Works about HYDRAZINES
Results: 949
SYNTHESIS AND BIOLOGICAL PROPERTIES OF THE SPIRO(BENZO[h]TRIAZOLO[3,4-b]QUINAZOLINE-7,1´-CYCLOPENTANE) DERVATIVES.
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- Electronic Journal of Natural Sciences, 2006, v. 7, n. 2, p. 9
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- Article
Replacement of Toxic Hydrazines in Satellite Propulsion with Greener Dinitramide‐Based Energetic Ionic Liquid Candidates.
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- Chemistry - A European Journal, 2024, v. 30, n. 31, p. 1, doi. 10.1002/chem.202303965
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Electrochemical N‐Aroylation of Sulfoximines by Using Benzoyl Hydrazines with H<sub>2</sub> Generation.
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- Chemistry - A European Journal, 2024, v. 30, n. 9, p. 1, doi. 10.1002/chem.202303444
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Hydrazine Sulfonic Acid, NH<sub>3</sub>NH(SO<sub>3</sub>), the Bigger Sibling of Sulfamic Acid.
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- Chemistry - A European Journal, 2024, v. 30, n. 1, p. 1, doi. 10.1002/chem.202302526
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Multistimuli‐Responsive Chromism of Vinylene‐Linked Bisflavin Based on the Aggregation and Redox Properties.
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- Chemistry - A European Journal, 2023, v. 29, n. 4, p. 1, doi. 10.1002/chem.202202257
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- Article
Cover Feature: Catalytic Reduction of Dinitrogen into Ammonia and Hydrazine by Using Chromium Complexes Bearing PCP‐Type Pincer Ligands (Chem. Eur. J. 25/2022).
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- Chemistry - A European Journal, 2022, v. 28, n. 25, p. 1, doi. 10.1002/chem.202200964
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Catalytic Reduction of Dinitrogen into Ammonia and Hydrazine by Using Chromium Complexes Bearing PCP‐Type Pincer Ligands**.
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- Chemistry - A European Journal, 2022, v. 28, n. 25, p. 1, doi. 10.1002/chem.202200557
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Ruthenium Nanoclusters and Single Atoms on α‐MoC/N‐Doped Carbon Achieves Low‐Input/Input‐Free Hydrogen Evolution via Decoupled/Coupled Hydrazine Oxidation.
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- Angewandte Chemie, 2024, v. 136, n. 30, p. 1, doi. 10.1002/ange.202316755
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Desulfurdioxidative N‐N Coupling of N‐Arylhydroxylamines and N‐Sulfinylanilines: Reaction Development and Mechanism.
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- Angewandte Chemie, 2024, v. 136, n. 26, p. 1, doi. 10.1002/ange.202406478
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Activating Interfacial Electron Redistribution in Lattice‐Matched Biphasic Ni<sub>3</sub>N‐Co<sub>3</sub>N for Energy‐Efficient Electrocatalytic Hydrogen Production via Coupled Hydrazine Degradation.
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- Angewandte Chemie, 2024, v. 136, n. 19, p. 1, doi. 10.1002/ange.202401364
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Ligand‐Promoted Iron‐Catalyzed Nitrene Transfer for the Synthesis of Hydrazines and Triazanes through N‐Amidation of Arylamines.
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- Angewandte Chemie, 2024, v. 136, n. 2, p. 1, doi. 10.1002/ange.202312465
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Nickel‐Catalyzed Asymmetric Synthesis of P‐Stereogenic Phosphanyl Hydrazine Building Blocks.
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- Angewandte Chemie, 2023, v. 135, n. 46, p. 1, doi. 10.1002/ange.202313112
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Cooperative Ni(Co)‐Ru‐P Sites Activate Dehydrogenation for Hydrazine Oxidation Assisting Self‐powered H<sub>2</sub> Production.
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- Angewandte Chemie, 2023, v. 135, n. 35, p. 1, doi. 10.1002/ange.202308800
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Innenrücktitelbild: Sonochemically‐Induced Reduction of Alkenes to Alkanes with Ammonia (Angew. Chem. 51/2022).
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- Angewandte Chemie, 2022, v. 134, n. 51, p. 1, doi. 10.1002/ange.202217292
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Dual Nanoislands on Ni/C Hybrid Nanosheet Activate Superior Hydrazine Oxidation‐Assisted High‐Efficiency H<sub>2</sub> Production.
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- Angewandte Chemie, 2022, v. 134, n. 2, p. 1, doi. 10.1002/ange.202113082
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Titelbild: Conversion of Ammonia to Hydrazine Induced by High‐Frequency Ultrasound (Angew. Chem. 48/2021).
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- Angewandte Chemie, 2021, v. 133, n. 48, p. 25369, doi. 10.1002/ange.202113427
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Conversion of Ammonia to Hydrazine Induced by High‐Frequency Ultrasound.
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- Angewandte Chemie, 2021, v. 133, n. 48, p. 25434, doi. 10.1002/ange.202109516
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- Article
Redox‐Mediated Ambient Electrolytic Nitrogen Reduction for Hydrazine and Ammonia Generation.
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- Angewandte Chemie, 2021, v. 133, n. 34, p. 18869, doi. 10.1002/ange.202105536
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Expanding the Versatility of Microbial Transglutaminase Using α‐Effect Nucleophiles as Noncanonical Substrates.
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- Angewandte Chemie, 2020, v. 132, n. 33, p. 13918, doi. 10.1002/ange.202001830
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Organocatalytic and Scalable Syntheses of Unsymmetrical 1,2,4,5‐Tetrazines by Thiol‐Containing Promotors.
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- Angewandte Chemie, 2019, v. 131, n. 4, p. 1118, doi. 10.1002/ange.201812550
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Detailed investigation of the reduction process of cupric oxide (CuO) to form metallic copper fine particles with a unique diameter.
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- Journal of Materials Science, 2010, v. 45, n. 23, p. 6433, doi. 10.1007/s10853-010-4728-5
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Thermal and mechanical profile of cast films from waterborne polyurethanes based on polyether block copolymers.
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- Journal of Materials Science, 2009, v. 44, n. 5, p. 1317, doi. 10.1007/s10853-009-3272-7
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Synthesis and Antimicrobial Activity of 3-Aryland 3-Arylmethyl-Cyclopenta[ c]Pyrazoles and -Cyclopenta[ d ]Isoxazoles.
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- Pharmaceutical Chemistry Journal, 2017, v. 50, n. 11, p. 721, doi. 10.1007/s11094-017-1519-1
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Synthesis and analgesic activity of the products of the interaction between 3-aroylpyrrolo[1,2- a]-quinoxaline-1,2,4(5 H)-triones with benzoic acid hydrazides.
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- Pharmaceutical Chemistry Journal, 2012, v. 45, n. 11, p. 660, doi. 10.1007/s11094-012-0697-0
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Synthesis and pharmacological activity of 2-arylaminonicotinic acid β-(3-carboxypropionyl)hydrazides.
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- Pharmaceutical Chemistry Journal, 2011, v. 45, n. 8, p. 472, doi. 10.1007/s11094-011-0658-z
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Synthesis of 4-amino-6-(hetaryl)pyridazin-3-ones as analogs of pyridazine-based cardiotonic agents.
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- Pharmaceutical Chemistry Journal, 2009, v. 43, n. 2, p. 87, doi. 10.1007/s11094-009-0249-4
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Indirect determination of N-acetyltransferase activity using ammonium metavanadate for evaluating isoniazide excretion with human urine.
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- Pharmaceutical Chemistry Journal, 2008, v. 42, n. 8, p. 488, doi. 10.1007/s11094-008-0157-z
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Synthesis and antimicrobial activity of substituted tetrahydroindazoles and cyclohexanones.
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- Pharmaceutical Chemistry Journal, 2007, v. 41, n. 6, p. 319, doi. 10.1007/s11094-007-0072-8
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Synthesis and Antimycobacterial Activity of Triazene Derivatives of N-Arylcarbamates.
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- Pharmaceutical Chemistry Journal, 2005, v. 39, n. 3, p. 126, doi. 10.1007/s11094-005-0099-7
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Synthesis and Antimicrobial Activity of Some (Nitro)furfurylidene-Containing Hexahydroindazoles.
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- Pharmaceutical Chemistry Journal, 2005, v. 39, n. 2, p. 76, doi. 10.1007/s11094-005-0086-z
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Synthesis and Antiinflammatory and Analgesic Activity of the Products of 3-Imino-(3H)-Furan-2-One Recyclization under the Action of Substituted Hydrazines.
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- Pharmaceutical Chemistry Journal, 2005, v. 39, n. 1, p. 11, doi. 10.1007/s11094-005-0069-0
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Structure of trans-diaqua-bis(3-hydroxybenzoylhydrazine)copper(II) sulfate monohydrate, [Cu(C<sub>7</sub>H<sub>8</sub>O<sub>2</sub>N<sub>2</sub>)<sub>2</sub>(OH<sub>2</sub>)<sub>2</sub>]SO<sub>4</sub>·H<sub>2</sub>O.
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- Journal of Structural Chemistry, 2008, v. 49, n. 2, p. 335, doi. 10.1007/s10947-008-0132-2
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Synthesis and structure of copper(II) trans-diaqua-bis(3-hydroxybenzoylhydrazine) nitrate dihydrate [Cu(C<sub>7</sub>H<sub>8</sub>O<sub>2</sub>N<sub>2</sub>)<sub>2</sub>(OH<sub>2</sub>)<sub>2</sub>](NO<sub>3</sub>)<sub>2</sub>2H<sub>2</sub>O.
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- Journal of Structural Chemistry, 2006, v. 47, n. 6, p. 1188, doi. 10.1007/s10947-006-0443-0
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Lipase‐catalyzed hydrazine insertion for the synthesis of N′‐alkyl benzohydrazides.
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- Biotechnology & Applied Biochemistry, 2023, v. 70, n. 1, p. 130, doi. 10.1002/bab.2335
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Reactivity of platinum nanoaggregates in catalytic reduction of U(VI) with hydrazine in acid solutions.
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- Radiochemistry, 2007, v. 49, n. 6, p. 603, doi. 10.1134/S1066362207060112
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Kinetics of Technetium Reactions: XV. Tc(IV) Oxidation with Persulfate Ions in HClO<sub>4</sub> Solution.
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- Radiochemistry, 2005, v. 47, n. 2, p. 163, doi. 10.1007/s11137-005-0065-y
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草酸银中银的还原重量法测定.
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- Precious Metals / Guijinshu, 2022, v. 43, p. 150
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Synthesis of fused dihydrobenzo [4,5]imidazo[1,2- a]pyrmido[5,4-e]pyrmidin-3(4H)-amine derivatives.
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- Al-Qadisiyah Journal of Pure Science, 2021, v. 26, n. 4, p. 34, doi. 10.29350/qjps.2021.26.4.1371
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Synthesis, Characterization, and Antimicrobial Activity of Carboxymethyl Chitosan-Graft-Poly(N-acryloyl,N′-cyanoacetohydrazide) Copolymers.
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- Journal of Carbohydrate Chemistry, 2012, v. 31, n. 3, p. 220, doi. 10.1080/07328303.2011.650338
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Synthesis of Ni/Al<sub>2</sub>O<sub>3</sub> catalysts via alkaline polyol method and hydrazine reduction method for the partial oxidation of methane.
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- Turkish Journal of Chemistry, 2021, v. 45, n. 4, p. 967, doi. 10.3906/kim-2012-46
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Synthesis and biological properties of novel 1-methyl-2-(2-(prop-2-yn-1-yloxy)benzylidene) hydrazine analogues.
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- Turkish Journal of Chemistry, 2018, v. 42, n. 2, p. 306, doi. 10.3906/kim-1701-42
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Response surface methodology optimization of electrode modification parameters toward hydrazine electrooxidation on Pd/MWCNT/GCE.
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- Manas Journal of Engineering, 2023, v. 11, n. 2, p. 204, doi. 10.51354/mjen.1312700
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Orthogonal Design of Fe−N<sub>4</sub> Active Sites and Hierarchical Porosity in Hydrazine Oxidation Electrocatalysts.
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- ChemElectroChem, 2022, v. 9, n. 10, p. 1, doi. 10.1002/celc.202200045
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Ultrasensitive, Sustainable, and Selective Electrochemical Hydrazine Detection by ALD‐Developed Two‐Dimensional WO<sub>3</sub>.
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- ChemElectroChem, 2018, v. 5, n. 2, p. 266, doi. 10.1002/celc.201700968
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- Article
Synthesis of Novel Pyrazolyl and Isoxazolyl 3-(Furan-2-yl)-5-Methyl-1-(4-Nitrophenyl)-1H-Pyrazol-4-yl Derivatives via Regioselectivity of the 1,3-Dipolar Cycloaddition.
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- Polycyclic Aromatic Compounds, 2024, v. 44, n. 4, p. 2212, doi. 10.1080/10406638.2023.2214284
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Synthesis and antiproliferative activity of some N ′-substituted 2,4-dihydroxybenzothiohydrazides.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, p. 166, doi. 10.1080/14756366.2016.1212192
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Synthesis and characterization of biologically significant 5,5'-(1,4-phenylene)bis(1-N-alkoxyphthalimido-3-aryl-2-pyrazoline) derivatives.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2008, v. 23, n. 6, p. 882, doi. 10.1080/14756360701442332
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Antitubercular activity of novel substituted 4, 5-dihydro-1H-1-pyrazolylmethanethiones.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2007, v. 22, n. 2, p. 183, doi. 10.1080/14756360601072437
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Inhibition of monoamine oxidase–A activity in rat brain by synthetic hydrazines: Structure-activity relationship (SAR).
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2005, v. 20, n. 3, p. 269, doi. 10.1080/14756360400026212
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Antibacterial Schiff Bases of Oxalyl-hydrazine/diamide Incorporating Pyrrolyl and Salicylyl Moieties and of Their Zinc(II) Complexes.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2002, v. 17, n. 1, p. 1, doi. 10.1080/14756360290005598
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