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Publications in Math-Net.Ru
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First synthesis of 1,10-phenanthroline-2,9-diamine dioxides, a novel family of phenanthroline-based ligands
Mendeleev Commun., 35:6 (2025), 720–722
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Piperidine- and 2-(p-tolyl)piperidine-derived DAPhen ligands: the aryl substituent unexpectedly suppresses the extraction efficiency
Mendeleev Commun., 35:5 (2025), 540–542
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Lanthanide complexes with (4,7-dichloro-1,10-phenanthroline-2,9-diyl)bis(pyrrolidin-1-ylmethanone): bifunctional materials for homogeneous catalysis and luminescent thermometry
Mendeleev Commun., 34:6 (2024), 825–827
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The chemistry of heterocycles in the 21st century
Usp. Khim., 93:7 (2024), 1–366
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First examples of 1,1-diazido-2-sulfonylalkenes
Mendeleev Commun., 33:6 (2023), 756–758
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Stereoselective epoxidation of 4-fluoro-4-nitrocyclohexenes
Mendeleev Commun., 33:4 (2023), 463–465
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The first example of fluoro-Meinwald rearrangement
Mendeleev Commun., 33:2 (2023), 188–190
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The green chemistry paradigm in modern organic synthesis
Usp. Khim., 92:12 (2023), 1–187
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Di- and polyazides. Synthesis, chemical transformations and practical applications
Usp. Khim., 92:1 (2023), 1–49
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Copper-containing polymethylsilsesquioxane nanocomposites in catalytic olefination reaction
Mendeleev Commun., 32:4 (2022), 478–481
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Diene-transmissive hetero-Diels–Alder reaction of distyryl thioketone
Mendeleev Commun., 32:3 (2022), 384–385
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[3,3]-Sigmatropic rearrangements: a variety of methods and recent advances
Usp. Khim., 91:8 (2022), 1–95
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Significant impact of lanthanide contraction on the structure of the phenanthroline complexes
Mendeleev Commun., 31:6 (2021), 853–855
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Arylhydrazones of α-keto esters via methanolysis of dichlorodiazabutadienes: synthesis and structural study
Mendeleev Commun., 31:5 (2021), 677–679
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Supramolecular organic frameworks derived from bromoaryl-substituted dichlorodiazabutadienes via Cl···Br halogen bonding
Mendeleev Commun., 31:2 (2021), 191–193
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New family of polydentate tetrazole-pyrazoline ligands prepared by the azido-Ugi reaction
Mendeleev Commun., 31:1 (2021), 48–50
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Hydrogen bonding in acetylene containing dichlorodiazaalkadienes
Mendeleev Commun., 30:5 (2020), 615–617
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Trifluoroacetyl substituted pyrazolotriazines: synthesis and pathways of formation
Mendeleev Commun., 30:2 (2020), 180–182
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Access to molecular complexity. Multicomponent reactions involving five or more components
Usp. Khim., 89:11 (2020), 1274–1336
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Recent advances in the chemistry of pyridazine — an important representative of six-membered nitrogen heterocycles
Usp. Khim., 89:4 (2020), 393–429
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PASE synthesis of 1-azolyl-1H-1,2,4-triazoles by the reaction of diazoazoles with ethyl isocyanoacetate
Mendeleev Commun., 29:6 (2019), 653–654
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Reaction of 3-azidoisoxazoles with active methylene compounds
Mendeleev Commun., 29:5 (2019), 529–530
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Diastereoselective vinylogous Mannich reaction of perfluoroalkylated cyclic imines with 2-trimethylsilyloxyfuran
Mendeleev Commun., 29:1 (2019), 57–58
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Organofluorine chemistry: promising growth areas and challenges
Usp. Khim., 88:5 (2019), 425–569
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Diazocarbonyl derivatives of amino acids: unique chiral building blocks for the synthesis of biologically active compounds
Usp. Khim., 88:3 (2019), 248–279
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Synthesis of chiral α-(tetrazol-1-yl)-substituted carboxylic acids
Mendeleev Commun., 28:4 (2018), 364–365
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Synthesis of azacycloalkane-1,2-fused pyrroles via alkylation of cyclic ketimines with α-bromo ketones
Mendeleev Commun., 28:3 (2018), 270–271
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Aza-Henry reaction with trifluoropiruvate ketimines
Mendeleev Commun., 28:2 (2018), 133–134
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Aza-Henry reaction with perfluoroalkylated cyclic ketimines
Mendeleev Commun., 28:1 (2018), 81–82
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Reaction of CF3-ynones with azides. An efficient regioselective and metal-free route to 4-trifluoroacetyl-1,2,3-triazoles
Mendeleev Commun., 28:1 (2018), 17–19
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Acetylene–azide click macrocyclization of peptides
Usp. Khim., 87:7 (2018), 619–635
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$^{18}\mathrm{F}$-Labelled catecholamine type radiopharmaceuticals in the diagnosis of neurodegenerative diseases and neuroendocrine tumours: approaches to synthesis and development prospects
Usp. Khim., 87:4 (2018), 350–373
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Cyanothioacetamide: a polyfunctional reagent with broad synthetic utility
Usp. Khim., 87:1 (2018), 1–27
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Copper catalyzed alkyne–azide cycloaddition with 3-propargyl- γ-butyrolactones
Mendeleev Commun., 27:6 (2017), 562–564
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Transformation of cyclic ketimines to oxaziridines and nitrones
Mendeleev Commun., 27:1 (2017), 29–30
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Oxidative Nef reaction of trifluoromethylated 2-nitroalkanamines
Mendeleev Commun., 26:6 (2016), 511–512
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Efficient synthesis of triazole-containing spiro dilactones
Mendeleev Commun., 26:1 (2016), 11–13
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Synthesis of 1,1,1-trifluorobut-3-yn-2-ones and their reactions with N-nucleophiles
Mendeleev Commun., 24:6 (2014), 342–344
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Computational study of the catalytic olefination reaction
Mendeleev Commun., 24:6 (2014), 340–341
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Synthesis of trifluoromethylated [1,4]diazepines from 1,1,1-trifluoroalk-3-yn-2-ones
Mendeleev Commun., 24:5 (2014), 269–271
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Development of new methods in modern selective organic synthesis: preparation of functionalized molecules with atomic precision
Usp. Khim., 83:10 (2014), 885–985
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Betulonic acid–peptide conjugates: synthesis and evaluation of anti-inflammatory activity
Mendeleev Commun., 23:5 (2013), 260–261
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Friedel–Crafts alkylation of natural amino acid-derived pyrroles with CF3-substituted cyclic imines
Mendeleev Commun., 23:2 (2013), 92–93
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R-α-Phenylglycinol and R-α-phenylglycinamide as novel chiral templates in diastereoselective Ugi reaction
Mendeleev Commun., 21:5 (2011), 245–246
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Cu and Au nanocomposites in catalytic olefination reaction
Mendeleev Commun., 20:4 (2010), 200–202
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α-Acyl lactams in the synthesis of physiologically active compounds
Usp. Khim., 78:5 (2009), 466–493
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A new synthesis of substituted 2-trifluoromethylindoles
Mendeleev Commun., 18:6 (2008), 327–328
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From thiophene to Sulflower
Mendeleev Commun., 18:4 (2008), 171–179
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Baylis–Hilman reaction for α,β-unsaturated trifluoromethyl ketones
Mendeleev Commun., 16:5 (2006), 273–274
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EWG-containing thiophene- and 2-thiolene-1,1-dioxides as promising electrophiles for organic synthesis
Mendeleev Commun., 16:4 (2006), 215–218
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Mild and regioselective straightforward synthesis of isomelatonin analogues
Mendeleev Commun., 16:4 (2006), 213–215
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Diastereoselective synthesis of α-hydroxydihydropyrans containing the CF3 group
Mendeleev Commun., 16:3 (2006), 180–182
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Stereoselective synthesis of 1-bromo-1-fluorostyrenes
Mendeleev Commun., 16:3 (2006), 179–180
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α-Pentafluoroethylated amines: a new synthetic approach
Mendeleev Commun., 16:3 (2006), 141–143
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Thiophene 1,1-dioxides as unique building blocks in modern organic synthesis and materials chemistry
Usp. Khim., 75:12 (2006), 1139–1174
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Olefination of carbonyl compounds: modern and classical methods
Usp. Khim., 73:10 (2004), 1039–1074
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Methods for the synthesis of α,β-unsaturated trifluoromethyl ketones and their use in organic synthesis
Usp. Khim., 68:6 (1999), 483–505
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