Works matching AU Bukharov, S.
Results: 51
Synthesis of Modified Sterically Hindered Phenols and Investigation of Their Ability to Protect Bacterial DNA Against UVB Damage.
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- Pharmaceutical Chemistry Journal, 2015, v. 48, n. 12, p. 787, doi. 10.1007/s11094-015-1196-x
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- Article
Synthesis, Toxicity, and Antituberculosis Activity of Isoniazid Derivatives Containing Sterically Hindered Phenols.
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- Pharmaceutical Chemistry Journal, 2014, v. 48, n. 1, p. 5, doi. 10.1007/s11094-014-1032-8
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- Article
Molecular and Crystal Structures of Ethyl-2-Amino-2-Bis(3,5-di-Tert-Butyl-4-Hydroxybenzyl)Ethanoate. Hydrogen Bonds in the Crystals of Sterically Hindered Phenols.
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- Journal of Structural Chemistry, 2024, v. 65, n. 2, p. 281, doi. 10.1134/S0022476624020069
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- Article
Synthesis and Structure of Hybrid Compounds Based on Phosphoryl Acetic Acid Hydrazide, Isatin, and Sterically Hindered Phenols.
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- Journal of Structural Chemistry, 2019, v. 60, n. 11, p. 1804, doi. 10.1134/S0022476619110143
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- Article
Molecular and Crystal Structure of Indole and Camfora with Sterically Hindered Phenol Fragments.
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- Journal of Structural Chemistry, 2019, v. 60, n. 2, p. 308, doi. 10.1134/S0022476619020197
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- Article
Molecular and Crystal Structure of Symmetric Sulfur-Containing Stericaly Hindered Trisphenols.
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- Journal of Structural Chemistry, 2019, v. 60, n. 2, p. 302, doi. 10.1134/S0022476619020185
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- Article
Crystal and Molecular Structural Features of Indolin-2-One Derivatives with Sterically Hindered Phenol Moieties.
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- Journal of Structural Chemistry, 2018, v. 59, n. 2, p. 439, doi. 10.1134/S0022476618020270
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- Article
The structure and intermolecular interactions of N,N′-bis-(3,5-di- tert-butyl-4-hydroxybenzyl)urea.
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- Journal of Structural Chemistry, 2006, v. 47, n. 4, p. 791, doi. 10.1007/s10947-006-0373-x
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- Article
The dilaton approach to evaluating the limiting mechanical properties of aramid fibres in high-speed pulsed loads.
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- Fibre Chemistry, 2006, v. 38, n. 6, p. 453, doi. 10.1007/s10692-006-0109-x
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- Article
Limiting and ultimate levels of the mechanical characteristics of aramid fibres in dynamic rupture.
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- Fibre Chemistry, 2006, v. 38, n. 6, p. 457, doi. 10.1007/s10692-006-0110-4
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- Article
Loop plasma and metallic antennas for mobile entities.
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- Radioelectronics & Communications Systems, 2014, v. 57, n. 3, p. 120, doi. 10.3103/S0735272714030030
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Calculation of partially filled resonator’s parameters during permittivity measurement.
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- Radioelectronics & Communications Systems, 2007, v. 50, n. 6, p. 343, doi. 10.3103/S0735272707060076
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- Article
Synthesis and Antitumour Activity of Hybrid Compounds Based on 4-Aminophenylarsonic Acid and Spatially Hindered Phenols.
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- Doklady Biochemistry & Biophysics, 2024, v. 519, n. 1, p. 534, doi. 10.1134/S1607672924701163
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- Article
Prebiotic Syntheses Under Shock in the Water – Formamide – Potassium Bicarbonate – Sodium Hydroxide System.
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- Origins of Life & Evolution of the Biosphere, 2019, v. 49, n. 1/2, p. 1, doi. 10.1007/s11084-019-09575-8
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Complexes of Ni II , Co II , Zn II , and Cu II with Promising Anti-Tuberculosis Drug: Solid-State Structures and DFT Calculations.
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- Inorganics, 2023, v. 11, n. 4, p. 167, doi. 10.3390/inorganics11040167
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Hydration of copper(II) amino acids complexes.
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- Journal of Computational Chemistry, 2018, v. 39, n. 14, p. 821, doi. 10.1002/jcc.25154
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The First Representatives of Phosphonium Salts Based on the Ammonium Acylhydrazone Scaffold: Synthesis and Biological Activity.
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- Russian Journal of General Chemistry, 2023, v. 93, p. S587, doi. 10.1134/S1070363223150240
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- Article
Synthesis and Antimicrobial Activity Evaluation of Ammonium Acylhydrazones Based on 4,6-Di-tert-butyl-2,3-dihydroxybenzaldehyde.
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- Russian Journal of General Chemistry, 2022, v. 92, n. 10, p. 1875, doi. 10.1134/S1070363222100012
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- Article
Kabachnik-Fields Reaction in the Synthesis of New Acetal-Containing Aminophosphine Oxides.
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- Russian Journal of General Chemistry, 2018, v. 88, n. 9, p. 1912, doi. 10.1134/S1070363218090244
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- Article
Synthesis and Antioxidant Activity of Sterically Hindered Phenol Derivatives of Carboxy- and Sulfobetaines.
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- Russian Journal of General Chemistry, 2018, v. 88, n. 1, p. 68, doi. 10.1134/S1070363218010103
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- Article
Isatin Derivatives Containing Sterically Hindered Phenolic Fragment and Water-Soluble Acyl Hydrazones on Their Basis: Synthesis and Antimicrobial Activity.
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- Russian Journal of General Chemistry, 2018, v. 88, n. 1, p. 57, doi. 10.1134/S1070363218010097
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- Article
Antiradical activity of benzazole-2-thiones.
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- Russian Journal of General Chemistry, 2017, v. 87, n. 9, p. 1919, doi. 10.1134/S1070363217090055
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- Article
Synthesis of sterically hindered phenols based on 7-amino-2,4-dimethylqunoline and 5,7-dimethyl-1,8-naphthyridin-2-amine.
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- 2017
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- Publication type:
- Letter
Reactions of benzazole-2-thiones with 3,5-di- tert-butyl-4-hydroxybenzyl acetate.
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- Russian Journal of General Chemistry, 2017, v. 87, n. 1, p. 22, doi. 10.1134/S1070363217010054
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- Article
Synthesis and antioxidant activity of modified sterically hindered phenols.
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- Russian Journal of General Chemistry, 2016, v. 86, n. 3, p. 602, doi. 10.1134/S1070363216030166
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- Article
Azo coupling of 2-hydroxymethyl-4- tert-butylphenol with sulfamoylbenzenediazonium chloride.
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- 2016
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- Publication type:
- Letter
Synthesis and antioxidant activity of 3,5-di- tert-butyl-4-hydroxyphenylthiomethyltetraalkylcalix[4]resorcinarenes.
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- Russian Journal of General Chemistry, 2015, v. 85, n. 9, p. 2087, doi. 10.1134/S107036321509011X
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- Article
Reaction of alkyl splitting of 4-acetylamino- N-(3,5-di- tert-butyl-4-hydroxybenzyl)-benzenesulfonamide.
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- Russian Journal of General Chemistry, 2015, v. 85, n. 2, p. 383, doi. 10.1134/S1070363215020061
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- Article
Condensation of certain selected 1-monoalkylisoindigo with 3,5-di- tert-butyl-4-hydroxybenzyl acetate.
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- 2015
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- Publication type:
- Letter
Antioxidant activity of isatin acylhydrazones with sterically hindered phenol fragments.
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- Russian Journal of General Chemistry, 2015, v. 85, n. 1, p. 53, doi. 10.1134/S1070363215010090
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- Article
New isatin acylhydrazones containing sterically hindered phenolic fragments.
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- 2014
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- Publication type:
- Letter
Synthesis, structure and antioxidant activity of sulfur-containing tetrakisphenol.
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- Russian Journal of General Chemistry, 2010, v. 80, n. 7, p. 1341, doi. 10.1134/S1070363210070200
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- Article
Synthesis and some properties of tetrakis-3,5-di- tert-butyl-4-hydroxybenzylated calix[4]resorcinols.
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- Russian Journal of General Chemistry, 2007, v. 77, n. 3, p. 458, doi. 10.1134/S1070363207030206
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- Article
Molecular structure of 2,4,6-tris(di- tert-butyl-4-hydroxybenzyl)resorcinol in the crystal and in solution, according to IR data.
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- Russian Journal of General Chemistry, 2006, v. 76, n. 6, p. 989, doi. 10.1134/S1070363206060247
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- Article
Structure and intermolecular interactions ofN-(3,5-di-tert-butyl-4-hydroxybenzyl)thioureas.
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- Russian Journal of General Chemistry, 2004, v. 74, n. 11, p. 1734, doi. 10.1007/s11176-005-0092-6
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- Article
Synthesis and structure of copper(II) 3-(3',5'-Di-tert-butyl-4'-hydroxybenzyl)acetylacetonate.
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- Russian Journal of General Chemistry, 2004, v. 74, n. 11, p. 1651, doi. 10.1007/s11176-005-0079-3
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- Article
Reactions of 3,5-di-tert-Butyl-4-hydroxybenzyl Acetate with Weakly Basic Nucleophiles.
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- Russian Journal of General Chemistry, 2003, v. 73, n. 3, p. 408, doi. 10.1023/A:1024910004024
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- Article
Influence of synergists: The influence of hydroperoxide decomposers on phenolic inhibitors consumption in oxidized polypropylene.
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- Journal of Applied Polymer Science, 2002, v. 85, n. 10, p. 2239, doi. 10.1002/app.10860
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- Article
Advanced sound absorbing materials to reduce noise and improve the environmental situation in production facilities and transportation.
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- Annals of the University of Oradea: Facsicle of Management & Technological Engineering, 2020, v. 30, n. 2, p. 174
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- Article
Development of comprehensive approaches to characterizing Cu<sup>II</sup> complexes: structures in solution and solid‐state, dynamic behavior, and bioactivity.
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- ChemistrySelect, 2023, v. 8, n. 48, p. 1, doi. 10.1002/slct.202303333
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- Article
α‐Umpolung/Michael Addition/Quaternization Tandem Reaction to provide α‐Imido‐β‐phosphonium Propanoates with Broad Spectrum of Biological Activity.
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- Chemistry & Biodiversity, 2024, v. 21, n. 3, p. 1, doi. 10.1002/cbdv.202302022
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- Article
PARAMETRIC SYNTHESIS OF STABILIZING NEUROMAGING TECHNOLOGICAL MODULE ON THE BASIS OF THE METHOD OF THE SPEED GRADIENT AND THE THEORY OF SLIDING REGIMES.
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- Advances in Differential Equations & Control Processes, 2019, v. 21, n. 1, p. 95, doi. 10.17654/DE021010095
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- Article
Synthesis and Antibacterial Activity of Sulfanilamides Containing Sterically Hindered Phenol Fragments.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 10, p. 1621, doi. 10.1134/S1070428021100080
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- Article
Effect of the Cationic Moiety on the Antimicrobial Activity of Sterically Hindered Isatin 3-Hydrazone Derivatives.
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- Russian Journal of Organic Chemistry, 2020, v. 56, n. 3, p. 555, doi. 10.1134/S107042802003032X
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- Article
Synthesis of acylhydrazones of sterically hindered hydroxybenzaldehydes based on phloroglucinol.
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- Russian Journal of Organic Chemistry, 2014, v. 50, n. 6, p. 805, doi. 10.1134/S1070428014060086
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- Article
Synthesis of hydrazones containing sterically hindered phenol groups and tetrathiacalix[4]arene fragment.
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- Russian Journal of Organic Chemistry, 2012, v. 48, n. 10, p. 1360, doi. 10.1134/S107042801210017X
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- Article
Synthesis of 3,5-di- tert-butyl-4-hydroxyphenylsulfanylmethyl-substituted tetramethylcalix[4]resorcinarenes.
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- Russian Journal of Organic Chemistry, 2010, v. 46, n. 7, p. 1097, doi. 10.1134/S1070428010070250
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- Article
Synthesis of sterically hindered phenolic compounds from indole and its derivatives.
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- Russian Journal of Organic Chemistry, 2007, v. 43, n. 12, p. 1797, doi. 10.1134/S1070428007120093
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- Article
Synthesis of 3-bromosubstituted 2-arylbornylenes by cross-coupling.
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- Russian Journal of Organic Chemistry, 2007, v. 43, n. 5, p. 747, doi. 10.1134/S107042800705017X
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- Article
Reaction of Tetramethylcalix[4]resorcinolarene with 3,5-Di-tert-butyl-4-hydroxybenzyl Acetate.
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- Russian Journal of Organic Chemistry, 2003, v. 39, n. 5, p. 689, doi. 10.1023/A:1026013430106
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- Article