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Mendeleev Communications, 2020, Volume 30, Issue 1, Pages 28–30
DOI: https://doi.org/10.1016/j.mencom.2020.01.009
(Mi mendc1090)
 

This article is cited in 8 scientific papers (total in 8 papers)

Communications

New route to bioactive 2-(hetero)arylethylamines via nucleophilic ring opening in fused 7-acyl-2,3-dihydroazepines

A. A. Zubenkoa, A. S. Morkovnikb, L. N. Divaevab, O. P. Demidovc, V. S. Sochnevb, I. G. Borodkinab, Yu. D. Drobina, A. A. Spasovd

a North-Caucasian Zonal Research Veterinary Institute, Novocherkassk, Russian Federation
b Institute of Physical and Organic Chemistry, Southern Federal University, Rostov-on-Don, Russian Federation
c North-Caucasus Federal University, Stavropol, Russian Federation
d Volgograd State Medical University, Volgograd, Russian Federation
Full-text PDF (527 kB) Citations (8)
Abstract: Nucleophilic heterocyclic ring opening in fused 7-acyl- H+ 1,2-dihydroazepines with o-phenylenediamine affords b-(hetero)arylethylamines.
Keywords: fused dihydroazepines, azepine–pyrazine recyclization, baryl(heteroaryl)ethylamines, bioactive amines, ring opening reactions.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (3.4 Mb)


Citation: 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
Linking options:
  • https://www.mathnet.ru/eng/mendc1090
  • https://www.mathnet.ru/eng/mendc/v30/i1/p28
  • This publication is cited in the following 8 articles:
    1. 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  mathnet  crossref
    2. 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 S2,S3- QUINOXALINE DERIVATIVES”, Journal of Volgograd State Medical University, 19:2 (2022), 135  crossref
    3. 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  crossref
    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  mathnet  crossref
    5. 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  mathnet  crossref
    6. 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  crossref
    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  mathnet  crossref
    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  mathnet  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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