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61
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Nikolaevskaya E.N.
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Chemistry of diazadiene type ligands with extra coordination groups. Prospects of reactivity
Coordination Chemistry Reviews. 2020.
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Electroreductive heterocyclization of ortho-piperidino substituted nitro(het)arenes
Mendeleev Communications. 2020.
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63
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Mikhal’chenko L.V.
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Electroreduction of Derivatives of N,N'-Dioxides of Phenazine and Quinoxaline in Nonaqueous Media and in the Presence of Proton Donors of Medium Strength
Russian Journal of Electrochemistry. 2020.
V.56. N5. P.388-395. DOI: 10.1134/s1023193520040102
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Saverina E.A.
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An environment-friendly approach to produce nanostructured germanium anodes for lithium-ion batteries
Green Chemistry. 2020.
V.22. N2. P.359-367. DOI: 10.1039/c9gc02348h
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65
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Saverina E.A.
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Porous Silicon Preparation by Electrochemical Etching in Ionic Liquids
ACS Sustainable Chemistry & Engineering. 2020.
V.8. N27. P.10259-10264. DOI: 10.1021/acssuschemeng.0c03133
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66
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Begunov R.S.
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A simple and convenient method for synthesizing dipyrido[1,2-a :1′,2′-a′]benzo[1,2-d:5,4-d]diimidazole-6,13-dione
Mendeleev Communications. 2019.
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67
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Filonova G.E.
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Antioxidant Properties of Adrenaline in the Presence of Ge‐132
European Journal of Organic Chemistry. 2019.
V.2019. N26. P.4128-4132. DOI: 10.1002/ejoc.201900331
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Germanium Dioxide and the Antioxidant Properties of Catechols
European Journal of Inorganic Chemistry. 2019.
V.2019. N5. P.676-681. DOI: 10.1002/ejic.201801259
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69
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Syroeshkin M.A.
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Angewandte Chemie International Edition. 2019.
V.58. N17. P.5532-5550. DOI: 10.1002/anie.201807247
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71
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Hypervalent iodine compounds for anti-Markovnikov-type iodo-oxyimidation of vinylarenes
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Five Roads That Converge at the Cyclic Peroxy-Criegee Intermediates: BF3-Catalyzed Synthesis of β-Hydroperoxy-β-peroxylactones
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73
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V.858. P.8-13. DOI: 10.1016/j.jorganchem.2018.01.004
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Farhati A.
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V.13. N9. P.902-908. DOI: 10.1002/cmdc.201700804
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Halogen-free GeO2 conversion: electrochemical reduction vs. complexation in (DTBC)2Ge[Py(CN)n] (n = 0…2) complexes
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Terent'ev A.O.
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Influence of the nature of solvent and substituents on the oxidation potential of 2,2,6,6-tetramethylpiperidine 1-oxyl derivatives
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V.66. N4. P.683-689. DOI: 10.1007/s11172-017-1792-x
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