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Публикации в базе данных Math-Net.Ru |
Цитирования |
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2025 |
| 1. |
A. A. Zubenko, V. S. Sochnev, A. S. Morkovnik, L. N. Divaeva, A. S. Burlov, A. E. Svyatogorova, E. N. Avagyan, “A new method for constructing pyrido[3',2':4,5]imidazo[1,2-<em>b</em>]pyridazine system and preparation of its derivatives”, Mendeleev Commun., 35:1 (2025), 24–26 |
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2023 |
| 2. |
A. A. Zubenko, L. N. Divaeva, A. S. Morkovnik, V. S. Sochnev, O. P. Demidov, V. V. Chekrysheva, A. I. Klimenko, A. E. Svyatogorova, “β-Carbolines as intermediates in indirect heteroarylation of tryptamines exemplified by the synthesis of 2-pyrazolyltryptamines”, Mendeleev Commun., 33:5 (2023), 645–647 |
1
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| 3. |
A. A. Zubenko, A. S. Morkovnik, L. N. Divaeva, V. S. Sochnev, O. P. Demidov, L. N. Fetisov, N. O. Andros, A. E. Svyatogorova, A. I. Klimenko, “New β-[o-(5-oxopyrazol-3-yl)aryl]ethylamines and their unusual metastable betaine form”, Mendeleev Commun., 33:2 (2023), 203–205 |
1
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2022 |
| 4. |
V. S. Sochnev, A. S. Morkovnik, A. A. Zubenko, L. N. Divaeva, O. P. Demidov, T. N. Gribanova, L. N. Fetisov, V. V. Chekrysheva, K. N. Kononenko, M. A. Bodryakova, A. I. Klimenko, G. S. Borodkin, I. A. Estrin, “Novel recyclization of 3,4-dihydroisoquinolines as an efficient route to a new type of heteroarylated derivatives of β-arylethylamines”, Mendeleev Commun., 32:6 (2022), 795–797 |
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| 5. |
A. A. Zubenko, A. S. Morkovnik, L. N. Divaeva, V. S. Sochnev, O. P. Demidov, A. I. Klimenko, L. N. Fetisov, A. N. Bodryakov, M. A. Bodryakova, G. S. Borodkin, “New type of recyclization in 3,4-dihydroisoquinolines in the synthesis of β-(o-indazolylaryl)ethylamines and their 7-azaindazolyl analogues”, Mendeleev Commun., 32:2 (2022), 265–267 |
4
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2021 |
| 6. |
V. S. Sochnev, T. A. Kuz'menko, A. S. Morkovnik, L. N. Divaeva, A. S. Podobina, A. A. Zubenko, P. B. Chepurnoy, G. S. Borodkin, A. I. Klimenko, “Nitration of 2,3-dihydroimidazo[1,2-a]benzimidazole and its N 9-substituted derivatives”, Mendeleev Commun., 31:4 (2021), 555–557 |
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| 7. |
A. A. Zubenko, V. S. Sochnev, V. G. Kartsev, L. N. Divaeva, O. P. Demidov, A. I. Klimenko, A. N. Bodryakov, M. A. Bodryakova, G. S. Borodkin, A. S. Morkovnik, “Systems with annulated thioxo azepinone moiety: an access through heterocyclic carbodithioate ring expansion”, Mendeleev Commun., 31:4 (2021), 545–547 |
2
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| 8. |
A. A. Zubenko, A. S. Morkovnik, L. N. Divaeva, O. P. Demidov, V. G. Kartsev, V. S. Sochnev, A. I. Klimenko, N. M. Dobaeva, G. S. Borodkin, A. N. Bodryakov, M. A. Bodryakova, L. N. Fetisov, “Thiourea assisted recyclization of 1-(chloromethyl)dihydroisoquinolines: a convenient route to β-(o-thiazolylaryl)ethylamines”, Mendeleev Commun., 31:1 (2021), 125–127 |
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2020 |
| 9. |
A. A. Zubenko, A. S. Morkovnik, L. N. Divaeva, O. P. Demidov, V. S. Sochnev, I. G. Borodkina, Yu. D. Drobin, A. A. Spasov, “New route to bioactive 2-(hetero)arylethylamines via nucleophilic ring opening in fused 7-acyl-2,3-dihydroazepines”, Mendeleev Commun., 30:1 (2020), 28–30 |
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2019 |
| 10. |
A. S. Morkovnik, A. A. Zubenko, L. N. Divaeva, V. G. Kartsev, G. S. Borodkin, A. I. Klimenko, “The novel structural modification of pyridoxal via its cyclization into 2-acyl- and 2-heteroarylfuro[2,3-c]pyridines”, Mendeleev Commun., 29:1 (2019), 116–118 |
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| 11. |
L. Yu. Ukhin, L. G. Kuz'mina, D. V. Alexeenko, L. V. Belousova, A. S. Morkovnik, G. S. Borodkin, T. N. Gribanova, “Uncommon condensations of 1,2,3-triketone 2-oximes with o-phenylenediamine”, Mendeleev Commun., 29:1 (2019), 111–113 |
1
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2018 |
| 12. |
A. A. Zubenko, A. S. Morkovnik, L. N. Divaeva, V. G. Kartsev, K. Yu. Suponitsky, A. I. Klimenko, “Synthesis of phenanthro[1,2-d]azepine derivatives containing a new heterocyclic system from the aporphine alkaloid glaucine”, Mendeleev Commun., 28:3 (2018), 320–322 |
6
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| 13. |
L. Yu. Ukhin, L. G. Kuz'mina, D. V. Alexeenko, L. V. Belousova, E. N. Shepelenko, V. A. Podshibyakin, A. S. Morkovnik, “Novel reactions of ninhydrin oxime with mercaptoalkanoic acids”, Mendeleev Commun., 28:3 (2018), 300–302 |
6
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| 14. |
A. A. Zubenko, A. S. Morkovnik, L. N. Divaeva, V. G. Kartsev, G. S. Borodkin, A. I. Klimenko, “Reaction of 2-methyl-3,4-dihydro-β-carbolin-2-ium iodide with acylmethyl halides controlled by electronic effects: a new route to 1,2-dihydroazepino[4,5-b]indoles”, Mendeleev Commun., 28:1 (2018), 83–85 |
7
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| 15. |
A. A. Zubenko, A. S. Morkovnik, L. N. Divaeva, V. G. Kartsev, L. G. Kuz'mina, G. S. Borodkin, A. I. Klimenko, “Recyclization of glaucine as a new route to litebamine derivatives”, Mendeleev Commun., 28:1 (2018), 58–60 |
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2016 |
| 16. |
Yu. V. Koshchienko, T. A. Kuz'menko, A. S. Morkovnik, M. A. Kiskin, G. G. Alexandrov, “Unexpected domino reaction of 3-alkyl-1,2,4-triazolo[1,5-a]benzimidazoles with butylmagnesium bromide leading to benzimidazolyl guanidines”, Mendeleev Commun., 26:4 (2016), 320–322 |
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2013 |
| 17. |
L. Yu. Ukhin, L. V. Belousova, E. N. Shepelenko, A. S. Morkovnik, “Synthesis of 6' H-spiro(indene-2,2' -[1,3]oxathiane)-1,3,5' -triones”, Mendeleev Commun., 23:6 (2013), 352–353 |
6
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2007 |
| 18. |
A. S. Morkovnik, L. N. Divaeva, Yu. V. Nelyubina, K. A. Lyssenko, I. S. Vasil'chenko, “Structure and tautomerism of 2-benzimidazolylthioureas”, Mendeleev Commun., 17:4 (2007), 224–226 |
4
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1997 |
| 19. |
A. S. Morkovnik, “Steric control in the ion radical nitration of 5-triphenylmethylbenzimidazolines using a silver/nitrite system”, Mendeleev Commun., 7:5 (1997), 175–176 |
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1995 |
| 20. |
A. S. Morkovnik, V. N. Khrustalev, S. V. Lindeman, Yu. T. Struchkov, Z. S. Morkovnik, “A New Class of Benzoin Condensation Catalysts: N,N′-Disubstituted o-Phenylenediamines”, Mendeleev Commun., 5:1 (1995), 11–12 |
3
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1988 |
| 21. |
А. С. Морковник, “Окислительно-восстановительная стадия в реакции нитрования”, Усп. хим., 57:2 (1988), 254–280 ; A. S. Morkovnik, “The Oxidation-reduction Stage in the Nitration Reaction”, Russian Chem. Reviews, 57:2 (1988), 144–160 |
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1979 |
| 22. |
А. С. Морковник, О. Ю. Охлобыстин, “Неорганические ион-радикалы и их органические реакции”, Усп. хим., 48:11 (1979), 1968–2006 ; A. S. Morkovnik, O. Yu. Okhlobystin, “Inorganic Radical-ions and Their Organic Reactions”, Russian Chem. Reviews, 48:11 (1979), 1055–1075 |
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