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Activation of C–O and C–N Bonds Using Non-Precious-Metal Catalysis
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Kinetic Modeling of the Nickel-Catalyzed Esterification of Amides
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Nickel-Catalyzed Reductive Transamidation of Secondary Amides with Nitroarenes
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Nickel-Catalyzed Suzuki–Miyaura Coupling of Aliphatic Amides
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Decarbonylative Borylation of Amides by Palladium Catalysis
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Directed ortho metalation. Tertiary amide and O-carbamate directors in synthetic strategies for polysubstituted aromatics
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Iron-Catalyzed Reactions in Organic Synthesis
inferredcites →https://doi.org/10.1021/cr0509861openalex-snapshot
Diazonium Salts as Substrates in Palladium-Catalyzed Cross-Coupling Reactions
inferredcites →https://doi.org/10.1021/cr100259topenalex-snapshot
Nickel-Catalyzed Cross-Couplings Involving Carbon−Oxygen Bonds
inferredcites →https://doi.org/10.1021/cr9000786openalex-snapshot
Cobalt-Catalyzed Cross-Coupling Reactions
inferredcites →https://doi.org/10.1021/cr990357popenalex-snapshot
Conjugated Polymers and Aromaticity
inferredcites →https://doi.org/10.1021/cs400633aopenalex-snapshot
Multistep One-Pot Reactions Combining Biocatalysts and Chemical Catalysts for Asymmetric Synthesis
inferredcites →https://doi.org/10.1021/cs501045vopenalex-snapshot
Nickel-Catalyzed Amination of Aryl Chlorides and Sulfamates in 2-Methyl-THF
inferredcites →https://doi.org/10.1021/ja00185a023openalex-snapshot
Enantiospecific and stereospecific rhodium(I)-catalyzed carbonylation and ring expansion of aziridines. Asymmetric synthesis of .beta.-lactams and the kinetic resolution of aziridines
inferredcites →https://doi.org/10.1021/ja00502a074openalex-snapshot
Nickel-induced conversion of carbon-oxygen into carbon-carbon bonds. One-step transformations of enol ethers into olefins and aryl ethers into biaryls
inferredcites →https://doi.org/10.1021/ja00515a028openalex-snapshot
Mechanism of oxidative addition. Reaction of nickel(0) complexes with aromatic halides
inferredcites →https://doi.org/10.1021/ja00531a016openalex-snapshot
Oxidative addition of aryl carboxylates to nickel(0) complexes involving cleavage of the acyl-oxygen bond
inferredcites →https://doi.org/10.1021/ja0103501openalex-snapshot
The Ruthenium-Catalyzed Reductive Decarboxylation of Esters: Catalytic Reactions Involving the Cleavage of Acyl−Oxygen Bonds of Esters
inferredcites →https://doi.org/10.1021/ja017086wopenalex-snapshot
A Mild and Efficient Catalytic Alkylative Monofunctionalization of Cyclic Anhydrides
inferredcites →https://doi.org/10.1021/ja017652nopenalex-snapshot
Interactions of Aziridines with Nickel Complexes: Oxidative-Addition and Reductive-Elimination Reactions that Break and Make C−N Bonds
inferredcites →https://doi.org/10.1021/ja027190topenalex-snapshot
Iron-Catalyzed Cross-Coupling Reactions
inferredcites →https://doi.org/10.1021/ja034908bopenalex-snapshot
The First Suzuki Cross-Couplings of Aryltrimethylammonium Salts
inferredcites →https://doi.org/10.1021/ja038752ropenalex-snapshot
Room-Temperature Ni(0)-Catalyzed Cross-Coupling Reactions of Aryl Arenesulfonates with Arylboronic Acids
inferredcites →https://doi.org/10.1021/ja044588bopenalex-snapshot
Highly Efficient Nickel-Catalyzed Cross-Coupling of Succinic and Glutaric Anhydrides with Organozinc Reagents
inferredcites →https://doi.org/10.1021/ja046528bopenalex-snapshot
A Palladium-Catalyzed Enantioselective Alkylative Desymmetrization of meso-Succinic Anhydrides
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Can Decarbonylation of Acyl Radicals Be Overcome in Radical Addition Reactions? En Route to a Solution Employing N-Acyl Oxazolidinones and SmI2/H2O
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Synthesis and Reactivity of Azapalladacyclobutanes
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Ligand-Dependent Catalytic Cycle and Role of Styrene in Nickel-Catalyzed Anhydride Cross-Coupling: Evidence for Turnover-Limiting Reductive Elimination
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Ruthenium-Catalyzed Carbon−Carbon Bond Formation via the Cleavage of an Unreactive Aryl Carbon−Nitrogen Bond in Aniline Derivatives with Organoboronates
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Rhodium-Catalyzed Enantioselective Desymmetrization of meso-3,5-Dimethyl Glutaric Anhydride: A General Strategy to syn-Deoxypolypropionate Synthons
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Suzuki−Miyaura Cross-Coupling of Aryl Carbamates and Sulfamates: Experimental and Computational Studies
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Decarbonylative C–H Coupling of Azoles and Aryl Esters: Unprecedented Nickel Catalysis and Application to the Synthesis of Muscoride A
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Nickel-Catalyzed Cross-Couplings of Benzylic Pivalates with Arylboroxines: Stereospecific Formation of Diarylalkanes and Triarylmethanes
inferredcites →https://doi.org/10.1021/ja4076716openalex-snapshot
Directed Nickel-Catalyzed Negishi Cross Coupling of Alkyl Aziridines
inferredcites →https://doi.org/10.1021/ja408856popenalex-snapshot
Electrophilic Rearrangements of Chiral Amides: A Traceless Asymmetric α-Allylation
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Isolation, Structure, and Reactivity of an Arylnickel(II) Pivalate Complex in Catalytic C–H/C–O Biaryl Coupling
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Mechanisms and Origins of Switchable Chemoselectivity of Ni-Catalyzed C(aryl)–O and C(acyl)–O Activation of Aryl Esters with Phosphine Ligands
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Nickel-Catalyzed Negishi Arylations of Propargylic Bromides: A Mechanistic Investigation
inferredcites →https://doi.org/10.1021/ja711449eopenalex-snapshot
Palladium-Catalyzed Carbonylation of Aryl Tosylates and Mesylates
inferredcites →https://doi.org/10.1021/ja801466topenalex-snapshot
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inferredcites →https://doi.org/10.1021/ja8056503openalex-snapshot
Biaryl Construction via Ni-Catalyzed C−O Activation of Phenolic Carboxylates
inferredcites →https://doi.org/10.1021/ja806244bopenalex-snapshot
Cross-Coupling Reactions of Aryl Pivalates with Boronic Acids
inferredcites →https://doi.org/10.1021/ja806569hopenalex-snapshot
Nickel-Catalyzed Decarbonylative Addition of Anhydrides to Alkynes
inferredcites →https://doi.org/10.1021/ja902829popenalex-snapshot
Cleavage of C−N Bonds in Aniline Derivatives on a Ruthenium Center and Its Relevance to Catalytic C−C Bond Formation
inferredcites →https://doi.org/10.1021/ja903091gopenalex-snapshot
Hydroxyphosphine Ligand for Nickel-Catalyzed Cross-Coupling through Nickel/Magnesium Bimetallic Cooperation
inferredcites →https://doi.org/10.1021/ja906477ropenalex-snapshot
Suzuki−Miyaura Coupling of Aryl Carbamates, Carbonates, and Sulfamates
inferredcites →https://doi.org/10.1021/ja907281fopenalex-snapshot
Cross-Coupling of Alkenyl/Aryl Carboxylates with Grignard Reagent via Fe-Catalyzed C−O Bond Activation
inferredcites →https://doi.org/10.1021/ja9928677openalex-snapshot
Configuration Energies of the d-Block Elements
inferredcites →https://doi.org/10.1021/jacs.0c01330openalex-snapshot
Nickel-Catalyzed Alkyl–Alkyl Cross-Electrophile Coupling Reaction of 1,3-Dimesylates for the Synthesis of Alkylcyclopropanes
inferredcites →https://doi.org/10.1021/jacs.5b02503openalex-snapshot
Electron-Deficient Olefin Ligands Enable Generation of Quaternary Carbons by Ni-Catalyzed Cross-Coupling
inferredcites →https://doi.org/10.1021/jacs.5b05308openalex-snapshot
Palladium-Catalyzed Intramolecular Insertion of Alkenes into the Carbon–Nitrogen Bond of β-Lactams
inferredcites →https://doi.org/10.1021/jacs.6b04086openalex-snapshot
Radical–Radical Cyclization Cascades of Barbiturates Triggered by Electron-Transfer Reduction of Amide-Type Carbonyls
inferredcites →https://doi.org/10.1021/jacs.6b11412openalex-snapshot
Mechanistic Study of an Improved Ni Precatalyst for Suzuki–Miyaura Reactions of Aryl Sulfamates: Understanding the Role of Ni(I) Species
inferredcites →https://doi.org/10.1021/jacs.6b12077openalex-snapshot
Dearomatizing Radical Cyclizations and Cyclization Cascades Triggered by Electron-Transfer Reduction of Amide-Type Carbonyls
inferredcites →https://doi.org/10.1021/jacs.6b12329openalex-snapshot
Palladium-Catalyzed Suzuki–Miyaura Coupling of Aryl Esters
inferredcites →https://doi.org/10.1021/jacs.6b13340openalex-snapshot
Stereodivergence in Asymmetric Catalysis
inferredcites →https://doi.org/10.1021/jacs.7b03159openalex-snapshot
The Suzuki–Miyaura Coupling of Nitroarenes
inferredcites →https://doi.org/10.1021/jacs.7b04973openalex-snapshot
Mechanism and Origins of Ligand-Controlled Stereoselectivity of Ni-Catalyzed Suzuki–Miyaura Coupling with Benzylic Esters: A Computational Study
inferredcites →https://doi.org/10.1021/jacs.7b06191openalex-snapshot
Ni-Catalyzed Alkene Carboacylation via Amide C–N Bond Activation
inferredcites →https://doi.org/10.1021/jacs.8b08779openalex-snapshot
Ni-Catalyzed Cross-Coupling of Dimethyl Aryl Amines with Arylboronic Esters under Reductive Conditions
inferredcites →https://doi.org/10.1021/jacs.9b05464openalex-snapshot
Different Strategies for Designing Dual-Catalytic Enantioselective Processes: From Fully Cooperative to Non-cooperative Systems
inferredcites →https://doi.org/10.1021/jm991167+openalex-snapshot
Synthesis and Cytostatic Activity of Substituted 6-Phenylpurine Bases and Nucleosides: Application of the Suzuki−Miyaura Cross-Coupling Reactions of 6-Chloropurine Derivatives with Phenylboronic Acids
inferredcites →https://doi.org/10.1021/jo00199a030openalex-snapshot
Transformation of carbon-oxygen into carbon-carbon bonds mediated by low-valent nickel species
inferredcites →https://doi.org/10.1021/jo00364a048openalex-snapshot
Directed ortho-lithiation of alkyl arenesulfonates
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What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Nickel‐Catalyzed Chemoselective Carbomagnesiation for Atroposelective Ring‐Opening Difunctionalization
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Mechanochemically Enabled Formal Reductive Cross‐Coupling Reaction Between Aryl Ethers and Aryl Fluorides
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Photo‐ and Cerium‐Mediated C─C Bond Cleavage for the Deconstructive Diversification of Cyclic Acids
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Biphenylene Coordination and Ring‐Opening by Alkali‐Metal Nickelates
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Catalytic Selective Deoxygenation and Deamination of Amides to Access Alkenes
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Reductive Arylation of Amides via a Nickel‐Catalyzed Suzuki–Miyaura‐Coupling and Transfer‐Hydrogenation Cascade
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Direct Synthesis of Ketones from Methyl Esters by Nickel‐Catalyzed Suzuki–Miyaura Coupling
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Temperature‐Controlled Mechanochemistry for the Nickel‐Catalyzed Suzuki–Miyaura‐Type Coupling of Aryl Sulfamates via Ball Milling and Twin‐Screw Extrusion.**
inferred← citeshttps://doi.org/10.1002/anie.202212213openalex-snapshot
Challenges and Breakthroughs in Selective Amide Activation
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Temperature‐Controlled Mechanochemistry Unlocks the Nickel‐Catalyzed Suzuki–Miyaura‐Type Coupling of Aryl Sulfamates at Different Scales
inferred← citeshttps://doi.org/10.1002/anie.202401756openalex-snapshot
Nickel‐Catalyzed Chemoselective Carbomagnesiation for Atroposelective Ring‐Opening Difunctionalization
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Mechanochemically Enabled Formal Reductive Cross‐Coupling Reaction Between Aryl Ethers and Aryl Fluorides
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Photo‐ and Cerium‐Mediated C─C Bond Cleavage for the Deconstructive Diversification of Cyclic Acids
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Biphenylene Coordination and Ring‐Opening by Alkali‐Metal Nickelates
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Catalytic Selective Deoxygenation and Deamination of Amides to Access Alkenes
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C−P Bond Formation by Nickel or Cobalt Catalyzed Coupling Reactions
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Understanding the Structure‐Activity Relationship of Ni‐Catalyzed Amide C−N Bond Activation using Distortion/Interaction Analysis
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Electrochemical Borylation of C−C and C−Het Bonds
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Facile Synthesis of Alkylidene Phthalides by Rhodium‐Catalyzed Domino C−H Acylation/Annulation of Benzamides with Aliphatic Carboxylic Acids
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Nickel‐Catalyzed Csp2−OMe Functionalization for Chemoselective Aromatic Homologation En Route to Nanographenes
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Skeletal Rearrangements of Amides via Breaking Inert Bonds
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Recent Developments in the Field of Air‐Stable Nickel(0) Precatalysts for Cross‐Coupling Reactions
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Nickel Catalyzed Selective Arylation of Geminal Dinitriles: Direct Access to α-Cyano Carbonyl Compounds
inferred← citeshttps://doi.org/10.1021/acs.joc.4c00103openalex-snapshot
[(NHC)Pd(OAc)2]: Highly Active Carboxylate Pd(II)–NHC (NHC = N-Heterocyclic Carbene) Precatalysts for Suzuki–Miyaura and Buchwald–Hartwig Cross-Coupling of Amides by N–C(O) Activation
inferred← citeshttps://doi.org/10.1021/acs.joc.6c00528openalex-snapshot
Reductant-Free NiF 2 /Picolinic Acid-Catalyzed Coupling–Cyclization of 2-Iodobenzamides with Malonates
inferred← citeshttps://doi.org/10.1021/acs.oprd.1c00054openalex-snapshot
N-Chloro-N-sodio-carbamates as a Practical Amidating Reagent for Scalable and Sustainable Amidation of Aldehydes under Visible Light
inferred← citeshttps://doi.org/10.1021/acs.oprd.4c00454openalex-snapshot
Development of an Inherently Safe and Scalable Nickel-Catalyzed Borylation Process of an Aryl Sulfamate
inferred← citeshttps://doi.org/10.1021/acs.organomet.0c00775openalex-snapshot
16-Electron Nickel(0)-Olefin Complexes in Low-Temperature C(sp2)–C(sp3) Kumada Cross-Couplings
inferred← citeshttps://doi.org/10.1021/acs.organomet.2c00016openalex-snapshot
Ni-Catalyzed Larock Indenone Annulation with Aliphatic- and Silyl-Substituted Alkynes Supported by Mechanistic Analysis
inferred← citeshttps://doi.org/10.1021/acs.organomet.2c00542openalex-snapshot
Understanding the Reaction Mechanism of Nickel-Catalyzed Enantioselective Arylative Activation of the Aromatic C–O Bond
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c04104openalex-snapshot
Palladium-Catalyzed Denitrative α-Arylation of Ketones with Nitroarenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c04281openalex-snapshot
N-Heterocyclic Carbene-Catalyzed Truce–Smiles Rearrangement of N-Arylacrylamides via the Cleavage of Unactivated C(aryl)–N Bonds
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c00940openalex-snapshot
Palladium-Catalyzed Intermolecular Alkene Carboacylation via Ester C–O Bond Activation
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c00940openalex-snapshot
Cobalt Bromide-Catalyzed Negishi-Type Cross-Coupling of Amides
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c01060openalex-snapshot
The Kumada–Tamao–Corriu Coupling Reaction Catalyzed by Rhodium–Aluminum Bimetallic Complexes
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c02113openalex-snapshot
Palladium-Mediated Carbonylative Suzuki Coupling for DNA-Encoded Library Synthesis
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c02420openalex-snapshot
Selective Conversion of Unactivated C–N Amide Bond to C–C bond via Steric and Electronic Resonance Destabilization
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c03414openalex-snapshot
Copper-Catalyzed Sulfinyl Cross-Coupling Reaction of Sulfinamides
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c03241openalex-snapshot
Nickel-Catalyzed Domino Reaction of α-Aryloxyacetonitriles with Arylboronic Acids: Synthesis of 2-Aroylbenzo[b]furans
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c04007openalex-snapshot
Electroreductive Ring-Opening Carboxylation of 1,3-Oxazolidin-2-ones with CO2 for Accessing β-Amino Acids
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c00225openalex-snapshot
Borylation of Stable C(sp3)–O Bonds of Alkyl Esters over Supported Au Catalysts
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c03375openalex-snapshot
Nickel Catalyzed Aryl–Aryl Bridging C–N Bond Activation of 2-Pyridylpyridones and 6-Purinylpyridones
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c04515openalex-snapshot
Formal Transesterification Reaction of But-3-enyl Esters Enabled by a Synergistic Nickel/Zinc Relay
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c04755openalex-snapshot
Visible-Light-Induced Esterification of Carboxylic Acids with Arylsulfonium Salts
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c00122openalex-snapshot
Ambient Temperature Cleavages of Amides in an Aqueous Medium for the Ipsilateral Effect of 1,8-Substituents on Naphthalene
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c00547openalex-snapshot
Photocatalytic Amine-Promoted Selective Hydrochlorination and sp3 C–O Acylation of Alkyne-Tethered Methyl Ethers with Aldehydes
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c01418openalex-snapshot
Nickel-Catalyzed Reductive Alkylation of Pyridines via C–N Bond Activation
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c03580openalex-snapshot
Nickel-Catalyzed Reductive Alkylation and Arylation of Arylallylamines via C–N Bond Cleavage
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c03937openalex-snapshot
Modular Amide Synthesis via Dual C–O and N–O Bond Cleavage: Palladium-Catalyzed Deoxygenative Carbonylation of Benzyl Alcohols with Nitroarenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c03986openalex-snapshot
Visible-Light-Driven Silylation of C(sp 2 )–O Bonds with Silylboranes via Nickel Catalysis
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c01710openalex-snapshot
Ruthenium-Catalyzed [4 + 2] Cycloaddition of Chromanone Dienes Using Triethylamine as an Ethylene Surrogate
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c02295openalex-snapshot
Iron-Catalyzed Direct Synthesis of Amides from Alcohols
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c03107openalex-snapshot
Skeletal Editing of α-Oxoketene- N , S -Acetals into Amides via Cooperative Base-Promoted/Copper-Catalyzed Amidation
inferred← citeshttps://doi.org/10.1021/acscatal.1c01102openalex-snapshot
Nickel-Catalyzed Cross-Electrophile Coupling between C(sp2)–F and C(sp2)–Cl Bonds by the Reaction of ortho-Fluoro-Aromatic Amides with Aryl Chlorides
inferred← citeshttps://doi.org/10.1021/acscatal.1c01840openalex-snapshot
Tungsten-Catalyzed Transamidation of Tertiary Alkyl Amides
inferred← citeshttps://doi.org/10.1021/acscatal.1c02790openalex-snapshot
Identifying the Imperative Role of Metal–Olefin Interactions in Catalytic C–O Reductive Elimination from Nickel(II)
inferred← citeshttps://doi.org/10.1021/acscatal.1c04705openalex-snapshot
Nickel and Palladium Catalysis: Stronger Demand than Ever
inferred← citeshttps://doi.org/10.1021/acscatal.1c05738openalex-snapshot
Palladium-NHC (NHC = N-heterocyclic Carbene)-Catalyzed Suzuki–Miyaura Cross-Coupling of Alkyl Amides
inferred← citeshttps://doi.org/10.1021/acscatal.2c06054openalex-snapshot
Enantioselective Alkylation of Unactivated C–O Bond: Solvent Molecule Affects Competing β-H Elimination and Reductive Elimination Dynamics
inferred← citeshttps://doi.org/10.1021/acscatal.3c00973openalex-snapshot
Deoxygenative Silylation of C(sp3)–O Bonds with Hydrosilane by Cooperative Catalysis of Gold Nanoparticles and Solid Acids
inferred← citeshttps://doi.org/10.1021/acscatal.3c03166openalex-snapshot
Broad-Scope Amination of Aryl Sulfamates Catalyzed by a Palladium Phosphine Complex
inferred← citeshttps://doi.org/10.1021/acscatal.3c03851openalex-snapshot
P,N Ligand in Ni-Catalyzed Cross-Coupling Reactions: A Promising Tool for π-Functionalization
inferred← citeshttps://doi.org/10.1021/acscatal.4c01809openalex-snapshot
Diversification of Pharmaceutical Manufacturing Processes: Taking the Plunge into the Non-PGM Catalyst Pool
inferred← citeshttps://doi.org/10.1021/acscatal.4c03945openalex-snapshot
Merging Pd(0)-Catalyzed Selective Cacyl–O Bond Activation of Enol Esters with π-Acid Catalysis: Net Hydroxyacylation of Aliphatic Alkynes with Carboxylic Acids
inferred← citeshttps://doi.org/10.1021/acscatal.5c02609openalex-snapshot
Desulfonylative Suzuki–Miyaura Cross-Coupling of Unactivated Aryl Sulfones through Ni Catalysis
inferred← citeshttps://doi.org/10.1021/jacs.1c03394openalex-snapshot
Iron-Catalyzed Tandem Cyclization of Diarylacetylene to a Strained 1,4-Dihydropentalene Framework for Narrow-Band-Gap Materials
inferred← citeshttps://doi.org/10.1021/jacs.1c09265openalex-snapshot
Nickel-Catalyzed Addition of C–C Bonds of Amides to Strained Alkenes: The 1,2-Carboaminocarbonylation Reaction
inferred← citeshttps://doi.org/10.1021/jacs.1c09797openalex-snapshot
Nickel-Catalyzed Enantioselective Arylative Activation of Aromatic C–O Bond
inferred← citeshttps://doi.org/10.1021/jacs.2c04513openalex-snapshot
Conformational Flexibility as a Tool for Enabling Site-Selective Functionalization of Unactivated sp3 C–O Bonds in Cyclic Acetals
inferred← citeshttps://doi.org/10.1021/jacs.2c12311openalex-snapshot
Diverse Alkyl–Silyl Cross-Coupling via Homolysis of Unactivated C(sp 3 )–O Bonds with the Cooperation of Gold Nanoparticles and Amphoteric Zirconium Oxides
inferred← citeshttps://doi.org/10.1021/jacs.3c05845openalex-snapshot
Nickel-Catalyzed Enantioconvergent Transformation of Anisole Derivatives via Cleavage of C–OMe Bond
inferred← citeshttps://doi.org/10.1021/jacs.3c12497openalex-snapshot
Ring Walking Mediated by Ni–Ni Species as a Vehicle for Enabling Distal C(sp2)–H Functionalization of Aryl Pivalates
inferred← citeshttps://doi.org/10.1021/jacs.5c09306openalex-snapshot
Unraveling the Dichotomy Exerted by Boron Reagents in Site-Selective Functionalization of C(sp2)– and C(sp3)–OMe Bonds
inferred← citeshttps://doi.org/10.1021/jacs.5c17878openalex-snapshot
Metal-Free Catalytic Cross-Coupling of Esters and Boranes
inferred← citeshttps://doi.org/10.1021/jacsau.3c00283openalex-snapshot
Distinguishing Competing Mechanistic Manifolds for C(acyl)–N Functionalization by a Ni/ N -Heterocyclic Carbene Catalyst System
inferred← citeshttps://doi.org/10.1021/jacsau.4c00128openalex-snapshot
Isolation and Reactivity of Arylnickel(II) Complexes in Nickel-Catalyzed Borylation of Aryl Fluorosulfates
inferred← citeshttps://doi.org/10.1021/jacsau.5c00371openalex-snapshot
Direct O 2 Activation by Ligand-Constrained Pnictogen Complexes: Contrasting Mechanisms and OAT Reactivity across the P, Sb, and Bi Triad
inferred← citeshttps://doi.org/10.1038/s41467-022-30693-xopenalex-snapshot
Enantioselective alkylative cross-coupling of unactivated aromatic C–O electrophiles
inferred← citeshttps://doi.org/10.1038/s41467-023-40979-3openalex-snapshot
Skeletal metalation of lactams through a carbonyl-to-nickel-exchange logic
inferred← citeshttps://doi.org/10.1038/s41467-024-44756-8openalex-snapshot
Amide C–N bonds activation by A new variant of bifunctional N-heterocyclic carbene
inferred← citeshttps://doi.org/10.1038/s41467-024-50897-7openalex-snapshot
Deoxygenative radical cross-coupling of C(sp3)−O/C(sp3)−H bonds promoted by hydrogen-bond interaction
inferred← citeshttps://doi.org/10.1039/d0cc08389eopenalex-snapshot
Cross-coupling reactions with esters, aldehydes, and alcohols
inferred← citeshttps://doi.org/10.1039/d0sc06056aopenalex-snapshot
Nickel-catalyzed C–O/N–H, C–S/N–H, and C–CN/N–H annulation of aromatic amides with alkynes: C–O, C–S, and C–CN activation
inferred← citeshttps://doi.org/10.1039/d1dt03286kopenalex-snapshot
C–O and C–C bond cleavage of α,β-unsaturated esters with the assistance of a gallane(pyridyl)iron complex
inferred← citeshttps://doi.org/10.1039/d1ob02349gopenalex-snapshot
An efficient and straightforward approach for accessing thionoesters via palladium-catalyzed C–N cleavage of thioamides
inferred← citeshttps://doi.org/10.1039/d1qo00656hopenalex-snapshot
Nickel-catalyzed Suzuki–Miyaura cross-coupling of C–F bonds
inferred← citeshttps://doi.org/10.1039/d1qo01240aopenalex-snapshot
Copper-catalyzed deaminative alkynylation of secondary amines with alkynes: selectivity switch in the synthesis of diverse propargylamines
inferred← citeshttps://doi.org/10.1039/d1ra07238bopenalex-snapshot
Nickel( ii )-catalyzed reductive silylation of alkenyl methyl ethers for the synthesis of alkyl silanes
inferred← citeshttps://doi.org/10.1039/d2cc01625gopenalex-snapshot
Cooperative catalysis-enabled C–N bond cleavage of biaryl lactams with activated isocyanides
inferred← citeshttps://doi.org/10.1039/d2cc06681eopenalex-snapshot
Breaking bonds and breaking rules: inert-bond activation by [( i Pr 3 P)Ni] 5 H 4 and catalytic stereospecific norbornene dimerization
inferred← citeshttps://doi.org/10.1039/d2ob00307dopenalex-snapshot
Solvent- and additive-free oxidative amidation of aldehydes using a recyclable oxoammonium salt
inferred← citeshttps://doi.org/10.1039/d2qo01700hopenalex-snapshot
Exploring visible light for carbon–nitrogen and carbon–oxygen bond formation via nickel catalysis
inferred← citeshttps://doi.org/10.1039/d2sc06152jopenalex-snapshot
Copper-catalyzed enantioselective diyne cyclization via C(sp 2 )–O bond cleavage
inferred← citeshttps://doi.org/10.1039/d3cc00520hopenalex-snapshot
Recent developments in nickel-catalyzed asymmetric cyclization and cycloaddition of carbonyl-alkynes, cyano-alkynes, and enynes
inferred← citeshttps://doi.org/10.1039/d3cc03078dopenalex-snapshot
Activation of robust bonds by carbonyl complexes of Mn, Fe and Co
inferred← citeshttps://doi.org/10.1039/d3qo00042gopenalex-snapshot
Ruthenium(0)-catalyzed cross-coupling of aryl methyl ethers with organoboranes by selective C–O cleavage
inferred← citeshttps://doi.org/10.1039/d3qo01730copenalex-snapshot
Interception of RCONCl 2 : late-stage hydrolysis and esterification of primary amides
inferred← citeshttps://doi.org/10.1039/d3ra02637jopenalex-snapshot
A sustainable metal and base-free direct amidation of esters using water as a green solvent
inferred← citeshttps://doi.org/10.1039/d3sc00301aopenalex-snapshot
Hypervalent iodine-promoted twofold oxidative coupling of amines with amides and thioamides: chemoselective pathway to oxazoles and thiazoles
inferred← citeshttps://doi.org/10.1039/d3sc05797fopenalex-snapshot
Enantioselective nickel-catalyzed Mizoroki–Heck cyclizations of amide electrophiles
inferred← citeshttps://doi.org/10.1039/d4cc01695eopenalex-snapshot
Electrochemical ring-opening carboxylation of cyclic carbonate with carbon dioxide
inferred← citeshttps://doi.org/10.1039/d4cc02815eopenalex-snapshot
Room temperature C–O bond cleavage of vinyl cyclic synthons via a metallaphotoredox approach
inferred← citeshttps://doi.org/10.1039/d4dt01829jopenalex-snapshot
Mechanistic insights on C(acyl)–N functionalisation mediated by late transition metals
inferred← citeshttps://doi.org/10.1039/d4nj00330fopenalex-snapshot
An efficient and straightforward approach for accessing sulfonamide/ N -sulfonyl succinic esters via potassium fluoride-promoted C–N cleavage of N -sulfonyl succinimide
inferred← citeshttps://doi.org/10.1039/d4sc00904eopenalex-snapshot
Mechanochemical synthesis of aromatic ketones: pyrylium tetrafluoroborate mediated deaminative arylation of amides
inferred← citeshttps://doi.org/10.1039/d5cc03991fopenalex-snapshot
Strategic advances in C–OCF 3 bond transformations
inferred← citeshttps://doi.org/10.1039/d5dt02077hopenalex-snapshot
Group 10 complexes of benzothiazolehydrazone- and imidazo[1,5- a ]pyridine-based ligands: structural artistry, biophysical study, and catalytic activity
inferred← citeshttps://doi.org/10.1039/d5ob00612kopenalex-snapshot
n Bu 4 NBr-catalyzed esterification of methoxyarenes with acyl bromide
inferred← citeshttps://doi.org/10.1039/d5ob01418bopenalex-snapshot
ortho -C–O arylation of aromatic amides with Grignard reagents through the Meyers reaction
inferred← citeshttps://doi.org/10.1039/d5qo01041aopenalex-snapshot
The mechanochemical production of biphenyls from nitrogen-containing organic compounds: amides, anilines, and sulfonamides
inferred← citeshttps://doi.org/10.1039/d5ra03168kopenalex-snapshot
Enhancing the antioxidant potential of a coumarin derivative via nickel complexation: synthesis, spectral insights, DFT analysis, and molecular docking
inferred← citeshttps://doi.org/10.1039/d6nj00431hopenalex-snapshot
Synthesis, structure, and catalytic- and bio-activity of some metal complexes and a coordination polymer featuring imidazo[1,5- a ]pyridine and chromen[4,3- b ]pyrrole-4-one
inferred← citeshttps://doi.org/10.1039/d6ob00695gopenalex-snapshot
Metalloradical and photoredox manifolds in manganese photocatalysis
inferred← citeshttps://doi.org/10.1055/a-1306-3228openalex-snapshot
C–O Bond Activation as a Strategy in Palladium-Catalyzed Cross-Coupling
inferred← citeshttps://doi.org/10.1055/a-2572-0925openalex-snapshot
Divergent Carbocyanation and Hydrocyanation of Alkynes Enabled by Photoinduced Nickel-Catalyzed Homolytic Bond Cleavage of C(sp3)–N Bond in Isonitriles
inferred← citeshttps://doi.org/10.1055/a-2913-0875openalex-snapshot
Aminoxyl-mediated Electrocatalytic Oxidative Amidation of Aldehydes with Pyrazoles
inferred← citeshttps://doi.org/10.1055/s-0042-1751485openalex-snapshot
Nickel-Catalyzed Transesterification of Methyl Esters
inferred← citeshttps://doi.org/10.1134/s1070428022120168openalex-snapshot
Palladium-Catalyzed Denitrative Mizoroki–Heck Reactions of Aryl or Alkyl Olefins with Nitrobenzenes
inferred← citeshttps://doi.org/10.1246/cl.200885openalex-snapshot
Nickel-catalyzed C–O/O–H Annulation of Salicylate Esters with Alkynes: Activation of C–O Bond in Esters
inferred← citeshttps://doi.org/10.12677/aac.2022.122010openalex-snapshot
Recent Progress in the Nickel-Catalyzed Inert C-O/C-H Cross-Coupling Reactions of Phenol Derivatives
inferred← citeshttps://doi.org/10.1515/pac-2021-0110openalex-snapshot
The exploration of deoxygenation reactions for alcohols and derivatives using earth-abundant reagents
inferred← citeshttps://doi.org/10.21203/rs.3.rs-4006707/v1openalex-snapshot
Deoxygenative radical cross-coupling of C(sp3)−O/C(sp3)−H bonds enabled by hydrogen-bond interaction
inferred← citeshttps://doi.org/10.21203/rs.3.rs-4565591/v1openalex-snapshot
Mechanically Enabled Formal Reductive Cross-Coupling Reaction of Two Inert Bonds
inferred← citeshttps://doi.org/10.26434/chemrxiv-2022-z1d96openalex-snapshot
Temperature-Controlled Mechanochemistry for the Nickel-Catalyzed Suzuki-Miyaura-Type Coupling of Aryl Sulfamates via Ball Milling and Twin-Screw Extrusion
inferred← citeshttps://doi.org/10.26434/chemrxiv-2023-prjc2openalex-snapshot
Ring-Walking Mediated by Ni–Ni Species as a Vehicle for Enabling Dis-tal C(sp2)–H Functionalization of Aryl Pivalates
inferred← citeshttps://doi.org/10.31274/td-20240329-824openalex-snapshot
Transition metal-catalyzed difunctionalization reactions
inferred← citeshttps://doi.org/10.6023/cjoc202105053openalex-snapshot
Transition Metal-Catalyzed C—P Bond Activation
inferred← citeshttps://doi.org/10.6023/cjoc202204034openalex-snapshot
Nickel-Catalyzed Heck Reaction of Cycloalkenes with Inert C—O Bonds of Aryl Carbonates and Aryl Sulfamates
inferred← citeshttps://doi.org/10.6023/cjoc202310004openalex-snapshot
Amide Hydrolysis Reaction Using tert-Butyl Nitrite
inferred← citeshttps://doi.org/10.6023/cjoc202406045openalex-snapshot
Recent Advances in Electrochemical Carboxylation of Inert Chemical Bonds with Carbon Dioxide
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