Works matching DE "NITROAROMATIC compounds"
Results: 902
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- Biotechnic & Histochemistry, 2003, v. 78, n. 6, p. 333, doi. 10.1080/10520290410001671353
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Synergistic Nanoscale Mn<sub>3</sub>O<sub>4</sub>‐CoO‐Co Heterojunctions for Boosting the Selectivity in Hydrogenation of Nitrostyrenes and Nitroarenes.
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- Chemistry - A European Journal, 2024, v. 30, n. 71, p. 1, doi. 10.1002/chem.202403236
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Photoredox/Bismuth Relay Catalysis Enabling Reductive Alkylation of Nitroarenes with Aldehydes.
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- Chemistry - A European Journal, 2024, v. 30, n. 40, p. 1, doi. 10.1002/chem.202401456
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Controlling Diastereoselectivity in Dearomatizing Diels‐Alder Reactions of Nitroarenes with 2‐Trimethylsilyloxycyclohexadiene.
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- Chemistry - A European Journal, 2024, v. 30, n. 34, p. 1, doi. 10.1002/chem.202303697
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Reduction‐Specified Coupling Reactions of Nitroarenes by Heterogeneous Cobalt Catalysis.
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- Chemistry - A European Journal, 2024, v. 30, n. 24, p. 1, doi. 10.1002/chem.202304373
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Direct Synthesis of Unprotected Indolines Through Intramolecular sp<sup>3</sup> C−H Amination Using Nitroarenes as Aryl Nitrene Precursors.
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- Chemistry - A European Journal, 2023, v. 29, n. 54, p. 1, doi. 10.1002/chem.202301978
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Denitrative Hydroxylation of Unactivated Nitroarenes.
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- Chemistry - A European Journal, 2023, v. 29, n. 16, p. 1, doi. 10.1002/chem.202203807
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Palladium‐Catalyzed Reductive Double Carbonylation of Nitroarenes with Aryl Halides Using Mo(CO)<sub>6</sub> as a Reductant and Carbonyl Source.
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- Chemistry - A European Journal, 2023, v. 29, n. 2, p. 1, doi. 10.1002/chem.202202880
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The effects of characteristics of substituents on toxicity of the nitroaromatics: HiT QSAR study.
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- Journal of Computer-Aided Molecular Design, 2008, v. 22, n. 10, p. 747, doi. 10.1007/s10822-008-9211-x
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Soapwort oxidoreductase is involved in trinitrotoluene detoxification.
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- Biologia Plantarum, 2007, v. 51, n. 2, p. 367
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A pillar[5]arene-based fluorescence sensor for nitroaromatic compound detection.
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- Journal of Molecular Science, 2024, v. 40, n. 1, p. 18, doi. 10.13563/j.cnki.jmolsci.2023.11.028
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Mechanistic insight into the sensing of nitroaromatic compounds by metal-organic frameworks.
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- Communications Chemistry, 2019, v. 2, n. 1, p. N.PAG, doi. 10.1038/s42004-019-0135-2
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Rapid evaluation of the substrate specificity of 3-nitrobenzoic acid dioxygenase MnbAB via colorimetric detection using Saltzman reagent.
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- Journal of Industrial Microbiology & Biotechnology, 2021, v. 48, n. 9/10, p. 1, doi. 10.1093/jimb/kuab064
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Development of Pyrene Embedded Luminophore via π‐linker: Room Temperature Phosphorescence (RTP) and Sensing towards Nitroaromatics (NACs).
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- ChemPhotoChem, 2024, v. 8, n. 11, p. 1, doi. 10.1002/cptc.202400046
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Aggregation Induced Emission (AIE)‐Active Poly(acrylates) for Electrofluorochromic Detection of Nitroaromatic Compounds.
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- ChemPhotoChem, 2022, v. 6, n. 11, p. 1, doi. 10.1002/cptc.202200168
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In Vitro Synthesis of 1,N<sup>6</sup>-Etheno-2-deoxyadenosine and 1, N²-E theno-2′-deoxygua nosine by 2, 4-dinitrophenol and 1,3-dinitropyrene in Presence of a Bacterial Nitroreductase.
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- Environmental Toxicology, 2007, v. 22, n. 2, p. 222, doi. 10.1002/tox.20253
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Accumulation of an Aromatic Amine, β-Phenethylamine, in Root Nodules of Adzuki Bean Vigna angularis.
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- Plant & Soil, 2006, v. 280, n. 1/2, p. 229, doi. 10.1007/s11104-005-3096-4
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Distinguishing between metabolically active and inactive roots by combined staining with 2,3,5-triphenyltetrazolium chloride and image colour analysis.
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- Plant & Soil, 2005, v. 271, n. 1/2, p. 75, doi. 10.1007/s11104-004-2027-0
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Investigating the Fate of Nitroaromatic (TNT) and Nitramine (RDX and HMX) Explosives in Fractured and Pristine Soils.
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- Journal of Environmental Quality, 2009, v. 38, n. 6, p. 2285, doi. 10.2134/jeq2008.0477
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Site-Specific Adsorption of 1,3-Dinitrobenzene to Bacterial Surfaces: A Mechanism of n-π Electron-Donor-Acceptor Interactions.
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- Journal of Environmental Quality, 2008, v. 37, n. 3, p. 824, doi. 10.2134/jeq2007.0236
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A tetraphenylethylene-based superphane for selective detection and adsorption of trace picric acid in aqueous media.
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- Supramolecular Chemistry, 2023, v. 34, n. 11/12, p. 497, doi. 10.1080/10610278.2024.2398575
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Photocatalytic properties and luminescent sensing of a new 2D layer coordination polymer.
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- Supramolecular Chemistry, 2019, v. 31, n. 5, p. 361, doi. 10.1080/10610278.2019.1592173
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New entities for sensory chemistry based on calix[4]arene-carbazole conjugates: from synthesis to applications.
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- Supramolecular Chemistry, 2013, v. 25, n. 12, p. 782, doi. 10.1080/10610278.2013.804185
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A fluorescence-based cyclodextrin sensor to detect nitroaromatic explosives.
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- Supramolecular Chemistry, 2010, v. 22, n. 1, p. 65, doi. 10.1080/10610270903378032
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Polyamide model compound containing the urea group as selective colorimetric sensing probe towards aromatic diamines.
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- Supramolecular Chemistry, 2009, v. 21, n. 5, p. 337, doi. 10.1080/10610270701882193
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Molecular Recognition of Aromatic Nitro Compounds at Cyclodextrin Dithiocarbamate-modified Electrodes.
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- Supramolecular Chemistry, 2003, v. 15, n. 6, p. 417, doi. 10.1080/1061027031000119684
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Influence of Ca(OH) 2 on the Extraction Efficiency of Nitroaromatic Compounds from Soils.
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- International Journal of Environmental Analytical Chemistry, 2003, v. 83, n. 9, p. 769, doi. 10.1080/03067310310001598391
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Seasonal Trends and Site Differences of Nitroaromatic Compounds in PM 2.5 in Sichuan Basin and Their Effects on Light Absorption of Brown Carbon.
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- Toxics, 2025, v. 13, n. 2, p. 124, doi. 10.3390/toxics13020124
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Design of Schiff Base-Like Postmetallocene Catalytic Systems for Polymerization of Olefins: III. Synthesis of 1,2-Bis-(arylimino)acenaphthenes Having Cyclic Substituents.
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- Russian Journal of Organic Chemistry, 2005, v. 41, n. 9, p. 1329, doi. 10.1007/s11178-005-0341-5
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Behavior of Benzoins and Hydroxy ketones in Acid Media: I. Reaction of 1-Aryl-2-(2,5-dimethylthiophen-3-yl)-2-hydroxyethanones with Thiols in Trifluoroacetic Acid.
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- Russian Journal of Organic Chemistry, 2005, v. 41, n. 1, p. 87, doi. 10.1007/s11178-005-0125-y
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Tetrazoles: XLVII. A route to tetrazole-containing dendrimers.
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- Russian Journal of Organic Chemistry, 2004, v. 40, n. 9, p. 1318, doi. 10.1007/s11178-005-0013-5
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Reaction of 4-Nitrochlorobenzene with 2-Methoxyphenylacetonitrile.
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- Russian Journal of Organic Chemistry, 2003, v. 39, n. 9, p. 1362, doi. 10.1023/B:RUJO.0000010231.69198.a0
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Colloidal and Nanosized Catalysts in Organic Synthesis: XXV. Reductive Alkylation of Nitroarenes with Alcohols in the Presence of a Supported Copper Nanocatalyst.
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- Russian Journal of General Chemistry, 2023, v. 93, n. 3, p. 457, doi. 10.1134/S1070363223030015
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Colloid and Nanosized Catalysts in Organic Synthesis: XXI. Reduction of Nitroarenes Catalyzed by Immobilized Nickel Nanoparticles.
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- Russian Journal of General Chemistry, 2019, v. 89, n. 8, p. 1549, doi. 10.1134/S1070363219080012
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Regiochemistry of Deoxygenation of Nitro-Containing Isatins with Tris(diethylamino)phosphine.
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- Russian Journal of General Chemistry, 2018, v. 88, n. 11, p. 2296, doi. 10.1134/S1070363218110087
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Catalytic Activity of Nickel Nanoparticles in the Reaction of Reduction of Nitroarenes.
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- Russian Journal of General Chemistry, 2018, v. 88, n. 3, p. 410, doi. 10.1134/S1070363218030064
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Modification of silica nanoparticles with stereisomers of p- tert-butylthiacalix[4]arene containing four 2-oxo-2-{[3-(triethoxysilyl)prop-1-yl]amino}ethoxy substituents at the lower rim.
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- Russian Journal of General Chemistry, 2017, v. 87, n. 9, p. 1969, doi. 10.1134/S1070363217090122
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Synthesis and reactivity of maleopimaric acid N-aryl(aralkyl)imidoamides.
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- Russian Journal of General Chemistry, 2016, v. 86, n. 4, p. 821, doi. 10.1134/S1070363216040101
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Colloid and nanosized catalysts in organic synthesis: IV. Reduction of nitroarenes with hydrazine hydrate catalyzed with metal nanoparticles.
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- Russian Journal of General Chemistry, 2014, v. 84, n. 8, p. 1515, doi. 10.1134/S107036321408012X
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Hydrogenation of unsaturated compounds in the presence of palladium-containing modified carbon nanofibers.
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- Russian Journal of General Chemistry, 2013, v. 83, n. 5, p. 928, doi. 10.1134/S1070363213050071
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Y-Shaped Fluorophores Based on N(2)-Aryl-1,2,3-triazoles: Synthesis and Study of Photophysical and Chemosensor Properties for the Detection of Nitroaromatic Compounds.
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- Doklady Chemistry, 2023, v. 512, n. 1, p. 232, doi. 10.1134/S0012500823600682
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Modification of PMMA/graphite nanocomposites through ion beam technique.
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- Radiation Effects & Defects in Solids: Incorporating Plasma Techniques & Plasma Phenomena, 2013, v. 168, n. 7/8, p. 512, doi. 10.1080/10420150.2012.763038
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Cobalt Nanoparticles Supported on TiO 2 for Highly Selective Formation of N -Benzylideneanilines from Nitroarenes and Benzaldehyde via Reductive Imination Reaction.
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- Catalysts (2073-4344), 2024, v. 14, n. 4, p. 272, doi. 10.3390/catal14040272
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Palladium Nanoparticles Incorporated Fumed Silica as an Efficient Catalyst for Nitroarenes Reduction via Thermal and Microwave Heating.
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- Catalysts (2073-4344), 2023, v. 13, n. 2, p. 445, doi. 10.3390/catal13020445
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Assembly of Smart Microgels and Hybrid Microgels on Graphene Sheets for Catalytic Reduction of Nitroarenes.
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- Catalysts (2073-4344), 2022, v. 12, n. 10, p. 1172, doi. 10.3390/catal12101172
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Carbon Quantum Dot-Titanium Doped Strontium Ferrite Nanocomposite: Visible Light Active Photocatalyst to Degrade Nitroaromatics.
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- Catalysts (2073-4344), 2022, v. 12, n. 10, p. 1126, doi. 10.3390/catal12101126
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A Reusable FeCl 3 ∙6H 2 O/Cationic 2,2′-Bipyridyl Catalytic System for Reduction of Nitroarenes in Water.
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- Catalysts (2073-4344), 2022, v. 12, n. 8, p. 924, doi. 10.3390/catal12080924
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Covalent Modification of Iron Phthalocyanine into Skeleton of Graphitic Carbon Nitride and Its Visible-Light-Driven Photocatalytic Reduction of Nitroaromatic Compounds.
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- Catalysts (2073-4344), 2022, v. 12, n. 7, p. N.PAG, doi. 10.3390/catal12070752
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Generation of Cobalt-Containing Nanoparticles on Carbon via Pyrolysis of a Cobalt Corrole and Its Application in the Hydrogenation of Nitroarenes.
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- Catalysts (2073-4344), 2022, v. 12, n. 1, p. 11, doi. 10.3390/catal12010011
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Pd on the Composite of Perlite and Allylamine- N -isopropylacrylamide Copolymer: A Thermo-Responsive Catalyst for Hydrogenation of Nitroarenes under Mild Reaction Condition.
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- Catalysts (2073-4344), 2021, v. 11, n. 11, p. 1334, doi. 10.3390/catal11111334
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