Works matching DE "TRIAZOLES synthesis"
Results: 362
Diphenylphosphoryl-Triazole-Tethered, AIEE-Type Conjugated Polymer as Optical Probe for Silver Ion in Relatively High-Water-Fraction Medium.
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- Macromolecular Chemistry & Physics, 2015, v. 216, n. 23, p. 2263, doi. 10.1002/macp.201500207
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Clustering and Dissolution of Triazole Branched Poly(ethyl methylacrylate).
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- Macromolecular Chemistry & Physics, 2015, v. 216, n. 11, p. 1251, doi. 10.1002/macp.201400621
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Synthesis and characterization of sulfonated polymers containing triazoles as low-humidity proton exchange membranes.
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- Journal of Polymer Research, 2014, v. 21, n. 8, p. 1, doi. 10.1007/s10965-014-0551-z
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Synthesis and Antioxidant Activity of New Neomenthyl and Caranyl Thiotriazoles.
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- Chemistry of Natural Compounds, 2018, v. 54, n. 5, p. 883, doi. 10.1007/s10600-018-2504-y
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Synthesis and Antioxidant Activity of Myrtanylthiotriazoles.
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- Chemistry of Natural Compounds, 2017, v. 53, n. 5, p. 895, doi. 10.1007/s10600-017-2150-9
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Synthesis of betulin derivatives containing triazole fragments.
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- Chemistry of Natural Compounds, 2013, v. 49, n. 2, p. 264, doi. 10.1007/s10600-013-0577-1
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Synthesis and antioxidant properties of new (2,4- and 3,4-dimethoxyphenyl)-1,2,4-triazoles.
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- Pharmacia (0428-0296), 2022, v. 69, n. 1, p. 135, doi. 10.3897/pharmacia.69.e74107
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Synthesis of New Substituted 1,2,4-Triazoles and 1,3,4-Thiadiazoles and Their Effects on DNA Methylation Level.
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- Russian Journal of General Chemistry, 2019, v. 89, n. 4, p. 673, doi. 10.1134/S1070363219040066
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Synthesis of New 1,4-Benzodioxanуl-1,2,4-triazole Derivatives.
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- Russian Journal of General Chemistry, 2018, v. 88, n. 4, p. 839, doi. 10.1134/S1070363218040345
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Modification of Diphenylphosphorylacetic Hydrazide with Thiosemicarbazide and Triazole Units.
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- Russian Journal of General Chemistry, 2017, v. 87, n. 12, p. 2794, doi. 10.1134/S1070363217120076
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Synthesis and antimicrobial activity of some novel benzofuran based 1,2,3-triazoles.
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- Russian Journal of General Chemistry, 2017, v. 87, n. 2, p. 322, doi. 10.1134/S1070363217020281
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Facile synthesis of novel (1-Aryl/alkyl-1 H-1,2,3-triazol- 4-yl)methyl-2-bromo-4-methylthiazole-5-carboxylates by Cu(I) catalyzed click reaction.
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- Russian Journal of General Chemistry, 2016, v. 86, n. 7, p. 1722, doi. 10.1134/S1070363216070306
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Geminally activated nitroethenes in reactions with sodium azide. Synthesis of functionalized 1,2,3-triazoles.
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- Russian Journal of General Chemistry, 2016, v. 86, n. 6, p. 1266, doi. 10.1134/S1070363216060086
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Synthesis, characterization, and antimicrobial activity of novel ( E)-1-(aryl)-3-{3, 5-dimethoxy-4-[(1-(aryl)-1 H-1,2,3-triazol-4-yl)methoxy]phenyl}prop-2-en-1-ones.
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- Russian Journal of General Chemistry, 2016, v. 86, n. 6, p. 1405, doi. 10.1134/S107036321606027X
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Synthesis and structures of 1,2,4-triazoles derivatives.
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- Russian Journal of General Chemistry, 2015, v. 85, n. 3, p. 746, doi. 10.1134/S1070363215030330
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Synthesis and structure of new 1,2,4-triazoles derived from p-hydroxybenzoic acid hydrazide.
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- Russian Journal of General Chemistry, 2015, v. 85, n. 1, p. 57, doi. 10.1134/S1070363215010107
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Synthesis of 3-(2-hydroxyphenyl)-1,5-dialkyl-1 H-1,2,4-triazoles and their Zn(II) complexes.
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- Doklady Chemistry, 2017, v. 472, n. 2, p. 30, doi. 10.1134/S0012500817020045
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Synthesis of 1,3-dioxacyclan-2-yl-substituted 1,2,3-triazoles.
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- Doklady Chemistry, 2017, v. 472, n. 1, p. 3, doi. 10.1134/S0012500817010025
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Synthesis, Molecular Docking Studies, and Antifungal Activity Evaluation of New Benzimidazole-Triazoles as Potential Lanosterol 14α-Demethylase Inhibitors.
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- Journal of Chemistry, 2017, p. 1, doi. 10.1155/2017/9387102
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General properties and comparison of the corrosion inhibition efficiencies of the triazole derivatives for mild steel.
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- Corrosion Reviews, 2018, v. 36, n. 6, p. 507, doi. 10.1515/corrrev-2018-0006
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SYNTHESIS AND CHARACTERIZATION OF SOME 3-(2-(5-PHENYL-1H-1,2,3-TRIAZOL-1-YL)ACETYL)-2H-CHROMEN-2-ONES, USING CLICK REACTION.
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- International Journal of Pharmaceutical, Chemical & Biological Sciences, 2017, v. 7, n. 3, p. 311
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Synthesis and Anticonvulsant Activity Evaluation of 3-alkoxy-4-( (hexyloxy/heptyloxy)phenyl)-4H-1,2,4 -triazole.
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- Iranian Journal of Pharmaceutical Research, 2015, v. 14, n. 1, p. 77
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One-Pot Synthesis of 4-Aryl- NH-1,2,3-Triazoles through Three-Component Reaction of Aldehydes, Nitroalkanes and NaN<sub>3</sub>.
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- Chinese Journal of Chemistry, 2017, v. 35, n. 12, p. 1808, doi. 10.1002/cjoc.201700367
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Recent Developments in Azide-Free Synthesis of 1,2,3-Triazoles.
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- Chinese Journal of Chemistry, 2017, v. 35, n. 12, p. 1797, doi. 10.1002/cjoc.201700459
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Copper( II) Acetylacetonate: An Efficient Catalyst for Huisgen-Click Reaction for Synthesis of 1,2,3-Triazoles in Water.
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- Chinese Journal of Chemistry, 2017, v. 35, n. 8, p. 1239, doi. 10.1002/cjoc.201700007
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An Efficient Copper-Catalyzed One-Pot Synthesis of 1-Aryl-1,2,3-triazoles from Arylboronic Acids in Water under Mild Conditions.
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- Chinese Journal of Chemistry, 2015, v. 33, n. 11, p. 1317, doi. 10.1002/cjoc.201500643
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Synthesis of 7-Triazole-substituted Camptothecin via Click Chemistry and Evaluation of in vitro Antitumor Activity.
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- Chinese Journal of Chemistry, 2014, v. 32, n. 2, p. 157, doi. 10.1002/cjoc.201300703
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Easy One-Pot Synthesis of 1-Monosubstituted Aliphatic 1,2,3-Triazoles from Aliphatic Halides, Sodium Azide and Propiolic Acid by a Click Cycloaddition/Decarboxylation Process.
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- Chinese Journal of Chemistry, 2013, v. 31, n. 8, p. 1011, doi. 10.1002/cjoc.201300155
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Effect of Hydrodynamic Conditions, Temperature and Immersion Times on the Corrosion Inhibition Efficiency of API 5L X52 Steel in 1M HCl Containing 1 H-1,2,4 or 1 H-1,2,3-triazoles.
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- Arabian Journal for Science & Engineering (Springer Science & Business Media B.V. ), 2017, v. 42, n. 1, p. 163, doi. 10.1007/s13369-016-2116-4
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On-line attenuated total reflection infrared (ATR-IR) spectroscopy combined with advanced chemometrics for investigating the synthesis process of 3,5-diamino-1,2,4-triazole.
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- Journal of the Iranian Chemical Society, 2017, v. 14, n. 4, p. 915, doi. 10.1007/s13738-016-1040-6
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One-pot three-component synthesis of 1,4-disubstituted 1 H-1,2,3-triazoles using green and recyclable cross-linked poly(4-vinylpyridine)-supported copper sulfate/sodium ascorbate in water/ t-BuOH system.
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- Journal of the Iranian Chemical Society, 2014, v. 11, n. 6, p. 1731, doi. 10.1007/s13738-014-0446-2
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Efficient, green and regioselective synthesis of 1,4,5-trisubstituted-1,2,3-triazoles in ionic liquid [bmim]BF and in task-specific basic ionic liquid [bmim]OH.
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- Journal of the Iranian Chemical Society, 2013, v. 10, n. 5, p. 883, doi. 10.1007/s13738-013-0224-6
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Determination of effective atomic numbers and electron densities for some synthesized triazoles from the measured total mass attenuation coefficients at different energies.
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- Canadian Journal of Physics, 2019, v. 97, n. 1, p. 86, doi. 10.1139/cjp-2017-0923
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Synthesis and Degradation of Schiff Bases Containing Heterocyclic Pharmacophore.
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- International Journal of Molecular Sciences, 2015, v. 16, n. 1, p. 1711, doi. 10.3390/ijms16011711
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Synthesis and Cytotoxic Activity of 1,2,3-Triazole Derivatives in Glioma Cell Cultures.
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- Pharmaceutical Chemistry Journal, 2015, v. 49, n. 5, p. 296, doi. 10.1007/s11094-015-1273-1
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Synthesis, Transformations, and Study of Some Biological Properties of New 3,4,5-Substituted 1,2,4-Triazoles.
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- Pharmaceutical Chemistry Journal, 2015, v. 49, n. 4, p. 231, doi. 10.1007/s11094-015-1261-5
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Synthesis and antitumor activity of new furyl-2-substituted 1,3,4-thiadiazoles and 1,2,4-triazoles.
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- Pharmaceutical Chemistry Journal, 2012, v. 45, n. 12, p. 705, doi. 10.1007/s11094-012-0706-3
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Syntheses and X-Ray crystal structures of aminated 4,4'-Bi-1,2,4-triazole salts.
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- Crystal Research & Technology, 2016, v. 51, n. 10, p. 595, doi. 10.1002/crat.201600161
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Synthesis and characterization of 2-amino-4,5-bis(tetrazol-5-yl)-1,2,3-triazole: A high-nitrogen energetic material with low sensitivities and high thermal stability.
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- Energetic Materials Frontiers, 2023, v. 4, n. 4, p. 221, doi. 10.1016/j.enmf.2023.12.002
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Synthesis of 1-Alkyl-5-amino-1,2,4-triazoles Based on Nucleophilic Substitution and Reduction Reactions.
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- Russian Journal of Organic Chemistry, 2018, v. 54, n. 10, p. 1537, doi. 10.1134/S1070428018100160
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Synthesis of Di- and Triterpenoid Ferrocenyltriazoles.
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- Russian Journal of Organic Chemistry, 2018, v. 54, n. 1, p. 126, doi. 10.1134/S1070428018010128
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Synthesis of 7-(2-R-pyrimidin-4-yl)- and 7-(2-R-[1,2,4]triazolo[1,5- a]pyrimidin-7-yl)-2,2,4,6-tetramethyl-1,2,3,4-tetrahydroquinolines.
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- Russian Journal of Organic Chemistry, 2017, v. 53, n. 7, p. 1060, doi. 10.1134/S1070428017070168
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Synthetic transformations of higher terpenoids: XXXVI. Synthesis of furanolabdanoid glycoconjugates with a 1,2,3-triazole linker.
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- Russian Journal of Organic Chemistry, 2017, v. 53, n. 1, p. 35, doi. 10.1134/S1070428017010079
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Cyclization of trifluoro- N-(prop-2-yn-1-yl)methanesulfonamides to N-(hydroxymethyl)-1,2,3-triazoles.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 7, p. 1032, doi. 10.1134/S1070428016070198
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Synthesis of N-(oxyran-2-ylmethyl)triazoles and -tetrazoles.
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- Russian Journal of Organic Chemistry, 2015, v. 51, n. 9, p. 1308, doi. 10.1134/S1070428015090171
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Synthesis of 4,5-dihydro-1 H-pyrazol-5-yl-substituted 1,2,3-triazoles.
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- Russian Journal of Organic Chemistry, 2015, v. 51, n. 3, p. 447, doi. 10.1134/S1070428015030306
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Synthesis of ferrocene conjugates with di- and triterpenes by click chemistry method.
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- Russian Journal of Organic Chemistry, 2014, v. 50, n. 8, p. 1180, doi. 10.1134/S1070428014080181
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Polarity and structure of diphosphorus-substituted isoxazole and 1,2,3-triazole.
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- Russian Journal of Organic Chemistry, 2013, v. 49, n. 9, p. 1369, doi. 10.1134/S1070428013090236
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Highly efficient synthesis of 4-trialkylsilyl(germyl)-1 H-1,2,3-triazole-5-carbaldehydes.
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- Russian Journal of Organic Chemistry, 2012, v. 48, n. 12, p. 1582, doi. 10.1134/S1070428012120196
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Synthesis and antibacterial activity of new 1,2,3-triazolylmethyl-2H-1,4-benzothiazin-3(4H)-one derivatives.
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- Chemistry Central Journal, 2018, v. 12, n. 1, p. 1, doi. 10.1186/s13065-018-0494-2
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