Works matching DE "HYDROXYLAMINE hydrochloride"
Results: 138
Modified synthesis of methyl (1 R,2 R,3 E,5 R)-3-(hydroxyimino)-5-methyl-2-(1-methylethyl)-cyclohexanecarboxylate from ( R)-4-menthen-3-one.
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- Chemistry of Natural Compounds, 2012, v. 48, n. 5, p. 789, doi. 10.1007/s10600-012-0383-1
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Synthetic transformations of higher terpenoids. XXVII.* Synthesis of 7-hydroxylabdanoids and their transformations.
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- Chemistry of Natural Compounds, 2012, v. 48, n. 2, p. 250, doi. 10.1007/s10600-012-0215-3
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Palladium-catalyzed relay hydroaminocarbonylation of alkenes with hydroxylamine hydrochloride as an ammonia equivalent.
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- Communications Chemistry, 2019, v. 2, n. 1, p. N.PAG, doi. 10.1038/s42004-019-0108-5
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Effect of fibre diameter on fabrication of modified PAN nanofibrous membranes and catalytic performance of their Fe complexes for dye degradation.
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- Journal of Industrial Textiles, 2018, v. 48, n. 1, p. 146, doi. 10.1177/1528083717725115
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Synthesis of some substituted 5 H-furo[3,2- g]chromene and benzofuran sulfonate derivatives as potent anti-HIV agents.
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- Russian Journal of General Chemistry, 2017, v. 87, n. 7, p. 1591, doi. 10.1134/S1070363217070246
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Esters of isoxazole- and isothiazolecarboxylic acids and oximes of β-isatin, isoxazole- and ferrocene-containing ketones and carborane alcohols.
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- Russian Journal of General Chemistry, 2013, v. 83, n. 3, p. 542, doi. 10.1134/S1070363213030225
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Urea-catalyzed multicomponent synthesis of 4-arylideneisoxazol-5(4H)-one derivatives under green conditions.
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- Research on Chemical Intermediates, 2023, v. 49, n. 3, p. 837, doi. 10.1007/s11164-022-04907-2
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SYNTHESIS AND ANTI-INFLAMMATORY, ANTIOXIDANT STUDIES OF NOVEL CHALCONES-BASED ISOXAZOLE DERIVATIVES.
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- Rasayan Journal of Chemistry, 2022, v. 15, n. 4, p. 2661, doi. 10.31788/RJC.2022.1547023
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A green and efficient synthesis of isoxazol-5(4 H)-one derivatives in water and a DFT study.
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- Journal of the Iranian Chemical Society, 2018, v. 15, n. 2, p. 455, doi. 10.1007/s13738-017-1246-2
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Solvent-free and atom efficient conversion of aldehydes into nitriles.
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- Green Chemistry Letters & Reviews, 2013, v. 6, n. 2, p. 149, doi. 10.1080/17518253.2012.728633
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Dual control over the reignition and combustion performance of hydroxylammonium nitrate-based gel propellants.
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- Energetic Materials Frontiers, 2024, v. 5, n. 3, p. 239, doi. 10.1016/j.enmf.2024.03.005
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1-Nitramino-5-aminotetrazole - A simple accessible highly energetic building block.
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- Energetic Materials Frontiers, 2022, v. 3, n. 3, p. 161, doi. 10.1016/j.enmf.2022.08.003
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Synthesis of Isoxazol-5-One Derivatives Catalyzed by Amine-Functionalized Cellulose.
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- Organics, 2024, v. 5, n. 4, p. 378, doi. 10.3390/org5040020
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Halogenation of Aldoximes. A Versatile Reaction for the Synthesis of Highly Functionalized Hydroximoyl Chlorides and Furazan N-Oxides.
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- Russian Journal of Organic Chemistry, 2023, v. 59, n. 12, p. 2221, doi. 10.1134/S1070428023120217
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Green Route for the Synthesis of 3,4-Disubstituted Isoxazol-5(4H)-ones Using GO@Fe(ClO<sub>4</sub>)<sub>3</sub> Nanocatalyst under Solvent-Free Conditions.
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- Russian Journal of Organic Chemistry, 2022, v. 58, n. 6, p. 830, doi. 10.1134/S1070428022060112
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Synthesis of 5-Chloroisoxazoles Derived from 2,2-Dichlorovinyl Ketones.
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- Russian Journal of Organic Chemistry, 2020, v. 56, n. 11, p. 1958, doi. 10.1134/S107042802011010X
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Synthesis and Transformations of 9-Substituted Imidazo[1,2-a]benzimidazole-2-carbaldehydes.
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- Russian Journal of Organic Chemistry, 2020, v. 56, n. 7, p. 1160, doi. 10.1134/S1070428020070064
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Transformations of 2-Ethyl-2-methyl-2,3-dihydro-1H-indole at the 3-Position.
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- Russian Journal of Organic Chemistry, 2020, v. 56, n. 1, p. 76, doi. 10.1134/S1070428020010133
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Synthesis, Structure, and Chemical Transformations of 2-Chloroprop-2-en-1-yl Sulfones.
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- Russian Journal of Organic Chemistry, 2019, v. 55, n. 12, p. 1912, doi. 10.1134/S1070428019120170
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Highly Efficient Microwave-assisted One-Pot Synthesis of Aromatic Nitriles from Aromatic Aldehydes.
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- Russian Journal of Organic Chemistry, 2019, v. 55, n. 5, p. 702, doi. 10.1134/S1070428019050191
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New Synthesis of 2-Oxoalkanamide Oximes.
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- Russian Journal of Organic Chemistry, 2019, v. 55, n. 4, p. 540, doi. 10.1134/S1070428019040201
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Recyclization of 5′-acetyl-2′-amino-6′-methyl-2-oxo-1,2-dihydrospiro[indole-3,4′-pyran]-3′-carbonitrile in reactions with some nitrogen binucleophiles.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 7, p. 1068, doi. 10.1134/S1070428016070290
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Synthesis of 1,5,9-trimethyl-6-thia-2-azabicyclo[3.2.2]nonan-3-one by the Ritter reaction.
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- Russian Journal of Organic Chemistry, 2014, v. 50, n. 12, p. 1851, doi. 10.1134/S1070428014120276
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SYNTHESIS, SPECTRAL CORRELATION STUDY, ANTIBACTERIAL AND ANTIFUNGAL ACTIVITIES OF SUBSTITUTED 5-(4-FLUOROPHENYL)-3-PHENYLISOXAZOLES.
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- Journal of Advanced Scientific Research, 2019, v. 10, n. 4, p. 156
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Direct Spectrophotometric Determination of Nickel (II) With p-Methoxyphenylazo-bis-acetoxime.
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- Journal of Advanced Scientific Research, 2012, v. 3, n. 2, p. 78
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Use of Sequential Extraction Methods to Evaluate the Environmental Impact of Trace Metal in the Iraqi Coastlines.
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- Basrah Journal of Agricultural Sciences, 2023, v. 36, n. 2, p. 17, doi. 10.37077/25200860.2023.36.2.02
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The crystal structure of (5-methyl-1,2,4- oxadiazol-3-yl)ferrocene, C<sub>13</sub>H<sub>12</sub>FeN<sub>2</sub>O.
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- Zeitschrift für Kristallographie / New Crystal Structures, 2017, v. 232, n. 4, p. 693, doi. 10.1515/ncrs-2017-0015
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Substituted quinolinones. Part 23. Synthesis of 6-ethyl-4,5-dioxo-5,6-dihydro-4H-pyrano[3,2-c]quinoline-3-carboxaldehyde and its chemical behavior towards hydroxylamine hydrochloride.
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- ARKIVOC: Online Journal of Organic Chemistry, 2013, p. 424
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Synthesis of Some New 1,2,4-Triazine and 1,2,5-Oxadiazine Derivatives with Antimicrobial Activity.
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- Heteroatom Chemistry, 2019, p. 1, doi. 10.1155/2019/2326514
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توزیع شکلهاي روي در تعدادي نمونه خاك آهکی از دشتهاي ماهیدشت و هلیلان استانهاي کرمانشاه و ایلام
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- Journal of Water & Soil Science, 2019, v. 22, n. 4, p. 331
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Roles of free radicals in NO oxidation by Fenton system and the enhancement on NO oxidation and H<sub>2</sub>O<sub>2</sub> utilization efficiency.
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- Environmental Technology, 2020, v. 41, n. 1, p. 109, doi. 10.1080/09593330.2018.1491638
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Pyrazole-oxime as reactivator for chlorpyrifos inhibited acetylcholinesterase: Synthesis and in vitro reactivation study.
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- Thai Journal of Pharmaceutical Sciences, 2023, v. 47, n. 1, p. 1
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Facile synthesis of 3-methyl-4-arylmethylene-isoxazol-5(4H)-ones catalysed by sodium silicate in an aqueous medium.
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- Journal of Chemical Research, 2011, v. 35, n. 10, p. 598, doi. 10.3184/174751911X13176501108975
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Synthesis and Myelostimulatory Activity of β-Cyclodextrin Complexes of 3,7-Diazabicyclo[3.3.1]Nonan-9-One Derivatives.
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- Pharmaceutical Chemistry Journal, 2020, v. 54, n. 6, p. 582, doi. 10.1007/s11094-020-02243-6
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Synthesis and Cytotoxic Activity of Indolo[2,3-a]Pyrrolo[3,4-c]Carbazole-5,7-Dione N-Glycosides Substituted on the Maleimide Nitrogen Atom.
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- Pharmaceutical Chemistry Journal, 2020, v. 54, n. 5, p. 455, doi. 10.1007/s11094-020-02222-x
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A REVIEW ON MUTATION BREEDING FOR THE IMPROVEMENT OF CROP PLANTS: PRESENT AND FUTURE.
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- Agriways, 2018, v. 6, n. 2, p. 50
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Silver nanoparticles: cytotoxic, apoptotic, and necrotic effects on MCF-7 cells.
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- Turkish Journal of Biology, 2013, v. 37, n. 5, p. 573, doi. 10.3906/biy-1302-21
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Facile and expedient synthesis of α,β-unsaturated isoxazol-5(4H)-ones under mild conditions.
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- Research on Chemical Intermediates, 2020, v. 46, n. 1, p. 943, doi. 10.1007/s11164-019-03999-7
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- Article
Facile, capable, atom-economical one-pot multicomponent strategy for the direct regioselective synthesis of novel isoxazolo[5,4-d]pyrimidines.
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- Research on Chemical Intermediates, 2019, v. 45, n. 5, p. 2673, doi. 10.1007/s11164-019-03757-9
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A novel dicationic ionic liquid as a highly effectual and dual-functional catalyst for the synthesis of 3-methyl-4-arylmethylene-isoxazole-5(4H)-ones.
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- Research on Chemical Intermediates, 2018, v. 44, n. 10, p. 6253, doi. 10.1007/s11164-018-3488-8
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Direct Synthesis of Nitriles from Aldehydes and Hydroxylamine Hydrochloride Catalyzed by a HAP@AEPH<sub>2</sub>-SO<sub>3</sub>H Nanocatalyst.
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- Australian Journal of Chemistry, 2017, v. 70, n. 1, p. 33, doi. 10.1071/CH16126
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Molecular Docking Studies, Synthesis of Novel Isoxazole Derivatives from 3-Methoxy Substituted Chalcone and Evaluation of their Anti-Inflammatory Activity.
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- Oriental Journal of Chemistry, 2023, v. 39, n. 3, p. 675, doi. 10.13005/ojc/390318
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Development and Validation of Estimation of Genotoxic Impurity (Hydroxylamine Hydrochloride Content) in Leflunomide by using RP-HPLC Technique.
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- Oriental Journal of Chemistry, 2021, v. 37, n. 2, p. 493, doi. 10.13005/ojc/370232
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Synthesis and antimicrobial activity of some novel fused heterocyclic moieties.
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- Organic Communications, 2013, v. 6, n. 2, p. 78
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Metal-organic frameworks encapsulating gold nanoclusters and carbon dots for ratiometric fluorescent detection of formaldehyde in real food samples, construction materials and indoor environments.
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- Microchimica Acta, 2025, v. 192, n. 2, p. 1, doi. 10.1007/s00604-025-06959-8
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- Article
Determination of iodate in iodized salt and water samples by shell-isolated nanoparticle-enhanced Raman spectroscopy.
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- Microchimica Acta, 2014, v. 181, n. 11/12, p. 1301, doi. 10.1007/s00604-014-1248-z
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- Article
Facile synthesis of light harvesting semiconductor bismuth oxychloride nano photo-catalysts for efficient removal of hazardous organic pollutants.
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- PLoS ONE, 2017, v. 12, n. 2, p. 1, doi. 10.1371/journal.pone.0172218
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- Article
Cyclocondensation of Hydroxylamine with 1,3-Bis(het)arylmonothio 1,3-Diketones and 1,3-Bis(het)aryl-3-(methylthio)-2-propenones: Synthesis of 3,5-Bis(het)arylisoxazoles with Complementary Regioselectivity.
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- European Journal of Organic Chemistry, 2014, v. 2014, n. 9, p. 1882, doi. 10.1002/ejoc.201301667
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Synthesis of crosslinked polyacrylonitrile via atom transfer radical polymerization with activators regenerated by electron transfer and use of the resin in mercury removal after modification.
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- Journal of Applied Polymer Science, 2012, v. 124, n. 3, p. 2179, doi. 10.1002/app.35240
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A green synthesis of nitrones in glycerol.
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- Journal of Chemical Sciences, 2019, v. 131, n. 10, p. N.PAG, doi. 10.1007/s12039-019-1677-7
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