Works matching DE "SELENIUM dioxide"
Results: 51
Topochemical, Single‐Crystal‐to‐Single‐Crystal [2+2] Photocycloadditions Driven by Chalcogen‐Bonding Interactions.
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- Angewandte Chemie, 2022, v. 134, n. 36, p. 1, doi. 10.1002/ange.202206249
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Atomically Dispersed Selenium Sites on Nitrogen‐Doped Carbon for Efficient Electrocatalytic Oxygen Reduction.
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- Angewandte Chemie, 2022, v. 134, n. 3, p. 1, doi. 10.1002/ange.202114441
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Chalkogenide durch Reduktion ihrer Dioxide in ultra‐alkalischen Medien.
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- Angewandte Chemie, 2021, v. 133, n. 41, p. 22744, doi. 10.1002/ange.202107642
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Enhanced Band Gap Energy and Electrochromic Behaviour of Selenium Incorporated Copper Thin Film.
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- Journal of Physical Science, 2016, v. 27, n. 2, p. 41, doi. 10.21315/jps2016.27.2.4
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Solvent-Dependent Facile Synthesis of Diaryl Selenides and Biphenols Employing Selenium Dioxide.
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- ChemistryOpen, 2016, v. 5, n. 2, p. 115, doi. 10.1002/open.201500206
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- Article
study of the biological activity of 4-(Para-Substituted phenyl)-1,2,3- Selenadiazole derivatives as anti-oxidant and anti-breast cancer.
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- Basrah Journal of Science / Magallat Al-Barat Li-L-ulum, 2020, v. 38, n. 3, p. 480, doi. 10.29072/basjs.202038
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Selenium Dioxide Promoted α‐Keto N‐Acylation of Sulfoximines Under Mild Reaction Conditions.
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- Asian Journal of Organic Chemistry, 2021, v. 10, n. 7, p. 1835, doi. 10.1002/ajoc.202100298
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Enhanced mesenchymal stem cell proliferation through complexation of selenium/titanium nanocomposites.
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- Journal of Materials Science: Materials in Medicine, 2019, v. 30, n. 2, p. 1, doi. 10.1007/s10856-019-6224-z
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Selenious acid‐doped polyaniline synthesis and characterization by chemical oxidative solid‐state polymerization of aniline with SeO<sub>2</sub> as an oxidizing agent.
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- Polymer International, 2022, v. 71, n. 7, p. 770, doi. 10.1002/pi.6338
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Development of Selenium-Silica Nanocomposites By Sol-Gel Process Utilizing Three Different Reducing Agents and Its Characterization.
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- Journal of Engineering Research, 2023, v. 20, n. 2, p. 130, doi. 10.53540/tjer.vol.20iss2pp130-137
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- Article
Radiation Shielding Tests of Crosslinked Polystyrene-b-Polyethyleneglycol Block Copolymers Blended with Nanostructured Selenium Dioxide and Boron Nitride Particles.
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- Nanomaterials (2079-4991), 2022, v. 12, n. 3, p. 297, doi. 10.3390/nano12030297
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A theoretical study on the mechanism and rate constants of luteolin and selenium dioxide.
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- Journal of Molecular Modeling, 2025, v. 31, n. 2, p. 1, doi. 10.1007/s00894-025-06291-1
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Thickness dependent variation in structural, optical and electrical properties of CdSe thin films.
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- Journal of Materials Science: Materials in Electronics, 2019, v. 30, n. 6, p. 5753, doi. 10.1007/s10854-019-00870-8
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Sol-gel synthesis, structural, morphological and optical properties of Se-doped SnO nanoparticles.
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- Journal of Materials Science: Materials in Electronics, 2016, v. 27, n. 3, p. 3103, doi. 10.1007/s10854-015-4263-x
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Magnetic selenium and nitrogen dual‐doped mesoporous carbon for immobilization of Pd nanoparticles: The utilitarian heterogeneous catalyst in Heck‐cross coupling reaction.
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- Applied Organometallic Chemistry, 2023, v. 37, n. 3, p. 1, doi. 10.1002/aoc.6988
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Synthesis of 2-arylideneimidazo[1,2-a]pyrazine-3,6,8(2H,5H,7H)-triones as a result of oxidation of 4-arylidene-2-methyl-1H-imidazol-5(4H)-ones with selenium dioxide.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 1, p. 116, doi. 10.1007/s10593-020-02634-3
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Oxidative rearrangement of 4 H-chromenes to 2-aroylbenzofurans in the presence of selenium dioxide.
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 9, p. 1053, doi. 10.1007/s10593-017-2169-7
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Synthesis of 2-arylidene-6,7-dihydroimidazo[1,2- a]pyrazine-3,8(2 H,5 H)-diones by oxidation of 4-arylidene-2-methyl-1 H-imidazol-5(4 H)-ones with selenium dioxide.
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 8, p. 930, doi. 10.1007/s10593-017-2149-y
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Synthesis of Thia- and Selenodiazoles Based on Acetosyringone and Its Glycosides.
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- Russian Journal of General Chemistry, 2023, v. 93, p. S219, doi. 10.1134/S1070363223140013
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- Article
Synthesis of Luteolin–Selenium Dioxide Complex under Acidic Catalysis.
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- Russian Journal of General Chemistry, 2022, v. 92, n. 8, p. 1534, doi. 10.1134/S1070363222080229
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Synthesis of Ethyl 4-(1,2,3-Selenodiazol-4-yl)-5-alkylsulfanyl- and -5-Phenylsulphonylmethylfuran-2-carboxylates.
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- Russian Journal of General Chemistry, 2022, v. 92, n. 1, p. 54, doi. 10.1134/S107036322201008X
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Synthesis of the Derivatives of 4-(1,2,3-Selenadiazol-4-yl)-5-methyl-2-furoate Functionalyzed at the Methyl Group.
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- Russian Journal of General Chemistry, 2020, v. 90, n. 12, p. 2489, doi. 10.1134/S1070363220120427
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Synthesis of 4-(2-Fluoro-4-hydroxyphenyl)-1,2,3-thia- and -Selenadiazoles and Glycosides on Their Base.
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- Russian Journal of General Chemistry, 2020, v. 90, n. 7, p. 1241, doi. 10.1134/S1070363220070117
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One-Pot Synthesis of Trifluoromethyl-Substituted Imidazobenz[1,2-d]- and -[1,2-c]isoxazoles.
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- Russian Journal of General Chemistry, 2020, v. 90, n. 4, p. 746, doi. 10.1134/S1070363220040295
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Synthesis of 2-Substituted 5-(1,2,3-Selenadiazol-4-yl)furan-3-carboxylic Acids Esters.
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- Russian Journal of General Chemistry, 2019, v. 89, n. 10, p. 2027, doi. 10.1134/S1070363219100074
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Synthesis of Glycosides with 4-(4-Hydroxyphenyl)-1,2,3-thia- and -selenadiazole Aglycones.
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- Russian Journal of General Chemistry, 2019, v. 89, n. 7, p. 1398, doi. 10.1134/S1070363219070089
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Reaction of isosteviol diterpenoid with selenium dioxide.
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- Russian Journal of General Chemistry, 2009, v. 79, n. 12, p. 2663, doi. 10.1134/S1070363209120184
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Thermochemical Route for Extraction and Recycling of Critical, Strategic and High Value Elements from By-Products and End-of-Life Materials, Part I: Treatment of a Copper By-Product in Air Atmosphere.
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- Materials (1996-1944), 2019, v. 12, n. 10, p. 1625, doi. 10.3390/ma12101625
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Facile and Selective Cross-Coupling of Phenols Using Selenium Dioxide.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 25, p. 4307, doi. 10.1002/ejoc.201600886
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Selenium dioxide catalysed oxidation of acetic acid hydrazide by bromate in aqueous hydrochloric acid medium.
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- Journal of Chemical Sciences, 2012, v. 124, n. 4, p. 821, doi. 10.1007/s12039-012-0286-5
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- Article
Self‐Healing SeO<sub>2</sub> Additives Enable Zinc Metal Reversibility in Aqueous ZnSO<sub>4</sub> Electrolytes.
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- Advanced Functional Materials, 2022, v. 32, n. 18, p. 1, doi. 10.1002/adfm.202112091
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Unveiled Supercapacitive Performance of Se‐doped Graphene Nanoarchitectonics Prepared via Supercritical Fluid Technique.
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- ChemNanoMat, 2023, v. 9, n. 9, p. 1, doi. 10.1002/cnma.202300209
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Investigating the antimicrobial, antioxidant and cytotoxic activities of the biological synthesized glutathione selenium nano-incorporation.
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- BioMetals, 2021, v. 34, n. 4, p. 815, doi. 10.1007/s10534-021-00309-w
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- Article
Scalable Synthesis of TRPV1 Antagonist Bipyridinyl Benzimidazole Derivative via the Suzuki–Miyaura Reaction and Selective SeO 2 Oxidation.
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- Molecules, 2023, v. 28, n. 2, p. 836, doi. 10.3390/molecules28020836
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Synthesis of (E)‐β‐Iodovinyl Sulfones via Photoredox Catalyzed Difunctionalization of Terminal Alkynes.
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- ChemPhotoChem, 2022, v. 6, n. 10, p. 1, doi. 10.1002/cptc.202200110
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Double‐shell and yolk‐shell structured ZnSe‐carbon nanospheres as anode materials for high‐performance potassium‐ion batteries.
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- International Journal of Energy Research, 2022, v. 46, n. 3, p. 3539, doi. 10.1002/er.7404
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- Article
ONE-POT SYNTHESIS OF Sb<sub>2</sub>Se<sub>3</sub> NANO WIRES USING SELENIUM DIOXIDE AS THE SELENIUM PRECURSOR IN AIR AND THEIR CHARACTERIZATION.
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- International Journal of Nanoscience, 2013, v. 12, n. 5, p. 1, doi. 10.1142/S0219581X13500403
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Modification of Azepanobetulin at the Isopropenyl Group.
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- Russian Journal of Organic Chemistry, 2020, v. 56, n. 9, p. 1582, doi. 10.1134/S1070428020090134
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3,28-Diacetoxylup-20(29)-ene-30-oic Acid and Its ω-Bromoalkyl Esters.
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- Russian Journal of Organic Chemistry, 2020, v. 56, n. 4, p. 626, doi. 10.1134/S1070428020040107
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Synthesis of bis(2-haloalkyl) selanes and selenides based on selenium dioxide and terminal alkenes.
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- Russian Journal of Organic Chemistry, 2017, v. 53, n. 12, p. 1809, doi. 10.1134/S1070428017120041
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Microwave synthesis of new azolyl-substituted thiazolo[5,4- d]thiazoles.
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- Russian Journal of Organic Chemistry, 2017, v. 53, n. 4, p. 550, doi. 10.1134/S107042801704008X
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Synthesis and some transformations of methyl [4-(oxoacetyl)phenyl]carbamate.
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- Russian Journal of Organic Chemistry, 2017, v. 53, n. 1, p. 82, doi. 10.1134/S1070428017010146
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Functionalization of methyl 3-acetyl-5-[(methoxycarbonyl)amino]-2-methyl-1 H-indole-1-carboxylate.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 6, p. 834, doi. 10.1134/S1070428016060129
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Synthesis of Derivatives (3-Oxobut-1-en-1-yl), [2-(1,2,3-Thiadiazol-4-yl)ethen-1-yl], and [2-(1,2,3-Selenodiazol-4-yl)ethen-1-yl]-5-tert-butylfurancarboxylic Acids.
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- Russian Journal of General Chemistry, 2024, v. 94, n. 11, p. 2889, doi. 10.1134/S1070363224110094
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Synthesis and Biological Activity of 2,6-Substituted Pyridoxine Derivatives. Unusual Catalytic Role of Selenium Dioxide in the Formation of Pyridinone Methides.
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- Russian Journal of General Chemistry, 2024, v. 94, n. 8, p. 1912, doi. 10.1134/S1070363224080036
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Phosphorylated 5-tert-Butyl-2 and 3-Furylalkenes: Synthesis and Heterocyclization.
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- Russian Journal of General Chemistry, 2024, v. 94, n. 6, p. 1279, doi. 10.1134/S1070363224060070
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Chemo- and regioselective oxidation of substituted 2,3,4,9-tetrahydro-1H-carbazoles.
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- Chemistry of Heterocyclic Compounds, 2022, v. 58, n. 8/9, p. 403, doi. 10.1007/s10593-022-03106-6
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Application of Ionic Liquid Choline Chloride in Electrolysis of Manganese.
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- Hydrometallurgy of China, 2024, v. 43, n. 6, p. 672, doi. 10.13355/j.cnki.sfyj.2024.06.012
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SeO<sub>2</sub> Microwires Designed as Low‐Temperature Abrupt Microelectronic Switches, Negative Resistance, and Negative Dielectric Constant Sources.
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- Physica Status Solidi. A: Applications & Materials Science, 2022, v. 219, n. 24, p. 1, doi. 10.1002/pssa.202200200
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Allylic oxidation of methyl 10-undecenoate and nucleophilic additions to methyl 9-oxo-10-undecenoate.
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- European Journal of Lipid Science & Technology, 2015, v. 117, n. 2, p. 255, doi. 10.1002/ejlt.201400238
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