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A greener route for the one-pot synthesis of 1,2,4,5-tetraarylated imidazoles

https://doi.org/10.1007/s00706-012-0724-6
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Outgoing claims: the papers this work cites, builds on, or argues with.

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Constitution des Lophins und des Amarins
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Ueber die Constitution des Lophins und verwandter Verbindungen
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Ferric Perchlorate Catalyzed One‐pot Synthesis of 1,2,3,4‐Tetrahydro‐2‐pyrimidinones and ‐thiones: an Expedient Protocol for the Biginelli Reaction
inferredcites →https://doi.org/10.1007/s00706-007-0736-9openalex-snapshot
Highly Efficient, Four Component, One-pot Synthesis of Tetrasubstituted Imidazoles Using a Catalytic Amount of FeCl3 · 6H2O
inferredcites →https://doi.org/10.1007/s11030-009-9197-xopenalex-snapshot
Wells–Dawson heteropolyacid supported on silica: a highly efficient catalyst for synthesis of 2,4,5-trisubstituted and 1,2,4,5-tetrasubstituted imidazoles
inferredcites →https://doi.org/10.1016/0014-2999(78)90117-6openalex-snapshot
Electroencephalographic study of the short-acting hypnotics etomidate and methohexital in dogs
inferredcites →https://doi.org/10.1016/j.bmcl.2005.09.072openalex-snapshot
The identification of potent and selective imidazole-based inhibitors of B-Raf kinase
inferredcites →https://doi.org/10.1016/j.catcom.2006.04.004openalex-snapshot
Solvent-free synthesis of tetrasubstituted imidazoles on silica gel/NaHSO4 support
inferredcites →https://doi.org/10.1016/j.cclet.2007.09.030openalex-snapshot
Solventless synthesis of 2-aryl-1-arylmethyl-1H-1,3-benzimidazoles catalyzed by Fe(ClO4)3 at room temperature
inferredcites →https://doi.org/10.1016/j.molcata.2006.06.013openalex-snapshot
Catalytic synthesis of 2,3-dihydro-1H-1,5-benzodiazepines by ferric perchlorate
inferredcites →https://doi.org/10.1016/j.molcata.2006.08.048openalex-snapshot
Highly efficient, four-component one-pot synthesis of tetrasubstituted imidazoles using Keggin-type heteropolyacids as green and reusable catalysts
inferredcites →https://doi.org/10.1016/j.molcata.2006.10.009openalex-snapshot
One-pot synthesis of highly substituted imidazoles using molecular iodine: A versatile catalyst
inferredcites →https://doi.org/10.1016/j.molcata.2006.10.048openalex-snapshot
Highly efficient, one-pot, solvent-free synthesis of tetrasubstituted imidazoles using HClO4–SiO2 as novel heterogeneous catalyst
inferredcites →https://doi.org/10.1016/j.molcata.2006.10.056openalex-snapshot
Potassium dodecatugstocobaltate trihydrate (K5CoW12O40·3H2O): A mild and efficient reusable catalyst for the one-pot synthesis of 1,2,4,5-tetrasubstituted imidazoles under conventional heating and microwave irradiation
inferredcites →https://doi.org/10.1016/j.tet.2009.10.019openalex-snapshot
l-Proline: an efficient catalyst for the one-pot synthesis of 2,4,5-trisubstituted and 1,2,4,5-tetrasubstituted imidazoles
inferredcites →https://doi.org/10.1016/j.tetlet.2006.05.097openalex-snapshot
A one-pot synthesis of 1,2,4,5-tetraarylimidazoles using molecular iodine as an efficient catalyst
inferredcites →https://doi.org/10.1016/j.tetlet.2008.02.053openalex-snapshot
An efficient and one-pot synthesis of 2,4,5-trisubstituted and 1,2,4,5-tetrasubstituted imidazoles catalyzed by InCl3·3H2O
inferredcites →https://doi.org/10.1016/j.tetlet.2008.02.100openalex-snapshot
BF3·SiO2: an efficient reagent system for the one-pot synthesis of 1,2,4,5-tetrasubstituted imidazoles
inferredcites →https://doi.org/10.1016/s0009-9236(99)70017-2openalex-snapshot
genotype–related efficacy of omeprazole for the treatment of infection caused by
inferredcites →https://doi.org/10.1016/s0022-3182(89)80212-2openalex-snapshot
Educational materials in review
inferredcites →https://doi.org/10.1016/s0040-4039(03)00018-2openalex-snapshot
A novel one-pot synthesis of tetrasubstituted imidazoles under solvent-free conditions and microwave irradiation
inferredcites →https://doi.org/10.1016/s0926-860x(01)00837-7openalex-snapshot
Direct conversion of methane into oxygenates
inferredcites →https://doi.org/10.1016/s0926-860x(02)00600-2openalex-snapshot
Selective oxidation of benzene to phenol with N2O by unsupported and supported FePO4 catalysts
inferredcites →https://doi.org/10.1016/s0960-894x(99)00081-5openalex-snapshot
Potent, orally absorbed glucagon receptor antagonists
inferredcites →https://doi.org/10.1016/s0960-894x(99)00112-2openalex-snapshot
Analogues of 4,5-bis(3,5-dichlorophenyl)-2-trifluoromethyl-1H-imidazole as potential antibacterial agents
inferredcites →https://doi.org/10.1021/jm00194a023openalex-snapshot
Antimycotic imidazoles. Part 4. Synthesis and antifungal activity of ketoconazole, a new potent orally active broad-spectrum antifungal agent
inferredcites →https://doi.org/10.1021/jm010523xopenalex-snapshot
Potent, Orally Active Heterocycle-Based Combretastatin A-4 Analogues: Synthesis, Structure−Activity Relationship, Pharmacokinetics, and In Vivo Antitumor Activity Evaluation
inferredcites →https://doi.org/10.1021/jo00077a033openalex-snapshot
Synthesis of imidazoles via hetero-Cope rearrangements
inferredcites →https://doi.org/10.1021/jo01227a004openalex-snapshot
THE ACTION OF AMMONIA ON BENZIL
inferredcites →https://doi.org/10.1038/290514a0openalex-snapshot
Selective antagonists of benzodiazepines
inferredcites →https://doi.org/10.1038/372739a0openalex-snapshot
A protein kinase involved in the regulation of inflammatory cytokine biosynthesis
inferredcites →https://doi.org/10.1039/b006201oopenalex-snapshot
One-pot synthesis of tetrasubstituted imidazoles catalyzed by zeolite HY and silica gel under microwave irradiation
inferredcites →https://doi.org/10.1177/030006057500300205openalex-snapshot
Cimetidine—A Non-Thiourea H 2 -Receptor Antagonist
inferredcites →https://doi.org/10.1515/hc.2006.12.5.369openalex-snapshot
IRON (III) PHOSPHATE DIHYDRATE - CATALYZED ONE-POT SYNTHESIS OF DIHYDROPYRIMIDINONES AND THIONES : AN IMPROVED PROCEDURE FOR THE BIGINELLI REACTION
inferredcites →https://doi.org/10.3987/com-10-12019openalex-snapshot
Anhydrous FePO4: A Green and Cost-Effective Catalyst for the One-Pot Three Component Synthesis of 2,4,5-Triarylated Imidazoles

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.3983581openalex-extracted
A new catalyst for the synthesis of 2-substituted perimidines catalyzed by FePO4[enter Paper Title]
inferred← citeshttps://doi.org/10.1002/adsc.201801381openalex-snapshot
Catalytic Synthesis of 1,2,4,5‐Tetrasubstituted 1 H ‐Imidazole Derivatives: State of the Art
inferred← citeshttps://doi.org/10.1002/chin.201307103openalex-snapshot
ChemInform Abstract: A Greener Route for the One‐Pot Synthesis of 1,2,4,5‐Tetraarylated Imidazoles
inferred← citeshttps://doi.org/10.1002/ejoc.201300688openalex-snapshot
Synthesis of 1,2‐Diaryl‐ and 1‐Aryl‐2‐alkylimidazoles with Sterically Demanding Substituents
inferred← citeshttps://doi.org/10.1016/j.jtusci.2014.01.007openalex-snapshot
Applications of microwave technology to rapid synthesis of substituted imidazoles on silica-supported SbCl3as an efficient heterogeneous catalyst
inferred← citeshttps://doi.org/10.1016/j.jtusci.2015.10.004openalex-snapshot
A new catalyst for the synthesis of 2-substituted perimidines catalysed by FePO4
inferred← citeshttps://doi.org/10.1080/10426507.2015.1100184openalex-snapshot
A practical and green approach towards synthesis of multisubstituted imidazoles using boric acid as efficient catalyst
inferred← citeshttps://doi.org/10.1080/15533174.2016.1216452openalex-snapshot
A one-pot synthesis of 1,2-dihydro-1-arylnaphtho[1,2-e][1,3]oxazine-3-ones catalyzed by iron(III) phosphate under solvent-free condition
inferred← citeshttps://doi.org/10.1134/s1070427214100176openalex-snapshot
Solvent-free synthesis of 4,4′-diaminotriarylmethanes-leuco malachite materials in the presence of FePO4
inferred← citeshttps://doi.org/10.1134/s1070428020050243openalex-snapshot
[Bmim]HSO4-Catalyzed Synthesis of Tetrasubstituted Imidazoles as Potential Mutant Isocitrate Dehydrogenase 1 Inhibitors
inferred← citeshttps://doi.org/10.1134/s1070428020060160openalex-snapshot
Synthesis of 8-Aryl-7H-acenaphtho[1,2-d]imidazoles Using Fe3O4 NPs@GO@C4H8SO3H as a Green and Recyclable Magnetic Nanocatalyst
inferred← citeshttps://doi.org/10.1134/s1070428022060112openalex-snapshot
Green Route for the Synthesis of 3,4-Disubstituted Isoxazol-5(4H)-ones Using GO@Fe(ClO4)3 Nanocatalyst under Solvent-Free Conditions
inferred← citeshttps://doi.org/10.1134/s1070428022090184openalex-snapshot
Synthesis of 3,4-Dihydropyrimidin-2(1H)-ones, -thione, and -selones, Catalyzed by TiO2 Nanoparticles
inferred← citeshttps://doi.org/10.22453/lsj-018.2.219-225openalex-snapshot
Four components synthesis of 1,2,3,4-tetrasubstituted pyrroles using iron (iii) phosphate as a green activator.
inferred← citeshttps://doi.org/10.3329/jsr.v15i1.60623openalex-snapshot
Samarium(III) Triflate as an Efficient and Reusable Catalyst for the Facile Synthesis of 1,2,4,5-Tetrasubstituted Imidazoles
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