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Design and identification of nano‐Mg‐[4‐methoxy phenyl‐salicylaldimine–methyl‐pyranopyrzole] Cl<sub>2</sub> and its catalytic application on the preparation of 1‐(α‐aminoalkyl)‐2‐naphthols.
- Published in:
- Applied Organometallic Chemistry, 2020, v. 34, n. 3, p. N.PAG, doi. 10.1002/aoc.5372
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- Article
Preparation and characterization of nano‐Co‐[4‐chlorophenyl‐salicylaldimine‐methyl pyranopyrazole]Cl<sub>2</sub> as a new Schiff base complex and catalyst for the solvent‐free synthesis of 1‐amidoalkyl‐2‐naphthols
- Published in:
- Applied Organometallic Chemistry, 2020, v. 34, n. 1, p. N.PAG, doi. 10.1002/aoc.5252
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- Article
Preparation and characterization of Cu (II) supported on poly(8‐hydroxyquinoline‐p‐styrene sulphonate) and its application as catalyst for the synthesis of hexahydroquinolines.
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- Applied Organometallic Chemistry, 2018, v. 32, n. 7, p. 1, doi. 10.1002/aoc.4368
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- Article
Synthesis, characterization and application of 3‐methyl‐1‐sulfonic acid imidazolium tetrachloroferrate as nanostructured catalyst for the tandem reaction of <italic>β</italic>‐naphthol with aromatic aldehydes and amide derivatives
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- Applied Organometallic Chemistry, 2018, v. 32, n. 2, p. 1, doi. 10.1002/aoc.4058
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- Article
Synthesis of pyranopyrazoles using nano-Fe-[phenylsalicylaldiminemethylpyranopyrazole]Cl<sub>2</sub> as a new Schiff base complex and catalyst.
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- Applied Organometallic Chemistry, 2018, v. 32, n. 1, p. n/a, doi. 10.1002/aoc.3968
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- Article
Nano–Mn‐[4‐nitrophenyl‐salicylaldimine‐methyl pyranopyrazole] Cl<sub>2</sub> as a new nanostructured Schiff base complex and catalyst for the synthesis of hexahydroquinolines.
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- Applied Organometallic Chemistry, 2017, v. 31, n. 12, p. 1, doi. 10.1002/aoc.3845
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- Article
Synthesis, characterization and application of nano-CoAl<sub>2</sub>O<sub>4</sub> as an efficient catalyst in the preparation of hexahydroquinolines.
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- Applied Organometallic Chemistry, 2017, v. 31, n. 12, p. 1, doi. 10.1002/aoc.3815
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- Article
Preparation of 1,2,4,5-tetrasubstituted imidazoles over magnetic core-shell titanium dioxide nanoparticles.
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- Applied Organometallic Chemistry, 2016, v. 30, n. 8, p. 691, doi. 10.1002/aoc.3491
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- Article
Synthesis of 4‐((2‐hydroxynaphthalen‐1‐yl)(aryl)methyl)‐5‐methyl‐2‐phenyl‐1H‐pyrazol‐3(2H)‐ones using nano‐Zn‐[2‐boromophenyl‐salicylaldimine‐methylpyranopyrazole]Cl<sub>2</sub> nanoparticles
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- Journal of the Chinese Chemical Society, 2019, v. 66, n. 5, p. 529, doi. 10.1002/jccs.201800215
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- Article
Catalytic Applications of Nano-Fe-[Phenyl-Salicylaldimine-Methylpyranopyrazole]Cl<sub>2</sub> as a Schiff Base Complex and Nanostructured Catalyst for the Synthesis of Hexahydroquinolines.
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- Journal of the Chinese Chemical Society, 2017, v. 64, n. 12, p. 1496, doi. 10.1002/jccs.201700211
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- Article
Solvent-free Synthesis of 1,8-Dioxo-octahydroxanthenes and Tetra-hydrobenzo[a]xanthene-11-ones over Poly( N,N′-dibromo- N-ethylnaphtyl-2,7-sulfonamide).
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- Journal of the Chinese Chemical Society, 2017, v. 64, n. 9, p. 1088, doi. 10.1002/jccs.201700082
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- Article
Mn-[4-Chlorophenyl-Salicylaldimine-Methylpyranopyrazole]Cl<sub>2</sub> as a Novel Nanostructured Schiff Base Complex and Catalyst.
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- Journal of the Chinese Chemical Society, 2017, v. 64, n. 7, p. 727, doi. 10.1002/jccs.201600890
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- Article
The Synthesis of 2,11-Diamino-4,9-diphenyl-4,9-dihydrobenzo [f] pyrano[3,2-h]chromene-3,10-dicarbonitrile Derivatives using Triethanolammonium Acetate as a Green Ionic Liquid.
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- Journal of the Chinese Chemical Society, 2017, v. 64, n. 7, p. 757, doi. 10.1002/jccs.201700019
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- Article
Nano-TiO<sub>2</sub> as an Efficient Catalyst for Tandem Knoevenagel-Michael-Cyclocondensation Reaction of Dimedone with Aromatic Aldehydes and Ammonium Acetate or Aromatic Amines under Solvent-free Conditions.
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- Journal of the Chinese Chemical Society, 2016, v. 63, n. 2, p. 165, doi. 10.1002/jccs.201500384
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Condensation of Aryl Aldehydes, 2-naphthol, and Thioacetamide Catalyzed by N-halo Reagents in Neutral Media.
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- Journal of the Chinese Chemical Society, 2015, v. 62, n. 10, p. 850, doi. 10.1002/jccs.201500125
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- Article
Water Mediated Domino Knoevenagel-Michael-cyclocondensation Reaction of Malononitrile, Various Aldehydes and Barbituric Acid Derivatives Using Boric Acid Aqueous Solution System Compared with Nano-titania Sulfuric Acid.
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- Journal of the Chinese Chemical Society, 2015, v. 62, n. 8, p. 675, doi. 10.1002/jccs.201500115
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- Article
Knoevenagel-Michael-cyclocondensation Tandem Reaction of Malononitrile, Various Aldehydes and Dimedone Catalyzed by Sulfonic Acid Functionalized Pyridinium Chloride as a New Ionic Liquid and Catalyst.
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- Journal of the Chinese Chemical Society, 2015, v. 62, n. 5, p. 398, doi. 10.1002/jccs.201400413
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- Article
Trityl Chloride (TrCl): Efficient and Homogeneous Organocatalyst for the Solvent-Free Synthesis of 14-Aryl-14 H-dibenzo[ a, j]xanthenes by in situ Formation of Carbocationic System.
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- Journal of the Chinese Chemical Society, 2012, v. 59, n. 7, p. 860, doi. 10.1002/jccs.201100719
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- Article
Cs<sub>2</sub>CO<sub>3</sub>/[bmim]Br as an Efficient, Green, and Reusable Catalytic System for the Synthesis of N-Alkyl Derivatives of Phthalimide under Mild Conditions.
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- Research Letters in Organic Chemistry, 2008, p. 1, doi. 10.1155/2008/419054
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Synthesis, characterization, and application of a triazene-based polysulfone as a dye adsorbent.
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- Journal of Applied Polymer Science, 2013, v. 129, n. 6, p. 3439, doi. 10.1002/app.39069
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- Article
[Msim]CuCl<sub>3</sub>: as an efficient catalyst for the preparation of 5-amino-1H-pyrazole-4-carbonitriles by anomeric based oxidation.
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- Zeitschrift für Naturforschung B: A Journal of Chemical Sciences, 2022, v. 77, n. 1, p. 87, doi. 10.1515/znb-2021-0153
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- Article
Three-component condensation reaction of various aldehydes, dimedone and malononitrile catalyzed by boric acid in water in comparison with multifunctional ionic liquids as green catalytic systems.
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- Zeitschrift für Naturforschung B: A Journal of Chemical Sciences, 2018, v. 73, n. 10, p. 707, doi. 10.1515/znb-2018-0101
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- Article
Ionic Liquid 3-Methyl-1-sulphonic Acid Imidazolium Chloride {[Msim]Cl}: A Highly Efficient, Mild and Green Catalyst for the Synthesis of β-Acetamido Ketones.
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- South African Journal of Chemistry, 2012, v. 65, p. 63
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- Article
Nano-Fe<sub>3</sub>O<sub>4</sub>/O<sub>2</sub>: Green, Magnetic and Reusable Catalytic System for the Synthesis of Benzimidazoles.
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- South African Journal of Chemistry, 2012, v. 65, p. 280
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- Article
Ionic Liquid 3-Methyl-1-sulphonic Acid Imidazolium Chloride {[Msim]Cl}: A Highly Efficient, Mild and Green Catalyst for the Synthesis of β-Acetamido Ketones.
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- South African Journal of Chemistry, 2012, v. 65, p. 63
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- Article
A Green Solventless Protocol for the Synthesis of β-Enaminones and β-Enamino Esters Using Silica Sulfuric Acid as a Highly Efficient, Heterogeneous and Reusable Catalyst.
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- E-Journal of Chemistry, 2010, v. 7, n. 4, p. 1546, doi. 10.1155/2010/829547
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- Article
An Efficient Solvent-Free Protocol for the Synthesis of 1-Amidoalkyl-2-naphthols using Silica-Supported Molybdatophosphoric Acid.
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- E-Journal of Chemistry, 2010, v. 7, n. 4, p. 1162, doi. 10.1155/2010/512392
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- Article
LiHSO<sub>4</sub>/SiO<sub>2</sub> as a New, Efficient and Reusable Catalytic System for the Chemoselective Conversion of Aldehydes to Acylals under Solvent-Free Conditions.
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- E-Journal of Chemistry, 2009, n. S1, p. S390, doi. 10.1155/2009/953175
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- Article
Bentonite Clay K-10 as an Efficient Reagent for the Synthesis of Quinoxaline Derivatives at Room Temperature.
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- E-Journal of Chemistry, 2009, n. S1, p. S247, doi. 10.1155/2009/354273
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- Article
Ionic liquid 1-butyl-3-methylimidazolium bromide ([bmim]Br): a green and neutral reaction media for the efficient, catalyst-free synthesis of quinoxaline derivatives.
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- Journal of the Serbian Chemical Society, 2010, v. 75, n. 10, p. 1315, doi. 10.2298/JSC091014109Z
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- Article
A Convenient Catalytic Method for the Synthesis of Pyridines with Henna and Pyrazole Moieties using Cooperative Vinylogous Anomeric‐Based Oxidation.
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- ChemistrySelect, 2022, v. 7, n. 23, p. 1, doi. 10.1002/slct.202200346
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- Article
Three‐Component Synthesis of Spiropyrans Using SBA‐15/En Bonded Phosphorous Acid [SBA‐15/Pr‐NH<sub>1‐y</sub>(CH<sub>2</sub>PO<sub>3</sub>H<sub>2</sub>)<sub>y</sub>‐Et‐NH<sub>2‐x</sub>(CH<sub>2</sub>PO<sub>3</sub>H<sub>2</sub>)<sub>x</sub>] as a New Nanoporous Heterogeneous Catalyst
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- ChemistrySelect, 2018, v. 3, n. 43, p. 12144, doi. 10.1002/slct.201802525
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- Article
Silica supported boric tri-sulfuric anhydride as a novel and efficient catalyst for solvent-free synthesis of coumarins via Pechmann condensation.
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- ARKIVOC: Online Journal of Organic Chemistry, 2012, p. 111
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- Article
Multicomponent synthesis of pyrimido[4,5-b] quinolines over a carbocationic catalytic system.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-43793-5
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- Article
Multicomponent synthesis of pyrimido[4,5-b] quinolines over a carbocationic catalytic system.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-43793-5
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- Article
Multicomponent synthesis of 2-amino-3-cyano pyridines catalyzed by Nano-[Fe-4BSP]Cl<sub>2</sub> as a new Schiff base complex and catalyst.
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- Research on Chemical Intermediates, 2023, v. 49, n. 11, p. 4771, doi. 10.1007/s11164-023-05097-1
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- Article
Nano-[Cu-4C3NSP](Cl)<sub>2</sub> as a new catalyst for the preparation of pyrimido[4,5-b]quinoline derivatives.
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- Research on Chemical Intermediates, 2023, v. 49, n. 2, p. 507, doi. 10.1007/s11164-022-04901-8
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- Article
Nano-[Mn-PSMP]Cl<sub>2</sub> as a new Schiff base complex and catalyst for the synthesis of N,N'-alkylidene bisamides.
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- Research on Chemical Intermediates, 2022, v. 48, n. 4, p. 1423, doi. 10.1007/s11164-022-04668-y
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- Article
The synthesis of 5-amino-1H-pyrazole-4-carbonitriles by anomeric based oxidative aromatization over [CSPy]ZnCl3 as a new catalyst.
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- Research on Chemical Intermediates, 2021, v. 47, n. 7, p. 2689, doi. 10.1007/s11164-021-04437-3
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- Article
Nano-Co-[4-chlorophenyl-salicylaldimine-pyranopyrimidine dione]Cl2 as a new Schiff base complex and catalyst for the one-pot synthesis of some 4H-pyrimido[2,1-b]benzazoles.
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- Research on Chemical Intermediates, 2020, v. 46, n. 12, p. 5567, doi. 10.1007/s11164-020-04279-5
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- Article
Fabrication, identification and application of Fe<sub>3</sub>O<sub>4</sub> bonded nicotinic acid-sulfonic acid chloride as a retrievable magnetic nanostructured catalyst for the one-pot synthesis of 1-carbamato-alkyl-2-naphthols.
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- Research on Chemical Intermediates, 2018, v. 44, n. 10, p. 5893, doi. 10.1007/s11164-018-3462-5
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- Article
Synthesis of spiropyran derivatives over 1-(carboxymethyl) pyridinium iodide as nanostructured pyridinium salt under aqueous media.
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- Canadian Journal of Chemistry, 2017, v. 95, n. 2, p. 194, doi. 10.1139/cjc-2016-0374
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- Article
Friedel-Crafts alkylation of 4-hydroxycoumarin over silica-bonded 1,4-diaza-bicyclo[2.2.2] octane-sulfonic acid chloride as nanostructured heterogeneous catalyst.
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- Canadian Journal of Chemistry, 2017, v. 95, n. 1, p. 16, doi. 10.1139/cjc-2016-0258
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- Article
Trityl chloride promoted the synthesis of 3-(2,6-diarylpyridin-4-yl)-1H-indoles and 2,4,6-triarylpyridines by in situ generation of trityl carbocation and anomeric based oxidation in neutral media.
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- Canadian Journal of Chemistry, 2016, v. 94, n. 7, p. 626, doi. 10.1139/cjc-2015-0629
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- Article
Solvent-free preparation of amidoalkyl phenols catalyzed by trityl chloride under neutral media.
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- Canadian Journal of Chemistry, 2015, v. 93, n. 11, p. 1245, doi. 10.1139/cjc-2015-0230
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- Article
A catalyst-free protocol for the green and efficient condensation of indoles with aldehydes in ionic liquids.
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- Canadian Journal of Chemistry, 2009, v. 87, n. 2, p. 416, doi. 10.1139/V08-172
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- Article
Triarylmethyl chlorides as novel, efficient, and mild organic catalysts for the synthesis of N-sulfonyl imines under neutral conditions.
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- Canadian Journal of Chemistry, 2008, v. 86, n. 5, p. 456, doi. 10.1139/V08-039
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- Article
Zinc oxide as a new, highly efficient, green, and reusable catalyst for microwave-assisted Michael addition of sulfonamides to α,β-unsaturated esters in ionic liquids.
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- Canadian Journal of Chemistry, 2007, v. 85, n. 6, p. 438, doi. 10.1139/V07-050
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- Article
A solvent-free protocol for facile condensation of indoles with carbonyl compounds using silica chloride as a new, highly efficient, and mild catalyst.
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- Canadian Journal of Chemistry, 2007, v. 85, n. 6, p. 416, doi. 10.1139/V07-051
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- Article