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Highly reusable support‐free copper(II) complex of para‐hydroxy‐substituted salen: Novel, efficient and versatile catalyst for C─N bond forming reactions

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What this work says

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

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Copper‐Mediated Cross‐Coupling Reactions

inferredcites →https://doi.org/10.1002/9783527626410openalex-snapshot

Solvent‐Free Organic Synthesis

inferredcites →https://doi.org/10.1002/adsc.200800317openalex-snapshot

Reusable Cobalt(III)‐Salen Complex Supported on Activated Carbon as an Efficient Heterogeneous Catalyst for Synthesis of 2‐Arylbenzimidazole Derivatives

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Copper Nanoparticles on Charcoal for Multicomponent Catalytic Synthesis of 1,2,3‐Triazole Derivatives from Benzyl Halides or Alkyl Halides, Terminal Alkynes and Sodium Azide in Water as a “Green” Solvent

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Immobilization of Porphyrinatocopper Nanoparticles onto Activated Multi‐Walled Carbon Nanotubes and a Study of its Catalytic Activity as an Efficient Heterogeneous Catalyst for a Click Approach to the Three‐Component Synthesis of 1,2,3‐Triazoles in Water

inferredcites →https://doi.org/10.1002/adsc.201300741openalex-snapshot

Suzuki–Miyaura Cross‐Coupling under Solvent‐Free Conditions

inferredcites →https://doi.org/10.1002/adsc.201400201openalex-snapshot

Stable Nickel(0) Phosphites as Catalysts for CN Cross‐Coupling Reactions

inferredcites →https://doi.org/10.1002/cssc.201100382openalex-snapshot

Epoxidation of Alkenes Catalyzed by Phenyl Group‐Modified, Periodic Mesoporous Organosilica‐Entrapped, Dimeric Manganese–Salen Complexes

inferredcites →https://doi.org/10.1002/ejoc.200300709openalex-snapshot

Mild Conditions for Copper‐Catalysed N‐Arylation of Pyrazoles

inferredcites →https://doi.org/10.1002/ejoc.200800351openalex-snapshot

Reusable Porphyrinatoiron(III) Complex Supported on Activated Silica as an Efficient Heterogeneous Catalyst for a Facile, One‐Pot, Selective Synthesis of 2‐Arylbenzimidazole Derivatives in the Presence of Atmospheric Air as a “Green” Oxidant at Ambient Temperature

inferredcites →https://doi.org/10.1002/ejoc.201100274openalex-snapshot

Cross‐Coupling Reactions of Aryl Halides with Amines, Phenols, and Thiols Catalyzed by an N,N′‐Dioxide–Copper(I) Catalytic System

inferredcites →https://doi.org/10.1007/bf02510042openalex-snapshot

Benzimidazole derivatives: Spectrum of pharmacological activity and toxicological properties (a review)

inferredcites →https://doi.org/10.1007/s00044-010-9533-9openalex-snapshot

Benzimidazole: a medicinally important heterocyclic moiety

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The therapeutic journey of benzimidazoles: A review

inferredcites →https://doi.org/10.1016/j.bmcl.2006.08.132openalex-snapshot

The development of 2-benzimidazole substituted pyrimidine based inhibitors of lymphocyte specific kinase (Lck)

inferredcites →https://doi.org/10.1016/j.ica.2013.05.028openalex-snapshot

A new palladium(II)–allyl complex containing a thioether-triazole ligand as active catalyst in Suzuki–Miyaura reaction. Use of tetraalkylammonium salts as promoters: Influence of the salt anion and cation on the catalytic activity

inferredcites →https://doi.org/10.1016/j.inoche.2011.05.019openalex-snapshot

A reusable polymer supported copper(I) complex for the C–N bond cross-coupling reaction

inferredcites →https://doi.org/10.1016/j.jorganchem.2013.10.046openalex-snapshot

Palladium(II) complexes featuring bidentate pyridine–triazole ligands: Synthesis, structures, and catalytic activities for Suzuki–Miyaura coupling reactions

inferredcites →https://doi.org/10.1016/j.molcata.2006.02.053openalex-snapshot

N-Arylation of nitrogen heterocycles with aryl halides and arylboronic acids catalyzed by cellulose supported copper(0)

inferredcites →https://doi.org/10.1016/j.molcata.2006.10.002openalex-snapshot

CuI/l-histidine catalyzed N-arylation of heterocycles

inferredcites →https://doi.org/10.1016/j.molcata.2012.03.017openalex-snapshot

Green synthesis of predominant (111) facet CuO nanoparticles: Heterogeneous and recyclable catalyst for N-arylation of indoles

inferredcites →https://doi.org/10.1016/j.molcata.2013.08.009openalex-snapshot

Synthesis and characterization of Cu(II) containing nanosilica triazine dendrimer: A recyclable nanocomposite material for the synthesis of benzimidazoles, benzothiazoles, bis-benzimidazoles and bis-benzothiazoles

inferredcites →https://doi.org/10.1016/j.molcata.2014.02.007openalex-snapshot

A highly active reusable polymer anchored copper catalyst for C-O, C-N and C-S cross coupling reactions

inferredcites →https://doi.org/10.1016/j.tet.2007.11.054openalex-snapshot

Copper-catalyzed amination of aryl halides with nitrogen-containing heterocycle using hippuric acid as the new ligand

inferredcites →https://doi.org/10.1016/j.tet.2008.02.082openalex-snapshot

CuI/L (L=pyridine-functionalized 1,3-diketones) catalyzed C–N coupling reactions of aryl halides with NH-containing heterocycles

inferredcites →https://doi.org/10.1016/j.tet.2009.03.061openalex-snapshot

An efficient, mild, and selective Ullmann-type N-arylation of indoles catalyzed by copper(I) complex

inferredcites →https://doi.org/10.1016/j.tet.2009.07.050openalex-snapshot

Benzotriazole: an efficient ligand for the copper-catalyzed N-arylation of indoles

inferredcites →https://doi.org/10.1016/j.tet.2009.10.014openalex-snapshot

Copper(I)-2-(2′-pyridyl)benzimidazole catalyzed N-arylation of indoles

inferredcites →https://doi.org/10.1016/j.tet.2011.05.025openalex-snapshot

Cu(OAc)2·H2O-catalyzed N-arylation of nitrogen-containing heterocycles

inferredcites →https://doi.org/10.1016/j.tet.2014.06.080openalex-snapshot

Synthesis of 1-aryl indoles via coupling reaction of indoles and aryl halides catalyzed by CuI/metformin

inferredcites →https://doi.org/10.1016/j.tetlet.2007.04.061openalex-snapshot

Benzotriazole: an excellent ligand for Cu-catalyzed N-arylation of imidazoles with aryl and heteroaryl halides

inferredcites →https://doi.org/10.1016/j.tetlet.2007.12.026openalex-snapshot

Ninhydrin: an efficient ligand for the Cu-catalyzed N-arylation of nitrogen-containing heterocycles with aryl halides

inferredcites →https://doi.org/10.1016/j.tetlet.2008.05.008openalex-snapshot

β-Ketoimine as an efficient ligand for copper-catalyzed N-arylation of nitrogen-containing heterocycles with aryl halides

inferredcites →https://doi.org/10.1016/j.tetlet.2011.02.050openalex-snapshot

Copper ferrite nanoparticle-mediated N-arylation of heterocycles: a ligand-free reaction

inferredcites →https://doi.org/10.1016/j.tetlet.2012.08.065openalex-snapshot

Solvent-free Heck and copper-free Sonogashira cross-coupling reactions catalyzed by a polystyrene-anchored Pd(II) phenyldithiocarbazate complex

inferredcites →https://doi.org/10.1016/j.tetlet.2013.12.053openalex-snapshot

N-arylation of indoles with aryl halides using copper/glycerol as a mild and highly efficient recyclable catalytic system

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/s0968-0896(03)00497-8openalex-snapshot

Synthesis and antiparasitic activity of albendazole and mebendazole analogues

inferredcites →https://doi.org/10.1021/cr9001098openalex-snapshot

Solvent-Free Heterocyclic Synthesis

inferredcites →https://doi.org/10.1021/ic902354eopenalex-snapshot

Click-Triazole N2 Coordination to Transition-Metal Ions Is Assisted by a Pendant Pyridine Substituent

inferredcites →https://doi.org/10.1021/ja027433hopenalex-snapshot

The Copper-Catalyzed N-Arylation of Indoles

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/jo201605vopenalex-snapshot

Synthesis of 2H-Indazoles by the [3 + 2] Dipolar Cycloaddition of Sydnones with Arynes

inferredcites →https://doi.org/10.1021/ol005728zopenalex-snapshot

Efficient Palladium-Catalyzed N-Arylation of Indoles

inferredcites →https://doi.org/10.1021/ol201409jopenalex-snapshot

Consecutive Condensation, C–N and N–N Bond Formations: A Copper- Catalyzed One-Pot Three-Component Synthesis of 2 H -Indazole

inferredcites →https://doi.org/10.1021/ol5012423openalex-snapshot

Regioselective Synthesis of 2 H -Indazoles Using a Mild, One-Pot Condensation–Cadogan Reductive Cyclization

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Highly Efficient Microwave-Assisted CO Aminocarbonylation with a Recyclable Pd(II)/TPP-β-Cyclodextrin Cross-Linked Catalyst

inferredcites →https://doi.org/10.1039/c001943gopenalex-snapshot

Recoverable chiral salen complexes for asymmetric catalysis: recent progress

inferredcites →https://doi.org/10.1039/c0cy00064gopenalex-snapshot

Well-defined copper(i) complexes for Click azide–alkyne cycloaddition reactions: one Click beyond

inferredcites →https://doi.org/10.1039/c0sc00107dopenalex-snapshot

Diamine ligands in copper-catalyzed reactions

inferredcites →https://doi.org/10.1039/c1cc13908hopenalex-snapshot

A general and efficient approach to 2H-indazoles and 1H-pyrazoles through copper-catalyzed intramolecular N–N bond formation under mild conditions

inferredcites →https://doi.org/10.1039/c2cy20590dopenalex-snapshot

Cu II –hydrotalcite catalyzed one-pot three component synthesis of 2H-indazoles by consecutive condensation, C–N and N–N bond formations

inferredcites →https://doi.org/10.1039/c2ob06942copenalex-snapshot

Copper(i) acetate-catalyzed azide–alkyne cycloaddition for highly efficient preparation of 1-(pyridin-2-yl)-1,2,3-triazoles

inferredcites →https://doi.org/10.1039/c3ra45298kopenalex-snapshot

CuO nanoparticle catalysed synthesis of 2H-indazoles under ligand free conditions

inferredcites →https://doi.org/10.1039/c4ob01483aopenalex-snapshot

Efficient cobalt-catalyzed C–N cross-coupling reaction between benzamide and aryl iodide in water

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Magnetically recoverable and reusable CuFe 2 O 4 nanoparticle-catalyzed synthesis of benzoxazoles, benzothiazoles and benzimidazoles using dioxygen as oxidant

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Copper/β-diketone-catalysed N-arylation of carbazoles

inferredcites →https://doi.org/10.1039/c6ra11678gopenalex-snapshot

CuI nanoparticles mediated expeditious synthesis of 2-substituted benzimidazoles using molecular oxygen as the oxidant

inferredcites →https://doi.org/10.1055/s-0033-1340979openalex-snapshot

Ligand-Free Copper(I) Oxide Nanoparticle Catalyzed Three-Component Synthesis of 2H-Indazole Derivatives from 2-Halobenzaldehydes, Amines and Sodium Azide in Polyethylene Glycol as a Green Solvent

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A Solvent-Free and One-Pot Strategy for Ecocompatible Synthesis of Substituted Benzofurans from Various Salicylaldehydes, Secondary Amines, and Nonactivated Alkynes Catalyzed by Copper(I) Oxide Nanoparticles

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2-Phenyl-2-(4-phenyl-1H-1,2,3-triazol-1-yl)ethanol as an Efficient and Versatile Auxiliary Ligand in Copper(II)-Catalyzed Buchwald–Hartwig and Sharpless–Meldal C–N Bond-Forming Reactions

inferredcites →https://doi.org/10.1080/00034983.1984.11811787openalex-snapshot

Benzimidazoles in the treatment of trichuriasis: a review

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Imidazole and Benzimidazole Derivatives as Chemotherapeutic Agents

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

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N‐Arylation of Nitrogen‐Containing Heterocycles with Cu(II) Complex of 4‐(2,2′:6′,2“‐Terpyridin‐4′‐yl)toluene as a Versatile and Efficient Catalyst

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Copper(I) Complex of Dihydro Bis(2‐Mercapto Benzimidazolyl) Borate as an Efficient Homogeneous Catalyst for the Synthesis of 2 H ‐Indazoles and 5‐Substituted 1 H ‐Tetrazoles

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