Works by Nugumanova, G.
Results: 24
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 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
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
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
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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- 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
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
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
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
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
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