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Ruthenium‐Catalyzed meta‐CAr–H Bond Difluoroalkylation of 2‐Phenoxypyridines
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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/ange.201202466openalex-snapshot
Cobalt‐Catalyzed Direct Arylation and Benzylation by CH/CO Cleavage with Sulfamates, Carbamates, and Phosphates
inferredcites →https://doi.org/10.1002/ange.201300763openalex-snapshot
Direct Synthesis of Fluorinated Heteroarylether Bioisosteres
inferredcites →https://doi.org/10.1002/ange.201403823openalex-snapshot
Nickel‐Catalyzed α‐Arylation of Ketones with Phenol Derivatives
inferredcites →https://doi.org/10.1002/ange.201504390openalex-snapshot
Ruthenium‐Catalyzed meta‐Selective CH Bromination
inferredcites →https://doi.org/10.1002/ange.201507100openalex-snapshot
Directed meta‐Selective Bromination of Arenes with Ruthenium Catalysts
inferredcites →https://doi.org/10.1002/ange.201611595openalex-snapshot
Ruthenium(II)‐Catalyzed meta C−H Mono‐ and Difluoromethylations by Phosphine/Carboxylate Cooperation
inferredcites →https://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
inferredcites →https://doi.org/10.1002/ange.201904288openalex-snapshot
meta‐Selective C−H Activation of Arenes at Room Temperature Using Visible Light: Dual‐Function Ruthenium Catalysis
inferredcites →https://doi.org/10.1002/anie.201202466openalex-snapshot
Cobalt‐Catalyzed Direct Arylation and Benzylation by CH/CO Cleavage with Sulfamates, Carbamates, and Phosphates
inferredcites →https://doi.org/10.1002/anie.201300763openalex-snapshot
Direct Synthesis of Fluorinated Heteroarylether Bioisosteres
inferredcites →https://doi.org/10.1002/anie.201403823openalex-snapshot
Nickel‐Catalyzed α‐Arylation of Ketones with Phenol Derivatives
inferredcites →https://doi.org/10.1002/anie.201504390openalex-snapshot
Ruthenium‐Catalyzed meta‐Selective CH Bromination
inferredcites →https://doi.org/10.1002/anie.201507100openalex-snapshot
Directed meta‐Selective Bromination of Arenes with Ruthenium Catalysts
inferredcites →https://doi.org/10.1002/anie.201611595openalex-snapshot
Ruthenium(II)‐Catalyzed meta C−H Mono‐ and Difluoromethylations by Phosphine/Carboxylate Cooperation
inferredcites →https://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
inferredcites →https://doi.org/10.1002/anie.201902258openalex-snapshot
Visible‐Light‐Enabled Ruthenium‐Catalyzed meta‐C−H Alkylation at Room Temperature
inferredcites →https://doi.org/10.1002/anie.201904288openalex-snapshot
meta‐Selective C−H Activation of Arenes at Room Temperature Using Visible Light: Dual‐Function Ruthenium Catalysis
inferredcites →https://doi.org/10.1002/chem.201404604openalex-snapshot
Ruthenium(II)‐Catalyzed Oxidative CH Alkenylations of Sulfonic Acids, Sulfonyl Chlorides and Sulfonamides
inferredcites →https://doi.org/10.1002/chem.201700354openalex-snapshot
Ruthenium‐Catalyzed meta‐Selective C−H Mono‐ and Difluoromethylation of Arenes through ortho‐Metalation Strategy
inferredcites →https://doi.org/10.1002/chem.201705499openalex-snapshot
The Hydrophobic Effect Applied to Organic Synthesis: Recent Synthetic Chemistry “in Water”
inferredcites →https://doi.org/10.1002/cmdc.201402555openalex-snapshot
Fluorine in Drug Design: A Case Study with Fluoroanisoles
inferredcites →https://doi.org/10.1016/j.jfluchem.2009.05.016openalex-snapshot
Nucleophilic, radical, and electrophilic (phenylsulfonyl)difluoromethylations
inferredcites →https://doi.org/10.1021/acs.orglett.6b02166openalex-snapshot
Nickel-Catalyzed Site-Selective C–H Bond Difluoroalkylation of 8-Aminoquinolines on the C5-Position
inferredcites →https://doi.org/10.1021/acs.orglett.6b02803openalex-snapshot
Nickel-Catalyzed Monofluoroalkylation of Arylsilanes via Hiyama Cross-Coupling
inferredcites →https://doi.org/10.1021/acs.orglett.7b00885openalex-snapshot
Synthesis of m-Alkylphenols via a Ruthenium-Catalyzed C–H Bond Functionalization of Phenol Derivatives
inferredcites →https://doi.org/10.1021/acs.orglett.7b00938openalex-snapshot
Palladium-Catalyzed Cross-Coupling of Ethyl Bromodifluoroacetate with Aryl Bromides or Triflates and Cross-Coupling of Ethyl Bromofluoroacetate with Aryl Iodides
inferredcites →https://doi.org/10.1021/acs.orglett.7b02439openalex-snapshot
Ruthenium-Catalyzed ortho/meta-Selective Dual C–H Bonds Functionalizations of Arenes
inferredcites →https://doi.org/10.1021/acscatal.7b01072openalex-snapshot
Ligand-Enabled Regioselectivity in the Oxidative Cross-coupling of Arenes with Toluenes and Cycloalkanes Using Ruthenium Catalysts: Tuning the Site-Selectivity from the ortho to meta Positions
inferredcites →https://doi.org/10.1021/acscatal.7b03648openalex-snapshot
Sequential meta-/ortho-C–H Functionalizations by One-Pot Ruthenium(II/III) Catalysis
inferredcites →https://doi.org/10.1021/acscatal.8b03695openalex-snapshot
Direct Decarboxylative Meta-Selective Acylation of Arenes via an Ortho-Ruthenation Strategy
inferredcites →https://doi.org/10.1021/cr5002386openalex-snapshot
Good Partnership between Sulfur and Fluorine: Sulfur-Based Fluorination and Fluoroalkylation Reagents for Organic Synthesis
inferredcites →https://doi.org/10.1021/cr500286dopenalex-snapshot
19 F Magnetic Resonance Imaging (MRI): From Design of Materials to Clinical Applications
inferredcites →https://doi.org/10.1021/ja208286bopenalex-snapshot
Ruthenium-Catalyzed Meta Sulfonation of 2-Phenylpyridines
inferredcites →https://doi.org/10.1021/ja401466yopenalex-snapshot
meta-Selective C–H Bond Alkylation with Secondary Alkyl Halides
inferredcites →https://doi.org/10.1021/ja5029793openalex-snapshot
Ni-Catalyzed Direct Reductive Amidation via C–O Bond Cleavage
inferredcites →https://doi.org/10.1021/ja503163kopenalex-snapshot
Highly Site-Selective Direct C–H Bond Functionalization of Phenols with α-Aryl-α-diazoacetates and Diazooxindoles via Gold Catalysis
inferredcites →https://doi.org/10.1021/jacs.5b08435openalex-snapshot
N-Acyl Amino Acid Ligands for Ruthenium(II)-Catalyzed meta-C–H tert-Alkylation with Removable Auxiliaries
inferredcites →https://doi.org/10.1021/jacs.6b03402openalex-snapshot
Meta-Selective CAr–H Nitration of Arenes through a Ru3(CO)12-Catalyzed Ortho-Metalation Strategy
inferredcites →https://doi.org/10.1021/jacs.9b00364openalex-snapshot
Oxidatively Induced Reductive Elimination: Exploring the Scope and Catalyst Systems with Ir, Rh, and Ru Complexes
inferredcites →https://doi.org/10.1021/jacs.9b06608openalex-snapshot
Three-Component Ruthenium-Catalyzed Direct Meta-Selective C–H Activation of Arenes: A New Approach to the Alkylarylation of Alkenes
inferredcites →https://doi.org/10.1021/jm1013693openalex-snapshot
Synopsis of Some Recent Tactical Application of Bioisosteres in Drug Design
inferredcites →https://doi.org/10.1021/ol500166dopenalex-snapshot
Copper-Mediated Direct Aryloxylation of Benzamides Assisted by an N,O-Bidentate Directing Group
inferredcites →https://doi.org/10.1021/om990232aopenalex-snapshot
Electrophilic Substitution Reactions at the Phenyl Ring of the Chelated 2-(2‘-Pyridyl)phenyl Ligand Bound to Ruthenium(II) or Osmium(II)
inferredcites →https://doi.org/10.1039/c3sc51489gopenalex-snapshot
Benzofuran synthesis via copper-mediated oxidative annulation of phenols and unactivated internal alkynes
inferredcites →https://doi.org/10.1039/c7qo00449dopenalex-snapshot
meta-Selective C–H difluoromethylation of various arenes with a versatile ruthenium catalyst
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/9783527834242.chf0033openalex-snapshot
Ruthenium‐Catalyzed Remote CH Functionalization of Directed Arenes
inferred← citeshttps://doi.org/10.1002/9783527834242.chf0034openalex-snapshot
Ru‐Catalyzed CC Bond Formation via CH Bond Cleavage
inferred← citeshttps://doi.org/10.1002/adsc.202001053openalex-snapshot
Recent Developments in Remote Meta‐C−H Bond Functionalizations
inferred← citeshttps://doi.org/10.1002/adsc.202001614openalex-snapshot
A Palladium(0)‐Catalyzed C4 Site‐Selective C−H Difluoroalkylation of Isoquinolin‐1(2H)‐Ones
inferred← citeshttps://doi.org/10.1002/ajoc.202100159openalex-snapshot
Ru(II)‐Catalyzed Difluoromethylations of 7‐Azaindoles: Access to Novel Fluoro‐7‐Azaindole Derivatives
inferred← citeshttps://doi.org/10.1002/ange.202007144openalex-snapshot
Regiodivergente C‐H‐ und decarboxylierende C‐C‐Alkylierung mittels Rutheniumkatalyse: ortho‐ versus meta‐Regioselektivität
inferred← citeshttps://doi.org/10.1002/anie.202007144openalex-snapshot
Regiodivergent C−H and Decarboxylative C−C Alkylation by Ruthenium Catalysis: ortho versus meta Position‐Selectivity
inferred← citeshttps://doi.org/10.1016/j.cclet.2026.112869openalex-snapshot
Visible-light-mediated Ru-catalyzed meta-alkylation enabled by Ru complex ligating by two κ2-bound aminopyrimidine
inferred← citeshttps://doi.org/10.1016/j.chempr.2024.12.005openalex-snapshot
Ruthenaphoto-catalyzed ortho-C−H alkylation with secondary alkyl halides: SET-enabled ruthenium(II/III/IV) manifold
inferred← citeshttps://doi.org/10.1016/j.jcat.2024.115351openalex-snapshot
Copper-catalyzed regioselective C−H alkylation of phenol derivatives with unactivated alkyl chlorides: Manifesting a Cu(I)/Cu(III) pathway
inferred← citeshttps://doi.org/10.1021/acs.chemrev.1c00220openalex-snapshot
Toolbox for Distal C–H Bond Functionalizations in Organic Molecules
inferred← citeshttps://doi.org/10.1021/acs.joc.0c01909openalex-snapshot
Ruthenium-Catalyzed Meta-Selective C-H Difluoromethylation of Phenol Derivatives
inferred← citeshttps://doi.org/10.1021/acs.joc.2c00332openalex-snapshot
meta-Allylation of Arenes via Ruthenium-Catalyzed Cross-Dehydrogenative Coupling
inferred← citeshttps://doi.org/10.1021/jacs.0c09545openalex-snapshot
Iron-Catalyzed Highly para-Selective Difluoromethylation of Arenes
inferred← citeshttps://doi.org/10.1039/d0cc02851gopenalex-snapshot
A directing group-assisted ruthenium-catalyzed approach to access meta -nitrated phenols
inferred← citeshttps://doi.org/10.1039/d0qo00567copenalex-snapshot
Promising reagents for difluoroalkylation
inferred← citeshttps://doi.org/10.1039/d1qo01544copenalex-snapshot
Recent advances in transition-metal catalyzed directed C–H functionalization with fluorinated building blocks
inferred← citeshttps://doi.org/10.1039/d2qo00666aopenalex-snapshot
Ruthenium-catalyzed meta -difluoromethylation of arene phosphines enabled by 1,3-dione
inferred← citeshttps://doi.org/10.1039/d5sc02780bopenalex-snapshot
Electroreductive room-temperature C–H activations with RuCl 3 · n H 2 O precatalyst via cathodic ruthenium( iii / ii ) manifold
inferred← citeshttps://doi.org/10.1055/a-1485-5156openalex-snapshot
Remote C–H Functionalizations by Ruthenium Catalysis
inferred← citeshttps://doi.org/10.6023/cjoc202212032openalex-snapshot
Visible Light-Catalyzed Synthesis of Difluoroalkylated Polycyclic Indoles
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