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Unified Strategy for Nickel-Catalyzed C-2 Alkylation of Indoles through Chelation Assistance

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Outgoing claims: the papers this work cites, builds on, or argues with.

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Transition Metal‐Catalysed, Direct and Site‐Selective N1‐, C2‐ or C3‐Arylation of the Indole Nucleus: 20 Years of Improvements
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User‐Friendly [(Diglyme)NiBr2]‐Catalyzed Direct Alkylations of Heteroarenes with Unactivated Alkyl Halides through CH Bond Cleavages
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Palladium‐Catalyzed Intermolecular C‐2 Alkenylation of Indoles Using Oxygen as the Oxidant
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Very Important Publication: Iridium‐Catalyzed Intramolecular Enantioselective CH Alkylation at the C‐2 Position of N‐Alkenylindoles
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Transition Metal‐Catalyzed CH Activation of Indoles
inferredcites →https://doi.org/10.1002/anie.200500468openalex-snapshot
Palladium‐Catalyzed Intermolecular Alkenylation of Indoles by Solvent‐Controlled Regioselective CH Functionalization
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Palladium‐Catalyzed Direct Arylation of (Hetero)Arenes with Aryl Boronic Acids
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Palladium(II)‐Catalyzed CH Activation/CC Cross‐Coupling Reactions: Versatility and Practicality
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Catalytic Functionalization of Indoles in a New Dimension
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Palladium(II)‐Catalyzed Regioselective Direct C2 Alkenylation of Indoles and Pyrroles Assisted by the N‐(2‐Pyridyl)sulfonyl Protecting Group
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Transition‐Metal‐Catalyzed Direct Arylation of (Hetero)Arenes by CH Bond Cleavage
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The Nickel/Copper‐Catalyzed Direct Alkylation of Heterocyclic CH Bonds
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Mild and Efficient C2‐Alkenylation of Indoles with Alkynes Catalyzed by a Cobalt Complex
inferredcites →https://doi.org/10.1002/anie.201201491openalex-snapshot
Copper‐Mediated and Copper‐Catalyzed Cross‐Coupling of Indoles and 1,3‐Azoles: Double CH Activation
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.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.201303556openalex-snapshot
8‐Aminoquinoline: A Powerful Directing Group in Metal‐Catalyzed Direct Functionalization of CH Bonds
inferredcites →https://doi.org/10.1002/anie.201309584openalex-snapshot
Nickel‐Catalyzed CH Alkylations: Direct Secondary Alkylations and Trifluoroethylations of Arenes
inferredcites →https://doi.org/10.1002/anie.201510743openalex-snapshot
A General Strategy for the Nickel‐Catalyzed C−H Alkylation of Anilines
inferredcites →https://doi.org/10.1002/anie.201511197openalex-snapshot
Phenyltrimethylammonium Salts as Methylation Reagents in the Nickel‐Catalyzed Methylation of C−H Bonds
inferredcites →https://doi.org/10.1002/chem.201001631openalex-snapshot
Palladium‐ and Nickel‐Catalyzed Direct Alkylation of Azoles with Unactivated Alkyl Bromides and Chlorides
inferredcites →https://doi.org/10.1002/chem.201301409openalex-snapshot
Cobalt‐Catalyzed CH Bond Functionalizations with Aryl and Alkyl Chlorides
inferredcites →https://doi.org/10.1002/chem.201405931openalex-snapshot
Ru‐Catalysed CH Arylation of Indoles and Pyrroles with Boronic Acids: Scope and Mechanistic Studies
inferredcites →https://doi.org/10.1016/j.tet.2013.06.095openalex-snapshot
Ligand-free Cu2O-catalyzed cross coupling of nitrogen heterocycles with iodopyridines
inferredcites →https://doi.org/10.1016/j.tet.2014.05.089openalex-snapshot
Controlling bacterial behavior with indole-containing natural products and derivatives
inferredcites →https://doi.org/10.1021/acs.organomet.6b00201openalex-snapshot
Synthesis of Quinoline-Based NNN-Pincer Nickel(II) Complexes: A Robust and Improved Catalyst System for C–H Bond Alkylation of Azoles with Alkyl Halides
inferredcites →https://doi.org/10.1021/acs.orglett.5b00535openalex-snapshot
Ruthenium-Catalyzed Heteroatom-Directed Regioselective C–H Arylation of Indoles Using a Removable Tether
inferredcites →https://doi.org/10.1021/acs.orglett.5b01232openalex-snapshot
Rh(III)-Catalyzed C–H Alkylation of Arenes Using Alkylboron Reagents
inferredcites →https://doi.org/10.1021/acs.orglett.6b00658openalex-snapshot
Dicumyl Peroxide as a Methylating Reagent in the Ni-Catalyzed Methylation of Ortho C–H Bonds in Aromatic Amides
inferredcites →https://doi.org/10.1021/acscatal.5b02344openalex-snapshot
Cobalt-Catalyzed C–H Activation
inferredcites →https://doi.org/10.1021/acscatal.6b01120openalex-snapshot
Nickel-Catalyzed C–H Alkynylation of Anilines: Expedient Access to Functionalized Indoles and Purine Nucleobases
inferredcites →https://doi.org/10.1021/ar5004626openalex-snapshot
Bidentate, Monoanionic Auxiliary-Directed Functionalization of Carbon–Hydrogen Bonds
inferredcites →https://doi.org/10.1021/ar800138aopenalex-snapshot
Cross-Coupling Reaction of Alkyl Halides with Grignard Reagents Catalyzed by Ni, Pd, or Cu Complexes with π-Carbon Ligand(s)
inferredcites →https://doi.org/10.1021/bi500175popenalex-snapshot
Noncompetitive Inhibition of Indolethylamine- N -methyltransferase by N , N -Dimethyltryptamine and N , N -Dimethylaminopropyltryptamine
inferredcites →https://doi.org/10.1021/cr020033sopenalex-snapshot
The Combinatorial Synthesis of Bicyclic Privileged Structures or Privileged Substructures
inferredcites →https://doi.org/10.1021/cr040639bopenalex-snapshot
Synthesis and Functionalization of Indoles Through Palladium-catalyzed Reactions
inferredcites →https://doi.org/10.1021/cr050521aopenalex-snapshot
Reserpine: A Challenge for Total Synthesis of Natural Products
inferredcites →https://doi.org/10.1021/cr0509760openalex-snapshot
Aryl−Aryl Bond Formation by Transition-Metal-Catalyzed Direct Arylation
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/cr900005nopenalex-snapshot
Rhodium-Catalyzed C−C Bond Formation via Heteroatom-Directed C−H Bond Activation
inferredcites →https://doi.org/10.1021/cr900032sopenalex-snapshot
Variolins and Related Alkaloids
inferredcites →https://doi.org/10.1021/cr900184eopenalex-snapshot
Palladium-Catalyzed Ligand-Directed C−H Functionalization Reactions
inferredcites →https://doi.org/10.1021/cr900211popenalex-snapshot
Marine Indole Alkaloids: Potential New Drug Leads for the Control of Depression and Anxiety
inferredcites →https://doi.org/10.1021/cs400066qopenalex-snapshot
Recent Advances in Iridium-Catalyzed Alkylation of C–H and N–H Bonds
inferredcites →https://doi.org/10.1021/cs401141kopenalex-snapshot
Origins of Selective C(sp2)–H Activation Using Transition Metal Complexes with N,N-Bidentate Directing Groups: A Combined Theoretical–Experimental Study
inferredcites →https://doi.org/10.1021/ja027822bopenalex-snapshot
The First Total Synthesis of Dragmacidin D
inferredcites →https://doi.org/10.1021/ja060809xopenalex-snapshot
Room Temperature Palladium-Catalyzed 2-Arylation of Indoles
inferredcites →https://doi.org/10.1021/ja107159bopenalex-snapshot
Regioselective Oxidative Arylation of Indoles Bearing N-Alkyl Protecting Groups: Dual C−H Functionalization via a Concerted Metalation−Deprotonation Mechanism
inferredcites →https://doi.org/10.1021/ja2055066openalex-snapshot
Palladium-Catalyzed Direct 2-Alkylation of Indoles by Norbornene-Mediated Regioselective Cascade C–H Activation
inferredcites →https://doi.org/10.1021/ja304068topenalex-snapshot
Nickel-Catalyzed Coupling Reactions of Alkyl Electrophiles, Including Unactivated Tertiary Halides, To Generate Carbon–Boron Bonds
inferredcites →https://doi.org/10.1021/ja3058138openalex-snapshot
Pd(II)-Catalyzed Regioselective 2-Alkylation of Indoles via a Norbornene-Mediated C–H Activation: Mechanism and Applications
inferredcites →https://doi.org/10.1021/ja308742xopenalex-snapshot
Ir(I)-Catalyzed C–H Bond Alkylation of C2-Position of Indole with Alkenes: Selective Synthesis of Linear or Branched 2-Alkylindoles
inferredcites →https://doi.org/10.1021/ja311669popenalex-snapshot
Nickel-Catalyzed Carbon–Carbon Bond-Forming Reactions of Unactivated Tertiary Alkyl Halides: Suzuki Arylations
inferredcites →https://doi.org/10.1021/ja312360copenalex-snapshot
Iridium-Catalyzed Intermolecular Asymmetric Hydroheteroarylation of Bicycloalkenes
inferredcites →https://doi.org/10.1021/ja401344eopenalex-snapshot
Nickel-Catalyzed Direct Alkylation of C–H Bonds in Benzamides and Acrylamides with Functionalized Alkyl Halides via Bidentate-Chelation Assistance
inferredcites →https://doi.org/10.1021/ja413131mopenalex-snapshot
Nickel-Catalyzed Site-Selective Alkylation of Unactivated C(sp3)–H Bonds
inferredcites →https://doi.org/10.1021/ja508718mopenalex-snapshot
Nickel-Catalyzed Negishi Arylations of Propargylic Bromides: A Mechanistic Investigation
inferredcites →https://doi.org/10.1021/ja710731aopenalex-snapshot
Room Temperature and Phosphine Free Palladium Catalyzed Direct C-2 Arylation of Indoles
inferredcites →https://doi.org/10.1021/jacs.5b04892openalex-snapshot
Oxidation of Ni(II) to Ni(IV) with Aryl Electrophiles Enables Ni-Mediated Aryl–CF 3 Coupling
inferredcites →https://doi.org/10.1021/jacs.5b08039openalex-snapshot
Anti-Markovnikov Hydroheteroarylation of Unactivated Alkenes with Indoles, Pyrroles, Benzofurans, and Furans Catalyzed by a Nickel– N -Heterocyclic Carbene System
inferredcites →https://doi.org/10.1021/jm200791zopenalex-snapshot
Development of Indole Compounds as Small Molecule Fusion Inhibitors Targeting HIV-1 Glycoprotein-41
inferredcites →https://doi.org/10.1021/jo501361kopenalex-snapshot
Cobalt-Catalyzed C–H Arylations, Benzylations, and Alkylations with Organic Electrophiles and Beyond
inferredcites →https://doi.org/10.1021/ol200601eopenalex-snapshot
Metal-Free Direct Arylations of Indoles and Pyrroles with Diaryliodonium Salts
inferredcites →https://doi.org/10.1021/ol2010648openalex-snapshot
Ruthenium-Catalyzed Direct C–H Bond Arylations of Heteroarenes
inferredcites →https://doi.org/10.1021/ol302070topenalex-snapshot
Palladium-Assisted Regioselective C–H Cyanation of Heteroarenes Using Isonitrile as Cyanide Source
inferredcites →https://doi.org/10.1021/ol500754hopenalex-snapshot
Mild Rh(III)-Catalyzed Direct C–H Bond Arylation of (Hetero)Arenes with Arylsilanes in Aqueous Media
inferredcites →https://doi.org/10.1021/ol501087mopenalex-snapshot
Mild and Phosphine-Free Iron-Catalyzed Cross-Coupling of Nonactivated Secondary Alkyl Halides with Alkynyl Grignard Reagents
inferredcites →https://doi.org/10.1021/ol503119zopenalex-snapshot
Cobalt-Catalyzed Enantioselective Directed C–H Alkylation of Indole with Styrenes
inferredcites →https://doi.org/10.1021/ol503395gopenalex-snapshot
Iron-Catalyzed Directed C2-Alkylation and Alkenylation of Indole with Vinylarenes and Alkynes
inferredcites →https://doi.org/10.1039/a909834hopenalex-snapshot
Recent developments in indole ring synthesis—methodology and applications
inferredcites →https://doi.org/10.1039/b606984nopenalex-snapshot
Direct transition metal-catalyzed functionalization of heteroaromatic compounds
inferredcites →https://doi.org/10.1039/c004871bopenalex-snapshot
A colorimetric and fluorescent turn-on chemosensor operative in aqueous media for Zn2+ based on a multifunctionalized spirobenzopyran derivative
inferredcites →https://doi.org/10.1039/c0cc00778aopenalex-snapshot
Metal-catalyzed direct alkylations of (hetero)arenes via C–H bond cleavages with unactivated alkyl halides
inferredcites →https://doi.org/10.1039/c0dt01141jopenalex-snapshot
A gadolinium(III) complex with 8-amidequinoline based ligand as copper(II) ion responsive contrast agent
inferredcites →https://doi.org/10.1039/c1sc00368bopenalex-snapshot
Nickel-catalyzed cross coupling of non-activated alkyl halides: a mechanistic perspective
inferredcites →https://doi.org/10.1039/c2ob26767eopenalex-snapshot
Rhodium-catalyzed regioselective amidation of indoles with sulfonyl azides via C–H bond activation
inferredcites →https://doi.org/10.1039/c3cc43915aopenalex-snapshot
Nickel-catalyzed alkyne annulation by anilines: versatile indole synthesis by C–H/N–H functionalization
inferredcites →https://doi.org/10.1039/c4cs00137kopenalex-snapshot
Arene C–H functionalisation using a removable/modifiable or a traceless directing group strategy
inferredcites →https://doi.org/10.1055/s-0028-1087951openalex-snapshot
Palladium-Catalyzed Direct C-3 Arylations of Indoles with an Air-Stable HASPO
inferredcites →https://doi.org/10.1055/s-0033-1338523openalex-snapshot
Regioselective Direct C–H Alkylation of NH Indoles and Pyrroles by a Palladium/Norbornene-Cocatalyzed Process
inferredcites →https://doi.org/10.1126/science.1141956openalex-snapshot
The Catalytic Cross-Coupling of Unactivated Arenes
inferredcites →https://doi.org/10.1246/bcsj.20140387openalex-snapshot
The Nickel(II)-Catalyzed Direct Benzylation, Allylation, Alkylation, and Methylation of C–H Bonds in Aromatic Amides Containing an 8-Aminoquinoline Moiety as the Directing Group
inferredcites →https://doi.org/10.3762/bjoc.8.174openalex-snapshot
C2-Alkylation of N-pyrimidylindole with vinylsilane via cobalt-catalyzed C–H bond activation

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Transition Metal‐Catalyzed C2 and C3 Functionalization of Indoles
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Recent Advances in Ni ‐Catalyzed Chelation‐Assisted Direct Functionalization of Inert C H Bonds
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CH Activation of Indoles
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Pd‐Catalyzed Tandem Coupling Reaction of 2‐gem‐Dibromovinylanilines and N‐Tosylhydrazones to Construct 2‐(1‐phenylvinyl)‐indoles
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Selective Synthesis of Secondary Amines from Nitriles by a User‐Friendly Cobalt Catalyst
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Palladium‐Catalyzed Picolinamide‐Directed Benzylic C(sp3)−H Chalcogenation with Diaryl Disulfides and Diphenyl Diselenide
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Copper‐Catalyzed Direct Arylation of Indoles and Related (Hetero)arenes: A Ligandless and Solvent‐free Approach
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A Copper‐ and Phosphine‐Free Nickel(II)‐Catalyzed Method for C−H Bond Alkynylation of Benzothiazoles and Related Azoles
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C−H Functionalization of Indoles by 3d Transition‐Metal Catalysis
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Rhodium(I)‐Catalyzed C2‐Selective Decarbonylative C−H Alkylation of Indoles with Alkyl Carboxylic Acids and Anhydrides
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Carbonylative Coupling of Alkyl Zinc Reagents with Benzyl Bromides Catalyzed by a Nickel/NN2 Pincer Ligand Complex
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Jenseits von Friedel und Crafts: dirigierte Alkylierung von C‐H‐Bindungen in Arenen
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Nickelaelektrokatalysierte, milde C‐H‐Alkylierungen bei Raumtemperatur
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Carbonylative Coupling of Alkyl Zinc Reagents with Benzyl Bromides Catalyzed by a Nickel/NN2 Pincer Ligand Complex
inferred← citeshttps://doi.org/10.1002/anie.201806629openalex-snapshot
Beyond Friedel and Crafts: Directed Alkylation of C−H Bonds in Arenes
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Nickel‐Catalyzed Asymmetric Hydrogenation for the Synthesis of a Key Intermediate of Sitagliptin
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Chemodivergent Dehydrogenative Coupling of Alcohols by 3d Metal Catalysts
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MnBr2-Catalyzed Direct and Site-Selective Alkylation of Indoles and Benzo[h]quinoline
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Silver-Catalyzed Direct Synthesis of Trifluoromethylated Enaminopyridines and Isoquinolinones Employing Trifluorodiazoethane
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Cobalt-Catalyzed Direct C–H Thiolation of Aromatic Amides with Disulfides: Application to the Synthesis of Quetiapine
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Iron-Catalyzed C(sp2)–H Alkylation of Indolines and Benzo[ h ]quinoline with Unactivated Alkyl Chlorides through Chelation Assistance
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Unactivated Alkyl Halides in Transition-Metal-Catalyzed C–H Bond Alkylation
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Direct Reductive Quinolyl β-C–H Alkylation by Multispherical Cavity Carbon-Supported Cobalt Oxide Nanocatalysts
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inferred← citeshttps://doi.org/10.1021/acscatal.8b04267openalex-snapshot
Nickel-Catalyzed Straightforward and Regioselective C–H Alkenylation of Indoles with Alkenyl Bromides: Scope and Mechanistic Aspect
inferred← citeshttps://doi.org/10.1021/acssuschemeng.0c07465openalex-snapshot
Mn(I)-Catalyzed Mechanochemical C–H Bond Activation: C-2 Selective Alkenylation of Indoles
inferred← citeshttps://doi.org/10.1021/jacs.4c05123openalex-snapshot
Speciation and Reactivity of Mono- and Binuclear Ni Intermediates in Aminoquinoline-Directed C–H Arylation and Benzylation
inferred← citeshttps://doi.org/10.1038/s41467-021-25222-1openalex-snapshot
Nickel-catalyzed deaminative Sonogashira coupling of alkylpyridinium salts enabled by NN2 pincer ligand
inferred← citeshttps://doi.org/10.1039/c7cc02808copenalex-snapshot
Rhodium-catalyzed C2 and C4 C–H activation/annulation of 3-(1H-indol-3-yl)-3-oxopropanenitriles with internal alkynes: a facile access to substituted and fused carbazoles
inferred← citeshttps://doi.org/10.1039/c7cc05532copenalex-snapshot
Nickel-catalyzed direct C–H trifluoroethylation of heteroarenes with trifluoroethyl iodide
inferred← citeshttps://doi.org/10.1039/c7nj00452dopenalex-snapshot
Development of (quinolinyl)amido-based pincer palladium complexes: a robust and phosphine-free catalyst system for C–H arylation of benzothiazoles
inferred← citeshttps://doi.org/10.1039/c7qo01086aopenalex-snapshot
Iron( ii )-catalyzed C-2 cyanomethylation of indoles and pyrroles via direct oxidative cross-dehydrogenative coupling with acetonitrile derivatives
inferred← citeshttps://doi.org/10.1039/c8cs00201kopenalex-snapshot
A comprehensive overview of directing groups applied in metal-catalysed C–H functionalisation chemistry
inferred← citeshttps://doi.org/10.1039/c8dt03210fopenalex-snapshot
Synthesis of quinolinyl-based pincer copper( ii ) complexes: an efficient catalyst system for Kumada coupling of alkyl chlorides and bromides with alkyl Grignard reagents
inferred← citeshttps://doi.org/10.1039/c8ra01377bopenalex-snapshot
Cobalt-catalyzed C(sp 3 )–H/C(sp 2 )–H oxidative coupling between alkanes and benzamides
inferred← citeshttps://doi.org/10.1039/c9sc01446bopenalex-snapshot
Nickel-catalyzed C–H alkylation of indoles with unactivated alkyl chlorides: evidence of a Ni( i )/Ni( iii ) pathway
inferred← citeshttps://doi.org/10.1039/d0cc03345fopenalex-snapshot
The copper( ii )-catalyzed and oxidant-promoted regioselective C-2 difluoromethylation of indoles and pyrroles
inferred← citeshttps://doi.org/10.1039/d0dt03593aopenalex-snapshot
Recent advances in pincer–nickel catalyzed reactions
inferred← citeshttps://doi.org/10.1039/d0ob02232bopenalex-snapshot
Removal and modification of directing groups used in metal-catalyzed C–H functionalization: the magical step of conversion into ‘conventional’ functional groups
inferred← citeshttps://doi.org/10.1039/d0qo00765jopenalex-snapshot
Synthesis of 2,3-disubstituted indoles via a tandem reaction
inferred← citeshttps://doi.org/10.1039/d1dt03967aopenalex-snapshot
Cyclometalated (NNC)Ru( ii ) complex catalyzed β-methylation of alcohols using methanol
inferred← citeshttps://doi.org/10.1039/d1nj01696bopenalex-snapshot
Transition metal-catalyzed C–H functionalizations of indoles
inferred← citeshttps://doi.org/10.1039/d1nj01698aopenalex-snapshot
Achiral and chiral NNN-pincer nickel complexes with oxazolinyl backbones: application in transfer hydrogenation of ketones
inferred← citeshttps://doi.org/10.1039/d2cy00027jopenalex-snapshot
Room temperature Z -selective hydrogenation of alkynes by hemilabile and non-innocent (NNN)Co( ii ) catalysts
inferred← citeshttps://doi.org/10.1039/d3nj00460kopenalex-snapshot
TiO 2 (P25) nanoparticle catalyzed C-alkylation and quinoline synthesis via the borrowing hydrogen method
inferred← citeshttps://doi.org/10.1039/d3qo01501gopenalex-snapshot
Rapid modular synthesis of indole ethers via dehydrogenative cross-coupling reaction of indoles and alcohols
inferred← citeshttps://doi.org/10.1039/d3ra02031bopenalex-snapshot
Iridium catalysed C2 site-selective methylation of indoles using a pivaloyl directing group through weak chelation-assistance
inferred← citeshttps://doi.org/10.1039/d4dt00282bopenalex-snapshot
Pd( ii ) complexes bearing NNS pincer ligands: unveiling potent cytotoxicity against breast and pancreatic cancer
inferred← citeshttps://doi.org/10.1039/d4dt00605dopenalex-snapshot
Reactions of cyclonickelated complexes with hydroxylamines and TEMPO˙: isolation of new TEMPOH adducts of Ni( ii ) and their reactivities with nucleophiles and oxidants
inferred← citeshttps://doi.org/10.1039/d4qo00063copenalex-snapshot
Advancement in the C–H bond alkylation of (hetero)arenes catalyzed by the most abundant transition metal–iron
inferred← citeshttps://doi.org/10.1039/d6qo00602gopenalex-snapshot
Transition metal-catalyzed monodentate directing group-assisted C–H functionalization: an overview of advances (2015–2024)
inferred← citeshttps://doi.org/10.1055/sos-sd-238-00266openalex-snapshot
1.14 Nickel-Catalyzed Directed C—H Functionalization
inferred← citeshttps://doi.org/10.1139/cjc-2017-0258openalex-snapshot
Rh(III)-catalyzed oxidative ortho-C–H alkylation of 2,4-diarylquinazoline with potassium alkyltrifluoroborates
inferred← citeshttps://doi.org/10.12677/jocr.2023.111001openalex-snapshot
Progress in Synthesis of Indole Derivatives
inferred← citeshttps://doi.org/10.3390/catal9010076openalex-snapshot
Benzothiazole Nickelation: An Obstacle to the Catalytic Arylation of Azoles by Cyclopentadienyl Nickel N-Heterocyclic Carbene Complexes
inferred← citeshttps://doi.org/10.3390/inorganics12080221openalex-snapshot
C–H Activation via Group 8–10 Pincer Complexes: A Mechanistic Approach
inferred← citeshttps://doi.org/10.3390/molecules29091917openalex-snapshot
Recent Advances in the Nickel-Catalyzed Alkylation of C-H Bonds
inferred← citeshttps://doi.org/10.70675/3d64a7ebzd169z4689za8a5z87e5499c2b19openalex-snapshot
From molecular catalysts to their incorporation in porous materials : the case of regiospecific aromatic CH arylation
inferred← citeshttps://doi.org/10.70675/feedc0b6z6a14z4f41za850ze2562d87a485openalex-snapshot
Réactions d'échange isotopique de nitriles : applications au radiomarquage par le carbone-14 de composés d'intérêt pharmaceutique
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