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Modern Synthetic Methods for Copper‐Mediated C(aryl)O, C(aryl)N, and C(aryl)S Bond Formation

https://doi.org/10.1002/anie.200300594

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Transition Metal Catalyzed Synthesis of Arylamines and Aryl Ethers from Aryl Halides and Triflates: Scope and Mechanism

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Palladium-Catalyzed Coupling Reactions of Aryl Chlorides

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Palladium-catalyzed amination of aryl halides and sulfonates

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Ultrasound effect on the synthesis of 4-alkyl-(aryl)aminobenzaldehydes

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Newer methods of arylation

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Tetrahedron report number 163

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Palladium-catalysed reactions of aryl halides with soft, non-organometallic nucleophiles

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Utilization of a copper-catalyzed diaryl ether synthesis for the preparation of verbenachalcone

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The chemistry of pentavalent organobismuth reagents. Part 14. Recent advances in the copper-catalyzed phenylation of amines

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inferredcites →https://doi.org/10.1016/s0040-4020(99)00752-8openalex-snapshot

N-aryl heterocycles via coupling reactions with arylboronic acids

inferredcites →https://doi.org/10.1016/s0040-4039(00)01650-6openalex-snapshot

First combined selective N- and C-arylations with boronic acids: application to the synthesis of 1,3-diarylindazoles

inferredcites →https://doi.org/10.1016/s0040-4039(00)02310-8openalex-snapshot

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Total synthesis of OF4949-III, a novel inhibitor of aminopeptidase B

inferredcites →https://doi.org/10.1016/s0040-4039(00)86664-2openalex-snapshot

Copper catalysed phenylation of indoles by triphenylbismuth BIS-trifluoroacetate

inferredcites →https://doi.org/10.1016/s0040-4039(00)92336-0openalex-snapshot

N-arylation of azoles and their benzo derivatives by p-tolyllead triacetate

inferredcites →https://doi.org/10.1016/s0040-4039(00)95284-5openalex-snapshot

N-phenylation of amino acid derivatives

inferredcites →https://doi.org/10.1016/s0040-4039(01)00510-xopenalex-snapshot

Copper-catalyzed general CN and CO bond cross-coupling with arylboronic acid

inferredcites →https://doi.org/10.1016/s0040-4039(01)00888-7openalex-snapshot

Formation of arylnitrogen bonds using a soluble copper(I) catalyst

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Microwave-enhanced Goldberg reaction: a novel route to N-arylpiperazinones and N-arylpiperazinediones

inferredcites →https://doi.org/10.1016/s0040-4039(01)81015-7openalex-snapshot

Copper salts catalysis of N-phenylation of amines by trivalent organobismuth compounds

inferredcites →https://doi.org/10.1016/s0040-4039(01)92420-7openalex-snapshot

Selective phenylation in mild conditions of one hydroxy group in glycols with triphenylbismuth diacetate: A new specific glycol reaction.

inferredcites →https://doi.org/10.1016/s0040-4039(02)00356-8openalex-snapshot

Copper-promoted CN bond cross-coupling with phenylstannane

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Palladium- and copper-catalyzed selective arylation of 5-aryltetrazoles by diaryliodonium salts

inferredcites →https://doi.org/10.1016/s0040-4039(02)01326-6openalex-snapshot

Regioselective arylation of N-tributylstannylated 5-substituted tetrazoles by diaryliodonium salts in the presence of Cu(OAc)2

inferredcites →https://doi.org/10.1016/s0040-4039(02)01327-8openalex-snapshot

Highly selective arylation of disubstituted hydrazines by pentavalent organobismuth reagents

inferredcites →https://doi.org/10.1016/s0040-4039(02)01708-2openalex-snapshot

Copper-catalyzed amination of aryl halides: single-step synthesis of triarylamines

inferredcites →https://doi.org/10.1016/s0040-4039(02)01725-2openalex-snapshot

Copper-catalyzed amidations of bromo substituted furans and thiophenes

inferredcites →https://doi.org/10.1016/s0040-4039(02)02073-7openalex-snapshot

A mild, convenient synthesis of sulfinic acid salts and sulfonamides from alkyl and aryl halides

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N-Arylation of α-aminoesters with p-tolylboronic acid promoted by copper(II) acetate

inferredcites →https://doi.org/10.1016/s0040-4039(03)00569-0openalex-snapshot

Copper-catalyzed N-arylation of sulfonamides with aryl bromides and iodides using microwave heating

inferredcites →https://doi.org/10.1016/s0040-4039(03)00576-8openalex-snapshot

Regioselective N-9 arylation of purines employing arylboronic acids in the presence of Cu(II)

inferredcites →https://doi.org/10.1016/s0040-4039(03)00703-2openalex-snapshot

Synthesis of diaryl ethers through the copper-catalyzed arylation of phenols with aryl halides using microwave heating

inferredcites →https://doi.org/10.1016/s0040-4039(03)00739-1openalex-snapshot

Copper promoted CN and CO bond cross-coupling with phenyl and pyridylboronates

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Copper-catalyzed amination of aromatic halides with 2-N,N-dimethylaminoethanol as solvent

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Copper(I)-catalyzed arylselenylation of aryl bromides and iodides

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Synthesis of symmetrical diaryl ethers from arylboronic acids mediated by copper(II) acetate

inferredcites →https://doi.org/10.1016/s0040-4039(96)02116-8openalex-snapshot

Promotion of reaction of NH boths with triarylbismuth and cupric acetate

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New N- and O-arylations with phenylboronic acids and cupric acetate

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New aryl/heteroaryl CN bond cross-coupling reactions via arylboronic acid/cupric acetate arylation

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Cupric acetate mediated N-arylation by arylboronic acids: A preliminary investigation into the scope of application

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Solid supported CN cross-coupling reactions

inferredcites →https://doi.org/10.1016/s0040-4039(99)00287-7openalex-snapshot

N-Phenylation of azole derivatives by triphenylbismuth derivatives/cupric acetate

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N-Aryl 2,6-Dimethoxybiphenylalanine Analogues as VLA-4 Antagonists

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Web alert Mechanisms Analytical techniques

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Rational Development of Practical Catalysts for Aromatic Carbon−Nitrogen Bond Formation

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Carbon−Heteroatom Bond-Forming Reductive Eliminations of Amines, Ethers, and Sulfides

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N-Arylation of Primary and Secondary Aliphatic Amines on Solid Supports

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Comprehensive Survey of Combinatorial Library Synthesis: 2001

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Comprehensive Survey of Combinatorial Library Synthesis: 2002

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N-Arylation of Sulfonamides on Solid Supports

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Studies directed toward the synthesis of vancomycin and related cyclic peptides

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Organic Compounds Of Boron

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Metal-Catalyzed Carbon−Sulfur Bond Formation

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Asymmetric transformation in synthesis: chiral amino acid enolate equivalents

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Copper-Promoted C−N Bond Cross-Coupling with Hypervalent Aryl Siloxanes and Room-Temperature N-Arylation with Aryl Iodide

inferredcites →https://doi.org/10.1021/ja00239a032openalex-snapshot

Mechanisms and models for copper mediated nucleophilic aromatic substitution. 2. Single catalytic species from three different oxidation states of copper in an Ullmann synthesis of triarylamines

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Mechanistic investigation of the copper-catalyzed reactions of diphenyliodonium salts

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Diaryliodonium Salts. II. The Phenylation of Organic and Inorganic Bases1,2

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Total Synthesis of Teicoplanin Aglycon

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A General and Efficient Copper Catalyst for the Amidation of Aryl Halides

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Total Synthesis of Anti-HIV Agent Chloropeptin I

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A General Copper-Catalyzed Synthesis of Diaryl Ethers

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Accelerating Effect Induced by the Structure of α-Amino Acid in the Copper-Catalyzed Coupling Reaction of Aryl Halides with α-Amino Acids. Synthesis of Benzolactam-V8

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N6,9-Disubstituted adenines: potent, selective antagonists at the A1 adenosine receptor

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Selective N-Arylation of Aminobenzanilides under Mild Conditions Using Triarylbismuthanes

inferredcites →https://doi.org/10.1021/jo00122a060openalex-snapshot

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Conversion of one hydroxy group in a diol to a phenyl ether with triphenylbismuth diacetate, a new glycol reaction showing strong axial preference in six-membered rings

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Regioselective Conversion of Arylboronic Acids to Phenols and Subsequent Coupling to Symmetrical Diaryl Ethers

inferredcites →https://doi.org/10.1021/jo0016780openalex-snapshot

The [Cu(OH)·TMEDA] 2 Cl 2 -Catalyzed Coupling of Arylboronic Acids with Imidazoles in Water

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Organic chemistry of L-tyrosine. 1. General synthesis of chiral piperazines from amino acids

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Total synthesis of K-13

inferredcites →https://doi.org/10.1021/jo01056a511openalex-snapshot

Oxidative Coupling of Acetylenes. II 1

inferredcites →https://doi.org/10.1021/jo010615uopenalex-snapshot

Catalytic Activities of Cu(II) Complexes with Nitrogen-Chelating Bidentate Ligands in the Coupling of Imidazoles with Arylboronic Acids

inferredcites →https://doi.org/10.1021/jo01091a039openalex-snapshot

Potential Purine Antagonists XXI. Preparation of Some 9-Phenyl-6-substituted Purines1

inferredcites →https://doi.org/10.1021/jo01299a020openalex-snapshot

Preparation of o-substituted benzoic acids by the copper(II)-catalyzed reaction of diphenyliodonium-2-carboxylate with anilines and other nucleophiles

inferredcites →https://doi.org/10.1021/jo016131fopenalex-snapshot

Facile Synthesis of N-Aryl Pyrroles via Cu(II)-Mediated Cross Coupling of Electron Deficient Pyrroles and Arylboronic Acids

inferredcites →https://doi.org/10.1021/jo026125zopenalex-snapshot

Aromatic Nucleophilic Substitution or CuI-Catalyzed Coupling Route to Martinellic Acid

inferredcites →https://doi.org/10.1021/jo026757lopenalex-snapshot

Several Convenient Methods for the Synthesis of 2-Amido Substituted Furans

inferredcites →https://doi.org/10.1021/jo0341463openalex-snapshot

Easy Access to Novel Substituted 6-Aminoimidazo[1,2-a]pyridines Using Palladium- and Copper-Catalyzed Aminations

inferredcites →https://doi.org/10.1021/jo0343376openalex-snapshot

Copper-Catalyzed Synthesis of Unsymmetrical Triarylphosphines

inferredcites →https://doi.org/10.1021/jo980451qopenalex-snapshot

Mild Aryl Ether Formation in the Semisynthesis of the Novel Macrolide Immunosuppressant L-732,531

inferredcites →https://doi.org/10.1021/jo981804oopenalex-snapshot

Ligand-Accelerated Catalysis of the Ullmann Condensation: Application to Hole Conducting Triarylamines

inferredcites →https://doi.org/10.1021/jo990114xopenalex-snapshot

The Directed Ortho Metalation−Ullmann Connection. A New Cu(I)-Catalyzed Variant for the Synthesis of Substituted Diaryl Ethers

inferredcites →https://doi.org/10.1021/jo9902751openalex-snapshot

New Efficient Method for the Total Synthesis of ( S , S )-Isodityrosine from Natural Amino Acids

inferredcites →https://doi.org/10.1021/jo990490hopenalex-snapshot

Synthesis of Alkoxylamines by Alkoxide Amination with 3,3‘-Di- tert -butyloxaziridine

inferredcites →https://doi.org/10.1021/np000501yopenalex-snapshot

Synthetic Derivatives of Abietic Acid with Radical Scavenging Activity

inferredcites →https://doi.org/10.1021/np000632zopenalex-snapshot

The Complestatins as HIV-1 Integrase Inhibitors. Efficient Isolation, Structure Elucidation, and Inhibitory Activities of Isocomplestatin, Chloropeptin I, New Complestatins, A and B, and Acid-Hydrolysis Products of Chloropeptin I

inferredcites →https://doi.org/10.1021/ol000033jopenalex-snapshot

An Efficient Diamine·Copper Complex-Catalyzed Coupling of Arylboronic Acids with Imidazoles

inferredcites →https://doi.org/10.1021/ol0003533openalex-snapshot

The Copper-Mediated Cross-Coupling of Phenylboronic Acids and N -Hydroxyphthalimide at Room Temperature: Synthesis of Aryloxyamines

inferredcites →https://doi.org/10.1021/ol005832gopenalex-snapshot

Copper-Mediated Cross-Coupling of Aryl Boronic Acids and Alkyl Thiols

inferredcites →https://doi.org/10.1021/ol015572iopenalex-snapshot

Intramolecular O-Arylation of Phenols with Phenylboronic Acids: Application to the Synthesis of Macrocyclic Metalloproteinase Inhibitors

inferredcites →https://doi.org/10.1021/ol0160396openalex-snapshot

Copper-Catalyzed Coupling of Arylboronic Acids and Amines

inferredcites →https://doi.org/10.1021/ol016258ropenalex-snapshot

CuI-Catalyzed Coupling Reaction of β-Amino Acids or Esters with Aryl Halides at Temperature Lower Than That Employed in the Normal Ullmann Reaction. Facile Synthesis of SB-214857

inferredcites →https://doi.org/10.1021/ol0168216openalex-snapshot

Synthesis of N-Aryl Hydrazides by Copper-Catalyzed Coupling of Hydrazides with Aryl Iodides

inferredcites →https://doi.org/10.1021/ol0170105openalex-snapshot

Formation of Aryl−Nitrogen, Aryl−Oxygen, and Aryl−Carbon Bonds Using Well-Defined Copper(I)-Based Catalysts

inferredcites →https://doi.org/10.1021/ol0171867openalex-snapshot

Copper-Catalyzed Coupling of Alkylamines and Aryl Iodides: An Efficient System Even in an Air Atmosphere

inferredcites →https://doi.org/10.1021/ol025548kopenalex-snapshot

Copper-Catalyzed Coupling of Aryl Iodides with Aliphatic Alcohols

inferredcites →https://doi.org/10.1021/ol025839topenalex-snapshot

Ullmann Diaryl Ether Synthesis: Rate Acceleration by 2,2,6,6-Tetramethylheptane-3,5-dione

inferredcites →https://doi.org/10.1021/ol0264105openalex-snapshot

A General Method for the Formation of Aryl−Sulfur Bonds Using Copper(I) Catalysts

inferredcites →https://doi.org/10.1021/ol026655hopenalex-snapshot

Copper-Catalyzed Arylation of β-Amino Alcohols

inferredcites →https://doi.org/10.1021/ol0266673openalex-snapshot

A General, Efficient, and Inexpensive Catalyst System for the Coupling of Aryl Iodides and Thiols

inferredcites →https://doi.org/10.1021/ol026902hopenalex-snapshot

Highly Efficient CuI-Catalyzed Coupling of Aryl Bromides with Oxazolidinones Using Buchwald's Protocol: A Short Route to Linezolid and Toloxatone

inferredcites →https://doi.org/10.1021/ol0269190openalex-snapshot

An Efficient Copper Catalyst for the Formation of Sulfones from Sulfinic Acid Salts and Aryl Iodides

inferredcites →https://doi.org/10.1021/ol026948aopenalex-snapshot

A Mild, Nonbasic Synthesis of Thioethers. The Copper-Catalyzed Coupling of Boronic Acids with N -Thio(alkyl, aryl, heteroaryl)imides

inferredcites →https://doi.org/10.1021/ol027061hopenalex-snapshot

Copper- and Palladium-Catalyzed Intramolecular Aryl Guanidinylation: An Efficient Method for the Synthesis of 2-Aminobenzimidazoles

inferredcites →https://doi.org/10.1021/ol0273396openalex-snapshot

Mild and Efficient Copper-Catalyzed Amination of Aryl Bromides with Primary Alkylamines

inferredcites →https://doi.org/10.1021/ol034454nopenalex-snapshot

Copper(II)-Catalyzed Ether Synthesis from Aliphatic Alcohols and Potassium Organotrifluoroborate Salts

inferredcites →https://doi.org/10.1021/ol0346436openalex-snapshot

Microwave-Assisted Synthesis of Diaryl Ethers without Catalyst

inferredcites →https://doi.org/10.1021/ol0346584openalex-snapshot

Mild Method for Ullmann Coupling Reaction of Amines and Aryl Halides

inferredcites →https://doi.org/10.1021/ol0346640openalex-snapshot

Copper-Catalyzed C−P Bond Construction via Direct Coupling of Secondary Phosphines and Phosphites with Aryl and Vinyl Halides

inferredcites →https://doi.org/10.1021/ol0350947openalex-snapshot

N,N-Dimethyl Glycine-Promoted Ullmann Coupling Reaction of Phenols and Aryl Halides

inferredcites →https://doi.org/10.1021/ol035227oopenalex-snapshot

Total Synthesis of Scytophycin C. 1. Stereoselective Syntheses of the C(1)−C(18) Segment and the C(19)−C(31) Segment

inferredcites →https://doi.org/10.1021/ol035355copenalex-snapshot

Copper-Catalyzed Coupling of Amides and Carbamates with Vinyl Halides

inferredcites →https://doi.org/10.1021/op010108eopenalex-snapshot

Application of ReactArray Robotics and Design of Experiments Techniques in Optimisation of Supported Reagent Chemistry

inferredcites →https://doi.org/10.1039/a705425dopenalex-snapshot

Synthesis of New Cyclopenta-acridinone and -phenothiazine Derivatives

inferredcites →https://doi.org/10.1039/a707937kopenalex-snapshot

The importance of nitrogen substituents in chiral amino thiol ligands for the asymmetric addition of diethylzinc to aromatic aldehydes

inferredcites →https://doi.org/10.1039/a805783dopenalex-snapshot

Phosphazene P4-But base for the Ullmann biaryl ether synthesis

inferredcites →https://doi.org/10.1039/b105420copenalex-snapshot

Cyclic ureas as ortho directing substituents

inferredcites →https://doi.org/10.1039/jr9490003424openalex-snapshot

715. The synthesis of thyroxine and related substances. Part V. A synthesis of L-thyroxine from L-tyrosine

inferredcites →https://doi.org/10.1055/s-1991-26496openalex-snapshot

Synthese von Bryophyten-Inhaltsstoffen 3. Neue Synthesen der Perrottetine E, F und G

inferredcites →https://doi.org/10.1055/s-1994-25569openalex-snapshot

Synthesis of SubstitutedN-Arylpiperidines via Organobismuth Derivatives

inferredcites →https://doi.org/10.1055/s-1997-789openalex-snapshot

Palladium-Catalyzed Amination of Aryl Halides: Mechanism and Rational Catalyst Design

inferredcites →https://doi.org/10.1055/s-1998-2189openalex-snapshot

2,5-Dimethylpyrrole Protection Facilitates Copper(I)-Mediated Methoxylations of Aryl Iodides in the Presence of Anilines

inferredcites →https://doi.org/10.1055/s-2000-7600openalex-snapshot

Synthesis of Hydrazines with Aromatic Substituents Using Triarylbismuth Reagents

inferredcites →https://doi.org/10.1055/s-2001-16780openalex-snapshot

Synthesis of SB-214857 using Copper Catalysed Amination of Arylbromides with l-Aspartic Acid

inferredcites →https://doi.org/10.1055/s-2002-19782openalex-snapshot

A Mild Copper-mediated Intramolecular Amination of Aryl Halides

inferredcites →https://doi.org/10.1055/s-2002-20457openalex-snapshot

Copper-catalyzed N-Arylation of Aryl Iodides with Benzamides or Nitrogen Heterocycles in the Presence of Ethylenediamine

inferredcites →https://doi.org/10.1055/s-2003-38749openalex-snapshot

Copper-Catalyzed Synthesisof Diaryl Selenide from Aryl Iodide and Diphenyl Diselenide UsingMagnesium Metal

inferredcites →https://doi.org/10.1055/s-2003-41407openalex-snapshot

Copper-Catalyzed Cross-Coupling of Aryl Halides and Thiols Using Microwave Heating

inferredcites →https://doi.org/10.1063/1.555839openalex-snapshot

Standard Electrode Potentials and Temperature Coefficients in Water at 298.15 K

inferredcites →https://doi.org/10.1080/00397910008087300openalex-snapshot

N-Phenylation ofN-Arylaminophthalimides with Triphenylbismuth and Cupric Acetate: A Convenient Synthesis of 1-Aryl-1- Phenylhydrazines

inferredcites →https://doi.org/10.1080/00397919508015448openalex-snapshot

A Convenient Synthesis of N-Arylanthranilic Acids Using Ultrasonics in the Ullmann-Goldberg Condensation

inferredcites →https://doi.org/10.1080/00397919708004076openalex-snapshot

Use of Organobismuth Derivatives for Arylation of Piperazines

inferredcites →https://doi.org/10.1081/scc-100105338openalex-snapshot

SYNTHESIS OF DIARYL ETHERS USING AN EASY-TO-PREPARE, AIR-STABLE, SOLUBLE COPPER(I) CATALYST

inferredcites →https://doi.org/10.1081/scc-120002702openalex-snapshot

HYPERVALENT IODINE IN SYNTHESIS. 77. AN EFFICIENT METHOD FOR THE SYNTHESIS OF N-ARYLINDOLES BY THE COPPER-CATALYZED N-ARYLATION OF INDOLE WITH DIARYLIODONIUM SALTS

inferredcites →https://doi.org/10.1081/scc-120016350openalex-snapshot

The Use of Ultrasound in the Synthesis of 2-Carboxy Substituted Diphenylethers Using Water as Solvent

inferredcites →https://doi.org/10.1139/v98-230openalex-snapshot

A versatile synthetic route to 1,5-dithiocins from o-mercapto aromatic aldehydes

inferredcites →https://doi.org/10.1248/cpb.31.1424openalex-snapshot

Studies on the antitumor cyclic hexapeptides obtained from Rubiae radix.

inferredcites →https://doi.org/10.1248/cpb.46.1274openalex-snapshot

Selective Muscarinic Antagonists. I. Synthesis and Antimuscarinic Properties of 4-Piperidyl Benzhydrylcarbamate Derivatives.

inferredcites →https://doi.org/10.1351/pac198759080937openalex-snapshot

Bismuth(V) reagents in organic synthesis

inferredcites →https://doi.org/10.1351/pac199971081417openalex-snapshot

Approaches to catalyst discovery. New carbon–heteroatom and carbon–carbon bond formation

inferredcites →https://doi.org/10.2174/1385272023374058openalex-snapshot

Recent Advances in Ullmann Reaction:Copper ( II ) Diacetate C at alysed N - ,O - and S - ArylationInvolving Polycoordinate Hetero atomic Derivatives

inferredcites →https://doi.org/10.3987/com-00-9013openalex-snapshot

Synthesis of New N-Alkyl- and N-Acyldioxinophenothiazine and Acridinone Derivatives

inferredcites →https://doi.org/10.3987/com-94-6963openalex-snapshot

Synthesis of Substituted Pyrazolo[3,4-b]- and Pyrazolo[4,3-c]phenothiazine Derivatives

inferredcites →https://doi.org/10.3987/com-98-s21openalex-snapshot

Synthesis and Cytotoxicity of Various Structural Types of Novel Cyclopropapyrroloindole(CPI) Derivatives

What points at this work

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

inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113264zenodo-depositor-declared

Undescribed diphenyl ethers betaethrins A-I from a desert plant endophytic strain of the fungus Phoma betae A.B. Frank (Didymellaceae)

inferred← citeshttps://doi.org/10.1002/047084289x.rc192.pub2openalex-snapshot

Copper

inferred← citeshttps://doi.org/10.1002/047084289x.rc229openalex-snapshot

Copper(I) Iodide

inferred← citeshttps://doi.org/10.1002/047084289x.rc229.pub2openalex-snapshot

Copper(I) Iodide

inferred← citeshttps://doi.org/10.1002/047084289x.rc251openalex-snapshot

Copper(I) Trifluoromethanesulfonate

inferred← citeshttps://doi.org/10.1002/047084289x.rc251.pub2openalex-snapshot

Copper(I) Trifluoromethanesulfonate

inferred← citeshttps://doi.org/10.1002/047084289x.ri079.pub2openalex-snapshot

Isopropenyllithium

inferred← citeshttps://doi.org/10.1002/047084289x.ri079.pub3openalex-snapshot

Isopropenyllithium

inferred← citeshttps://doi.org/10.1002/0471264180.or085.01openalex-snapshot

Copper‐Catalyzed Amination of Aryl and Alkenyl Electrophiles

inferred← citeshttps://doi.org/10.1002/0471264229.os083.05openalex-snapshot

Copper‐Catalyzed Electrophilic Amination of Diorganozinc Reagents: 4‐Phenylmorpholine

inferred← citeshttps://doi.org/10.1002/0471264229.os085.22openalex-snapshot

Synthesis of Aminoarenethiolato‐Copper(I) Complexes

inferred← citeshttps://doi.org/10.1002/0471264229.os088.35openalex-snapshot

An IntramolecularAmination of Aryl Halides with a Combination of Copper (I) Iodide and Cesium Acetate: Preparation of 5,6‐Dimethoxyindole‐1,2‐Dicarboxylic Acid 1‐Benzyl Ester 2‐Methyl Ester

inferred← citeshttps://doi.org/10.1002/9780470638859.conrr350openalex-snapshot

Jourdan‐Ullmann Reaction

inferred← citeshttps://doi.org/10.1002/9780470682531.pat0437openalex-snapshot

NMR of Organocopper Compounds

inferred← citeshttps://doi.org/10.1002/9781118092828.ch3openalex-snapshot

Indoles

inferred← citeshttps://doi.org/10.1002/9781118094365.ch11openalex-snapshot

Organic Synthetic Methods Using Copper Oxygen Chemistry

inferred← citeshttps://doi.org/10.1002/9781118299715.ch10openalex-snapshot

Phosphaalkenes

inferred← citeshttps://doi.org/10.1002/9781118309872.ch1openalex-snapshot

Transition Metal Catalysis in the Pharmaceutical Industry

inferred← citeshttps://doi.org/10.1002/9781118309872.ch2openalex-snapshot

Selected Applications of Transition Metal‐Catalyzed Carbon–Carbon Cross‐Coupling Reactions in the Pharmaceutical Industry

inferred← citeshttps://doi.org/10.1002/9781118309872.ch3openalex-snapshot

Selected Applications of Pd‐ and Cu‐Catalyzed Carbon–Heteroatom Cross‐Coupling Reactions in the Pharmaceutical Industry

inferred← citeshttps://doi.org/10.1002/9781118342886.ch3openalex-snapshot

Metal‐Catalyzed C–Heteroatom Cross‐Coupling Reactions

inferred← citeshttps://doi.org/10.1002/9781118690659.ch1openalex-snapshot

Modern Ullmann–Goldberg Chemistry: Arylation of N‐Nucleophiles with Aryl Halides

inferred← citeshttps://doi.org/10.1002/9781118690659.ch10openalex-snapshot

Copper‐Mediated Aryl–Aryl Bond Formation Leading to Biaryls: A Century after the Ullmann Breakthrough

inferred← citeshttps://doi.org/10.1002/9781118690659.ch12openalex-snapshot

Copper‐Catalyzed Alkynylation and Alkenylation Reactions of Alkynyl Derivatives: New Access to Diynes and Enynes

inferred← citeshttps://doi.org/10.1002/9781118690659.ch15openalex-snapshot

Copper‐Mediated Cyclization Reactions: New Entries to Heterocycles

inferred← citeshttps://doi.org/10.1002/9781118690659.ch2openalex-snapshot

Ullmann Condensation Today: Arylation of Alcohols and Thiols with Aryl Halides

inferred← citeshttps://doi.org/10.1002/9781118690659.ch20openalex-snapshot

Reusable Catalysts for Copper‐Mediated Cross‐Coupling Reactions under Heterogeneous Conditions

inferred← citeshttps://doi.org/10.1002/9781118690659.ch4openalex-snapshot

Alternative and Emerging Reagents for the Arylation of Heteronucleophiles

inferred← citeshttps://doi.org/10.1002/9781118690659.ch6openalex-snapshot

Aromatic/Vinylic Finkelstein Reaction

inferred← citeshttps://doi.org/10.1002/9781118690659.ch7openalex-snapshot

Insights into the Mechanism of Modern Ullmann–Goldberg Coupling Reactions

inferred← citeshttps://doi.org/10.1002/9781118690659.ch8openalex-snapshot

Modern Copper‐Catalyzed Hurtley Reaction: Efficient C‐Arylation of CH‐Acid Derivatives

inferred← citeshttps://doi.org/10.1002/9781118754887.ch20openalex-snapshot

Transition Metal‐Mediated Carbon–Heteroatom Cross‐Coupling (C—N, C—O, C—S, C—Se, C—Te, C—P, C—As, C—Sb, and C—B Bond Forming Reactions)

inferred← citeshttps://doi.org/10.1002/9781118754887.ch6openalex-snapshot

Nucleophilic Aromatic Substitution

inferred← citeshttps://doi.org/10.1002/9781118788981.ch1openalex-snapshot

Catalysis In C–Cl Activation

inferred← citeshttps://doi.org/10.1002/9781118909911.ch17openalex-snapshot

Reaction of Iodo Compounds

inferred← citeshttps://doi.org/10.1002/9781119015789.ch1openalex-snapshot

Introduction to Practical Functional Group Synthesis

inferred← citeshttps://doi.org/10.1002/9781119015789.ch2openalex-snapshot

Preparation of Alcohols, Ethers, and Related Compounds

inferred← citeshttps://doi.org/10.1002/9781119015789.ch5openalex-snapshot

Synthesis of Thioethers, Sulfones, and Related Compounds

inferred← citeshttps://doi.org/10.1002/9781119304197.ch13openalex-snapshot

Oxidative Couplings with C─H Bonds Forming C─P and C─S Bonds

inferred← citeshttps://doi.org/10.1002/9781119304197.ch3openalex-snapshot

Green Oxidative Synthesis of Ethers, Esters, and Organic Halides

inferred← citeshttps://doi.org/10.1002/9781119942863.ch2openalex-snapshot

Coupling Reactions

inferred← citeshttps://doi.org/10.1002/9783527619467.ch3openalex-snapshot

Functionalized Organoborane Derivatives in Organic Synthesis

inferred← citeshttps://doi.org/10.1002/9783527619467.ch4openalex-snapshot

Polyfunctional Magnesium Organometallics for Organic Synthesis

inferred← citeshttps://doi.org/10.1002/9783527627325.ch4openalex-snapshot

Copper‐Catalyzed Arylations of Amines and Alcohols with Boron‐Based Arylating Reagents

inferred← citeshttps://doi.org/10.1002/9783527628698.hgc004openalex-snapshot

Microwave‐Accelerated Homogeneous Catalysis in Water

inferred← citeshttps://doi.org/10.1002/9783527630516.ch2openalex-snapshot

The Bioinorganic and Organometallic Chemistry of Copper(III)

inferred← citeshttps://doi.org/10.1002/9783527631582.ch9openalex-snapshot

Copper‐Catalyzed Ligand Promoted Ullmann‐Type Coupling Reactions

inferred← citeshttps://doi.org/10.1002/9783527633388.ch8openalex-snapshot

Transition Metal‐Catalyzed Synthesis of Monocyclic Five‐Membered Aromatic Heterocycles

inferred← citeshttps://doi.org/10.1002/9783527633388.ch9openalex-snapshot

Transition Metal‐Catalyzed Synthesis of Fused Five‐Membered Aromatic Heterocycles

inferred← citeshttps://doi.org/10.1002/9783527635993.ch9openalex-snapshot

Metal‐Catalyzed Cross‐Coupling Reactions

inferred← citeshttps://doi.org/10.1002/9783527639328.ch6openalex-snapshot

Recent Advances in Chan–Lam Coupling Reaction: Copper‐Promoted C–Heteroatom Bond Cross‐Coupling Reactions with Boronic Acids and Derivatives

inferred← citeshttps://doi.org/10.1002/9783527639328.ch7openalex-snapshot

Transition Metal‐Catalyzed Desulfitative Coupling of Thioorganic Compounds with Boronic Acids

inferred← citeshttps://doi.org/10.1002/9783527646586.ch10openalex-snapshot

Copper Catalysis in Arene and Heteroarene Functionalization through C–H Bond Activation

inferred← citeshttps://doi.org/10.1002/9783527651733.ch6openalex-snapshot

Cross Coupling Reactions

inferred← citeshttps://doi.org/10.1002/9783527655588.ch1openalex-snapshot

Mechanistic Aspects of Metal‐Catalyzed C,C‐ and C,X‐Bond Forming Reactions

inferred← citeshttps://doi.org/10.1002/9783527655588.ch13openalex-snapshot

Palladium‐Catalyzed Aromatic Carbon–Nitrogen Bond Formation

inferred← citeshttps://doi.org/10.1002/9783527658909.ch01openalex-snapshot

Copper‐Catalyzed Coupling for a Green Process

inferred← citeshttps://doi.org/10.1002/9783527658909.ch10openalex-snapshot

Copper‐Catalyzed CN Coupling on Large Scale: An Industrial Case Study

inferred← citeshttps://doi.org/10.1002/9783527672707.ch2openalex-snapshot

Amine, Phenol, Alcohol, and Thiol Arylation

inferred← citeshttps://doi.org/10.1002/9783527673223.ch11openalex-snapshot

Halide Exchange Reactions Mediated by Transition Metals

inferred← citeshttps://doi.org/10.1002/9783527680986.ch4openalex-snapshot

Bonding Including Heteroatoms via Oxidative Coupling

inferred← citeshttps://doi.org/10.1002/9783527805624.ch10openalex-snapshot

Alcohol as a Reagent in Homogeneous Catalysis

inferred← citeshttps://doi.org/10.1002/9783527809080.cataz01327openalex-snapshot

Avendano‐modified Ullmann reaction

inferred← citeshttps://doi.org/10.1002/9783527809080.cataz01492openalex-snapshot

Barton‐modified Ullmann reaction

inferred← citeshttps://doi.org/10.1002/9783527809080.cataz01571openalex-snapshot

Batey‐modified Ullmann reaction

inferred← citeshttps://doi.org/10.1002/9783527809080.cataz01767openalex-snapshot

Beringer‐Kang reaction

inferred← citeshttps://doi.org/10.1002/9783527809080.cataz03405openalex-snapshot

Chan‐Evans‐Lam‐modified Ullmann reaction

inferred← citeshttps://doi.org/10.1002/9783527809080.cataz07458openalex-snapshot

Goldberg (modified Ullmann) reaction

inferred← citeshttps://doi.org/10.1002/9783527809080.cataz09616openalex-snapshot

Lam‐modified Ullmann reactions

inferred← citeshttps://doi.org/10.1002/9783527826186.ch10openalex-snapshot

Recent Advances in the Synthesis of Arylamines in the Light of Application in Pharmaceutical and Chemical Industry

inferred← citeshttps://doi.org/10.1002/9783527826445.ch20openalex-snapshot

Application of Cu ‐Mediated Reactions in the Synthesis of Natural Products

inferred← citeshttps://doi.org/10.1002/9783527826445.ch7openalex-snapshot

Microwave‐Assisted Cu ‐Catalyzed Organic Reactions

inferred← citeshttps://doi.org/10.1002/9783527834242.chf0057openalex-snapshot

Copper‐Catalyzed sp 3 CH Bond Functionalization

inferred← citeshttps://doi.org/10.1002/adsc.200404011openalex-snapshot

Highly Selective Copper‐Catalyzed Monoarylation of Aniline

inferred← citeshttps://doi.org/10.1002/adsc.200404182openalex-snapshot

A Domino Copper‐Catalyzed CN and CO Cross‐Coupling for the Conversion of Primary Amides into Benzoxazoles

inferred← citeshttps://doi.org/10.1002/adsc.200404279openalex-snapshot

A General Copper‐Promoted Coupling of Sulfoximines with Vinyl Bromides

inferred← citeshttps://doi.org/10.1002/adsc.200505158openalex-snapshot

Industrial‐Scale Palladium‐Catalyzed Coupling of Aryl Halides and Amines –A Personal Account

inferred← citeshttps://doi.org/10.1002/adsc.200505207openalex-snapshot

Alkyl‐ and Arylthiolation of Aryl Halides Catalyzed by Fluorinated Bis‐Imino‐Nickel NNN Pincer Complexes [NiCl2{C5H3N‐2,6‐(CHNArf)2}]

inferred← citeshttps://doi.org/10.1002/adsc.200505385openalex-snapshot

Mild Conditions for Copper‐Catalyzed Coupling Reaction of Phenols and Aryl Iodides and Bromides

inferred← citeshttps://doi.org/10.1002/adsc.200600566openalex-snapshot

Desulfitative Carbon–Carbon Cross‐Coupling of Thioamide Fragments with Boronic Acids

inferred← citeshttps://doi.org/10.1002/adsc.200600628openalex-snapshot

Nitrogen Ligands in Copper‐Catalyzed Arylation of Phenols: Structure/Activity Relationships and Applications

inferred← citeshttps://doi.org/10.1002/adsc.200606198openalex-snapshot

An Inexpensive and Efficient Copper Catalyst for N‐Arylation of Amines, Amides and Nitrogen‐Containing Heterocycles

inferred← citeshttps://doi.org/10.1002/adsc.200700133openalex-snapshot

Applicability Aspects of Transition Metal‐Catalyzed Aromatic Amination Protocols in Medicinal Chemistry

inferred← citeshttps://doi.org/10.1002/adsc.200700408openalex-snapshot

Ligand‐Free Copper‐Catalyzed N‐Arylation of Nitrogen Nucleophiles

inferred← citeshttps://doi.org/10.1002/adsc.200700480openalex-snapshot

Cadmium(II)‐Catalyzed CN Cross‐Coupling of Amines with Aryl Iodides

inferred← citeshttps://doi.org/10.1002/adsc.200700508openalex-snapshot

Iron‐Catalyzed CN Cross‐Coupling of Sulfoximines with Aryl Iodides

inferred← citeshttps://doi.org/10.1002/adsc.200700535openalex-snapshot

Highly Practical “Ligand‐Free‐Like” Copper‐Catalyzed N‐Arylation of Azoles in Lower Nitrile Solvents

inferred← citeshttps://doi.org/10.1002/adsc.200800291openalex-snapshot

Copper‐Catalyzed Cycloaddition of Sulfonyl Azides with Alkynes to Synthesize N‐Sulfonyltriazoles ‘on Water’ at Room Temperature

inferred← citeshttps://doi.org/10.1002/adsc.200800360openalex-snapshot

Efficient and Versatile Sol‐Gel Immobilized Copper Catalyst for Ullmann Arylation of Phenols

inferred← citeshttps://doi.org/10.1002/adsc.200800417openalex-snapshot

Evaluation of Aromatic Amination Catalyzed by Palladium on Carbon: A Practical Synthesis of Triarylamines

inferred← citeshttps://doi.org/10.1002/adsc.200800517openalex-snapshot

Ligand‐Free Iron/Copper Cocatalyzed Alkynylation Coupling Reactions

inferred← citeshttps://doi.org/10.1002/adsc.200800730openalex-snapshot

Copper‐Catalyzed N ‐Arylation of Hindered Substrates Under Mild Conditions

inferred← citeshttps://doi.org/10.1002/adsc.200800746openalex-snapshot

Efficient Cross‐Coupling Reactions of Nitrogen Nucleophiles with Aryl Halides in Water

inferred← citeshttps://doi.org/10.1002/adsc.200800757openalex-snapshot

Copper‐Catalyzed Preparation of γ‐Alkylidenebutenolides and Isocoumarins under Mild Palladium‐Free Conditions

inferred← citeshttps://doi.org/10.1002/adsc.200900004openalex-snapshot

Copper‐Catalyzed N‐Arylation/Hydroamin(d)ation Domino Synthesis of Indoles and its Application to the Preparation of a Chek1/KDR Kinase Inhibitor Pharmacophore

inferred← citeshttps://doi.org/10.1002/adsc.200900059openalex-snapshot

Transition Metal‐Catalysed, Direct and Site‐Selective N1‐, C2‐ or C3‐Arylation of the Indole Nucleus: 20 Years of Improvements

inferred← citeshttps://doi.org/10.1002/adsc.200900065openalex-snapshot

Efficient Copper‐Catalyzed Synthesis of N‐Alkylanthranilic Acids via an ortho‐Substituent Effect of the Carboxyl Group of 2‐Halobenzoic Acids at Room Temperature

inferred← citeshttps://doi.org/10.1002/adsc.200900095openalex-snapshot

Iron‐Catalyzed Ligand‐Free Carbon‐Selenium (or Tellurium) Coupling of Arylboronic Acids with Diselenides and Ditellurides

inferred← citeshttps://doi.org/10.1002/adsc.200900101openalex-snapshot

Copper‐Catalyzed Synthesis of 1,2,4‐Benzothiadiazine 1,1‐Dioxide Derivatives by Coupling of 2‐Halobenzenesulfonamides with Amidines

inferred← citeshttps://doi.org/10.1002/adsc.200900327openalex-snapshot

An Efficient Copper‐Catalyzed Amination of Aryl Halides by Aqueous Ammonia

inferred← citeshttps://doi.org/10.1002/adsc.200900438openalex-snapshot

First Copper‐Catalyzed Intramolecular Amidation in Substituted 4‐Iodopyrazoles Leading to the Synthesis of Pyrazolo[4,3‐b]‐ pyridin‐5‐ones

inferred← citeshttps://doi.org/10.1002/adsc.200900450openalex-snapshot

Iron‐Catalyzed Tandem Reactions of 2‐Halobenzenamines with Isothiocyanates Leading to 2‐Aminobenzothiazoles

inferred← citeshttps://doi.org/10.1002/adsc.200900481openalex-snapshot

Nano‐Iron Oxide as a Recyclable Catalyst for Intramolecular CN Cross‐Coupling Reactions under Ligand‐Free Conditions: One‐Pot Synthesis of 1,4‐Dihydroquinoline Derivatives

inferred← citeshttps://doi.org/10.1002/adsc.200900501openalex-snapshot

Palladium on Charcoal as a Recyclable Catalyst for CS Cross‐Coupling of Thiols with Aryl Halides under Ligand‐Free Conditions

inferred← citeshttps://doi.org/10.1002/adsc.200900775openalex-snapshot

Copper‐Catalyzed Highly Regioselective Oxidative CH Bond Amidation of 2‐Arylpyridine Derivatives and 1‐Methylindoles

inferred← citeshttps://doi.org/10.1002/adsc.200900836openalex-snapshot

The First General and Selective Palladium(II)‐Catalyzed Alkoxycarbonylation of Arylboronates: Interplay among Benzoquinone‐Ligated Palladium(0) Complex, Organoboron, and Alcohol Solvent

inferred← citeshttps://doi.org/10.1002/adsc.200900887openalex-snapshot

A Simple Copper‐Catalyzed Cascade Synthesis of 2‐Amino‐1H‐indole‐3‐carboxylate Derivatives

inferred← citeshttps://doi.org/10.1002/adsc.201000144openalex-snapshot

Regioselective Functionalization of the Imidazole Ring via Transition Metal‐Catalyzed CN and CC Bond Forming Reactions

inferred← citeshttps://doi.org/10.1002/adsc.201000383openalex-snapshot

Copper(I)‐Catalyzed Cascade Synthesis of 2‐Arylsulfanyl‐ arylcyanamides

inferred← citeshttps://doi.org/10.1002/adsc.201000465openalex-snapshot

One‐Pot Synthesis of Triazolothiadiazepine 1,1‐Dioxide Derivatives via Copper‐Catalyzed Tandem [3+2] Cycloaddition/N‐Arylation

inferred← citeshttps://doi.org/10.1002/adsc.201000575openalex-snapshot

Dimethyl Sulfoxide/Potassium Hydroxide: A Superbase for the Transition Metal‐Free Preparation of Cross‐Coupling Products

inferred← citeshttps://doi.org/10.1002/adsc.201000708openalex-snapshot

Ligand‐Free Copper‐Catalyzed Amination of Heteroaryl Halides with Alkyl‐ and Arylamines

inferred← citeshttps://doi.org/10.1002/adsc.201000723openalex-snapshot

Base‐Mediated Direct Arylation of Pyrrole Derivatives

inferred← citeshttps://doi.org/10.1002/adsc.201000800openalex-snapshot

Palladium‐ and Copper‐Catalyzed Site Selective Monoamination of Dibromobenzoic Acid

inferred← citeshttps://doi.org/10.1002/adsc.201000905openalex-snapshot

Commentary on “A New, Efficient and Recyclable Lanthanum(III) Oxide‐Catalyzed CN Cross‐Coupling” by S. Narayana Murthy, B. Madhav, V. Prakash Reddy, and Y. V. D. Nageswar, Adv. Synth. Catal. 2010, 352, 3241–3245

inferred← citeshttps://doi.org/10.1002/adsc.201000977openalex-snapshot

Fe3O4@mesoporouspolyaniline: A Highly Efficient and Magnetically Separable Catalyst for Cross‐Coupling of Aryl Chlorides and Phenols

inferred← citeshttps://doi.org/10.1002/adsc.201100153openalex-snapshot

Copper‐Catalyzed Coupling of Arylboronic Acids with Potassium Cyanate: A New Approach to the Synthesis of Aryl Carbamates

inferred← citeshttps://doi.org/10.1002/adsc.201100580openalex-snapshot

Copper‐Catalyzed Domino Synthesis of Benzimidazo[2,1‐b]quin‐ azolin‐12(6H)‐ones Using Cyanamide as a Building Block

inferred← citeshttps://doi.org/10.1002/adsc.201100788openalex-snapshot

A Highly Efficient Palladium‐Catalyzed One‐Pot Synthesis of Unsymmetrical Aryl Alkyl Thioethers under Mild Conditions in Water

inferred← citeshttps://doi.org/10.1002/adsc.201100808openalex-snapshot

Copper‐Catalyzed Ultrasound‐Expedited N‐Arylation of Sulfoximines using Diaryliodonium Salts

inferred← citeshttps://doi.org/10.1002/adsc.201100892openalex-snapshot

Multiple Oxidative Dehydrogenative Functionalization of Arylacetaldehydes Using Molecular Oxygen as Oxidant Leading to 2‐Oxo‐acetamidines

inferred← citeshttps://doi.org/10.1002/adsc.201100925openalex-snapshot

Copper‐Catalyzed Coupling of (E)‐Bromostilbene with Phenols/Azole: ESI‐MS Detection of Intermediates by Using an Ionically‐Tagged Ligand

inferred← citeshttps://doi.org/10.1002/adsc.201100946openalex-snapshot

Copper‐Catalyzed Aerobic Oxidative Synthesis of 5‐Substituted Imidazo/Benzimidazoquinazolinones through Intramolecular CH Amination

inferred← citeshttps://doi.org/10.1002/adsc.201100951openalex-snapshot

Copper‐Catalyzed Domino Synthesis of Isoquinolino[2,3‐a]quinazolinones

inferred← citeshttps://doi.org/10.1002/adsc.201200296openalex-snapshot

Synthesis of Aryl Carbamates via Copper‐Catalyzed Coupling of Aryl Halides with Potassium Cyanate

inferred← citeshttps://doi.org/10.1002/adsc.201200408openalex-snapshot

Desulfurization Strategy in the Construction of Azoles Possessing Additional Nitrogen, Oxygen or Sulfur using a Copper(I) Catalyst

inferred← citeshttps://doi.org/10.1002/adsc.201200430openalex-snapshot

Cesium Carbonate‐Promoted Hydroamidation of Alkynes: Enamides, Indoles and the Effect of Iron(III) Chloride

inferred← citeshttps://doi.org/10.1002/adsc.201200547openalex-snapshot

Zinc‐Catalyzed Organic Synthesis: CC, CN, CO Bond Formation Reactions

inferred← citeshttps://doi.org/10.1002/adsc.201200574openalex-snapshot

General, Green, and Scalable Synthesis of Imines from Alcohols and Amines by a Mild and Efficient Copper‐Catalyzed Aerobic Oxidative Reaction in Open Air at Room Temperature

inferred← citeshttps://doi.org/10.1002/adsc.201200600openalex-snapshot

An Ullmann CO Coupling Reaction Catalyzed by Magnetic Copper Ferrite Nanoparticles

inferred← citeshttps://doi.org/10.1002/adsc.201200752openalex-snapshot

Synthesis of Chiral Amino Acid Anilides by Ligand‐Free Copper‐Catalyzed Selective N‐Arylation of Amino Acid Amides

inferred← citeshttps://doi.org/10.1002/adsc.201200784openalex-snapshot

Copper‐Catalyzed Tandem CC/CO Bond‐Forming Reactions of ortho‐Halo‐β‐chlorostyrenes with Ketones: Synthesis of 4‐Trifluoromethylbenzoxepines

inferred← citeshttps://doi.org/10.1002/adsc.201200944openalex-snapshot

Cooperative Catalysis with Aldehydes and Copper: Development and Application in Aerobic Oxidative CH Amination at Room Temperature

inferred← citeshttps://doi.org/10.1002/adsc.201201022openalex-snapshot

Copper‐Catalyzed C‐Arylation and Denitrogenation of Tetrazoles: Domino Synthesis of 1,3‐Diaminoisoquinoline Derivatives

inferred← citeshttps://doi.org/10.1002/adsc.201300044openalex-snapshot

Copper‐Catalyzed Selective Oxidative Acylation of Secondary Anilines with Ethyl Glyoxalate: Domino Synthesis of Indoline‐2,3‐diones

inferred← citeshttps://doi.org/10.1002/adsc.201300157openalex-snapshot

Copper‐Catalyzed Intermolecular Oxidative Cyclization of Halo‐ alkynes: Synthesis of 2‐Halo‐substituted Imidazo[1,2‐a]pyridines, Imidazo[1,2‐a]pyrazines and Imidazo[1,2‐a]pyrimidines

inferred← citeshttps://doi.org/10.1002/adsc.201300261openalex-snapshot

Magnetically Separable CuFe2O4 Nanoparticles Catalyzed Ligand‐Free CS Coupling in Water: Access to (E)‐ and (Z)‐Styrenyl‐, Heteroaryl and Sterically Hindered Aryl Sulfides

inferred← citeshttps://doi.org/10.1002/adsc.201300271openalex-snapshot

Synthesis of Carbazoles via One‐Pot Copper‐Catalyzed Amine Insertion into Cyclic Diphenyleneiodoniums as a Strategy to Generate a Drug‐Like Chemical Library

inferred← citeshttps://doi.org/10.1002/adsc.201300372openalex-snapshot

Synthesis of Functionalized Naphthalenes by Copper(I)‐Catalyzed Annulation between 3‐(2‐Halobenzyl)pentane‐2,4‐diones and β‐Keto Esters, Malonates and Cyanoacetates

inferred← citeshttps://doi.org/10.1002/adsc.201300416openalex-snapshot

Copper Oxide Nanoparticles Supported on Graphene Oxide‐ Catalyzed S‐Arylation: An Efficient and Ligand‐Free Synthesis of Aryl Sulfides

inferred← citeshttps://doi.org/10.1002/adsc.201300456openalex-snapshot

Copper(I) Iodide‐Catalysed Aerobic Oxidative Synthesis of Imidazo[1,2‐a]pyridines from 2‐Aminopyridines and Methyl Ketones

inferred← citeshttps://doi.org/10.1002/adsc.201300475openalex-snapshot

Copper‐Catalyzed Domino Synthesis of 4‐Oxopyrimido[1,2‐a]indole Derivatives

inferred← citeshttps://doi.org/10.1002/adsc.201300485openalex-snapshot

Nickel‐Catalyzed Coupling of Fluoroarenes and Amines

inferred← citeshttps://doi.org/10.1002/adsc.201300503openalex-snapshot

Copper‐Catalyzed Synthesis of α‐Naphthols from Enol Esters

inferred← citeshttps://doi.org/10.1002/adsc.201300728openalex-snapshot

Concise Synthesis of 1‐Naphthols under Mild Conditions through a Copper‐Catalyzed Arylation of Methyl Ketones

inferred← citeshttps://doi.org/10.1002/adsc.201300815openalex-snapshot

Iodine‐Catalyzed Intramolecular Oxidative Thiolation of Vinylic Carbon‐Hydrogen Bonds via Tandem Iodocyclization and Dehydroiodination: Construction of 2‐Methylene‐3‐thiophenones

inferred← citeshttps://doi.org/10.1002/adsc.201300900openalex-snapshot

Copper(II)‐Catalyzed Aerobic Oxidative Coupling between Chalcone and 2‐Aminopyridine via CH Amination: An Expedient Synthesis of 3‐Aroylimidazo[1,2‐a]pyridines

inferred← citeshttps://doi.org/10.1002/adsc.201301001openalex-snapshot

Copper‐Catalyzed Decarboxylative CN Triple Bond Formation: Direct Synthesis of Benzonitriles from Phenylacetic Acids Under O2 Atmosphere

inferred← citeshttps://doi.org/10.1002/adsc.201400017openalex-snapshot

Catalytic Isonitrile Insertions and Condensations Initiated by RNC–X Complexation

inferred← citeshttps://doi.org/10.1002/adsc.201400032openalex-snapshot

Metal‐Free Preparation of Cycloalkyl Aryl Sulfides via Di‐ tert ‐butyl Peroxide‐Promoted Oxidative C( sp 3 )H Bond Thiolation of Cycloalkanes

inferred← citeshttps://doi.org/10.1002/adsc.201400203openalex-snapshot

Recent Advances in Catalytic Functionalization of N ‐Oxide Compounds via CH Bond Activation

inferred← citeshttps://doi.org/10.1002/adsc.201400306openalex-snapshot

Palladium‐Catalyzed Intramolecular Oxidative CH Sulfuration of Aryl Thiocarbamates

inferred← citeshttps://doi.org/10.1002/adsc.201400376openalex-snapshot

Exploring the in situ Utilization of Cyclic Imine Intermediates Generated by Isocyanoacetate Cycloaddition: Convergent Assembly of cis‐3a,8a‐Hexahydropyrrolo[2,3‐b]indole Scaffolds

inferred← citeshttps://doi.org/10.1002/adsc.201400659openalex-snapshot

Copper‐Catalyzed Cross Dehydrogenative Coupling of N,N‐Disubstituted Formamides and Phenols: A Direct Access to Carbamates

inferred← citeshttps://doi.org/10.1002/adsc.201400881openalex-snapshot

Synthesis of Free NH 2‐(Aminomethyl)indoles through Copper‐Catalyzed Reaction of 3‐(ortho‐Trifluoroacetamidophenyl)‐1‐propargylic Alcohols with Amines and Palladium/Copper‐ Cocatalyzed Domino Three‐Component Sonogashira Cross‐Coupling/Cyclization/Substitution Reactions

inferred← citeshttps://doi.org/10.1002/adsc.201400929openalex-snapshot

Arylthiolation of Arylamine Derivatives with (Arylthio)‐ pyrrolidine‐2,5‐diones

inferred← citeshttps://doi.org/10.1002/adsc.201400980openalex-snapshot

Chemo‐Controlled Cross‐Coupling of Di(hetero)aryl Disulfides with Grignard Reagents: CC vs. CS Bond Formation

inferred← citeshttps://doi.org/10.1002/adsc.201500457openalex-snapshot

Nickel–Copper‐Catalyzed C(sp2)N Cross‐Coupling of Cyclic and Bridged Amides: An Access to Cyclic Enamides and Alkenyl Vince Lactams

inferred← citeshttps://doi.org/10.1002/adsc.201500538openalex-snapshot

Assembly of Enantioenriched cis‐3a,8a‐Hexahydropyrrolo[2,3‐b]indole Scaffolds by Silver(I)‐Catalyzed Asymmetric Domino Reaction of Isocyanoacetates in the Presence of Cinchona‐Derived Chiral Phosphorus Ligands

inferred← citeshttps://doi.org/10.1002/adsc.201500577openalex-snapshot

Copper‐Catalyzed Domino Synthesis of Benzo[4,5]imidazo[1,2‐a]pyrimidin‐4(10H)‐ones using Cyanamide as a Building Block

inferred← citeshttps://doi.org/10.1002/adsc.201501099openalex-snapshot

Oxidative Coupling of Enamines and Disulfides via Tetrabutylammonium Iodide/ tert‐ Butyl Hydroperoxide‐Mediated Intermolecular Oxidative C( sp 2 )S Bond Formation Under Transition Metal‐Free Conditions

inferred← citeshttps://doi.org/10.1002/adsc.201600316openalex-snapshot

Simple N‐Heterocyclic Carbenes as Ligands in Ullmann‐Type Ether and Thioether Formations

inferred← citeshttps://doi.org/10.1002/adsc.201600405openalex-snapshot

N‐Benzyldithiocarbamate Salts as Sulfur Sources to Access Tricyclic Thioheterocycles Mediated by Copper Species

inferred← citeshttps://doi.org/10.1002/adsc.201600642openalex-snapshot

Copper‐Catalyzed Three‐Component One‐Pot Synthesis of Aryl Sulfides with Sulfur Powder under Aqueous Conditions

inferred← citeshttps://doi.org/10.1002/adsc.201600656openalex-snapshot

Indium‐Catalyzed Formal N‐Arylation and N‐Alkylation of Pyrroles with Amines

inferred← citeshttps://doi.org/10.1002/adsc.201600775openalex-snapshot

Copper‐Mediated Tandem C( sp 2 )–H Sulfenylation and Annulation of Arenes with 2‐Mercaptoimidazoles: Regio‐ and Site‐selective Access to Polycyclic Fused Imidazo[2,1‐ b ][1,3]thiazinones

inferred← citeshttps://doi.org/10.1002/adsc.201700004openalex-snapshot

Hypervalent Iodine‐Promoted Aromatization of Exocyclic β‐Enaminones for the Synthesis of meta‐N,N‐Diarylaminophenols

inferred← citeshttps://doi.org/10.1002/adsc.201700026openalex-snapshot

Copper(I) Oxide/N,N′‐Bis[(2‐furyl)methyl]oxalamide‐Catalyzed Coupling of (Hetero)aryl Halides and Nitrogen Heterocycles at Low Catalytic Loading

inferred← citeshttps://doi.org/10.1002/adsc.201700234openalex-snapshot

Copper‐Catalyzed One‐pot Synthesis of Pyrimidines from Amides, N,N′‐dimethylformamide dimethylacetal, and Enamines

inferred← citeshttps://doi.org/10.1002/adsc.201700535openalex-snapshot

Making Copper(0) Nanoparticles in Glycerol: A Straightforward Synthesis for a Multipurpose Catalyst

inferred← citeshttps://doi.org/10.1002/adsc.201700785openalex-snapshot

Iridium(III)‐Catalyzed Selective and Mild C‐H Amidation of Cyclic N‐Sulfonyl Ketimines with Organic Azides

inferred← citeshttps://doi.org/10.1002/adsc.201700949openalex-snapshot

Copper‐Mediated Thiolation of Unactivated Heteroaryl C−H Bonds with Disulfides under Ligand‐ and Metal‐Oxidant‐Free Conditions

inferred← citeshttps://doi.org/10.1002/adsc.201701144openalex-snapshot

Direct ortho‐Acyloxylation of Arenes and Alkenes by Cobalt Catalysis

inferred← citeshttps://doi.org/10.1002/adsc.201701640openalex-snapshot

A Tunable Route to Prepare α,β‐Unsaturated Esters and α,β‐Unsaturated‐γ‐Keto Esters through Copper‐Catalyzed Coupling of Alkenyl Boronic Acids with Phosphorus Ylides

inferred← citeshttps://doi.org/10.1002/adsc.201800090openalex-snapshot

Rhodium‐Catalyzed Direct and Selective ortho C−H Chalcogenation of N‐(Hetero)aryl‐7‐azaindoles

inferred← citeshttps://doi.org/10.1002/adsc.201800504openalex-snapshot

Synthesis of Arylamines via Non‐Aerobic Dehydrogenation Using a Palladium/Carbon‐Ethylene System

inferred← citeshttps://doi.org/10.1002/adsc.201800919openalex-snapshot

Palladium‐Catalyzed Synthesis of Indolines from Aroyloxycarbamates through a Tandem Decarboxylative Amination/Heck/Annulation Reaction

inferred← citeshttps://doi.org/10.1002/adsc.201801510openalex-snapshot

Iodine(III) Enabled Dehydrogenative Aryl C−S Coupling by in situ Generated Sulfenium Ion

inferred← citeshttps://doi.org/10.1002/adsc.201901008openalex-snapshot

(Thio)etherification of Quinoxalinones under Visible‐Light Photoredox Catalysis

inferred← citeshttps://doi.org/10.1002/adsc.201901009openalex-snapshot

Transition‐Metal‐Free Three‐Component Synthesis of Tertiary Aryl Amines from Nitro Compounds, Boronic Acids, and Trialkyl Phosphites

inferred← citeshttps://doi.org/10.1002/adsc.202000786openalex-snapshot

Construction of Boronated γ‐Lactams via Palladium‐Catalyzed Intramolecular Boryldifluoroalkylation of Alkenes

inferred← citeshttps://doi.org/10.1002/adsc.202001176openalex-snapshot

Photocatalysis in Dual Catalysis Systems for Carbon‐Nitrogen Bond Formation

inferred← citeshttps://doi.org/10.1002/adsc.202001358openalex-snapshot

Recent Advances in Cross‐Dehydrogenative Couplings (CDC) of C−H Bond in Aqueous Media

inferred← citeshttps://doi.org/10.1002/adsc.202100089openalex-snapshot

Solvent‐Dependent Chemoselective and Stereoselective Approach to Synthesis of Spiro‐γ‐Lactams with Potent Anticancer Activity

inferred← citeshttps://doi.org/10.1002/adsc.202100236openalex-snapshot

A Metal‐Free Direct Arene C−H Amination

inferred← citeshttps://doi.org/10.1002/adsc.202100558openalex-snapshot

Recent Advances in Cobalt‐Catalyzed, Directing‐Group‐Assisted C−H Bond Amidation Reactions

inferred← citeshttps://doi.org/10.1002/adsc.202100594openalex-snapshot

Copper‐Catalysed Electrophilic Amination of Aryl(alkenyl) Boronic Acids with Nitrogen‐Containing Hypervalent Iodine (III) Reagent

inferred← citeshttps://doi.org/10.1002/adsc.202200572openalex-snapshot

Palladium‐Catalyzed Sequential C−H Activation/Amination of 2‐Iodobiphenyls with Benzoisoxazoles for Synthesis of Carbazoles

inferred← citeshttps://doi.org/10.1002/adsc.202200780openalex-snapshot

Pincer‐Ruthenium Catalyzed Oxygen Mediated Dehydrative Etherification of Alcohols and Ortho‐Alkylation of Phenols

inferred← citeshttps://doi.org/10.1002/adsc.202200945openalex-snapshot

Selective Intermolecular Dual Amino‐Trifluoromethylation of Alkenes by High‐Valent Cu(III)−CF3 Compounds

inferred← citeshttps://doi.org/10.1002/adsc.202400909openalex-snapshot

Bidentate NHC‐Containing Ligands for Copper Catalysed Synthesis of Functionalised Diaryl Ethers

inferred← citeshttps://doi.org/10.1002/adsc.70026openalex-snapshot

Photoredox/Nickel Dual Catalytic C(sp2)S Cross‐coupling of Bromoanilines Enabled by Mineral Acids

inferred← citeshttps://doi.org/10.1002/adsc.70812openalex-snapshot

Selective Electroreductive N ‐Alkylation of Nitroarenes

inferred← citeshttps://doi.org/10.1002/advs.201801368openalex-snapshot

Synthesis of a Novel Disperse Reactive Dye Involving a Versatile Bridge Group for the Sustainable Coloration of Natural Fibers in Supercritical Carbon Dioxide

inferred← citeshttps://doi.org/10.1002/ajoc.201300074openalex-snapshot

Silver‐Nitrate‐Catalyzed N‐Arylation of Amines and O‐Arylations of Phenols and Alcohols

inferred← citeshttps://doi.org/10.1002/ajoc.201400027openalex-snapshot

N1‐Selective Oxidative CN Coupling of Azoles with Pyrroles Using a Hypervalent Iodine Reagent

inferred← citeshttps://doi.org/10.1002/ajoc.201402136openalex-snapshot

Efficient Copper Catalyzed CN Coupling Reaction in Water by Using 2‐Hydroxybenzohydrazides as Ligands

inferred← citeshttps://doi.org/10.1002/ajoc.201402154openalex-snapshot

Transition‐Metal‐Free Syntheses of Pyridine‐Containing Thioethers Through Two‐Fold CS Bond Formation

inferred← citeshttps://doi.org/10.1002/ajoc.201402169openalex-snapshot

Metal‐Free Preparation of 6‐Alkylthiophenanthridines via Oxidative CS and CC Bond Formation from 2‐Isocyanobiphenyls and Disulfides

inferred← citeshttps://doi.org/10.1002/ajoc.201500062openalex-snapshot

Unimolecular 4‐Hydroxypiperidines: New Ligands for Copper‐Catalyzed N‐Arylation

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