenzielle Katalyse
inferred← citeshttps://doi.org/10.1002/ange.200802526openalex-snapshot
Iron‐Mediated Direct Arylation of Unactivated Arenes
inferred← citeshttps://doi.org/10.1002/ange.200804517openalex-snapshot
Palladiumkatalysierte direkte Arylierungen von Heteroarenen mit Tosylaten und Mesylaten
inferred← citeshttps://doi.org/10.1002/ange.200806358openalex-snapshot
Iridium Catalysis for CH Bond Arylation of Heteroarenes with Iodoarenes
inferred← citeshttps://doi.org/10.1002/ange.200900454openalex-snapshot
Iron‐Catalyzed Chemoselective ortho Arylation of Aryl Imines by Directed CH Bond Activation
inferred← citeshttps://doi.org/10.1002/ange.200902458openalex-snapshot
Rutheniumkatalysierte regioselektive direkte Alkylierungen von Arenen mit nichtaktivierten Alkylhalogeniden unter C‐H‐Bindungsspaltung
inferred← citeshttps://doi.org/10.1002/ange.200902996openalex-snapshot
Übergangsmetallkatalysierte direkte Arylierungen von (Hetero)Arenen durch C‐H‐Bindungsbruch
inferred← citeshttps://doi.org/10.1002/ange.201002987openalex-snapshot
A Versatile Palladium/Triphosphane System for Direct Arylation of Heteroarenes with Chloroarenes at Low Catalyst Loading
inferred← citeshttps://doi.org/10.1002/ange.201005990openalex-snapshot
Palladium(II)‐Catalyzed CH Bond Arylation of Electron‐Deficient Arenes at Room Temperature
inferred← citeshttps://doi.org/10.1002/ange.201104035openalex-snapshot
Direct Arylation of 6‐Phenylpurine and 6‐Arylpurine Nucleosides by Ruthenium‐Catalyzed CH Bond Activation
inferred← citeshttps://doi.org/10.1002/ange.201104544openalex-snapshot
Use of Hemilabile N,N Ligands in Nitrogen‐Directed Iridium‐Catalyzed Borylations of Arenes
inferred← citeshttps://doi.org/10.1002/ange.201301663openalex-snapshot
Ruthenium‐Catalyzed Carbonylative CC Coupling in Water by Directed CH Bond Activation
inferred← citeshttps://doi.org/10.1002/ange.201304884openalex-snapshot
Twofold Unsymmetrical CH Functionalization of PyrDipSi‐Substituted Arenes: A General Method for the Synthesis of Substituted meta‐Halophenols
inferred← citeshttps://doi.org/10.1002/ange.201605877openalex-snapshot
N−H Imine as a Powerful Directing Group for Cobalt‐Catalyzed Olefin Hydroarylation
inferred← citeshttps://doi.org/10.1002/ange.201607270openalex-snapshot
ortho‐C−H Arylation of Benzoic Acids with Aryl Bromides and Chlorides Catalyzed by Ruthenium
inferred← citeshttps://doi.org/10.1002/ange.201609631openalex-snapshot
Bioorthogonal Diversification of Peptides through Selective Ruthenium(II)‐Catalyzed C–H Activation
inferred← citeshttps://doi.org/10.1002/ange.201611595openalex-snapshot
Ruthenium(II)‐Catalyzed meta C−H Mono‐ and Difluoromethylations by Phosphine/Carboxylate Cooperation
inferred← citeshttps://doi.org/10.1002/ange.201701523openalex-snapshot
Domino N‐/C‐Arylation via In Situ Generation of a Directing Group: Atom‐Efficient Arylation Using Diaryliodonium Salts
inferred← citeshttps://doi.org/10.1002/ange.201802748openalex-snapshot
Electrooxidative Ruthenium‐Catalyzed C−H/O−H Annulation by Weak O‐Coordination
inferred← citeshttps://doi.org/10.1002/ange.201813191openalex-snapshot
Enantioselective Aluminum‐Free Alkene Hydroarylations through C−H Activation by a Chiral Nickel/JoSPOphos Manifold
inferred← citeshttps://doi.org/10.1002/ange.201901856openalex-snapshot
Mizellare Katalyse für Ruthenium(II)‐katalysierte C‐H‐Arylierung: Schwache Koordination ermöglicht C‐H‐Aktivierung in H2O
inferred← citeshttps://doi.org/10.1002/ange.201909457openalex-snapshot
Aren‐freie Ruthenium(II/IV)‐katalysierte gegabelte Arylierungen für oxidative C‐H/C‐H‐Funktionalisierungen
inferred← citeshttps://doi.org/10.1002/ange.202006164openalex-snapshot
C7‐Indol‐Amidierung und ‐Alkenylierung durch Ruthenium(II)‐ Katalyse
inferred← citeshttps://doi.org/10.1002/ange.202208620openalex-snapshot
Distale C−H‐Glykosylierung durch Ruthenium(II)‐Katalyse: Modularer Aufbau vonmeta‐C‐Aryl‐Glykosiden
inferred← citeshttps://doi.org/10.1002/ange.202212595openalex-snapshot
Ruthenium(II)/Imidazolidincarbonsäure‐katalysierte C−H‐Alkylierung für zentrale und axiale Doppelenantioinduktion
inferred← citeshttps://doi.org/10.1002/ange.202400845openalex-snapshot
Photoinduzierte Ruthenium‐katalysierte C−H Arylierungspolymerisation bei Raumtemperatur
inferred← citeshttps://doi.org/10.1002/ange.202402060openalex-snapshot
Ruthenium(II)‐katalysierter Late‐Stage Einbau von N‐Aryltriazolen und ‐tetrazolen mit Sulfoniumsalzen per C−H‐Aktivierung
inferred← citeshttps://doi.org/10.1002/ange.202508139openalex-snapshot
Arene‐Ruthenium(II)‐Carboxylate für C–H‐Alkylierungen und Arylierungen bei Annährend Raumtemperatur
inferred← citeshttps://doi.org/10.1002/anie.200501860openalex-snapshot
Efficient Aryl–(Hetero)Aryl Coupling by Activation of CCl and CF Bonds Using Nickel Complexes of Air‐Stable Phosphine Oxides
inferred← citeshttps://doi.org/10.1002/anie.200504450openalex-snapshot
Catalytic Arylation Reactions by CH Bond Activation with Aryl Tosylates
inferred← citeshttps://doi.org/10.1002/anie.200600111openalex-snapshot
Chemoselective Benzylic CH Activations for the Preparation of Condensed N‐Heterocycles
inferred← citeshttps://doi.org/10.1002/anie.200602222openalex-snapshot
A Diaminochlorophosphine for Palladium‐Catalyzed Arylations of Amines and Ketones
inferred← citeshttps://doi.org/10.1002/anie.200603833openalex-snapshot
Domino NH/CH Bond Activation: Palladium‐Catalyzed Synthesis of Annulated Heterocycles Using Dichloro(hetero)arenes
inferred← citeshttps://doi.org/10.1002/anie.200604988openalex-snapshot
An Efficient Bimetallic Rhodium Catalyst for the Direct Arylation of Unactivated Arenes
inferred← citeshttps://doi.org/10.1002/anie.200701727openalex-snapshot
Ruthenium(IV) Alkylidenes as Precatalysts for Direct Arylations of Alkenes with Aryl Chlorides and an Application to Sequential Catalysis
inferred← citeshttps://doi.org/10.1002/anie.200802526openalex-snapshot
Iron‐Mediated Direct Arylation of Unactivated Arenes
inferred← citeshttps://doi.org/10.1002/anie.200804517openalex-snapshot
Palladium‐Catalyzed Direct Arylations of Heteroarenes with Tosylates and Mesylates
inferred← citeshttps://doi.org/10.1002/anie.200806358openalex-snapshot
Iridium Catalysis for CH Bond Arylation of Heteroarenes with Iodoarenes
inferred← citeshttps://doi.org/10.1002/anie.200900454openalex-snapshot
Iron‐Catalyzed Chemoselective ortho Arylation of Aryl Imines by Directed CH Bond Activation
inferred← citeshttps://doi.org/10.1002/anie.200902458openalex-snapshot
Ruthenium‐Catalyzed Regioselective Direct Alkylation of Arenes with Unactivated Alkyl Halides through CH Bond Cleavage
inferred← citeshttps://doi.org/10.1002/anie.200902996openalex-snapshot
Transition‐Metal‐Catalyzed Direct Arylation of (Hetero)Arenes by CH Bond Cleavage
inferred← citeshttps://doi.org/10.1002/anie.201002987openalex-snapshot
A Versatile Palladium/Triphosphane System for Direct Arylation of Heteroarenes with Chloroarenes at Low Catalyst Loading
inferred← citeshttps://doi.org/10.1002/anie.201005990openalex-snapshot
Palladium(II)‐Catalyzed CH Bond Arylation of Electron‐Deficient Arenes at Room Temperature
inferred← citeshttps://doi.org/10.1002/anie.201104035openalex-snapshot
Direct Arylation of 6‐Phenylpurine and 6‐Arylpurine Nucleosides by Ruthenium‐Catalyzed CH Bond Activation
inferred← citeshttps://doi.org/10.1002/anie.201104544openalex-snapshot
Use of Hemilabile N,N Ligands in Nitrogen‐Directed Iridium‐Catalyzed Borylations of Arenes
inferred← citeshttps://doi.org/10.1002/anie.201301663openalex-snapshot
Ruthenium‐Catalyzed Carbonylative CC Coupling in Water by Directed CH Bond Activation
inferred← citeshttps://doi.org/10.1002/anie.201304884openalex-snapshot
Twofold Unsymmetrical CH Functionalization of PyrDipSi‐Substituted Arenes: A General Method for the Synthesis of Substituted meta‐Halophenols
inferred← citeshttps://doi.org/10.1002/anie.201605877openalex-snapshot
N−H Imine as a Powerful Directing Group for Cobalt‐Catalyzed Olefin Hydroarylation
inferred← citeshttps://doi.org/10.1002/anie.201607270openalex-snapshot
ortho ‐C−H Arylation of Benzoic Acids with Aryl Bromides and Chlorides Catalyzed by Ruthenium
inferred← citeshttps://doi.org/10.1002/anie.201609631openalex-snapshot
Bioorthogonal Diversification of Peptides through Selective Ruthenium(II)‐Catalyzed C–H Activation
inferred← citeshttps://doi.org/10.1002/anie.201611595openalex-snapshot
Ruthenium(II)‐Catalyzed meta C−H Mono‐ and Difluoromethylations by Phosphine/Carboxylate Cooperation
inferred← citeshttps://doi.org/10.1002/anie.201701523openalex-snapshot
Domino N‐/C‐Arylation via In Situ Generation of a Directing Group: Atom‐Efficient Arylation Using Diaryliodonium Salts
inferred← citeshttps://doi.org/10.1002/anie.201802748openalex-snapshot
Electrooxidative Ruthenium‐Catalyzed C−H/O−H Annulation by Weak O ‐Coordination
inferred← citeshttps://doi.org/10.1002/anie.201813191openalex-snapshot
Enantioselective Aluminum‐Free Alkene Hydroarylations through C−H Activation by a Chiral Nickel/JoSPOphos Manifold
inferred← citeshttps://doi.org/10.1002/anie.201901856openalex-snapshot
Micellar Catalysis for Ruthenium(II)‐Catalyzed C−H Arylation: Weak‐Coordination‐Enabled C−H Activation in H 2 O
inferred← citeshttps://doi.org/10.1002/anie.201909457openalex-snapshot
Arene‐Free Ruthenium(II/IV)‐Catalyzed Bifurcated Arylation for Oxidative C−H/C−H Functionalizations
inferred← citeshttps://doi.org/10.1002/anie.202006164openalex-snapshot
C7‐Indole Amidations and Alkenylations by Ruthenium(II) Catalysis
inferred← citeshttps://doi.org/10.1002/anie.202208620openalex-snapshot
Remote C−H Glycosylation by Ruthenium(II) Catalysis: Modular Assembly ofmeta‐C‐Aryl Glycosides
inferred← citeshttps://doi.org/10.1002/anie.202212595openalex-snapshot
Ruthenium(II)/Imidazolidine Carboxylic Acid‐Catalyzed C−H Alkylation for Central and Axial Double Enantio‐Induction
inferred← citeshttps://doi.org/10.1002/anie.202400845openalex-snapshot
Photo‐Induced Ruthenium‐Catalyzed C−H Arylation Polymerization at Ambient Temperature
inferred← citeshttps://doi.org/10.1002/anie.202402060openalex-snapshot
Ruthenium(II)‐Catalyzed Late‐Stage Incorporation of N ‐Aryl Triazoles and Tetrazoles with Sulfonium Salts via C−H Activation
inferred← citeshttps://doi.org/10.1002/anie.202508139openalex-snapshot
Arene Ruthenium(II) Carboxylates for C─H Alkylations and Arylations at Near Room Temperature
inferred← citeshttps://doi.org/10.1002/aoc.1392openalex-snapshot
Ruthenium N‐heterocyclic–carbene catalyzed diarylation of arene CH bond
inferred← citeshttps://doi.org/10.1002/aoc.4794openalex-snapshot
Reactivity of 4‐phenylthiazoles in ruthenium catalyzed direct arylations
inferred← citeshttps://doi.org/10.1002/asia.200600398openalex-snapshot
Chemoselective C(sp3)H Bond Activation for the Preparation of Condensed N‐Heterocycles
inferred← citeshttps://doi.org/10.1002/asia.201600954openalex-snapshot
C−H Bond Activation/Arylation Catalyzed by Arene–Ruthenium–Aniline Complexes in Water
inferred← citeshttps://doi.org/10.1002/asia.202100513openalex-snapshot
Ruthenium Catalyzed Intramolecular C−X (X=C, N, O, S) Bond Formation via C−H Functionalization: An Overview
inferred← citeshttps://doi.org/10.1002/asia.202300569openalex-snapshot
2‐Hydroxypyridine‐based Ligands as Promoter in Ruthenium(II) Catalyzed C‐H Bond Activation/Arylation Reactions
inferred← citeshttps://doi.org/10.1002/cctc.201200155openalex-snapshot
Palladium(II)‐Catalyzed Regioselective Ortho Arylation of sp2 CH Bonds of N‐Aryl‐2‐amino Pyridine Derivatives
inferred← citeshttps://doi.org/10.1002/cctc.201300031openalex-snapshot
Direct CH bond Arylation in Water Promoted by (O,O)‐ and (O,N)‐Chelate Ruthenium(II) Catalysts
inferred← citeshttps://doi.org/10.1002/cctc.201300752openalex-snapshot
Ruthenium(II)‐catalysed Functionalisation of CH Bonds via a Six‐membered Cyclometallate: Monoarylation of Aryl 2‐pyridyl Ketones
inferred← citeshttps://doi.org/10.1002/cctc.201402020openalex-snapshot
Synthesis of (Poly)fluorobiphenyls through Metal‐catalyzed CH Bond Activation/Arylation of (Poly)fluorobenzene Derivatives
inferred← citeshttps://doi.org/10.1002/cctc.201700494openalex-snapshot
Synthesis and Reactivity of 2‐Arylquinazoline Halidoruthenacycles in Arylation Reactions
inferred← citeshttps://doi.org/10.1002/cctc.202000493openalex-snapshot
Secondary Phosphine Oxides: Bifunctional Ligands in Catalysis
inferred← citeshttps://doi.org/10.1002/cctc.202001338openalex-snapshot
Palladium−Ruthenium Catalyst Complementarity Strengthens Ortho‐Directed C−H Bond Arylation of 2‐Arylpyrazines
inferred← citeshttps://doi.org/10.1002/chem.200902612openalex-snapshot
RuCl3⋅x H2O‐Catalyzed Direct Arylation of Arenes with Aryl Chlorides in the Presence of Triphenylphosphine
inferred← citeshttps://doi.org/10.1002/chem.200903564openalex-snapshot
Recyclable Solid Ruthenium Catalysts for the Direct Arylation of Aromatic CH Bonds
inferred← citeshttps://doi.org/10.1002/chem.201000032openalex-snapshot
Kumada–Corriu Cross‐Couplings with 2‐Pyridyl Grignard Reagents
inferred← citeshttps://doi.org/10.1002/chem.201200406openalex-snapshot
Ruthenium‐Catalyzed Hydroarylation of Methylenecyclopropanes through CH Bond Cleavage: Scope and Mechanism
inferred← citeshttps://doi.org/10.1002/chem.201203813openalex-snapshot
Autocatalytic Intermolecular versus Intramolecular Deprotonation in CH Bond Activation of Functionalized Arenes by Ruthenium(II) or Palladium(II) Complexes
inferred← citeshttps://doi.org/10.1002/chem.201301025openalex-snapshot
Ruthenium‐Catalyzed Direct CH Amidation of Arenes Including Weakly Coordinating Aromatic Ketones
inferred← citeshttps://doi.org/10.1002/chem.201304314openalex-snapshot
Regioselective Ruthenium‐Catalyzed Carbonylative Direct Arylation of Five‐Membered and Condensed Heterocycles
inferred← citeshttps://doi.org/10.1002/chem.201403019openalex-snapshot
Triazole‐Assisted Ruthenium‐Catalyzed CH Arylation of Aromatic Amides
inferred← citeshttps://doi.org/10.1002/chem.201501831openalex-snapshot
Late‐Stage Peptide Diversification by Bioorthogonal Catalytic CH Arylation at 23 °C in H 2 O
inferred← citeshttps://doi.org/10.1002/chem.201504851openalex-snapshot
Single‐Component Phosphinous Acid Ruthenium(II) Catalysts for Versatile C−H Activation by Metal–Ligand Cooperation
inferred← citeshttps://doi.org/10.1002/chem.201605068openalex-snapshot
Ruthenium‐Catalyzed C−H Arylation of Benzoic Acids and Indole Carboxylic Acids with Aryl Halides
inferred← citeshttps://doi.org/10.1002/chem.201804734openalex-snapshot
Ruthenium(IV) Intermediates in C−H Activation/Annulation by Weak O‐Coordination
inferred← citeshttps://doi.org/10.1002/chin.200545112openalex-snapshot
Phosphine Oxides as Preligands in Ruthenium‐Catalyzed Arylations via C—H Bond Functionalized Using Aryl Chlorides.
inferred← citeshttps://doi.org/10.1002/cssc.200800248openalex-snapshot
Palladium‐Catalysed Direct 3‐ or 4‐Arylation of 2,5‐Disubstituted Pyrrole Derivatives: An Economically and Environmentally Attractive Procedure
inferred← citeshttps://doi.org/10.1002/cssc.200900014openalex-snapshot
Ruthenium‐Catalyzed Direct Arylations of N‐Aryl 1,2,3‐Triazoles with Aryl Chlorides as Electrophiles
inferred← citeshttps://doi.org/10.1002/ejic.200700420openalex-snapshot
Activated Aryl Chlorides: Useful Partners for the Coupling with 2‐Substituted Thiazoles in the Palladium‐Catalysed C‐H Activation/Functionalisation Reaction
inferred← citeshttps://doi.org/10.1002/ejic.200801189openalex-snapshot
Synthesis, Characterization and Catalytic Activity of New N‐Heterocyclic Bis(carbene)ruthenium Complexes
inferred← citeshttps://doi.org/10.1002/ejic.201701382openalex-snapshot
A Phosphino‐Carboxylic Acid‐Based Ru Dimeric Complex
inferred← citeshttps://doi.org/10.1002/ejic.201701446openalex-snapshot
Ligand‐Tuned C–H Bond Activation/Arylation of 2‐Arylpyridines over Pyridine‐Based N , O/N , N Ligated Ruthenium–Arene Complexes
inferred← citeshttps://doi.org/10.1002/ejic.201900218openalex-snapshot
Ruthenium‐Catalyzed C‐H Bond Activation/Arylation Accelerated by Biomass‐Derived Ligands
inferred← citeshttps://doi.org/10.1002/ejoc.201201127openalex-snapshot
Acetamide as Cocatalyst for the Nitrogen‐Directed Coupling of Arenes with Aryl Chlorides through Ruthenium‐Catalyzed C–H Activation
inferred← citeshttps://doi.org/10.1002/ejoc.201301620openalex-snapshot
Iron‐Mediated Direct Arylation of Unactivated Arenes in Air
inferred← citeshttps://doi.org/10.1002/ejoc.201403268openalex-snapshot
Direct Arylation of Imidazo[1,5‐a]azines Through Ruthenium and Palladium Catalysis
inferred← citeshttps://doi.org/10.1002/ejoc.201600742openalex-snapshot
Amino Acid Ligands for Ruthenium(II)‐Catalyzed C–H Arylation of Aryltetrazoles with Chlorides: Expedient Access to Antihypertension Drugs
inferred← citeshttps://doi.org/10.1002/ejoc.201701022openalex-snapshot
Solvent and Base in One: Tetra‐n‐butylammonium Acetate as a Multi‐Purpose Ionic Liquid Medium for Ru‐Catalyzed Directed Mono‐ and Di‐o‐C–H Arylation Reactions
inferred← citeshttps://doi.org/10.1002/ejoc.202000749openalex-snapshot
Regiodivergent Late‐Stage Pd‐ or Ru‐Catalyzed C–H Bond Functionalization Applied to the Straightforward Synthesis of N ‐Methylated Diflufenican Derivatives
inferred← citeshttps://doi.org/10.1002/ejoc.202100717openalex-snapshot
Carboxylic Acid Promoted, Redox‐Neutral Ru‐Catalyzed C−H Allylation of Aromatic Ketones
inferred← citeshttps://doi.org/10.1002/ijch.201000043openalex-snapshot
Air‐Stable Bifunctional HASPO Preligands for Metal‐Catalyzed Cross‐Couplings and Direct C–H Bond Arylations
inferred← citeshttps://doi.org/10.1002/ijch.202300048openalex-snapshot
Nature's Blueprint: Chelation‐Assisted C−H Functionalization for Selective and Efficient Reactions in Aqueous Media
inferred← citeshttps://doi.org/10.1002/qua.26475openalex-snapshot
Theoretical insights into the mechanism of rhodium‐catalyzed, PIII‐directed regioselective CH arylation of indole with anhydride
inferred← citeshttps://doi.org/10.1002/tcr.20108openalex-snapshot
Pd‐catalyzed asymmetric allylic substitution reactions using P‐chirogenic diaminophosphine oxides: DIAPHOXs
inferred← citeshttps://doi.org/10.1002/tcr.201800142openalex-snapshot
Reactions in Water – A Greener Approach Using Ruthenium Catalysts
inferred← citeshttps://doi.org/10.1007/128_2009_10openalex-snapshot
Palladium and Copper Catalysis in Regioselective, Intermolecular Coupling of C–H and C–Hal Bonds
inferred← citeshttps://doi.org/10.1007/128_2009_12openalex-snapshot
Rhodium-Catalyzed C–H Bond Arylation of Arenes
inferred← citeshttps://doi.org/10.1007/128_2009_9openalex-snapshot
Ruthenium-Catalyzed Direct Arylations Through C–H Bond Cleavages
inferred← citeshttps://doi.org/10.1007/3418_2007_062openalex-snapshot
Chelation-Assisted Arylation via C–H Bond Cleavage
inferred← citeshttps://doi.org/10.1007/3418_2014_85openalex-snapshot
Ruthenium(II)-Catalysed sp2 C–H Bond Functionalization by C–C Bond Formation
inferred← citeshttps://doi.org/10.1007/3418_2015_134openalex-snapshot
Ruthenium(II)-Catalysed Functionalisation of C–H Bonds with Alkenes: Alkenylation versus Alkylation
inferred← citeshttps://doi.org/10.1007/978-4-431-54604-7_6openalex-snapshot
Reasons Why Organometallic Intramolecular-Coordination Five-Membered Ring Compounds Are Extremely Easily Synthesized Through Cyclometalation Reactions
inferred← citeshttps://doi.org/10.1007/s10563-010-9104-6openalex-snapshot
Development of Ceria-Supported Ruthenium Catalysts Effective for Various Synthetic Reactions
inferred← citeshttps://doi.org/10.1007/s11244-014-0244-1openalex-snapshot
Sequential Ruthenium(II)-Acetate Catalyzed C–H Bond Diarylation in NMP or Water and Hydrosilylation of Imines
inferred← citeshttps://doi.org/10.1007/s11426-022-1541-5openalex-snapshot
Aromatic and olefinic C-H alkenylation by catalysis with spirocyclic NHC Ru(IV) pincer complex
inferred← citeshttps://doi.org/10.1007/s12039-010-0016-9openalex-snapshot
Palladium-catalysed ortho arylation of acetanilides
inferred← citeshttps://doi.org/10.1016/b0-08-045047-4/00125-4openalex-snapshot
Synthetic Reactions via C–H Bond Activation: C–C and C–E Bond Formation
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00329-3openalex-snapshot
3.23 Carbon–Carbon σ-Bond Formation via CH Bond Functionalization
inferred← citeshttps://doi.org/10.1016/b978-0-12-820206-7.00036-6openalex-snapshot
Impurities in Organometallic Catalysis
inferred← citeshttps://doi.org/10.1016/bs.acat.2023.07.002openalex-snapshot
Carbanion-functionalized phosphines: New design elements for catalyst development
inferred← citeshttps://doi.org/10.1016/bs.adomc.2017.03.002openalex-snapshot
Biaryl Synthesis via C–H Bond Activation
inferred← citeshttps://doi.org/10.1016/j.ccr.2007.03.011openalex-snapshot
Transition metals in organic synthesis: Highlights for the year 2005
inferred← citeshttps://doi.org/10.1016/j.ccr.2009.07.023openalex-snapshot
Catalytic C–C coupling through C–H arylation of arenes or heteroarenes
inferred← citeshttps://doi.org/10.1016/j.ccr.2011.11.007openalex-snapshot
Secondary phosphine oxides: Versatile ligands in transition metal-catalyzed cross-coupling reactions
inferred← citeshttps://doi.org/10.1016/j.ccr.2019.02.014openalex-snapshot
The chemistry of Group 8 metal complexes with phosphinous acids and related P OH ligands
inferred← citeshttps://doi.org/10.1016/j.ccr.2020.213602openalex-snapshot
Ruthenium-catalyzed C–H bond functionalization in cascade and one-pot transformations
inferred← citeshttps://doi.org/10.1016/j.checat.2024.101146openalex-snapshot
Next-generation functional surfactant for mild C−H arylation under micellar conditions
inferred← citeshttps://doi.org/10.1016/j.ica.2011.09.030openalex-snapshot
Pt mediated C–H activation: Formation of a six membered platinacycle via Csp3-H activation
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2009.08.030openalex-snapshot
Synthesis and catalytic properties of novel ruthenium N-heterocyclic-carbene complexes
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2011.06.009openalex-snapshot
Ruthenium-catalyzed coupling reaction of 2,3,5-trisubstituted furans with aryl halides through C–H bond cleavages
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2015.02.050openalex-snapshot
Cycloruthenation of aryl imines and N-heteroaryl benzenes via C–H bond activation with Ru(II) and acetate partners
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2020.121555openalex-snapshot
New half-sandwich (η6-p-cymene)ruthenium(II) complexes with benzothiazole hydrazone Schiff base ligand: Synthesis, structural characterization and catalysis in transamidation of carboxamide with primary amines
inferred← citeshttps://doi.org/10.1016/j.tet.2007.10.117openalex-snapshot
Annulation of internal alkynes through a hydroamination/aza-Heck reaction sequence for the regioselective synthesis of indoles
inferred← citeshttps://doi.org/10.1016/j.tet.2007.12.060openalex-snapshot
Nitrogen-directed ortho-arylation and -heteroarylation of aromatic rings catalyzed by ruthenium complexes
inferred← citeshttps://doi.org/10.1016/j.tet.2008.01.050openalex-snapshot
[RuCl3(H2O)n]-catalyzed direct arylations
inferred← citeshttps://doi.org/10.1016/j.tet.2008.01.053openalex-snapshot
Direct coupling of arenes and iodoarenes catalyzed by a rhodium complex with a strongly π-accepting phosphite ligand
inferred← citeshttps://doi.org/10.1016/j.tet.2010.11.069openalex-snapshot
Catalytic asymmetric synthesis using P-chiral diaminophosphine oxide preligands: DIAPHOXs
inferred← citeshttps://doi.org/10.1016/j.tet.2012.03.117openalex-snapshot
Catalytic C–H bond arylation of aryl imines and oxazolines in water with ruthenium(II)-acetate catalyst
inferred← citeshttps://doi.org/10.1016/j.tet.2013.01.006openalex-snapshot
Carboxylate-assisted ruthenium(II)-catalyzed C–H arylations of 5-aryl tetrazoles: step-economical access to Valsartan
inferred← citeshttps://doi.org/10.1016/j.tet.2015.10.042openalex-snapshot
Quinazoline-directed regioselective arylation via palladium catalysis: synthesis of 2-(1-biaryl)-4-arylquinazolines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.11.209openalex-snapshot
Palladium bis(2,2,6,6-tetramethyl-3,5-heptanedionate): an efficient catalyst for regioselective C-2 arylation of heterocycles
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.10.061openalex-snapshot
Direct synthesis of ortho-dihalogenated arylpyrimidines using calcium halides as halogen sources
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.11.020openalex-snapshot
Diaminophosphine oxides as preligands for Ni-catalyzed Suzuki cross-coupling reactions of aryl chlorides with arylboronic acids
inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.153831openalex-snapshot
Visible light-activated ruthenium-catalysed direct arylation at ambient temperature
inferred← citeshttps://doi.org/10.1016/j.tetlet.2025.155956openalex-snapshot
Ruthenium(II)-catalyzed 1,3,5-triazine group directed C H amidation of anilines with dioxazolones
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.6b01115openalex-snapshot
Ruthenium-Catalyzed Oxidative Homocoupling of Arylboronic Acids in Water: Ligand Tuned Reactivity and Mechanistic Study
inferred← citeshttps://doi.org/10.1021/acs.joc.0c01010openalex-snapshot
Sulfoximine-Assisted Unsymmetrical Twofold C–H Functionalization of Arenes
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02872openalex-snapshot
MIA-Directed 2-Pyridione-Enabled Selective Ortho-C–H Arylation of Phenylalanine: A Mechanistic Study
inferred← citeshttps://doi.org/10.1021/acs.joc.2c00815openalex-snapshot
Ruthenium-Catalyzed Pyridine-Directed Aryl C–H Glycosylation with Glycosyl Chlorides
inferred← citeshttps://doi.org/10.1021/acs.joc.3c00689openalex-snapshot
Intramolecular Hydroarylation of Arenes via Imidazole-Directed C–H Activation in Aqueous Methanol Using Rhodium(III) as the Catalyst and Mechanistic Study
inferred← citeshttps://doi.org/10.1021/acs.joc.4c01588openalex-snapshot
RuII–Catalyzed C–H Activated Diverse Cyclization with Transformation of Substrate-DG to Functional Groups: Synthesis of Functionalized Indoles and Indenones
inferred← citeshttps://doi.org/10.1021/acs.joc.6b00634openalex-snapshot
Ru(II)-Catalyzed Direct C(sp 2 )–H Activation/Selenylation of Arenes with Selenyl Chlorides
inferred← citeshttps://doi.org/10.1021/acs.joc.8b00229openalex-snapshot
Ruthenium-Catalyzed Decarboxylative C–H Alkenylation in Aqueous Media: Synthesis of Tetrahydropyridoindoles
inferred← citeshttps://doi.org/10.1021/acs.joc.9b01756openalex-snapshot
Selective Monoarylation of Aromatic Ketones via C–H Bond Cleavage by Trialkylphosphine Ruthenium Catalysts
inferred← citeshttps://doi.org/10.1021/acs.oprd.8b00141openalex-snapshot
Arene Ruthenium Catalyst MCAT-53 for the Synthesis of Heterobiaryl Compounds in Water through Aromatic C–H Bond Activation
inferred← citeshttps://doi.org/10.1021/acs.organomet.1c00578openalex-snapshot
Dimenthylphosphine P-Oxide as a Synthetic Platform for Bulky and Chiral Ligands with Dimenthylphosphino Donor Groups
inferred← citeshttps://doi.org/10.1021/acs.organomet.6b00308openalex-snapshot
Nondirected C–H Activation of Arenes with Cp*Ir(III) Acetate Complexes: An Experimental and Computational Study
inferred← citeshttps://doi.org/10.1021/acs.organomet.7b00531openalex-snapshot
Intramolecular C–H Activation Reactions of Ru(NHC) Complexes Combined with H2 Transfer to Alkenes: A Theoretical Elucidation of Mechanisms and Effects of Ligands on Reactivities
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