Образец цитирования:
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
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc1090
https://www.mathnet.ru/rus/mendc/v30/i1/p28
Эта публикация цитируется в следующих 8 статьяx:
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
Dmitry V. Maltsev, Alexander A. Spasov, Maria O. Skripka, Mikhail V. Miroshnikov, Lyudmila N. Divaeva, Anatoly S. Morkovnik, Alexander A. Zubenko, Alexander I. Klimenko, “ASSESSMENT OF ANXIOLYTIC POTENTIAL OF NEW С2,С3- QUINOXALINE DERIVATIVES”, Journal of Volgograd State Medical University, 19:2 (2022), 135
Dmitriy V. Maltsev, Maria O. Skripka, Alexander A. Spasov, Pavel M. Vassiliev, Maxim A. Perfiliev, Lyudmila N. Divaeva, Alexander A. Zubenko, Anatolii S. Morkovnik, Alexander I. Klimenko, Mikhail V. Miroshnikov, Vladlen G. Klochkov, Laura R. Ianalieva, “Design, Synthesis and Pharmacological Evaluation of Novel C2,C3-Quinoxaline Derivatives as Promising Anxiolytic Agents”, IJMS, 23:22 (2022), 14401
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
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
A. A. Zubenko, A. S. Morkovnik, L. N. Divaeva, V. S. Sochnev, O. P. Demidov, A. N. Bodryakov, L. N. Fetisov, K. N. Kononenko, M. A. Bodryakova, A. I. Klimenko, “New Azepine-Furan Spirocyclic Structures in the Reaction of
4-Aroyl-1,2-dihydrobenzo[d]azepines and
2-Aroyl-4,5-dihydrophenanthreno[1,2-d]azepine
with Formaldehyde”, Russ J Gen Chem, 91:5 (2021), 792
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
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