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Publications in Math-Net.Ru |
Citations |
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2024 |
| 1. |
Ya. V. Demyanov, I. Yu. Bagryanskaya, A. V. Artem'ev, “Cu<sup>I</sup> and Ag<sup>I</sup> scorpionate-like complexes based on sterically hindered tris(6-methyl-2-pyridyl)phosphine oxide”, Mendeleev Commun., 34:6 (2024), 812–814  |
| 2. |
S. B. Kalashnikov, A. S. Vinogradov, I. Yu. Bagryanskaya, T. V. Mezhenkova, “Synthesis of 5-methyl-4-polyfluoroaryl-1,3-thiazol-2-amines”, Mendeleev Commun., 34:2 (2024), 277–278 |
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2023 |
| 3. |
Ya. V. Demyanov, M. I. Rakhmanova, I. Yu. Bagryanskaya, A. V. Artem'ev, “Cu<sub>4</sub>I<sub>4</sub>-cubane cluster based on tris(<i>p</i>-anisyl)arsine: Synthesis, crystal structure and photophysical properties”, Mendeleev Commun., 33:4 (2023), 484–486 |
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2022 |
| 4. |
Ya. V. Demyanov, M. I. Rakhmanova, I. Yu. Bagryanskaya, A. V. Artem'ev, “1D Cu<sup>I</sup> coordination polymers based on triphenylarsine and <i>N</i>,<i>N'</i>-ditopic co-ligands: synthesis, crystal structure and TADF properties”, Mendeleev Commun., 32:5 (2022), 649–651 |
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2021 |
| 5. |
M. Yu. Petyuk, I. Yu. Bagryanskaya, O. I. Artyushin, V. K. Brel, A. V. Artem'ev, “Dinuclear Re<sup>I</sup> complex based on 1,2,4,5-tetrakis(diphenylphosphino)- pyridine: synthesis and luminescence properties”, Mendeleev Commun., 31:6 (2021), 810–812 |
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2020 |
| 6. |
M. I. Rogovoy, M. P. Davydova, I. Yu. Bagryanskaya, A. V. Artem'ev, “Efficient one-pot synthesis of diphenyl(pyrazin-2-yl)phosphine and its Ag<sup>I</sup>, Au<sup>I</sup> and Pt<sup>II</sup> complexes”, Mendeleev Commun., 30:3 (2020), 305–307 |
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2017 |
| 7. |
D. O. Prima, E. V. Vorontsova, A. G. Makarov, A. Yu. Makarov, I. Yu. Bagryanskaya, T. F. Mikhailovskaya, Yu. G. Slizhov, A. V. Zibarev, “Halogenated (F, Cl) 1,3-benzodiazoles, 1,2,3-benzotriazoles, 2,1,3-benzothia(selena)diazoles and 1,4-benzodiazines inducing Hep2 cell apoptosis”, Mendeleev Commun., 27:5 (2017), 439–442 |
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| 8. |
E. S. Vasilyev, I. Yu. Bagryanskaya, A. V. Tkachev, “Syntheses of chiral nopinane-annelated pyridines of <i>C</i><sub>2</sub> and <i>D</i><sub>2</sub>-symmetry: X-ray structures of the fused derivatives of 4,5-diazafluorene, 4,5-diaza-9<i>H</i>-fluoren-9-one, and 9,9’-bi-4,5-diazafluorenylidene”, Mendeleev Commun., 27:2 (2017), 128–130 |
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| 9. |
Yu. M. Volkova, A. Yu. Makarov, S. B. Zikirin, A. M. Genaev, I. Yu. Bagryanskaya, A. V. Zibarev, “3,1,2,4-Benzothiaselenadiazine and related heterocycles: synthesis and transformation into Herz-type radicals”, Mendeleev Commun., 27:1 (2017), 19–22 |
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2016 |
| 10. |
B. A. Trofimov, L. P. Nikitina, K. V. Belyaeva, L. V. Andriyankova, A. G. Mal'kina, I. Yu. Bagryanskaya, A. V. Afonin, I. A. Ushakov, “Insertion of 1,3-diphenylprop-2-yn-1-one into imidazo[4,5-<i>b</i>]pyridines in the presence of water: one-pot synthesis of pyrido[2,3-<i>b</i>][1,4]diazocin-9-ones”, Mendeleev Commun., 26:1 (2016), 16–18 |
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2015 |
| 11. |
E. A. Chulanova, I. G. Irtegova, N. V. Vasilieva, I. Yu. Bagryanskaya, N. P. Gritsan, A. V. Zibarev, “Novel long-lived π-heterocyclic radical anion: a hybrid of 1,2,5-thiadiazo- and 1,2,3-dithiazolidyls”, Mendeleev Commun., 25:5 (2015), 336–338 |
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2014 |
| 12. |
G. T. Sukhanov, G. V. Sakovich, Yu. V. Filippova, I. Yu. Bagryanskaya, A. G. Sukhanova, “Regioselective quaternization of <i>N</i>-alkyl-4-nitro- 1,2,3-triazoles in ButOH–HClO<sub>4</sub> system”, Mendeleev Commun., 24:5 (2014), 280–282 |
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2011 |
| 13. |
A. G. Makarov, T. D. Grayfer, A. Yu. Makarov, I. Yu. Bagryanskaya, V. G. Vasiliev, A. V. Zibarev, “Reactivity of extended chalcogen–nitrogen π-systems: compounds Ar–Se–N=S=N–Se–Ar”, Mendeleev Commun., 21:6 (2011), 320–322 |
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2005 |
| 14. |
Yu. V. Shklyaev, V. A. Glushkov, M. A. El'tsov, Yu. V. Gatilov, I. Yu. Bagryanskaya, A. G. Tolstikov, “Synthesis of regioisomeric (<i>S</i>)-(+)-3,3,4-trimethyl-8-methoxy-3,4-dihydrobenzo[<i>h</i>]-isoquinolin-1(2<i>H</i>)-one and (<i>S</i>)-(+)-1,2,2-trimethyl-8-methoxy-1,2-dihydrobenzo[<i>f</i>]-isoquinolin-4(3<i>H</i>)-one by the Ritter reaction”, Mendeleev Commun., 15:3 (2005), 125–127 |
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| 15. |
A. Yu. Makarov, S. N. Kim, N. P. Gritsan, I. Yu. Bagryanskaya, Yu. V. Gatilov, A. V. Zibarev, “Interaction of 1,2,3-benzodithiazolyls (Herz radicals) with dioxygen”, Mendeleev Commun., 15:1 (2005), 14–17 |
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2003 |
| 16. |
A. Yu. Makarov, I. Yu. Bagryanskaya, Yu. V. Gatilov, M. M. Shakirov, A. V. Zibarev, “Unexpected water addition to fluorinated 1,3λ<sup>4</sup>δ<sup>2</sup>,2,4-benzodithiadiazines with the formation of 2-amino-<i>N</i>-sulfinylbenzenesulfenamides”, Mendeleev Commun., 13:1 (2003), 19–21 |
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2002 |
| 17. |
I. Yu. Bagryanskaya, Yu. V. Gatilov, M. M. Shakirov, A. V. Zibarev, “The first stable R–N=S=N–H sulfur diimide”, Mendeleev Commun., 12:5 (2002), 167–168 |
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2000 |
| 18. |
P. A. Petukhov, I. Yu. Bagryanskaya, Yu. V. Gatilov, A. V. Tkachev, “Novel terpene-based chiral bis-α-aminooximes and the corresponding macrocycles: X-ray structure of a ring-fused 5,7-dioxa-1,4,8,11-tetraazacyclotrideca-3,8-diene derivative”, Mendeleev Commun., 10:6 (2000), 209–210 |
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1999 |
| 19. |
I. Yu. Bagryanskaya, Yu. V. Gatilov, A. V. Zibarev, “Configurations of 1,3-bis(aryl)-1,3-diaza-2-thiaallenes in the crystal state”, Mendeleev Commun., 9:4 (1999), 157–158 |
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1994 |
| 20. |
I. Yu. Bagryanskaya, Yu. V. Gatilov, M. M. Shakirov, A. V. Zibarev, “<i>Z</i>,<i>Z</i> Isomers of Polyfluorinated 1,3-Bis(aryl)-1,3-diaza-2-thiaallenes, (ArN=)<sub>2</sub>S, in the Crystal and in Solution”, Mendeleev Commun., 4:5 (1994), 167–169 |
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| 21. |
I. Yu. Bagryanskaya, Yu. V. Gatilov, M. M. Shakirov, A. V. Zibarev, “<i>Z,Z</i> Isomers of Sterically Hindered 1,3-Bis(aryl)-1,3-diaza-2-thiaallenes, (ArN=)<sub>2</sub>S, in the Crystal and in Solution”, Mendeleev Commun., 4:4 (1994), 136–137 |
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1992 |
| 22. |
A. M. Chibiryaev, I. Yu. Bagryanskaya, Yu. V. Gatilov, A. V. Tkachev, “An Unusual Dimerization in the Nitrosation Reaction of a Caryophyllene-type α,β-Unsaturated Oxime”, Mendeleev Commun., 2:3 (1992), 82–83 |
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