|
|
|
Publications in Math-Net.Ru |
Citations |
|
2023 |
| 1. |
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
|
| 2. |
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-[<i>o</i>-(5-oxopyrazol-3-yl)aryl]ethylamines and their unusual metastable betaine form”, Mendeleev Commun., 33:2 (2023), 203–205 |
1
|
|
2022 |
| 3. |
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 |
3
|
| 4. |
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
|
|
2021 |
| 5. |
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-<i>a</i>]benzimidazole and its <i>N</i> 9-substituted derivatives”, Mendeleev Commun., 31:4 (2021), 555–557 |
6
|
| 6. |
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
|
| 7. |
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-(<i>o</i>-thiazolylaryl)ethylamines”, Mendeleev Commun., 31:1 (2021), 125–127 |
4
|
|
2019 |
| 8. |
A. S. Morkovnik, A. A. Zubenko, L. N. Divaeva, V. G. Kartsev, G. S. Borodkin, A. I. Klimenko, “The novel structural modification of pyridoxal <i>via</i> its cyclization into 2-acyl- and 2-heteroarylfuro[2,3-<i>c</i>]pyridines”, Mendeleev Commun., 29:1 (2019), 116–118 |
3
|
|
2018 |
| 9. |
A. A. Zubenko, A. S. Morkovnik, L. N. Divaeva, V. G. Kartsev, K. Yu. Suponitsky, A. I. Klimenko, “Synthesis of phenanthro[1,2-<i>d</i>]azepine derivatives containing a new heterocyclic system from the aporphine alkaloid glaucine”, Mendeleev Commun., 28:3 (2018), 320–322 |
7
|
| 10. |
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-<i>b</i>]indoles”, Mendeleev Commun., 28:1 (2018), 83–85 |
7
|
| 11. |
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 |
8
|
|
| Organisations |
|
| |
|
|
Contact us: