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Publications in Math-Net.Ru
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Benzo[c][1,2,5]thiadiazole doubly fused with thieno[2',3':4,5]thieno[3,2-b]pyrroles as a key building block for non-fullerene acceptors of Y6 series
Mendeleev Commun., 35:5 (2025), 503–511
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Herz chemistry and its applications in small-molecule functional materials science: achievements, challenges, and prospects
Usp. Khim., 94:1 (2025), 1–35
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Wolmershäuser radicals: Chemistry and materials science
Mendeleev Commun., 33:4 (2023), 439–447
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How electron delocalization influences the electron-withdrawing properties of isomeric benzobischalcogenadiazoles
Mendeleev Commun., 33:3 (2023), 372–375
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New D–A–D luminophores of the [1,2,5]thiadiazolo[3,4-d]pyridazine series
Mendeleev Commun., 32:3 (2022), 371–373
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Chalcogen exchange in chalcogen–nitrogen π-heterocycles
Mendeleev Commun., 31:4 (2021), 433–441
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Progress in the chemistry of nitrogen-, oxygen- and sulfur-containing heterocyclic systems
Usp. Khim., 89:1 (2020), 55–124
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Bis[1,2,5]oxadiazolo[3,4-c:3’,4’-e]pyridazine 4,5-dioxide as a synthetic equivalent of 4,4’-dinitroso-3,3’-bifurazan
Mendeleev Commun., 27:5 (2017), 448–450
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Influence of structural factors on the photovoltaic properties of dye-sensitized solar cells
Usp. Khim., 85:10 (2016), 1146–1183
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A short and efficient synthesis of 5,5’ -bi-1,2,3-dithiazoles
Mendeleev Commun., 25:6 (2015), 427–428
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[1,4]Dithiino[2,3-c:5,6-c’ ]bis[1,2,5]oxadiazole di-N-oxide: synthesis and oxidation to mono- and bis-S-oxides
Mendeleev Commun., 25:5 (2015), 339–340
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Sulfur monochloride in organic synthesis
Usp. Khim., 83:3 (2014), 225–250
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Reactivity of 1,2-dithioles
Usp. Khim., 81:7 (2012), 638–661
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Synthesis of 17-(1,2,3-dithiazole) androstene derivatives
Mendeleev Commun., 21:4 (2011), 186–187
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Stable heterocyclic radicals
Usp. Khim., 80:7 (2011), 679–692
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4,6-Dinitrobenzo[c]isothiazole: synthesis and 1,3-dipolar cycloaddition to azomethine ylide
Mendeleev Commun., 20:6 (2010), 353–354
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Synthesis of 2-iminothiophen-3(2H)-ones from 3H-1,2-dithiol-3-ones
Mendeleev Commun., 20:5 (2010), 282–284
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[(4-Sulfanylidene-4H-1λ4,3,2-dithiazol-5-yl)sulfanyl]formic acid derivatives: synthesis from 5-oxo[1,3]dithiolo[4,5-d][1,3,2]dithiazol-1-ium chloride and structural characterization
Mendeleev Commun., 20:5 (2010), 279–281
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Unexpected formation of 5,5-diethoxy-5H-1,2,3-dithiazoles from 5H-1,2,3-dithiazole-5-thiones
Mendeleev Commun., 20:4 (2010), 212–214
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Identification of the [1,3]dithiolo[4,5-d]dithiazolyl radical
Mendeleev Commun., 20:2 (2010), 80–82
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Synthesis of 1,2,5-thiadiazole-3(2H)-thiones and 1,2,5-thiadiazol-3(2H)-ones from 1,2,3-dithiazoles
Mendeleev Commun., 19:2 (2009), 84–86
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Design of sulfur heterocycles with sulfur monochloride: synthetic possibilities and prospects
Mendeleev Commun., 19:2 (2009), 55–61
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Synthesis and properties of 1,2,3-dithiazoles
Usp. Khim., 77:6 (2008), 551–577
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1,2,3,4,5-Pentathiepines and 1,2,3,4,5-pentathiepanes
Usp. Khim., 76:3 (2007), 219–236
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Thienopentathiepins and pentathiepinofuran
Mendeleev Commun., 16:6 (2006), 289–290
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Synthesis of 1,3,4-thiadiazolines from 1,2-dithiole-3-thiones
Mendeleev Commun., 15:2 (2005), 55–56
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New routes to 1,2-dithiole-3-thiones and 3-imines
Mendeleev Commun., 15:1 (2005), 20–21
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Regioselective synthesis of pentathiepino-fused pyrroles and indoles
Mendeleev Commun., 14:3 (2004), 91–92
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4,5-Dichloro-1,2-dithiole-3-thione in the synthesis of benzimidazole, benzoxazole and benzothiazole derivatives of 1,3-dithioles
Mendeleev Commun., 13:2 (2003), 50–51
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Direct conversion of N-ethylamines into functionalised amides by S2Cl2
Mendeleev Commun., 11:5 (2001), 167–168
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New reactions of Hünig's base with S2Cl2: formation of monocyclic 1,2-dithioles
Mendeleev Commun., 11:5 (2001), 165–166
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Substitution of the Nitro Group in Chloronitrofuroxan by N- and O-Trimethylsilyl Derivatives
Mendeleev Commun., 4:4 (1994), 135
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3,4-Dinitrofuroxan—the First Example of a Pernitro Heterocycle
Mendeleev Commun., 3:5 (1993), 209–210
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Diazotisation of Weakly Basic Aromatic and Heterocyclic Amines in Strongly Acid Media
Usp. Khim., 52:5 (1983), 777–786
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