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Photochemical Synthesis of Anilines via Ni-Catalyzed Coupling of Aryl Halides with Ammonium Salts

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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/adsc.200900587openalex-snapshot
Recent Applications of Palladium‐Catalyzed Coupling Reactions in the Pharmaceutical, Agrochemical, and Fine Chemical Industries
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An Expeditious Copper‐Catalyzed Access to 3‐Aminoquinolinones, 3‐Aminocoumarins and Anilines using Sodium Azide
inferredcites →https://doi.org/10.1002/adsc.201701539openalex-snapshot
Controlled Transformations of Aryl Halides in a Flow System: Selective Synthesis of Aryl Azides and Aniline Derivatives
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A Review on the Latest Progress of Chan‐Lam Coupling Reaction
inferredcites →https://doi.org/10.1002/ajoc.201700115openalex-snapshot
Cooperation of a Nickel–Bipyridine Complex with Light for Benzylic C−H Arylation of Toluene Derivatives
inferredcites →https://doi.org/10.1002/anie.200802569openalex-snapshot
A Very Simple Copper‐Catalyzed Synthesis of Anilines by Employing Aqueous Ammonia
inferredcites →https://doi.org/10.1002/anie.201000526openalex-snapshot
A P,N‐Ligand for Palladium‐Catalyzed Ammonia Arylation: Coupling of Deactivated Aryl Chlorides, Chemoselective Arylations, and Room Temperature Reactions
inferredcites →https://doi.org/10.1002/anie.201410875openalex-snapshot
Nickel‐Catalyzed Monoarylation of Ammonia
inferredcites →https://doi.org/10.1002/anie.201500404openalex-snapshot
Nickel‐Catalyzed Amination of Aryl Chlorides with Ammonia or Ammonium Salts
inferredcites →https://doi.org/10.1002/anie.201604429openalex-snapshot
Highly Chemoselective Iridium Photoredox and Nickel Catalysis for the Cross‐Coupling of Primary Aryl Amines with Aryl Halides
inferredcites →https://doi.org/10.1002/anie.201701690openalex-snapshot
Selected Copper‐Based Reactions for C−N, C−O, C−S, and C−C Bond Formation
inferredcites →https://doi.org/10.1002/anie.201809431openalex-snapshot
Alkyl Carbon–Carbon Bond Formation by Nickel/Photoredox Cross‐Coupling
inferredcites →https://doi.org/10.1002/anie.201904795openalex-snapshot
The Buchwald–Hartwig Amination After 25 Years
inferredcites →https://doi.org/10.1002/anie.201916398openalex-snapshot
General Paradigm in Photoredox Nickel‐Catalyzed Cross‐Coupling Allows for Light‐Free Access to Reactivity
inferredcites →https://doi.org/10.1002/anie.202003359openalex-snapshot
Light‐Promoted Nickel Catalysis: Etherification of Aryl Electrophiles with Alcohols Catalyzed by a Ni II ‐Aryl Complex
inferredcites →https://doi.org/10.1002/anie.202012877openalex-snapshot
Light‐Promoted C–N Coupling of Aryl Halides with Nitroarenes
inferredcites →https://doi.org/10.1002/anie.202013852openalex-snapshot
Nickel‐Catalyzed C‐Heteroatom Cross‐Coupling Reactions under Mild Conditions via Facilitated Reductive Elimination
inferredcites →https://doi.org/10.1002/anie.202100270openalex-snapshot
Visible‐Light‐Induced Homolysis of Earth‐Abundant Metal‐Substrate Complexes: A Complementary Activation Strategy in Photoredox Catalysis
inferredcites →https://doi.org/10.1002/anie.202108587openalex-snapshot
Chiral Arylated Amines via C−N Coupling of Chiral Amines with Aryl Bromides Promoted by Light
inferredcites →https://doi.org/10.1002/anie.202203176openalex-snapshot
An Integrated Carbon Nitride‐Nickel Photocatalyst for the Amination of Aryl Halides Using Sodium Azide
inferredcites →https://doi.org/10.1002/chem.200802678openalex-snapshot
A General Palladium‐Catalyzed Amination of Aryl Halides with Ammonia
inferredcites →https://doi.org/10.1002/chem.200902316openalex-snapshot
A Highly Versatile Catalyst System for the Cross‐Coupling of Aryl Chlorides and Amines
inferredcites →https://doi.org/10.1002/chem.201100984openalex-snapshot
Recyclable Catalysts for Palladium‐Catalyzed Aminations of Aryl Halides
inferredcites →https://doi.org/10.1002/chem.201203640openalex-snapshot
An Examination of the Palladium/Mor‐DalPhos Catalyst System in the Context of Selective Ammonia Monoarylation at Room Temperature
inferredcites →https://doi.org/10.1002/chem.202000052openalex-snapshot
A Unified and Practical Method for Carbon–Heteroatom Cross‐Coupling using Nickel/Photo Dual Catalysis
inferredcites →https://doi.org/10.1002/chem.202003974openalex-snapshot
Photoactive Nickel Complexes in Cross‐Coupling Catalysis
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Ullmann‐Ma Reaction: Development, Scope and Applications in Organic Synthesis †
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Nickel‐Catalyzed Amination of Aryl Carbamates with Ammonia
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Stable Isotope Techniques in Early Drug Development: An Economic Evaluation
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Performance of Human Mass Balance Studies with Stable Isotope‐Labeled Drug and Continuous Flow‐Isotope Ratio Mass Spectrometry: A Progress Report
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Synthesis of isotopically labelled compounds at Schering‐Plough, an historical perspective
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Synthesis and spectroscopic characterisation of 3‐chloroperbenzoic acid‐17O,18O, nitrosobenzene‐17O,18O and nitrosobenzene‐15N
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Pharmacokinetics of the 13C labeled anticancer agent temozolomide detected in vivo by selective cross‐polarization transfer
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Absorption spectroscopy of octahedral nickel(II) complexes: A case study of interactions between multiple electronic excited states
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An Ammonia Equivalent for the Palladium-Catalyzed Amination of Aryl Halides and Triflates
inferredcites →https://doi.org/10.1016/s0040-4039(97)10877-2openalex-snapshot
Allyl amines as ammonia equivalents in the preparation of anilines and heteroarylamines
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Catalytic syntheses of aromatic amines
inferredcites →https://doi.org/10.1021/acs.chemrev.1c00403openalex-snapshot
Visible Light-Induced Transition Metal Catalysis
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Applications of Palladium-Catalyzed C–N Cross-Coupling Reactions
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Reduction of Nitro Compounds Using 3d-Non-Noble Metal Catalysts
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Palladium-Catalyzed Cross-Coupling Reactions: A Powerful Tool for the Synthesis of Agrochemicals
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Analysis of Past and Present Synthetic Methodologies on Medicinal Chemistry: Where Have All the New Reactions Gone?
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General Method for the Amination of Aryl Halides with Primary and Secondary Alkyl Amines via Nickel Photocatalysis
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Recent Developments in the Reduction of Aromatic and Aliphatic Nitro Compounds to Amines
inferredcites →https://doi.org/10.1021/acs.oprd.9b00161openalex-snapshot
The 25th Anniversary of the Buchwald–Hartwig Amination: Development, Applications, and Outlook
inferredcites →https://doi.org/10.1021/acs.organomet.6b00830openalex-snapshot
Selective Cross-Coupling of (Hetero)aryl Halides with Ammonia To Produce Primary Arylamines using Pd-NHC Complexes
inferredcites →https://doi.org/10.1021/acs.organomet.8b00605openalex-snapshot
Probing the Influence of PAd-DalPhos Ancillary Ligand Structure on Nickel-Catalyzed Ammonia Cross-Coupling
inferredcites →https://doi.org/10.1021/acs.orglett.2c00203openalex-snapshot
Photochemically Enabled, Ni-Catalyzed Cyanation of Aryl Halides
inferredcites →https://doi.org/10.1021/acs.orglett.5b03230openalex-snapshot
Assembly of Primary (Hetero)Arylamines via CuI/Oxalic Diamide-Catalyzed Coupling of Aryl Chlorides and Ammonia
inferredcites →https://doi.org/10.1021/acs.orglett.7b00901openalex-snapshot
Discovery of N -(Naphthalen-1-yl)- N ′-alkyl Oxalamide Ligands Enables Cu-Catalyzed Aryl Amination with High Turnovers
inferredcites →https://doi.org/10.1021/acscatal.2c04213openalex-snapshot
Photo-Initiated Nickel Catalysis (PiNiC): Unmasking Dimethylnickel with Light
inferredcites →https://doi.org/10.1021/acscatal.7b03215openalex-snapshot
Transition-Metal-Catalyzed Monoarylation of Ammonia
inferredcites →https://doi.org/10.1021/cr00009a001openalex-snapshot
Transition metal and enzyme catalyzed reactions involving reactions with ammonia and amines
inferredcites →https://doi.org/10.1021/cr300503ropenalex-snapshot
Visible Light Photoredox Catalysis with Transition Metal Complexes: Applications in Organic Synthesis
inferredcites →https://doi.org/10.1021/ja01567a049openalex-snapshot
Confirmation of the Intramolecular Nature of the Hofmann “Haloamide” Reaction by Double Labeling
inferredcites →https://doi.org/10.1021/ja064005topenalex-snapshot
Palladium-Catalyzed Coupling of Ammonia and Lithium Amide with Aryl Halides
inferredcites →https://doi.org/10.1021/ja0717414openalex-snapshot
Pd-Catalyzed Amidations of Aryl Chlorides Using Monodentate Biaryl Phosphine Ligands: A Kinetic, Computational, and Synthetic Investigation
inferredcites →https://doi.org/10.1021/ja074681aopenalex-snapshot
Selective Palladium-Catalyzed Arylation of Ammonia: Synthesis of Anilines as Well as Symmetrical and Unsymmetrical Di- and Triarylamines
inferredcites →https://doi.org/10.1021/ja076762copenalex-snapshot
Indirect, Reversible High-Density Hydrogen Storage in Compact Metal Ammine Salts
inferredcites →https://doi.org/10.1021/ja1023404openalex-snapshot
Slow Reductive Elimination from Arylpalladium Parent Amido Complexes
inferredcites →https://doi.org/10.1021/ja903049zopenalex-snapshot
Palladium-Catalyzed Coupling of Ammonia with Aryl Chlorides, Bromides, Iodides, and Sulfonates: A General Method for the Preparation of Primary Arylamines
inferredcites →https://doi.org/10.1021/jacs.0c00286openalex-snapshot
The Quest for the Ideal Base: Rational Design of a Nickel Precatalyst Enables Mild, Homogeneous C–N Cross-Coupling
inferredcites →https://doi.org/10.1021/jacs.0c00781openalex-snapshot
3 d-d Excited States of Ni(II) Complexes Relevant to Photoredox Catalysis: Spectroscopic Identification and Mechanistic Implications
inferredcites →https://doi.org/10.1021/jacs.0c05901openalex-snapshot
Mechanistic Analysis of Metallaphotoredox C–N Coupling: Photocatalysis Initiates and Perpetuates Ni(I)/Ni(III) Coupling Activity
inferredcites →https://doi.org/10.1021/jacs.2c00462openalex-snapshot
Oxidative Addition of Aryl Halides to a Ni(I)-Bipyridine Complex
inferredcites →https://doi.org/10.1021/jacs.2c01356openalex-snapshot
Elucidating the Mechanism of Excited-State Bond Homolysis in Nickel–Bipyridine Photoredox Catalysts
inferredcites →https://doi.org/10.1021/jacs.6b04789openalex-snapshot
Photochemical Nickel-Catalyzed C–H Arylation: Synthetic Scope and Mechanistic Investigations
inferredcites →https://doi.org/10.1021/jacs.6b08397openalex-snapshot
Direct C(sp 3 )–H Cross Coupling Enabled by Catalytic Generation of Chlorine Radicals
inferredcites →https://doi.org/10.1021/jacs.7b13281openalex-snapshot
Long-Lived Charge-Transfer States of Nickel(II) Aryl Halide Complexes Facilitate Bimolecular Photoinduced Electron Transfer
inferredcites →https://doi.org/10.1021/jacs.8b03744openalex-snapshot
C–N Cross-Coupling via Photoexcitation of Nickel–Amine Complexes
inferredcites →https://doi.org/10.1021/jacs.8b11262openalex-snapshot
Elucidation of a Redox-Mediated Reaction Cycle for Nickel-Catalyzed Cross Coupling
inferredcites →https://doi.org/10.1021/jacs.8b12142openalex-snapshot
Oxalic Diamides and tert-Butoxide: Two Types of Ligands Enabling Practical Access to Alkyl Aryl Ethers via Cu-Catalyzed Coupling Reaction
inferredcites →https://doi.org/10.1021/jacs.9b11049openalex-snapshot
Energy Transfer to Ni-Amine Complexes in Dual Catalytic, Light-Driven C–N Cross-Coupling Reactions
inferredcites →https://doi.org/10.1021/jacs.9b12835openalex-snapshot
Transient Absorption Spectroscopy Offers Mechanistic Insights for an Iridium/Nickel-Catalyzed C–O Coupling
inferredcites →https://doi.org/10.1021/jf000055kopenalex-snapshot
Development of an Enzyme-Linked Immunosorbent Assay for the Fungicide Imazalil in Citrus Fruits
inferredcites →https://doi.org/10.1021/jm00305a014openalex-snapshot
Preparation and antimycotic properties of derivatives of 1-phenethylimidazole
inferredcites →https://doi.org/10.1021/jo010613+openalex-snapshot
Amination Reactions of Aryl Halides with Nitrogen-Containing Reagents Mediated by Palladium/Imidazolium Salt Systems
inferredcites →https://doi.org/10.1021/jo701573wopenalex-snapshot
Fluorous-Tagged Carbamates for the Pd-Catalyzed Amination of Aryl Halides
inferredcites →https://doi.org/10.1021/jo800818eopenalex-snapshot
Copper-Catalyzed Synthesis of Primary Arylamines via Cascade Reactions of Aryl Halides with Amidine Hydrochlorides
inferredcites →https://doi.org/10.1021/jo9006738openalex-snapshot
CuI/4-Hydro- l -proline as a More Effective Catalytic System for Coupling of Aryl Bromides with N-Boc Hydrazine and Aqueous Ammonia
inferredcites →https://doi.org/10.1021/jo990408iopenalex-snapshot
Room-Temperature Palladium-Catalyzed Amination of Aryl Bromides and Chlorides and Extended Scope of Aromatic C−N Bond Formation with a Commercial Ligand
inferredcites →https://doi.org/10.1021/ol005654ropenalex-snapshot
Palladium-Catalyzed Intermolecular Coupling of Aryl Halides and Amides
inferredcites →https://doi.org/10.1021/ol016333yopenalex-snapshot
Palladium-Catalyzed Synthesis of Arylamines from Aryl Halides and Lithium Bis(trimethylsilyl)amide as an Ammonia Equivalent
inferredcites →https://doi.org/10.1021/ol0166808openalex-snapshot
New Ammonia Equivalents for the Pd-Catalyzed Amination of Aryl Halides
inferredcites →https://doi.org/10.1021/ol0262688openalex-snapshot
Improved Functional Group Compatibility in the Palladium-Catalyzed Synthesis of Aryl Amines
inferredcites →https://doi.org/10.1021/ol027119sopenalex-snapshot
Palladium-Catalyzed Amination of Aryl Halides on Solid Support
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Zinc Trimethylsilylamide as a Mild Ammonia Equivalent and Base for the Amination of Aryl Halides and Triflates
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Mild and Highly Selective Palladium-Catalyzed Monoarylation of Ammonia Enabled by the Use of Bulky Biarylphosphine Ligands and Palladacycle Precatalysts
inferredcites →https://doi.org/10.1021/ol501739gopenalex-snapshot
Palladium-Catalyzed Amination of Aryl Chlorides and Bromides with Ammonium Salts
inferredcites →https://doi.org/10.1021/om300683copenalex-snapshot
The Complementary Competitors: Palladium and Copper in C–N Cross-Coupling Reactions
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Kiloscale Buchwald–Hartwig Amination: Optimized Coupling of Base-Sensitive 6-Bromoisoquinoline-1-carbonitrile with (S)-3-Amino-2-methylpropan-1-ol
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Microwave-assisted Pd(0)-catalyzed amination of aryl halides on solid support
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Challenging nickel-catalysed amine arylations enabled by tailored ancillary ligand design
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The merger of transition metal and photocatalysis
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Overcoming limitations in dual photoredox/nickel-catalysed C–N cross-couplings due to catalyst deactivation
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Ammonium salts as an inexpensive and convenient nitrogen source in the Cu-catalyzed amination of aryl halides at room temperature
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Efficient copper-catalyzed coupling of aryl chlorides, bromides and iodides with aqueous ammonia
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Visible light photoredox catalysis: applications in organic synthesis
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Efficient synthesis of aminopyridine derivatives by copper catalyzed amination reactions
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d-Glucosamine as a green ligand for copper catalyzed synthesis of primary aryl amines from aryl halides and ammonia
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d-Glucosamine as an efficient ligand for the copper-catalyzed selective synthesis of anilines from aryl halides and NaN3
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Copper catalysed Ullmann type chemistry: from mechanistic aspects to modern development
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Visible-light radical reaction designed by Ru- and Ir-based photoredox catalysis
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A chiral nickel DBFOX complex as a bifunctional catalyst for visible-light-promoted asymmetric photoredox reactions
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15 N labeling and analysis of 13 C– 15 N and 1 H– 15 N couplings in studies of the structures and chemical transformations of nitrogen heterocycles
inferredcites →https://doi.org/10.1039/d1cc01734aopenalex-snapshot
Synthesis of 15 N-labeled heterocycles via the cleavage of C–N bonds of anilines and glycine- 15 N
inferredcites →https://doi.org/10.1039/d2sc01264bopenalex-snapshot
State-of-the-art accounts of hyperpolarized 15 N-labeled molecular imaging probes for magnetic resonance spectroscopy and imaging
inferredcites →https://doi.org/10.1055/s-0036-1590819openalex-snapshot
Nickel-Catalyzed Cross-Coupling of Ammonia or Primary Alkylamines with (Hetero)aryl Sulfamates, Carbamates, or Pivalates
inferredcites →https://doi.org/10.1124/dmd.113.055715openalex-snapshot
Investigations into the Mechanisms of Pyridine Ring Cleavage in Vismodegib
inferredcites →https://doi.org/10.1126/science.1253647openalex-snapshot
Single-electron transmetalation in organoboron cross-coupling by photoredox/nickel dual catalysis
inferredcites →https://doi.org/10.1126/science.1255525openalex-snapshot
Merging photoredox with nickel catalysis: Coupling of α-carboxyl sp 3 -carbons with aryl halides
inferredcites →https://doi.org/10.1126/science.aal2490openalex-snapshot
Photosensitized, energy transfer-mediated organometallic catalysis through electronically excited nickel(II)
inferredcites →https://doi.org/10.2165/00003495-197816030-00001openalex-snapshot
Econazole
inferredcites →https://doi.org/10.2165/00003495-199448040-00009openalex-snapshot
Loratadine
inferredcites →https://doi.org/10.2165/11203920-000000000-00000openalex-snapshot
Fenofibric Acid
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Light-Promoted Nickel Catalysis: Etherification of Aryl Electro-philes with Alcohols Catalyzed by Ni(II)/Aryl Complex

What points at this work

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

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Photoredox/Nickel Dual-Catalysis-Enabled Regioselective Cyclization of Alkenes with Alkyl Chlorides
inferred← citeshttps://doi.org/10.1002/adsc.202300761openalex-snapshot
Selective Monoarylation of Ammonium Triflate with Aryl Chlorides Catalyzed by [Pd(β‐MeNAP)Br]2 and AdBrettPhos
inferred← citeshttps://doi.org/10.1002/adsc.70188openalex-snapshot
Primary Amination of Enones Using Inorganic Ammonium Salts and Nitrogen Isotope Incorporation
inferred← citeshttps://doi.org/10.1002/adsc.70302openalex-snapshot
Light‐Induced Nickel‐Carboxylate Facilitates C–O Coupling
inferred← citeshttps://doi.org/10.1002/ange.202314355openalex-snapshot
Werner Salt as Nickel and Ammonia Source for Photochemical Synthesis of Primary Aryl Amines
inferred← citeshttps://doi.org/10.1002/ange.202314508openalex-snapshot
Photoexcitation of Distinct Divalent Palladium Complexes in Cross‐Coupling Amination Under Air
inferred← citeshttps://doi.org/10.1002/ange.202504459openalex-snapshot
Electrochemical Amination of Aryl Halides with NH 3
inferred← citeshttps://doi.org/10.1002/ange.4978376openalex-snapshot
α‐Trifluoromethyl Substituted α‐Hydroxyhydrazides as Dianionic Ligands Enable Cu‐Catalyzed Aryl Amination With Higher Turnovers
inferred← citeshttps://doi.org/10.1002/anie.202314355openalex-snapshot
Werner Salt as Nickel and Ammonia Source for Photochemical Synthesis of Primary Aryl Amines
inferred← citeshttps://doi.org/10.1002/anie.202314508openalex-snapshot
Photoexcitation of Distinct Divalent Palladium Complexes in Cross‐Coupling Amination Under Air
inferred← citeshttps://doi.org/10.1002/anie.202504459openalex-snapshot
Electrochemical Amination of Aryl Halides with NH 3
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Recent Advance in Single Nickel Photocatalysis for Carbon‐Heteroatom Bond Formation
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Ni‐Catalyzed Photochemical C−N Coupling of Amides with (Hetero)aryl Chlorides
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Nucleophilic Amination of Aryl Halides with an Azanide Surrogate
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Advances in Copper and Nickel C─N and C─O Cross‐Couplings of (Hetero)Aryl Chlorides Enabled by Ancillary Ligand Development
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Nickel Metallaphotoredox Buchwald–Hartwig Amination Reactions: A Perspective on Irradiation Light Wavelength
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Recent Developments on Carbon‐Heteroatom Coupling in Aryl and Heteroaryl Rings Under Visible Light Irradiation
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Recent developments for the synthesis of stable isotopically labeled compounds
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Earth-abundant Ni(II)-based molecular photoredox catalysts: Emerging platform for sustainable cross coupling reactions
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Lignin-based hyper-cross-linked resin as an adsorbent for aniline from aqueous solution
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Nickel-catalyzed amination of aryl halides: An exogenous ligand-free approach to primary arylamines using TMSN3
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Microwave-assisted synthesis of primary aryl/heteroarylamines via one-pot reductive amination: A convenient and efficient synthetic route
inferred← citeshttps://doi.org/10.1016/j.mcat.2023.113806openalex-snapshot
Photoredox/nickel dual-catalysis-enabled synthesis of N-heterocycles from alkyl chlorides and alkenes
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Regioselectivity for nucleophilic substitutions of aryl halides with DMF in deep eutectic solvent
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Leveraging the Redox Promiscuity of Nickel To Catalyze C–N Coupling Reactions
inferred← citeshttps://doi.org/10.1021/acs.joc.5c00867openalex-snapshot
Visible-Light-Induced Nickel/Organoboron Dual Catalysis for the Synthesis of Primary Aryl Amines
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Catalytic C–N Bond-Forming Processes from Inorganic Ammonium Salts
inferred← citeshttps://doi.org/10.1021/acs.joc.5c02127openalex-snapshot
Photochemical Ni-Catalyzed Selective Mono- N -Arylation
inferred← citeshttps://doi.org/10.1021/acs.joc.6c00211openalex-snapshot
cis -Diphosphine Ethene Ligand–Ni(II)ArCl Complexes Catalyze Primary Amination of Aryl Chlorides
inferred← citeshttps://doi.org/10.1021/acs.joc.6c01242openalex-snapshot
Photochemical Ni-Catalyzed Cross-Coupling of Aryl Bromides with Hydrazides
inferred← citeshttps://doi.org/10.1021/acs.joc.6c01352openalex-snapshot
Visible-Light-Mediated C–N Cross-Coupling through Direct Sensitization of the Ni–BINAM Complex
inferred← citeshttps://doi.org/10.1021/acs.organomet.3c00506openalex-snapshot
Ni-Catalyzed Photochemial Sulfamidation of Aryl Chlorides with Soluble Organic Amine as Base
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c01047openalex-snapshot
Light-Promoted Ni-Catalyzed Cross-Coupling of Aryl Chlorides with Hydrazides: Application to the Synthesis of Rizatriptan
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c01079openalex-snapshot
Photoinduced Homolysis of the Ni–P Bond via Ligand to Metal Charge Transfer for C–P Bond Formation in Nickel Catalysis
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c01219openalex-snapshot
Photoexcited NiII–Aryl Complex-Mediated Giese Reaction of Aryl Bromides
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c01474openalex-snapshot
Visible-Light-Activated Nickel Thiolates for C–S Couplings
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c01694openalex-snapshot
Nickel/Photoredox-Catalyzed Direct Amidation of Aldehydes with Nitroarenes via Fully Catalytic Process
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c02119openalex-snapshot
Photoinduced Copper-Catalyzed Aminoalkylation of Amino-Pendant Olefins
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c00147openalex-snapshot
Excited-State Nickel-Catalyzed Amination of Aryl Bromides: Synthesis of Diphenylamines and Primary Anilines
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c00641openalex-snapshot
Pd-Catalyzed Coupling of Aryl Chloride, Isocyanides, and Thiocarboxylate To Synthesize Thioamides
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c05128openalex-snapshot
A One-Pot Three-Step Cu-Catalyzed Protocol to Construct Dibenzo[1,4]diazepine Derivatives and Their Analogs with Cyclopropylamine as a Surrogate of Ammonia
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c05346openalex-snapshot
Room-Temperature Decarboxylative Amination of Electron-Deficient (Hetero)Aromatic Carboxylic Acids
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c00011openalex-snapshot
Photochemical Ni-Catalyzed Enabled C–O Coupling of Aryl Halides with Phenols
inferred← citeshttps://doi.org/10.1021/acscatal.4c00788openalex-snapshot
Light-Promoted Efficient Generation of Fe(I) to Initiate Amination
inferred← citeshttps://doi.org/10.1021/acscatal.4c01283openalex-snapshot
Thermal Nickel-Catalyzed Carbon–Oxygen Cross-Coupling of (Hetero)aryl Halides with Alcohols Enabled by the Use of a Silane Reductant Approach
inferred← citeshttps://doi.org/10.1021/acscatal.4c02036openalex-snapshot
Mechanisms of Photoredox Catalysis Featuring Nickel–Bipyridine Complexes
inferred← citeshttps://doi.org/10.1021/acscatal.4c02624openalex-snapshot
Pd-Methylnaphthyl-tBuBrettPhos Complexes as Efficient and Selective Catalysts for the Monoarylation of Ammonia and Hydrazine
inferred← citeshttps://doi.org/10.1021/acscatal.5c07964openalex-snapshot
Advances in NiI/NiIII-Catalyzed C(sp2)–Heteroatom Cross-Couplings
inferred← citeshttps://doi.org/10.1021/acscentsci.5c01770openalex-snapshot
Shaking Up Photochemistry: The Future Frontiers of Mechanophotocatalysis
inferred← citeshttps://doi.org/10.1021/jacs.4c08130openalex-snapshot
Adaptive Photochemical Amination via Co(II) Catalysis
inferred← citeshttps://doi.org/10.1038/s41467-025-61812-zopenalex-snapshot
General method for carbon–heteroatom cross-coupling reactions via semiheterogeneous red-light metallaphotocatalysis
inferred← citeshttps://doi.org/10.1038/s41467-026-70925-yopenalex-snapshot
Photoinduced Mn catalysis for efficient platform for C-heteroatom bond coupling of aryl halides
inferred← citeshttps://doi.org/10.1038/s41586-026-10991-wopenalex-snapshot
Phosphine-mediated azine C–H couplings with water and ammonia
inferred← citeshttps://doi.org/10.1039/d3sc06618eopenalex-snapshot
Dual role of nitroarenes as electrophiles and arylamine surrogates in Buchwald–Hartwig-type coupling for C–N bond construction
inferred← citeshttps://doi.org/10.1039/d4cc06395copenalex-snapshot
Synthesis of chiral N -free sulfinamides by asymmetric condensation of stable sulfinates and ammonium salts
inferred← citeshttps://doi.org/10.1039/d4gc06307dopenalex-snapshot
Electrochemically enabled nickel-catalyzed controllable synthesis of monoaryl or diaryl amines from aryl halides and trimethylsilyl azides
inferred← citeshttps://doi.org/10.1039/d4qo00116hopenalex-snapshot
Selective photochemical synthesis of primary arylamines and symmetric diarylamines via amination of aryl bromides using Ni(NH 3 ) 6 Cl 2 as a nitrogen source and catalyst
inferred← citeshttps://doi.org/10.1039/d4qo00966eopenalex-snapshot
Catalytic reduction of trifluoromethylated alkyl bromides and synthesis of alkylated heterocycles under visible light irradiation: synergetic action of a halogen bond and Ni catalysis
inferred← citeshttps://doi.org/10.1039/d5qo01442eopenalex-snapshot
Dehydrogenative aromatization of cyclohexanone derivatives for the synthesis of site-selective substituted phenols and anilines
inferred← citeshttps://doi.org/10.1055/a-2307-8257openalex-snapshot
Transition-Metal-Catalyzed Direct Arylation of Ammonia
inferred← citeshttps://doi.org/10.1055/a-2344-5677openalex-snapshot
Latest Developments on Palladium- and Nickel-Catalyzed Cross-Couplings Using Aryl Chlorides: Suzuki–Miyaura and Buchwald–Hartwig Reactions
inferred← citeshttps://doi.org/10.1360/ssc-2024-0116openalex-snapshot
Red light induced nickel catalyzed aryl C−N coupling reaction
inferred← citeshttps://doi.org/10.26434/chemrxiv-2023-p8qvxopenalex-snapshot
Ni-catalyzed asymmetric C-P cross-coupling reaction via Ni(I)/Ni(III) two-electron pathway
inferred← citeshttps://doi.org/10.6023/cjoc202400009openalex-snapshot
Werner Salt as Nickel and Ammonia Source for Photochemical Synthesis of Primary Aryl Amines
inferred← citeshttps://doi.org/10.6023/cjoc202405038openalex-snapshot
Recent Progress on Light-Mediated C—N Bond-Forming Processes from Ammonia and Equivalents
inferred← citeshttps://doi.org/10.6023/cjoc202511014openalex-snapshot
Photoexcitation-Enabled C(sp 2 )—N Coupling of Aryl Halides with Sulfonamides Catalyzed by Earth-Abundant Nickel
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