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Publications in Math-Net.Ru |
Citations |
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2025 |
| 1. |
A. Yu. Gavrilova, T. A. Solodovnikova, A. A. Stepanov, N. V. Zyk, “Synthesis of frame pyrazolines based on azabicyclo[2.2.1]heptenes and nitrilimines”, Mendeleev Commun., 35:4 (2025), 467–469 |
| 2. |
N. Yu. Zyk, A. Yu. Kolchanova, N. S. Volkova, A. A. Uspenskaia, D. A. Skvortsov, E. K. Beloglazkina, N. V. Zyk, A. G. Majouga, A. E. Machulkin, “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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2024 |
| 3. |
D. O. Shkil, E. Yu. Yamansarov, B. N. Tarasevich, S. V. Kovalev, O. N. Metelkina, E. T. Yamansarova, N. V. Zyk, E. K. Beloglazkina, A. G. Majouga, “Mild and efficient catalyst for nitrodopamine synthesis: from milligram to multi-gram scales”, Mendeleev Commun., 34:2 (2024), 268–269 |
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2023 |
| 4. |
N. Yu. Zyk, S. A. Petrov, M. V. Zavertkina, A. A. Uspenskaya, P. A. Krasnikov, N. S. Dashkova, E. K. Beloglazkina, A. G. Majouga, N. V. Zyk, A. E. Machulkin, “Choice of the optimal synthetic approach for the polypeptide ligands of prostatic specific membrane antigen preparation”, Mendeleev Commun., 33:4 (2023), 472–475 |
6
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2022 |
| 5. |
V. K. Novotortsev, D. M. Kuandykov, M. E. Kukushkin, N. V. Zyk, E. K. Beloglazkina, “Synthesis of 5-methylidene-2-thio- and 2-selenohydantoins from isothiocyanates or isoselenocyanates and l-serine”, Mendeleev Commun., 32:6 (2022), 769–770 |
6
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| 6. |
V. E. Filatov, D. A. Iuzabchuk, B. N. Tarasevich, N. V. Zyk, E. K. Beloglazkina, “A convenient <i>E</i>-diastereoselective synthesis of <i>NH</i>-isatin <i>N′-</i>arylimines <i>via</i> the aza-Wittig reaction”, Mendeleev Commun., 32:5 (2022), 634–636 |
| 7. |
T. A. Solodovnikova, N. V. Zyk, A. Yu. Gavrilova, “Reaction of 2-azabicyclo[2.2.1]heptenes with nitrile oxides”, Mendeleev Commun., 32:4 (2022), 549–550 |
3
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| 8. |
A. A. Barashkin, V. S. Polyakov, N. L. Shikut, A. D. Putilova, A. R. Gorovoy, A. D. Degtiarev, V. A. Tafeenko, B. N. Tarasevich, N. V. Zyk, E. K. Beloglazkina, “Diastereoselective cycloaddition of isatin azomethine ylides to 5-arylidene-2-thiohydantoins bearing 3-positioned chiral substituent”, Mendeleev Commun., 32:2 (2022), 221–223 |
16
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| 9. |
M. E. Kukushkin, N. A. Karpov, D. E. Shybanov, N. V. Zyk, E. K. Beloglazkina, “A convenient synthesis of 3-aryl-5-methylidene-2-thiohydantoins”, Mendeleev Commun., 32:1 (2022), 126–128 |
11
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2021 |
| 10. |
D. E. Shybanov, M. E. Kukushkin, V. A. Tafeenko, N. V. Zyk, Yu. K. Grishin, V. A. Roznyatovsky, E. K. Beloglazkina, “Different addition modes of cyclopentadiene and furan at methylidene(thio)hydantoins”, Mendeleev Commun., 31:2 (2021), 246–247 |
11
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2020 |
| 11. |
V. K. Novotortsev, M. E. Kukushkin, V. A. Tafeenko, N. V. Zyk, E. K. Beloglazkina, “New spiro-linked indolinone pyrrolidine selenoxoimidazolones”, Mendeleev Commun., 30:3 (2020), 320–321 |
10
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| 12. |
N. I. Vorozhtsov, D. D. Korablina, L. A. Sviridova, V. A. Tafeenko, A. A. Moiseeva, N. V. Zyk, E. K. Beloglazkina, “Unusual complexation of 1-phenylthiocarbamoyl-3-(pyridin-2-yl)pyrazoline with copper(<sc>ii</sc>) chloride”, Mendeleev Commun., 30:2 (2020), 244–245 |
2
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2019 |
| 13. |
E. S. Barskaya, A. V. Rzheutskiy, A. A. Moiseeva, V. A. Tafeenko, N. V. Zyk, E. K. Beloglazkina, “Binuclear copper(II) complex with 2-imidazolylbenzothiazole and bridged chloride ligands”, Mendeleev Commun., 29:4 (2019), 444–446 |
8
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| 14. |
O. B. Bondarenko, Z. M. Garaev, A. I. Komarov, L. I. Kuznetsova, S. V. Gutorova, D. A. Skvortsov, N. V. Zyk, “Nitrosylsulfuric acid in the synthesis of 5-chloroisoxazoles from 1,1-dichlorocyclopropanes”, Mendeleev Commun., 29:4 (2019), 419–420 |
3
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2018 |
| 15. |
I. A. Salimova, A. V. Yudina, A. V. Mironov, A. G. Majouga, N. V. Zyk, E. K. Beloglazkina, “A convenient synthesis of copper(II) bis[5-(pyridin-2-yl-methylidene)-2-thiohydantoin] complexes”, Mendeleev Commun., 28:5 (2018), 524–526 |
4
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2017 |
| 16. |
Ya. A. Ivanenkov, S. Yu. Maklakova, E. K. Beloglazkina, N. V. Zyk, A. G. Nazarenko, A. G. Tonevitsky, V. E. Kotelianski, A. G. Majouga, “Development of liver cell-targeted drug delivery systems: experimental approaches”, Usp. Khim., 86:8 (2017), 750–776 ; Russian Chem. Reviews, 86:8 (2017), 750–776 |
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2015 |
| 17. |
E. K. Beloglazkina, E. S. Barskaya, A. G. Majouga, N. V. Zyk, “The first tris(imidazolylbenzothiazole) copper(II) complex”, Mendeleev Commun., 25:2 (2015), 148–149 |
8
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2014 |
| 18. |
E. K. Beloglazkina, O. Yu. Kuznetsova, A. G. Majouga, A. A. Moiseeva, N. V. Zyk, “Copper(II) complex with (4<i>Z</i>,4<i>Z’)</i>-1,1<i>’</i>-[disulfanediylbis(ethane-2,1-diyl)]-bis[2-methylthio-4-(pyridin-2-ylmethylidene)-1<i>H</i>-imidazol-5(4<i>H</i>)-one] onto a gold electrode surface – a catalyst of electrochemical reduction of nitrite in water solution”, Mendeleev Commun., 24:1 (2014), 37–39 |
10
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2012 |
| 19. |
O. N. Zefirova, T. Yu. Baranova, K. A. Lyssenko, N. A. Zefirov, N. V. Zyk, P. M. Vassiliev, D. S. Yakovlev, A. A. Spasov, “Synthesis and biological testing of conformationally restricted serotonin analogues with bridgehead moieties”, Mendeleev Commun., 22:2 (2012), 75–77 |
6
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| 20. |
A. N. Chernysheva, E. K. Beloglazkina, A. A. Moiseeva, R. L. Antipin, N. V. Zyk, N. S. Zefirov, “Co<sup>II</sup> complex of <i>N-</i>[2-(phenylseleno)cyclohexyl]<i>-N-</i>(pyridin-2-ylmethylene) amine: Synthesis, electrochemistry and catalysis of triphenylphosphine and norbornene oxidation by nitrous oxide”, Mendeleev Commun., 22:2 (2012), 70–72 |
17
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| 21. |
E. K. Beloglazkina, A. G. Majouga, R. B. Romashkina, N. V. Zyk, N. S. Zefirov, “Gold nanoparticles modified with coordination compounds of metals: synthesis and application”, Usp. Khim., 81:1 (2012), 65–90 ; Russian Chem. Reviews, 81:1 (2012), 65–90 |
41
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2011 |
| 22. |
O. B. Bondarenko, A. Yu. Gavrilova, D. S. Murodov, N. V. Zyk, N. S. Zefirov, “New system for nitrosation of alkyl-substituted <i>gem</i>-dichlorocyclopropanes”, Mendeleev Commun., 21:4 (2011), 188–189 |
8
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| 23. |
R. B. Romashkina, E. K. Beloglazkina, A. N. Khlobystov, A. G. Majouga, D. A. Pichugina, V. I. Terenin, N. V. Zyk, N. S. Zefirov, “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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2010 |
| 24. |
P. V. Gorelkin, D. S. Mukhin, A. G. Majouga, R. B. Romashkina, E. K. Beloglazkina, I. V. Yaminskii, N. V. Zyk, “New self-assembled monolayer coated cantilever for histidine-tag protein immobilization”, Mendeleev Commun., 20:6 (2010), 329–331 |
5
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| 25. |
P. G. Rudakovskaya, E. K. Beloglazkina, A. G. Majouga, N. V. Zyk, “Synthesis and characterization of terpyridine-type ligand-protected gold-coated Fe<sub>3</sub>O<sub>4</sub> nanoparticles”, Mendeleev Commun., 20:3 (2010), 158–160 |
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2009 |
| 26. |
A. G. Majouga, E. K. Beloglazkina, I. V. Yudin, R. D. Rakhimov, A. N. Khlobystov, N. V. Zyk, “First example of the ring-opening transformation of thiazolidines to iminothiols on gold surface”, Mendeleev Commun., 19:2 (2009), 92–93 |
1
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| 27. |
E. K. Beloglazkina, A. G. Majouga, A. A. Moiseeva, N. V. Zyk, N. S. Zefirov, “Oxidation of triphenylphosphine and norbornene by nitrous oxide in the presence of Co<sup>II</sup>LCl<sub>2</sub> [L = 3-phenyl-5-(2-pyridylmethylidene)-2-thiohydantoin]: the first example of Co<sup>II</sup>-catalyzed alkene oxidation by N<sub>2</sub>O”, Mendeleev Commun., 19:2 (2009), 69–71 |
20
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| 28. |
O. B. Bondarenko, A. Yu. Gavrilova, V. V. Polunina, Z. A. Starikova, N. V. Zyk, N. S. Zefirov, “Unexpected mode of reactivity in nitrosation of <i>cis</i>-1,1-dichloro-2,3-diphenylcyclopropane with NOCl·2SO<sub>3</sub>”, Mendeleev Commun., 19:1 (2009), 12–13 |
6
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| 29. |
T. Yu. Baranova, N. V. Averina, N. V. Zyk, N. S. Zefirov, K. A. Lyssenko, M. Yu. Antipin, O. N. Zefirova, “Synthesis of indole derivatives fused with bicyclo[3.2.1]octane framework”, Mendeleev Commun., 19:1 (2009), 10–11 |
6
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2008 |
| 30. |
O. N. Zefirova, E. V. Nurieva, H. Lemcke, A. A. Ivanov, N. V. Zyk, D. G. Weiss, S. A. Kuznetsov, N. S. Zefirov, “Design, synthesis and bioactivity of simplified taxol analogues on the basis of bicyclo[3.3.1]nonane derivatives”, Mendeleev Commun., 18:4 (2008), 183–185 |
22
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| 31. |
S. Z. Vatsadze, A. G. Golikov, A. P. Kriven'ko, N. V. Zyk, “Chemistry of cross-conjugated dienones”, Usp. Khim., 77:8 (2008), 707–727 ; Russian Chem. Reviews, 77:8 (2008), 661–681 |
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2007 |
| 32. |
O. N. Zefirova, E. V. Nurieva, V. N. Nuriev, K. A. Potekhin, A. V. Maleev, N. V. Zyk, N. S. Zefirov, “Crystal structure of the tritylated product of 3-hydroxymethylbicyclo[3.3.1]nonan-2-on-7-ol ethylene acetal cyclization”, Mendeleev Commun., 17:6 (2007), 332–334 |
1
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| 33. |
S. Z. Vatsadze, A. G. Majouga, E. K. Beloglazkina, A. V. Mironov, N. V. Zyk, “First organic-inorganic hybrid material based on AgNO<sub>3</sub> and 3-pyridine containing 2-thiohydantoin”, Mendeleev Commun., 17:2 (2007), 77–79 |
4
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2006 |
| 34. |
N. A. Frolova, S. Z. Vatsadze, N. Yu. Vetokhina, V. E. Zavodnik, N. V. Zyk, “New C-arylation reaction found during a study on the interaction of aldohydrazones and arenediazonium chlorides”, Mendeleev Commun., 16:5 (2006), 251–254 |
6
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2005 |
| 35. |
A. G. Majouga, E. K. Beloglazkina, S. Z. Vatsadze, A. A. Moiseeva, F. S. Moiseev, K. P. Butin, N. V. Zyk, “The first example of a reversibly reducible Co<sup>II</sup> complex with an anionic 2-thiohydantoin-type ligand”, Mendeleev Commun., 15:2 (2005), 48–50 |
11
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| 36. |
N. N. Romanova, A. G. Gravis, N. V. Zyk, “Microwave irradiation in organic synthesis”, Usp. Khim., 74:11 (2005), 1059–1105 ; Russian Chem. Reviews, 74:11 (2005), 969–1013 |
38
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| 37. |
K. P. Butin, E. K. Beloglazkina, N. V. Zyk, “Metal complexes with non-innocent ligands”, Usp. Khim., 74:6 (2005), 585–609 ; Russian Chem. Reviews, 74:6 (2005), 531–553 |
132
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2004 |
| 38. |
A. G. Majouga, E. K. Beloglazkina, S. Z. Vatsadze, A. A. Moiseeva, K. P. Butin, N. V. Zyk, “Synthesis, structure and electrochemistry of Co<sup>II</sup>LCl<sub>2</sub>·0.5MeCN {L = [2-(methylthio)-3-phenyl-5-(pyridin-2-ylmethylene)-3,5-dihydro-4<i>H</i>-imidazol-4-one]}”, Mendeleev Commun., 14:3 (2004), 115–117 |
17
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2003 |
| 39. |
N. V. Zyk, E. K. Beloglazkina, M. A. Belova, N. S. Dubinina, “Methods for the synthesis of vinyl sulfides”, Usp. Khim., 72:9 (2003), 864–883 ; Russian Chem. Reviews, 72:9 (2003), 769–786 |
93
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1999 |
| 40. |
S. Z. Vatsadze, D. P. Krut'ko, N. V. Zyk, N. S. Zefirov, A. V. Churakov, J. A. Howard, “First <sup>1</sup>H NMR observation of chair–boat conformers in bispidinone system. Molecular structure of 3,7-diisopropyl-1,5-diphenyl-3,7-diazabicyclo-[3.3.1]nonane-9-one”, Mendeleev Commun., 9:3 (1999), 103–105 |
9
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1996 |
| 41. |
O. B. Bondarenko, L. G. Saginova, N. V. Zyk, “Synthesis and properties of sultines, cyclic esters of sulfinic acids”, Usp. Khim., 65:2 (1996), 156–177 ; Russian Chem. Reviews, 65:2 (1996), 147–166 |
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