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Публикации в базе данных Math-Net.Ru
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Synthesis of a pteroic-based conjugate with ibuprofen moiety and macrocyclic chelator DOTA-GA
Mendeleev Commun., 35:6 (2025), 670–672
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Platinum(IV) prodrugs with heavy-atom-free BODIPY in axial position: instant photoactivation, enhanced biosafety and improved phototoxicity
Mendeleev Commun., 35:5 (2025), 595–597
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A novel molecular platform for co-delivery of monomethyl auristatin E and ispinesib to prostate cancer cells
Mendeleev Commun., 35:4 (2025), 440–443
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Facile, efficient and green phthalimide synthesis in supercritical carbon dioxide
Mendeleev Commun., 35:3 (2025), 341–343
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Novel platinum(IV) prodrugs with tetraacetylriboflavin axial ligand possessing enhanced light-induced toxicity
Mendeleev Commun., 35:3 (2025), 282–284
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Fluorescent conjugates of PSMA-targeting ligand with cyanine dyes: synthetic approaches and photochemical properties
Mendeleev Commun., 35:2 (2025), 172–175
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The Huisgen’s cycloaddition of BODIPY acetylene and ferrocene azides in supercritical CO2
Mendeleev Commun., 34:4 (2024), 552–554
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Mild and efficient catalyst for nitrodopamine synthesis: from milligram to multi-gram scales
Mendeleev Commun., 34:2 (2024), 268–269
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BODIPY: синтез, модификация, применение в сенсорике и биомедицине
Усп. хим., 93:10 (2024), 1–115
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Синтез и биологические свойства малых молекул — лигандов неканонических структур ДНК и РНК
Усп. хим., 93:9 (2024), 1–41
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Успехи в химии гетероциклических соединений в 21 веке
Усп. хим., 93:7 (2024), 1–366
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Choice of the optimal synthetic approach for the polypeptide ligands of prostatic specific membrane antigen preparation
Mendeleev Commun., 33:4 (2023), 472–475
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Selective Fmoc and Cbz protection of aromatic amino group in the presence of similar aliphatic function in liquid CO2
Mendeleev Commun., 33:1 (2023), 14–16
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Парадигма зеленой химии в современном органическом синтезе
Усп. хим., 92:12 (2023), 1–187
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Пролекарства на основе Pt(IV) как альтернатива препаратам Pt(II): синтез и биологическое действие
Усп. хим., 92:10 (2023), 1–58
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Synthesis of 5-methylidene-2-thio- and 2-selenohydantoins from isothiocyanates or isoselenocyanates and l-serine
Mendeleev Commun., 32:6 (2022), 769–770
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A convenient E-diastereoselective synthesis of NH-isatin N′-arylimines via the aza-Wittig reaction
Mendeleev Commun., 32:5 (2022), 634–636
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Diastereoselective cycloaddition of isatin azomethine ylides to 5-arylidene-2-thiohydantoins bearing 3-positioned chiral substituent
Mendeleev Commun., 32:2 (2022), 221–223
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A convenient synthesis of 3-aryl-5-methylidene-2-thiohydantoins
Mendeleev Commun., 32:1 (2022), 126–128
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Different addition modes of cyclopentadiene and furan at methylidene(thio)hydantoins
Mendeleev Commun., 31:2 (2021), 246–247
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Координационные соединения биогенных металлов как цитотоксические агенты для терапии злокачественных новообразований
Усп. хим., 90:12 (2021), 1566–1623
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Influence of the dipeptide linker configuration on the activity of PSMA ligands
Mendeleev Commun., 30:6 (2020), 756–759
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New spiro-linked indolinone pyrrolidine selenoxoimidazolones
Mendeleev Commun., 30:3 (2020), 320–321
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Unusual complexation of 1-phenylthiocarbamoyl-3-(pyridin-2-yl)pyrazoline with copper(ii) chloride
Mendeleev Commun., 30:2 (2020), 244–245
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Synthesis of allobetulin-based asialoglycoprotein receptor-targeted glycoconjugates
Mendeleev Commun., 29:5 (2019), 526–528
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Binuclear copper(II) complex with 2-imidazolylbenzothiazole and bridged chloride ligands
Mendeleev Commun., 29:4 (2019), 444–446
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A convenient synthesis of copper(II) bis[5-(pyridin-2-yl-methylidene)-2-thiohydantoin] complexes
Mendeleev Commun., 28:5 (2018), 524–526
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Synthesis and electrochemical study of 2-carbamoyl-4,5-dihydro-1,3,4-thiadiazole-containing ligands and their complexes with Cuii, Coii and Niii
Mendeleev Commun., 28:1 (2018), 79–80
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Sequence of bromination of (E)-4,4-dimethyl- 6-isobutylidenecyclohex-2-en-1-one
Mendeleev Commun., 27:5 (2017), 495–497
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Экспериментальные направления в разработке средств направленной доставки лекарственных препаратов в клетки печени
Усп. хим., 86:8 (2017), 750–776
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Direct reagentless detection of the affinity binding of recombinant His-tagged firefly luciferase with a nickel-modified gold electrode
Mendeleev Commun., 25:4 (2015), 290–292
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The first tris(imidazolylbenzothiazole) copper(II) complex
Mendeleev Commun., 25:2 (2015), 148–149
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Copper(II) complex with (4Z,4Z’)-1,1’-[disulfanediylbis(ethane-2,1-diyl)]-bis[2-methylthio-4-(pyridin-2-ylmethylidene)-1H-imidazol-5(4H)-one] onto a gold electrode surface – a catalyst of electrochemical reduction of nitrite in water solution
Mendeleev Commun., 24:1 (2014), 37–39
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CoII complex of N-[2-(phenylseleno)cyclohexyl]-N-(pyridin-2-ylmethylene) amine: Synthesis, electrochemistry and catalysis of triphenylphosphine and norbornene oxidation by nitrous oxide
Mendeleev Commun., 22:2 (2012), 70–72
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Наночастицы золота, модифицированные координационными соединениями металлов: синтез и применение
Усп. хим., 81:1 (2012), 65–90
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Copper(ii) coordination compounds as building blocks for the formation of gold nanoparticle dimers
Mendeleev Commun., 21:3 (2011), 129–131
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New self-assembled monolayer coated cantilever for histidine-tag protein immobilization
Mendeleev Commun., 20:6 (2010), 329–331
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Synthesis and characterization of terpyridine-type ligand-protected gold-coated Fe3O4 nanoparticles
Mendeleev Commun., 20:3 (2010), 158–160
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First example of the ring-opening transformation of thiazolidines to iminothiols on gold surface
Mendeleev Commun., 19:2 (2009), 92–93
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Oxidation of triphenylphosphine and norbornene by nitrous oxide in the presence of CoIILCl2 [L = 3-phenyl-5-(2-pyridylmethylidene)-2-thiohydantoin]: the first example of CoII-catalyzed alkene oxidation by N2O
Mendeleev Commun., 19:2 (2009), 69–71
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First organic-inorganic hybrid material based on AgNO3 and 3-pyridine containing 2-thiohydantoin
Mendeleev Commun., 17:2 (2007), 77–79
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The first example of a reversibly reducible CoII complex with an anionic 2-thiohydantoin-type ligand
Mendeleev Commun., 15:2 (2005), 48–50
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Металлокомплексы с неинноцентными лигандами
Усп. хим., 74:6 (2005), 585–609
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Synthesis, structure and electrochemistry of CoIILCl2·0.5MeCN {L = [2-(methylthio)-3-phenyl-5-(pyridin-2-ylmethylene)-3,5-dihydro-4H-imidazol-4-one]}
Mendeleev Commun., 14:3 (2004), 115–117
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Методы синтеза винилсульфидов
Усп. хим., 72:9 (2003), 864–883
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