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Публикации в базе данных Math-Net.Ru |
Цитирования |
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2022 |
| 1. |
S. N. Sirakanyan, E. K. Hakobyan, D. Spinelli, A. Geronikaki, V. G. Kartsev, H. A. Yegoryan, A. A. Hovakimyan, “Synthesis of new heterocyclic systems fused at pyrazolo[3,4-c]-2,7-naphthyridine core”, Mendeleev Commun., 32:3 (2022), 393–394   |
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2021 |
| 2. |
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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| 3. |
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 |
4
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2019 |
| 4. |
R. F. Fatykhov, M. I. Savchuk, E. S. Starnovskaya, M. V. Bobkina, D. S. Kopchuk, E. V. Nosova, G. V. Zyryanov, I. A. Khalymbadzha, O. N. Chupakhin, V. N. Charushin, V. G. Kartsev, “Nucleophilic substitution of hydrogen–the Boger reaction sequence as an approach towards 8-(pyridin-2-yl)coumarins”, Mendeleev Commun., 29:3 (2019), 299–300 |
25
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| 5. |
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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2018 |
| 6. |
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 |
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| 7. |
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 |
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| 8. |
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
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2012 |
| 9. |
D. S. Baranov, A. A. Ryabichev, V. I. Mamatyuk, Yu. V. Gatilov, V. G. Kartsev, S. F. Vasilevskii, “Synthesis of 2-amino-5,5-dialkyl-4-arylmethylidene-2-oxazolines from 2-alkyl-4-arylbut-3-yn-2-ols and guanidine”, Mendeleev Commun., 22:2 (2012), 114–116 |
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2007 |
| 10. |
C. Rabong, C. Valla, V. G. Kartsev, U. Jordis, “Stereochemical outcome of the T-reaction employing chiral bicyclic amines”, Mendeleev Commun., 17:6 (2007), 318–320 |
12
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2006 |
| 11. |
K. A. Krasnov, V. G. Kartsev, V. N. Khrustalev, “Interaction of barbituric acids with o-dialkylaminobenzaldehydes”, Mendeleev Commun., 16:1 (2006), 52–54 |
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1999 |
| 12. |
В. Г. Дрюк, В. Г. Карцев, “Механизм направляющего влияния функциональных групп и геометрии молекул реагентов на пероксидное эпоксидирование алкенов”, Усп. хим., 68:3 (1999), 206–226 ; V. G. Dryuk, V. G. Kartsev, “Mechanism of the directing influence of functional groups and the geometry of reactant molecules on peroxide epoxidation of alkenes”, Russian Chem. Reviews, 68:3 (1999), 183–201  |
15
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1993 |
| 13. |
N. N. Sveshnikov, A. A. Fomichov, I. V. Vystorop, V. G. Kartsev, “Inter-ring Long-range Spin-Spin Proton Coupling in some 8-Hydroxyquinoline Derivatives”, Mendeleev Commun., 3:3 (1993), 107–108 |
5
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1992 |
| 14. |
S. V. Chapyshev, V. G. Kartsev, “New Rearrangement in the o-Methoxycarbonyl-ω-diazoacetophenone Series”, Mendeleev Commun., 2:1 (1992), 8–10 |
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1991 |
| 15. |
В. Г. Карцев, “Новые направления в создании пестицидов с низкой экологической нагрузкой”, Усп. хим., 60:3 (1991), 553–554 ; V. G. Kartsev, “New trends in the creation of pesticides with a low ecological stress”, Russian Chem. Reviews, 60:3 (1991), 264–265 |
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