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Catalytic CC, CN, and CO Ullmann‐Type Coupling Reactions

https://doi.org/10.1002/anie.200804497

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Design and Evolution of Copper Apatite Catalysts for N-Arylation of Heterocycles with Chloro- and Fluoroarenes

inferredcites →https://doi.org/10.1021/ja050120copenalex-snapshot

The Role of Chelating Diamine Ligands in the Goldberg Reaction: A Kinetic Study on the Copper-Catalyzed Amidation of Aryl Iodides

inferredcites →https://doi.org/10.1021/ja063063bopenalex-snapshot

Highly Selective Room-Temperature Copper-Catalyzed C−N Coupling Reactions

inferredcites →https://doi.org/10.1021/ja066505sopenalex-snapshot

Enhanced Catalytic Properties of Copper in O- and N-Arylation and Vinylation Reactions, Using Phosphorus Dendrimers as Ligands

inferredcites →https://doi.org/10.1021/ja066991jopenalex-snapshot

Enantioselective Arylation of 2-Methylacetoacetates Catalyzed by CuI/trans-4-Hydroxy- l -proline at Low Reaction Temperatures

inferredcites →https://doi.org/10.1021/ja068926fopenalex-snapshot

N- versus O-Arylation of Aminoalcohols: Orthogonal Selectivity in Copper-Based Catalysts

inferredcites →https://doi.org/10.1021/ja073633nopenalex-snapshot

A Concept of Supported Amino Acid Ionic Liquids and Their Application in Metal Scavenging and Heterogeneous Catalysis

inferredcites →https://doi.org/10.1021/ja076668wopenalex-snapshot

Copper Complexes of Anionic Nitrogen Ligands in the Amidation and Imidation of Aryl Halides

inferredcites →https://doi.org/10.1021/ja802123popenalex-snapshot

Carbon−Nitrogen Bond Formation Involving Well-Defined Aryl−Copper(III) Complexes

inferredcites →https://doi.org/10.1021/ja803179sopenalex-snapshot

Orthogonal Pd- and Cu-Based Catalyst Systems for C- and N-Arylation of Oxindoles

inferredcites →https://doi.org/10.1021/ja971901jopenalex-snapshot

A General Copper-Catalyzed Synthesis of Diaryl Ethers

inferredcites →https://doi.org/10.1021/ja981662fopenalex-snapshot

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

inferredcites →https://doi.org/10.1021/jo00069a040openalex-snapshot

Synthesis of aryl- and vinylacetylene derivatives by copper-catalyzed reaction of aryl and vinyl iodides with terminal alkynes

inferredcites →https://doi.org/10.1021/jo00938a044openalex-snapshot

Nucleophilic replacement of two halogens in dihalobenzenes without the intermediacy of monosubstitution products

inferredcites →https://doi.org/10.1021/jo01035a046openalex-snapshot

Mechanism of the Ullmann Condensation1

inferredcites →https://doi.org/10.1021/jo01047a008openalex-snapshot

The Substitution of Aryl Iodides with Cuprous Acetylides. A Synthesis of Tolanes and Heterocyclics 1

inferredcites →https://doi.org/10.1021/jo048761yopenalex-snapshot

Organosoluble Copper Clusters as Precatalysts for Carbon−Heteroelement Bond-Forming Reactions: Microwave and Conventional Heating

inferredcites →https://doi.org/10.1021/jo049658bopenalex-snapshot

Copper−Diamine-Catalyzed N -Arylation of Pyrroles, Pyrazoles, Indazoles, Imidazoles, and Triazoles

inferredcites →https://doi.org/10.1021/jo0504464openalex-snapshot

Amino Acid Promoted CuI-Catalyzed C−N Bond Formation between Aryl Halides and Amines or N-Containing Heterocycles

inferredcites →https://doi.org/10.1021/jo051221wopenalex-snapshot

Copper-Catalyzed Arylation of Amines Using Diphenyl Pyrrolidine-2-phosphonate as the New Ligand

inferredcites →https://doi.org/10.1021/jo051640topenalex-snapshot

A Soluble Base for the Copper-Catalyzed Imidazole N-Arylations with Aryl Halides

inferredcites →https://doi.org/10.1021/jo0606960openalex-snapshot

Mild and Nonracemizing Conditions for Ullmann-type Diaryl Ether Formation between Aryl Iodides and Tyrosine Derivatives

inferredcites →https://doi.org/10.1021/jo061572qopenalex-snapshot

2-Aminopyrimidine-4,6-diol as an Efficient Ligand for Solvent-Free Copper-Catalyzed N-Arylations of Imidazoles with Aryl and Heteroaryl Halides

inferredcites →https://doi.org/10.1021/jo062059fopenalex-snapshot

Highly Efficient Copper-Catalyzed N-Arylation of Nitrogen-Containing Heterocycles with Aryl and Heteroaryl Halides

inferredcites →https://doi.org/10.1021/jo062060eopenalex-snapshot

CuBr/rac-BINOL-Catalyzed N-Arylations of Aliphatic Amines at Room Temperature

inferredcites →https://doi.org/10.1021/jo062194sopenalex-snapshot

Copper-Catalyzed Double N-Alkenylation of Amides: An Efficient Synthesis of Di- or Trisubstituted N-Acylpyrroles

inferredcites →https://doi.org/10.1021/jo0623742openalex-snapshot

CuI-Catalyzed Suzuki−Miyaura and Sonogashira Cross-Coupling Reactions Using DABCO as Ligand

inferredcites →https://doi.org/10.1021/jo070443mopenalex-snapshot

A β-Keto Ester as a Novel, Efficient, and Versatile Ligand for Copper(I)-Catalyzed C−N, C−O, and C−S Coupling Reactions

inferredcites →https://doi.org/10.1021/jo070517uopenalex-snapshot

Total Synthesis of the Cyclopeptide Alkaloid Abyssenine A. Application of Inter- and Intramolecular Copper-Mediated Coupling Reactions in Organic Synthesis

inferredcites →https://doi.org/10.1021/jo070547xopenalex-snapshot

Assembly of Conjugated Enynes and Substituted Indoles via CuI/Amino Acid-Catalyzed Coupling of 1-Alkynes with Vinyl Iodides and 2-Bromotrifluoroacetanilides

inferredcites →https://doi.org/10.1021/jo070807aopenalex-snapshot

Copper-Catalyzed N-Arylation of Imidazoles and Benzimidazoles

inferredcites →https://doi.org/10.1021/jo0712289openalex-snapshot

Simple Copper Salt-Catalyzed N-Arylation of Nitrogen-Containing Heterocycles with Aryl and Heteroaryl Halides

inferredcites →https://doi.org/10.1021/jo0712291openalex-snapshot

An Ullmann Coupling of Aryl Iodides and Amines Using an Air-Stable Diazaphospholane Ligand

inferredcites →https://doi.org/10.1021/jo701384nopenalex-snapshot

Sequential Cu-Catalyzed Amidation-Base-Mediated Camps Cyclization: A Two-Step Synthesis of 2-Aryl-4-quinolones from o-Halophenones

inferredcites →https://doi.org/10.1021/jo7015983openalex-snapshot

N-Hydroxyimides as Efficient Ligands for the Copper-Catalyzed N-Arylation of Pyrrole, Imidazole, and Indole

inferredcites →https://doi.org/10.1021/jo702024popenalex-snapshot

An Improved Cu-Based Catalyst System for the Reactions of Alcohols with Aryl Halides

inferredcites →https://doi.org/10.1021/jo8008676openalex-snapshot

Pyrrole-2-carboxylic Acid as a Ligand for the Cu-Catalyzed Reactions of Primary Anilines with Aryl Halides

inferredcites →https://doi.org/10.1021/jo972184eopenalex-snapshot

Synthesis of 1,2,3,4-Tetrahydroisoquinolines Containing Electron-Withdrawing Groups

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/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/ol025548kopenalex-snapshot

Copper-Catalyzed Coupling of Aryl Iodides with Aliphatic Alcohols

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/ol035378ropenalex-snapshot

2-Aryl and 2-Heteroaryl Indoles from 1-Alkynes ando-Iodotrifluoroacetanilide through a Domino Copper-Catalyzed Coupling−Cyclization Process

inferredcites →https://doi.org/10.1021/ol0360041openalex-snapshot

Copper-Mediated Synthesis of N -Acyl Vinylogous Carbamic Acids and Derivatives: Synthesis of the Antibiotic CJ-15,801

inferredcites →https://doi.org/10.1021/ol036290gopenalex-snapshot

A General and Mild Ullmann-Type Synthesis of Diaryl Ethers

inferredcites →https://doi.org/10.1021/ol036381dopenalex-snapshot

Divergent and Stereocontrolled Synthesis of the Enamide Side Chains of Oximidines I/II/III, Salicylihalamides A/B, Lobatamides A/D, and CJ-12,950

inferredcites →https://doi.org/10.1021/ol049464iopenalex-snapshot

CuI/ N , N -Dimethylglycine-Catalyzed Coupling of Vinyl Halides with Amides or Carbamates

inferredcites →https://doi.org/10.1021/ol049706eopenalex-snapshot

Copper-Catalyzed Synthesis of 1,3-Enynes

inferredcites →https://doi.org/10.1021/ol050395xopenalex-snapshot

Synthesis of Allenamides by Copper-Catalyzed Coupling of Allenyl Halides with Amides, Carbamates, and Ureas

inferredcites →https://doi.org/10.1021/ol0505555openalex-snapshot

Synthesis of Lactams via Copper-Catalyzed Intramolecular Vinylation of Amides

inferredcites →https://doi.org/10.1021/ol0518838openalex-snapshot

CuI/ l -Proline-Catalyzed Coupling Reactions of Aryl Halides with Activated Methylene Compounds

inferredcites →https://doi.org/10.1021/ol052113zopenalex-snapshot

Aminoarenethiolate−Copper(I)-Catalyzed Amination of Aryl Bromides

inferredcites →https://doi.org/10.1021/ol0608505openalex-snapshot

4,7-Dimethoxy-1,10-phenanthroline: An Excellent Ligand for the Cu-Catalyzed N-Arylation of Imidazoles

inferredcites →https://doi.org/10.1021/ol062339hopenalex-snapshot

1,1,1-Tris(hydroxymethyl)ethane as a New, Efficient, and Versatile Tripod Ligand for Copper-Catalyzed Cross-Coupling Reactions of Aryl Iodides with Amides, Thiols, and Phenols

inferredcites →https://doi.org/10.1021/ol062904gopenalex-snapshot

Cu-Catalyzed N- and O-Arylation of 2-, 3-, and 4-Hydroxypyridines and Hydroxyquinolines

inferredcites →https://doi.org/10.1021/ol062978sopenalex-snapshot

Copper-Catalyzed Vinylation of Hydrazides. A Regioselective Entry to Highly Substituted Pyrroles

inferredcites →https://doi.org/10.1021/ol0700409openalex-snapshot

Copper-in-Charcoal (Cu/C) Promoted Diaryl Ether Formation

inferredcites →https://doi.org/10.1021/ol070102vopenalex-snapshot

Rapid and Efficient Microwave-Assisted Copper(0)-Catalyzed Ullmann Coupling Reaction: General Access to Anilinoanthraquinone Derivatives

inferredcites →https://doi.org/10.1021/ol070271fopenalex-snapshot

Highly Convergent Route to Cyclopeptide Alkaloids. Total Synthesis of Ziziphine N

inferredcites →https://doi.org/10.1021/ol0709578openalex-snapshot

CuI-Mediated Cross-Coupling of Aryl Halides with Oximes: A Direct Access to O -Aryloximes

inferredcites →https://doi.org/10.1021/ol0713887openalex-snapshot

Novel CuO Nanoparticle Catalyzed C−N Cross Coupling of Amines with Iodobenzene

inferredcites →https://doi.org/10.1021/ol701473popenalex-snapshot

Room-Temperature Copper-Catalyzed α-Arylation of Malonates

showing the first 200 of 243 · page through all 243

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4647246openalex-extracted

Light-Switchable N-Alkylation Using Amine-Functionalized Mof

inferred← citeshttps://doi.org/10.1002/0471264229.os096.13openalex-snapshot

Discussion Addendum for: Synthesis of Ynamides by Copper‐Mediated Coupling of 1,1‐Dibromo‐1‐Alkenes with Nitrogen Nucleophiles. Preparation of 4‐Methyl‐N‐(2‐Phenylethynyl)‐N‐(Phenylmethyl)Benzenesulfonamide

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.ch18openalex-snapshot

Copper‐Catalyzed C–C Bond Formation in Natural Product Synthesis: Elegant and Efficient Solutions to a Key Bond Disconnection

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.ch5openalex-snapshot

Beyond Ullmann–Goldberg Chemistry: Vinylation, Alkynylation, and Allenylation of Heteronucleophiles

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

Insights into the Mechanism of Modern Ullmann–Goldberg Coupling Reactions

inferred← citeshttps://doi.org/10.1002/9781118754887.ch24openalex-snapshot

Reactivity and Selectivity in Transition Metal‐Catalyzed, Nondirected Arene Functionalizations

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

Reaction of Iodo Compounds

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.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/10.1002/9783527346028.ch13openalex-snapshot

Theoretical Study of Cu‐Catalysis

inferred← citeshttps://doi.org/10.1002/9783527648283.ch7openalex-snapshot

Cross‐Coupling Reactions in Aqueous Media

inferred← citeshttps://doi.org/10.1002/9783527651351.ch3openalex-snapshot

Perfluoroalkylation

inferred← citeshttps://doi.org/10.1002/9783527651733.ch10openalex-snapshot

New Trends in Organometallic Catalysts

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

Palladium‐Catalyzed Aromatic Carbon–Nitrogen Bond Formation

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

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

inferred← citeshttps://doi.org/10.1002/9783527671229.ch08openalex-snapshot

NHC–Copper Complexes and their Applications

inferred← citeshttps://doi.org/10.1002/9783527675944.ch11openalex-snapshot

Application of Organozinc Reagents in Oxidative Coupling Reactions

inferred← citeshttps://doi.org/10.1002/9783527678211.ch1openalex-snapshot

Mechanisms of Metal‐Mediated C–N Coupling Processes: A Synergistic Relationship between Gas‐Phase Experiments and Computational Chemistry

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

Alcohol as a Reagent in Homogeneous Catalysis

inferred← citeshttps://doi.org/10.1002/9783527826131.ch8openalex-snapshot

Manganese‐Catalyzed Cross‐Coupling Processes

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

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

inferred← citeshttps://doi.org/10.1002/9783527834242.chf0028openalex-snapshot

Rhodium‐Catalyzed External Oxidant Free CH Amination and Amidation

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

Copper‐Catalyzed sp 3 CH Bond Functionalization

inferred← citeshttps://doi.org/10.1002/9783527844852.ch11openalex-snapshot

Metal‐Catalyzed Denitrogenative Transformations of Pyridotriazoles

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.200900887openalex-snapshot

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

inferred← citeshttps://doi.org/10.1002/adsc.201000311openalex-snapshot

Extremely Efficient Cross‐Coupling of Benzylic Halides with Aryltitanium Tris(isopropoxide) Catalyzed by Low Loadings of a Simple Palladium(II) Acetate/Tris(p‐tolyl)phosphine System

inferred← citeshttps://doi.org/10.1002/adsc.201000323openalex-snapshot

A General and Practical Access to Chiral Quinoxalinones with Low Copper‐Catalyst Loading

inferred← citeshttps://doi.org/10.1002/adsc.201000475openalex-snapshot

An Economical, Green Pathway to Biaryls: Palladium Nanoparticles Catalyzed Ullmann Reaction in Ionic Liquid/ Supercritical Carbon Dioxide System

inferred← citeshttps://doi.org/10.1002/adsc.201000603openalex-snapshot

Selective C3C3 Oxidative Cross‐Coupling between Unactivated Anilines and Indoles

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.201000825openalex-snapshot

Copper‐Catalyzed Aromatic Trifluoromethylation via Group Transfer from Fluoral Derivatives

inferred← citeshttps://doi.org/10.1002/adsc.201100172openalex-snapshot

Palladium/Copper‐Catalyzed Di‐α‐arylation of Acetic Acid Esters

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.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.201200164openalex-snapshot

One‐Pot Tandem Synthesis of 2‐Arylbenzoxazole Derivatives via Copper‐Catalyzed CN and CO Bond Formation

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.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.201200625openalex-snapshot

Palladium‐Catalyzed CH Bond Acetoxylation: An Approach to ortho‐Substituted Hydroxy[2.2]paracyclophane Derivatives

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.201200876openalex-snapshot

Phosphine‐Free Palladium‐Catalyzed Decarboxylative Coupling of Alkynylcarboxylic Acids with Aryl and Heteroaryl Halides

inferred← citeshttps://doi.org/10.1002/adsc.201201010openalex-snapshot

Ligandless Copper‐Catalyzed Coupling of Heteroaryl Bromides with Gaseous Ammonia

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.201201033openalex-snapshot

Copper‐Catalyzed Domino SN2′/Coupling Reaction: A Versatile and Facile Synthesis of Cyclic Compounds from Baylis–Hillman Acetates

inferred← citeshttps://doi.org/10.1002/adsc.201201133openalex-snapshot

Rhodium(III)‐Catalyzed C( sp 2 )H Activation and Electrophilic Amidation with N ‐Fluorobenzenesulfonimide

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.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.201300333openalex-snapshot

Copper(I) Iodide/Boron Trifluoride Etherate‐Cocatalyzed Aerobic Dehydrogenative Reactions Applied in the Synthesis of Substituted Heteroaromatic Imidazo[1,2‐a]pyridines

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.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.201300503openalex-snapshot

Copper‐Catalyzed Synthesis of α‐Naphthols from Enol Esters

inferred← citeshttps://doi.org/10.1002/adsc.201300618openalex-snapshot

Copper‐Catalyzed Synthesis of 1,3‐Butadienylphosphine Oxides and Chemoselective Phosphoryl Reduction to Stereodefined 1,3‐Butadienylphosphines

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.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.201301010openalex-snapshot

Copper Pincer Complexes as Advantageous Catalysts for the Heteroannulation of ortho‐Halophenols and Alkynes

inferred← citeshttps://doi.org/10.1002/adsc.201400189openalex-snapshot

Zeo‐Click Synthesis: Copper‐Zeolite‐Catalyzed Synthesis of Ynamides

inferred← citeshttps://doi.org/10.1002/adsc.201400295openalex-snapshot

Direct Oxidative Arylation of C(sp3)H Bonds Adjacent to Oxygen of Ethers and Alcohols

inferred← citeshttps://doi.org/10.1002/adsc.201400381openalex-snapshot

Heterogeneous Copper‐Catalyzed Cascade Three‐Component Reaction of Amines, Carbon Disulfide and 2‐Iodoanilines Leading to 2‐Aminobenzothiazoles

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.201400763openalex-snapshot

Copper‐Catalyzed Oxidative Ring Closure of ortho‐Cyanoanilides with Hypervalent Iodonium Salts: Arylation–Ring Closure Approach to Iminobenzoxazines

inferred← citeshttps://doi.org/10.1002/adsc.201400785openalex-snapshot

Room‐Temperature Copper‐Catalyzed Arylation of Dimethylamine and Methylamine in Neat Water

inferred← citeshttps://doi.org/10.1002/adsc.201400904openalex-snapshot

Multicomponent Syntheses based upon Copper‐Catalyzed Alkyne‐Azide Cycloaddition

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.201500044openalex-snapshot

A Metal‐Free Approach Toward Saturated N‐Propargyl Heterocycles via an Annulation/Decarboxylative Coupling Sequence

inferred← citeshttps://doi.org/10.1002/adsc.201500477openalex-snapshot

Synthesis of Chiral 3‐Substituted 1,3,4,5‐Tetrahydro‐1,4‐benzo‐ diazepin‐2‐ones via a Domino Copper‐Catalyzed SN2/Coupling Reaction

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.201501036openalex-snapshot

Iridium(III)‐Catalyzed Direct CH Sulfonamidation of 2‐Aryl‐1,2,3‐triazole N‐Oxides with Sulfonyl Azides

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.201600035openalex-snapshot

Copper‐Catalyzed CNH 2 Arylation of 2‐Aminobenzimidazoles and Related C‐Amino‐NH‐azoles

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.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.201600947openalex-snapshot

Copper‐Catalyzed Remote C−H Amination of Quinolines with N‐Fluorobenzenesulfonimide

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.201701124openalex-snapshot

Iron‐catalyzed C(5)−H Imidation of Azole with N‐Fluorobenzenesulfonimide

inferred← citeshttps://doi.org/10.1002/adsc.201701389openalex-snapshot

Nondirecting Group sp3 C−H Activation for Synthesis of Bibenzyls via Homo‐coupling as Catalyzed by Reduced Graphene Oxide Supported PtPd@Pt Porous Nanospheres

inferred← citeshttps://doi.org/10.1002/adsc.201701522openalex-snapshot

Conversion of Primary Amines to Symmetrical Secondary and Tertiary Amines using a Co‐Rh Heterobimetallic Nanocatalyst

inferred← citeshttps://doi.org/10.1002/adsc.201800161openalex-snapshot

Mechanochemical Cobalt‐Catalyzed C−H Bond Functionalizations by Ball Milling

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.201800743openalex-snapshot

Magnetic Nanoparticle Anchored Deep Eutectic Solvents as a Catalyst for the Etherification and Amination of Naphthols

inferred← citeshttps://doi.org/10.1002/adsc.201801221openalex-snapshot

Domino Reactions Initiated by Copper‐Catalyzed Aryl‐I Bond Thiolation For the Switchable Synthesis of 2,3‐Dihydrobenzothiazinones and Benzoisothiazolones

inferred← citeshttps://doi.org/10.1002/adsc.201900532openalex-snapshot

Base Metal Catalysis in Directed C(sp3)−H Functionalisation

inferred← citeshttps://doi.org/10.1002/adsc.201900626openalex-snapshot

Regio‐ and Stereoselective Synthesis of Enynyl‐Aryl Ethers Enabled by Copper/Iodide Tandem Catalysis

inferred← citeshttps://doi.org/10.1002/adsc.201900643openalex-snapshot

Copper‐Catalyzed Domino Synthesis of Sulfur‐Containing Heterocycles Using Carbon Disulfide as a Building Block

inferred← citeshttps://doi.org/10.1002/adsc.201900732openalex-snapshot

Visible‐Light‐Induced Alkoxylation of Quinoxalin‐2(1H)‐ones with Alcohols for the Synthesis of Heteroaryl Ethers

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.202001254openalex-snapshot

Room Temperature Benzofused Lactam Synthesis Enabled by Cobalt(III)‐Catalyzed C(sp2)−H Amidation

inferred← citeshttps://doi.org/10.1002/adsc.202100769openalex-snapshot

A Unified Approach for Divergent Synthesis of Heterocycles via TMSOTf‐Catalyzed Formal [3+2] Cycloaddition of Electron‐Rich Alkynes

inferred← citeshttps://doi.org/10.1002/adsc.202200877openalex-snapshot

Tandem Copper(I)‐Catalyzed N‐Arylation–1,4‐Conjugate Addition to Access Tetrahydroacridinones

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.202300144openalex-snapshot

CH‐Functionalization of Heterocycles with the Formation of C−O, C−N, C−S/Se, and C−P Bonds by Intermolecular Addition of Heteroatom‐Centered Radicals

inferred← citeshttps://doi.org/10.1002/adsc.202300217openalex-snapshot

Copper‐Catalyzed C(sp3)− Functionalization and Annulation of 2‐Bromoaryl Oximes with Active Methylene Compounds towards Synthesis of Isoquinoline N‐Oxides

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.202401498openalex-snapshot

CuF 2 ‐Catalyzed C‐N Cross‐Coupling of Aryl Silanes: Expanding the Scope of Chan‐Lam Type Reaction

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/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.201402085openalex-snapshot

One‐Pot Copper‐Catalyzed Aerobic Decarboxylative Coupling of Phenylacetic Acids with o‐Aminobenzenes and Dioxygen as the Oxidant Leading to Benzoxazoles and Benzothiazoles

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.201500062openalex-snapshot

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

inferred← citeshttps://doi.org/10.1002/ajoc.201600219openalex-snapshot

Copper‐Catalyzed C(sp2)–C(sp3) Cross‐Dehydrogenative Coupling of Quinones with Cyclic Alkanes: One‐Step Access to Parvaquone and its Analogs

inferred← citeshttps://doi.org/10.1002/ajoc.201600596openalex-snapshot

Construction of Tertiary Amides: NiII‐Catalyzed N‐Arylation of Secondary Acyclic Amides (2‐Picolinamides) with Aryl Halides

inferred← citeshttps://doi.org/10.1002/ajoc.201700357openalex-snapshot

Molecular Iodine‐Promoted Transimination for the Synthesis of 6‐Phenylpyrido[2′,1′:2,3]imidazo[4,5‐c]quinoline and 6‐(Pyridin‐2‐yl)pyrido[2′,1′:2,3]imidazo[4,5‐c]quinolines

inferred← citeshttps://doi.org/10.1002/ajoc.201700525openalex-snapshot

Palladium‐Catalyzed ortho‐Alkoxylation of Tertiary Benzamides: H2SO4 as an Effective Additive

inferred← citeshttps://doi.org/10.1002/ajoc.201800154openalex-snapshot

A Copper‐Catalyzed Domino Reaction of Alkynyl Bromides and Oxazolidine‐2‐thiones: Synthesis of Thiazol‐2‐ones

inferred← citeshttps://doi.org/10.1002/ajoc.201900273openalex-snapshot

N‐(4‐Thiazolylmethyl)Morpholine N‐Oxide as N,O‐Bidentate Ligand for Copper‐Catalyzed Ullmann‐Type N‐Arylation of Azoles/Amines with Aryl Halides

inferred← citeshttps://doi.org/10.1002/ajoc.201900641openalex-snapshot

Iron‐Catalyzed Chemoselective C−N Coupling Reaction: A Protecting‐Group‐Free Amination of Aryl Halides Bearing Amino or Hydroxy Groups

inferred← citeshttps://doi.org/10.1002/ajoc.201900666openalex-snapshot

Visible Light‐ and Heat‐Promoted C−O Coupling Reaction of Phenols and Aryl Halides

inferred← citeshttps://doi.org/10.1002/ajoc.202000334openalex-snapshot

Iron‐Catalyzed Cross‐Coupling Reactions for the Construction of Carbon‐Heteroatom Bonds

inferred← citeshttps://doi.org/10.1002/ajoc.202000367openalex-snapshot

Recent Progress in the C−N Bond Formation via High‐Valent Group 9 Cp*M(III)‐Catalyzed Directed sp2 C−H Activation

inferred← citeshttps://doi.org/10.1002/ajoc.202200014openalex-snapshot

Tf 2 O‐Mediated Regioselective C(sp 2 )−H Sulfenylation of Enaminones Using Methyl Sulfoxides as Sulfur Sources

inferred← citeshttps://doi.org/10.1002/ajoc.202200023openalex-snapshot

Modern Development in Copper‐ and Nickel‐Catalyzed Cross‐Coupling Reactions: Formation of Carbon‐Carbon and Carbon‐Heteroatom bonds under Microwave Irradiation Conditions

inferred← citeshttps://doi.org/10.1002/ajoc.202200331openalex-snapshot

Transition‐metal‐catalyzed Heteroannulation Reactions in Aqueous Medium

inferred← citeshttps://doi.org/10.1002/ajoc.202200454openalex-snapshot

Copper‐catalyzed C(sp3)−H/N−H Cross Dehydrogenative Coupling Between Toluene Derivatives and Picolinamides

inferred← citeshttps://doi.org/10.1002/ajoc.202400397openalex-snapshot

Site‐Selective Synthetic Modifications of the Cinchona Alkaloids

inferred← citeshttps://doi.org/10.1002/ajoc.70445openalex-snapshot

N ‐Directed Rh‐Catalyzed Regioselective Amidation of Quinoxaline‐2(1 H )‐ones Using Dioxazolones

inferred← citeshttps://doi.org/10.1002/ange.200903639openalex-snapshot

A Very Simple Copper‐Catalyzed Synthesis of Phenols Employing Hydroxide Salts

inferred← citeshttps://doi.org/10.1002/ange.200905646openalex-snapshot

Assembly of Substituted Phenothiazines by a Sequentially Controlled CuI/ L ‐Proline‐Catalyzed Cascade CS and CN Bond Formation

inferred← citeshttps://doi.org/10.1002/ange.200905855openalex-snapshot

Efficient Synthesis of Aryl Fluorides

inferred← citeshttps://doi.org/10.1002/ange.201000526openalex-snapshot

A P,N‐Ligand for Palladium‐Catalyzed Ammonia Arylation: Coupling of Deactivated Aryl Chlorides, Chemoselective Arylations, and Room Temperature Reactions

inferred← citeshttps://doi.org/10.1002/ange.201003764openalex-snapshot

Palladium‐Catalyzed Cross‐Coupling of Aryl Chlorides and Tosylates with Hydrazine

inferred← citeshttps://doi.org/10.1002/ange.201005787openalex-snapshot

Domino Condensation/S‐Arylation/Heterocyclization Reactions: Copper‐Catalyzed Three‐Component Synthesis of 2‐N‐Substituted Benzothiazoles

inferred← citeshttps://doi.org/10.1002/ange.201007194openalex-snapshot

Dreikomponentensynthese von Indionen durch eine Glyoxylierungs‐Stephens‐Castro‐Kupplungs‐Sequenz

inferred← citeshttps://doi.org/10.1002/ange.201007302openalex-snapshot

Transition‐Metal‐Free Intramolecular Ullmann‐Type O‐Arylation: Synthesis of Chromone Derivatives

inferred← citeshttps://doi.org/10.1002/ange.201100096openalex-snapshot

Effiziente und selektive Monomethylierung kontra N‐H‐Bindungsaktivierung von Ammoniak: atomares Zink als Abgangsgruppe in einer SN2‐Reaktion von “nacktem” Zn(CH3)+ und NH3

inferred← citeshttps://doi.org/10.1002/ange.201100631openalex-snapshot

Allyl‐, Allenyl‐, and Propargyl‐Transfer Reactions through Cleavage of CC Bonds Catalyzed by an N‐Heterocyclic Carbene/Copper Complex: Synthesis of Multisubstituted Pyrroles

inferred← citeshttps://doi.org/10.1002/ange.201100633openalex-snapshot

A Broadly Applicable Copper Reagent for Trifluoromethylations and Perfluoroalkylations of Aryl Iodides and Bromides

inferred← citeshttps://doi.org/10.1002/ange.201102984openalex-snapshot

Organokatalytische, oxidative, intramolekulare C‐H‐Bindungsaminierung und metallfreie Kreuzaminierung nichtaktivierter Arene bei Raumtemperatur

inferred← citeshttps://doi.org/10.1002/ange.201103945openalex-snapshot

Kupferkatalysierte aerobe oxidative C‐H‐Funktionalisierungen: Trends und Erkenntnisse zum Mechanismus

inferred← citeshttps://doi.org/10.1002/ange.201104082openalex-snapshot

Copper‐Catalyzed Intramolecular Oxidative 6‐exo‐trig Cyclization of 1,6‐Enynes with H2O and O2

inferred← citeshttps://doi.org/10.1002/ange.201105020openalex-snapshot

Copper‐Catalyzed Oxidative CO Coupling by Direct CH Bond Activation of Formamides: Synthesis of Enol Carbamates and 2‐Carbonyl‐Substituted Phenol Carbamates

inferred← citeshttps://doi.org/10.1002/ange.201106719openalex-snapshot

Copper(I) Enolate Complexes in α‐Arylation Reactions: Synthesis, Reactivity, and Mechanism

inferred← citeshttps://doi.org/10.1002/ange.201106786openalex-snapshot

Copper‐Catalyzed Cross‐Coupling Interrupted by an Opportunistic Smiles Rearrangement: An Efficient Domino Approach to Dibenzoxazepinones

inferred← citeshttps://doi.org/10.1002/ange.201200480openalex-snapshot

Synthesis of Hindered Anilines: Copper‐Catalyzed Electrophilic Amination of Aryl Boronic Esters

inferred← citeshttps://doi.org/10.1002/ange.201200698openalex-snapshot

Catalytic Aerobic Synthesis of Aromatic Ethers from Non‐Aromatic Precursors

inferred← citeshttps://doi.org/10.1002/ange.201202149openalex-snapshot

Catalyst‐Free N‐Arylation Using Unactivated Fluorobenzenes

inferred← citeshttps://doi.org/10.1002/ange.201204710openalex-snapshot

Catalyst‐Controlled Chemoselective Arylation of 2‐Aminobenzimidazoles

inferred← citeshttps://doi.org/10.1002/ange.201206024openalex-snapshot

Direct Copper‐Catalyzed α‐Arylation of Benzyl Phenyl Ketones with Aryl Iodides: Route towards Tamoxifen

inferred← citeshttps://doi.org/10.1002/ange.201208755openalex-snapshot

Synthese von Arylethern aus Benzoaten über carboxylatdirigierte C‐H‐aktivierende Alkoxylierung mit gekoppelter Protodecarboxylierung

inferred← citeshttps://doi.org/10.1002/ange.201300382openalex-snapshot

Übergangsmetallfreie Aminierung von Arylboronsäuren und deren Derivaten

inferred← citeshttps://doi.org/10.1002/ange.201303702openalex-snapshot

Copper‐Catalyzed Dehydrogenative Coupling of Arenes with Alcohols

inferred← citeshttps://doi.org/10.1002/ange.201304188openalex-snapshot

A General, Practical Palladium‐Catalyzed Cyanation of (Hetero)Aryl Chlorides and Bromides

inferred← citeshttps://doi.org/10.1002/ange.201304380openalex-snapshot

Synthese von funktionalisierten Indolen und Azaindolen durch intramolekulare Kupfer‐vermittelte Carbomagnesierung von Inamiden

inferred← citeshttps://doi.org/10.1002/ange.201305970openalex-snapshot

Copper‐Catalyzed Domino Cycloaddition/CN Coupling/Cyclization/(CH Arylation): An Efficient Three‐Component Synthesis of Nitrogen Polyheterocycles

inferred← citeshttps://doi.org/10.1002/ange.201404120openalex-snapshot

Development of CN Coupling Using Mechanochemistry: Catalytic Coupling of Arylsulfonamides and Carbodiimides

inferred← citeshttps://doi.org/10.1002/ange.201405575openalex-snapshot

Enantioselective Formation of Cyano‐Bearing All‐Carbon Quaternary Stereocenters: Desymmetrization by Copper‐Catalyzed N‐Arylation

inferred← citeshttps://doi.org/10.1002/ange.201500074openalex-snapshot

Visible‐Light‐Mediated Chan–Lam Coupling Reactions of Aryl Boronic Acids and Aniline Derivatives

inferred← citeshttps://doi.org/10.1002/ange.201500902openalex-snapshot

Alkyl Aryl Ether Bond Formation with PhenoFluor

inferred← citeshttps://doi.org/10.1002/ange.201503882openalex-snapshot

Copper‐Catalyzed Intramolecular Desymmetric Aryl CO Coupling for the Enantioselective Construction of Chiral Dihydrobenzofurans and Dihydrobenzopyrans

inferred← citeshttps://doi.org/10.1002/ange.201506579openalex-snapshot

Photoinduced Copper‐Catalyzed Regioselective Synthesis of Indoles: Three‐Component Coupling of Arylamines, Terminal Alkynes, and Quinones

inferred← citeshttps://doi.org/10.1002/ange.201506751openalex-snapshot

Formal Direct Cross‐Coupling of Phenols with Amines

inferred← citeshttps://doi.org/10.1002/ange.201508571openalex-snapshot

Interface Engineering in Two‐Dimensional Heterostructures: Towards an Advanced Catalyst for Ullmann Couplings

inferred← citeshttps://doi.org/10.1002/ange.201508746openalex-snapshot

Synthesis of Carbazole Alkaloids by Ring‐Closing Metathesis and Ring Rearrangement–Aromatization

inferred← citeshttps://doi.org/10.1002/ange.201601035openalex-snapshot

CuI/Oxalamide Catalyzed Couplings of (Hetero)aryl Chlorides and Phenols for Diaryl Ether Formation

inferred← citeshttps://doi.org/10.1002/ange.201605132openalex-snapshot

C−N Bond Formation from a Masked High‐Valent Copper Complex Stabilized by Redox Non‐Innocent Ligands

inferred← citeshttps://doi.org/10.1002/ange.201611024openalex-snapshot

Silver‐Catalyzed Chemoselective [4+2] Annulation of Two Isocyanides: A General Route to Pyridone‐Fused Carbo‐ and Heterocycles

inferred← citeshttps://doi.org/10.1002/ange.201701690openalex-snapshot

Ausgewählte Kupfer‐katalysierte Reaktionen für die Bildung von C‐N‐, C‐O‐, C‐S‐ und C‐C‐Bindungen

inferred← citeshttps://doi.org/10.1002/ange.201706293openalex-snapshot

Copper‐Catalyzed Amination of Congested and Functionalized α‐Bromocarboxamides with either Amines or Ammonia at Room Temperature

inferred← citeshttps://doi.org/10.1002/ange.201709681openalex-snapshot

Access to Chiral Hydropyrimidines through Palladium‐Catalyzed Asymmetric Allylic C−H Amination

inferred← citeshttps://doi.org/10.1002/ange.201709766openalex-snapshot

Photokatalyse mit sichtbarem Licht: Welche Bedeutung hat sie für die organische Synthese?

inferred← citeshttps://doi.org/10.1002/ange.201712618openalex-snapshot

From Anilines to Aryl Ethers: A Facile, Efficient, and Versatile Synthetic Method Employing Mild Conditions

inferred← citeshttps://doi.org/10.1002/ange.201904795openalex-snapshot

The Buchwald–Hartwig Amination After 25 Years

inferred← citeshttps://doi.org/10.1002/ange.201913930openalex-snapshot

Nickelaelektro‐katalysierte C‐H‐Alkoxylierung mit sekundären Alkoholen: oxidationsinduzierte reduktive Eliminierung an Nickel(III)

inferred← citeshttps://doi.org/10.1002/ange.201916710openalex-snapshot

Visible‐Light‐Enabled Direct Decarboxylative N‐Alkylation

inferred← citeshttps://doi.org/10.1002/ange.202015654openalex-snapshot

Oxalohydrazide Ligands for Copper‐Catalyzed C−O Coupling Reactions with High Turnover Numbers

inferred← citeshttps://doi.org/10.1002/ange.202103803openalex-snapshot

Low‐Temperature Nickel‐Catalyzed C−N Cross‐Coupling via Kinetic Resolution Enabled by a Bulky and Flexible Chiral N‐Heterocyclic Carbene Ligand

inferred← citeshttps://doi.org/10.1002/ange.202315701openalex-snapshot

Synthesis of N‐Acylsulfenamides from (Hetero)Aryl Iodides and Boronic Acids by One‐Pot Sulfur‐Arylation and Dealkylation

inferred← citeshttps://doi.org/10.1002/ange.202400333openalex-snapshot

Room‐Temperature Copper‐Catalyzed Etherification of Aryl Bromides

inferred← citeshttps://doi.org/10.1002/ange.202412299openalex-snapshot

Anilines Formation via Molybdenum‐Catalyzed Intermolecular Reaction of Ynones with Allylic Amines

inferred← citeshttps://doi.org/10.1002/ange.202504156openalex-snapshot

Adaptive Defluoroamination of Aryl Fluorides: Harnessing the Catalytic Potential of a Unique Zinc Amide Compound

inferred← citeshttps://doi.org/10.1002/ange.202511311openalex-snapshot

Ligand‐Controlled Stereodivergent Manganese‐Catalyzed Hydroalkoxylation of Alkynylnitriles to Access ( E )‐ and ( Z )‐3‐Alkoxyvinylnitriles

inferred← citeshttps://doi.org/10.1002/ange.8724182openalex-snapshot

Oxygen‐Radical Capture Enabled Nickel‐Catalyzed Carbon(sp 2 )‐Heteroatom Coupling of Two Nucleophiles

inferred← citeshttps://doi.org/10.1002/anie.1753273openalex-snapshot

A Modular Approach to N ‐Fluoroalkyl Amides via Nitrene Insertion Into Fluoroalkylcopper(I)

inferred← citeshttps://doi.org/10.1002/anie.200903639openalex-snapshot

A Very Simple Copper‐Catalyzed Synthesis of Phenols Employing Hydroxide Salts

inferred← citeshttps://doi.org/10.1002/anie.200905646openalex-snapshot

Assembly of Substituted Phenothiazines by a Sequentially Controlled CuI/ L ‐Proline‐Catalyzed Cascade CS and CN Bond Formation

inferred← citeshttps://doi.org/10.1002/anie.200905855openalex-snapshot

Efficient Synthesis of Aryl Fluorides

inferred← citeshttps://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

inferred← citeshttps://doi.org/10.1002/anie.201003764openalex-snapshot

Palladium‐Catalyzed Cross‐Coupling of Aryl Chlorides and Tosylates with Hydrazine

inferred← citeshttps://doi.org/10.1002/anie.201005787openalex-snapshot

Domino Condensation/S‐Arylation/Heterocyclization Reactions: Copper‐Catalyzed Three‐Component Synthesis of 2‐N‐Substituted Benzothiazoles

inferred← citeshttps://doi.org/10.1002/anie.201007194openalex-snapshot

Three‐Component Synthesis of Ynediones by a Glyoxylation/Stephens–Castro Coupling Sequence

inferred← citeshttps://doi.org/10.1002/anie.201007302openalex-snapshot

Transition‐Metal‐Free Intramolecular Ullmann‐Type O‐Arylation: Synthesis of Chromone Derivatives

inferred← citeshttps://doi.org/10.1002/anie.201100096openalex-snapshot

Efficient and Selective Gas‐Phase Monomethylation versus NH Bond Activation of Ammonia by “Bare” Zn(CH3)+: Atomic Zinc as a Leaving Group in an SN2 Reaction

inferred← citeshttps://doi.org/10.1002/anie.201100631openalex-snapshot

Allyl‐, Allenyl‐, and Propargyl‐Transfer Reactions through Cleavage of CC Bonds Catalyzed by an N‐Heterocyclic Carbene/Copper Complex: Synthesis of Multisubstituted Pyrroles

inferred← citeshttps://doi.org/10.1002/anie.201100633openalex-snapshot

A Broadly Applicable Copper Reagent for Trifluoromethylations and Perfluoroalkylations of Aryl Iodides and Bromides

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