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Efficient Synthesis of Triarylamines Catalyzed by Copper(I) Diazabutadiene Complexes

https://doi.org/10.1002/cjoc.201400787

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1 of the 31 references listed on this page is in the Retraction Watch database as retracted (export 2026-11-04): 10.1039/b308034j (notice 2004-09-27).

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What this work says

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

inferredcites →https://doi.org/10.1002/anie.200300594openalex-snapshot

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

inferredcites →https://doi.org/10.1002/anie.200490023openalex-snapshot

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

inferredcites →https://doi.org/10.1002/anie.200903158openalex-snapshot

Room‐Temperature Copper‐Catalyzed Carbon–Nitrogen Coupling of Aryl Iodides and Bromides Promoted by Organic Ionic Bases

inferredcites →https://doi.org/10.1002/cber.19711040115openalex-snapshot

Kupfer(I)‐diazabutadien‐halogenide

inferredcites →https://doi.org/10.1002/chem.200501473openalex-snapshot

A Versatile and Efficient Ligand for Copper‐Catalyzed Formation of CN, CO, and PC Bonds: Pyrrolidine‐2‐Phosphonic Acid Phenyl Monoester

inferredcites →https://doi.org/10.1002/chem.200800436openalex-snapshot

Copper‐ or Iron‐Catalyzed Arylation of Phenols from respectively Aryl Chlorides and Aryl Iodides

inferredcites →https://doi.org/10.1002/cjoc.201200247openalex-snapshot

Copper‐Catalyzed Synthesis of Triarylamines from Aryl Halides and Arylamines

inferredcites →https://doi.org/10.1002/cjoc.201200623openalex-snapshot

Highly Efficient CN Bond Forming Reactions in Water Catalyzed by Copper(I) Iodide with Calix[4]arene Supported Amino Acid Ionic Liquid

inferredcites →https://doi.org/10.1016/j.ccr.2004.09.014openalex-snapshot

Copper in cross-coupling reactions

inferredcites →https://doi.org/10.1016/j.molcata.2003.09.038openalex-snapshot

Synthesis of triarylamines by copper-catalyzed amination of aryl halides

inferredcites →https://doi.org/10.1016/j.tet.2006.02.062openalex-snapshot

Highly efficient and practical phosphoramidite–copper catalysts for amination of aryl iodides and heteroaryl bromides with alkylamines and N(H)-heterocycles

inferredcites →https://doi.org/10.1016/j.tetlet.2005.08.146openalex-snapshot

Amination and amidation of aryl iodides catalyzed by copper(I)–phenanthroline complexes

inferredcites →https://doi.org/10.1016/j.tetlet.2006.10.103openalex-snapshot

Diazabutadiene: a simple and efficient ligand for copper-catalyzed N-arylation of aromatic amines

inferredcites →https://doi.org/10.1016/j.tetlet.2007.11.012openalex-snapshot

Copper-catalyzed synthesis of primary arylamines from aryl halides and 2,2,2-trifluoroacetamide

inferredcites →https://doi.org/10.1016/s0040-4020(01)92830-3openalex-snapshot

Glyoxal derivatives—I

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

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

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/10.1021/cr0505268openalex-snapshot

Selected Patented Cross-Coupling Reaction Technologies

inferredcites →https://doi.org/10.1021/cr100379jopenalex-snapshot

Bond Formations between Two Nucleophiles: Transition Metal Catalyzed Oxidative Cross-Coupling Reactions

inferredcites →https://doi.org/10.1021/cr300527gopenalex-snapshot

Aerobic Copper-Catalyzed Organic Reactions

inferredcites →https://doi.org/10.1021/cr8002505openalex-snapshot

Copper-Mediated Coupling Reactions and Their Applications in Natural Products and Designed Biomolecules Synthesis

inferredcites →https://doi.org/10.1021/ic50221a064openalex-snapshot

Binuclear copper(I) complexes which reversibly react with carbon monoxide. 1. Di-.mu.-halogeno-bis(2,2'-bipyridine)dicopper(I) and its derivatives

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

inferredcites →https://doi.org/10.1021/ja0260465openalex-snapshot

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

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

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

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/om700573hopenalex-snapshot

Theoretical Study on Copper(I)-Catalyzed Cross-Coupling between Aryl Halides and Amides

inferredcites →https://doi.org/10.1039/b308034jopenalex-snapshot

Novel CuI/tributyl phosphine catalyst system for amination of aryl chloridesElectronic supplementary information (ESI) available: experimental and analytical details (G.C. and NMR analysis). See http://www.rsc.org/suppdata/cc/b3/b308034j/

inferredcites →https://doi.org/10.1039/c0dt00674bopenalex-snapshot

The mechanism of the modified Ullmann reaction

inferredcites →https://doi.org/10.1055/s-2006-951510openalex-snapshot

Aromatic Amination of Aryl Bromides Catalysed by Copper/β-Diketone Catalysts: The Effect of Concentration

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.4768767openalex-extracted

Coupling reaction catalyzed by copper(I) complex bearing (E)-4-(((1H-pyrrol-2-yl)methylene)amino)-1,5-dimethyl-2-phenyl-1H-pyrazol-3(2H)-one and triphenylphosphine

inferred← citeshttps://doi.org/10.2139/ssrn.4829364openalex-extracted

Coupling reaction catalyzed by copper(I) complex bearing (E)-4-(((1H-pyrrol-2-yl)methylene)amino)-1,5-dimethyl-2-phenyl-1H-pyrazol-3(2H)-one and triphenylphosphine

inferred← citeshttps://doi.org/10.1002/cjoc.201700276openalex-snapshot

PdCl2(Ph3P)2/Salicylaldimine Catalyzed Diarylation of Anilines with Unactivated Aryl Chlorides

inferred← citeshttps://doi.org/10.1002/open.201800114openalex-snapshot

Electronic and Geometric Structures of Paramagnetic Diazadiene Complexes of Lithium and Sodium

inferred← citeshttps://doi.org/10.1016/j.ica.2019.119228openalex-snapshot

Copper complexes of 1,4-diazabutadiene ligands: Tuning of metal oxidation state and, application in catalytic C-C and C-N bond formation

inferred← citeshttps://doi.org/10.1016/j.jorganchem.2021.121994openalex-snapshot

Heterometallic antimony(V)-zinc and antimony(V)-copper complexes comprising catecholate and diazadiene as redox active centers

inferred← citeshttps://doi.org/10.1016/j.poly.2019.07.033openalex-snapshot

Heteroleptic copper(I) complexes incorporating sterically demanding diazabutadiene ligands (DABs). Synthesis, spectroscopic characterization and solid state structural analysis

inferred← citeshttps://doi.org/10.1016/j.tet.2017.01.050openalex-snapshot

n-Butyllithium-mediated synthesis of N-aryl tertiary amines by reactions of fluoroarenes with secondary amines at room temperature

inferred← citeshttps://doi.org/10.1039/d0gc01329copenalex-snapshot

Metal-free green synthesis of aryl amines in magnetized distilled water: experimental aspects and molecular dynamics simulation

inferred← citeshttps://doi.org/10.1055/sos-sd-127-00451openalex-snapshot

27.27 Product Class 27: 1,2-Diimines

inferred← citeshttps://doi.org/10.12794/metadc2416008openalex-snapshot

Experimental and Computational Investigations of Transition Metal Carbene and Chelating Ligand Complexes for Catalytic Applications

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