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Mendeleev Communications, 2018, Volume 28, Issue 1, Pages 83–85
DOI: https://doi.org/10.1016/j.mencom.2018.01.028
(Mi mendc1672)
 

This article is cited in 7 scientific papers (total in 7 papers)

Communications

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

A. A. Zubenkoa, A. S. Morkovnikb, L. N. Divaevab, V. G. Kartsevc, G. S. Borodkinb, A. I. Klimenkod

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 'InterBioScreen Ltd.', Chernogolovka, Moscow Region, Russian Federation
d Don State Agrarian University, Novocherkassk, Russian Federation
Full-text PDF (359 kB) Citations (7)
Abstract: 2-Methyl-3,4-dihydro-β-carbolin-2-ium iodide in the reaction with aryl halomethyl ketones is converted into 4- or/and 5-acyl-1,2-dihydroazepino[4,5-b]indoles depending on the electron donating effect of substituents in the aryl moiety of the halomethyl ketone.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (315.7 Kb)


Citation: 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
Linking options:
  • https://www.mathnet.ru/eng/mendc1672
  • https://www.mathnet.ru/eng/mendc/v28/i1/p83
  • This publication is cited in the following 7 articles:
    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  mathnet  crossref
    2. 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
    3. 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  mathnet  crossref
    4. A. A. Zubenko, A. S. Morkovnik, L. N. Divaeva, V. G. Kartsev, A. A. Anisimov, K. Yu. Suponitsky, “Pyridine—Azepine Structural Modification of 3,4-Dihydro-nor-isoharmine”, Russ J Org Chem, 55:1 (2019), 74  crossref
    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  mathnet  crossref
    6. S. Gundala, M. R. Guda, A. F. Khasanov, D. S. Kopchuk, A. P. Krinochkin, S. Santra, G. V. Zyryanov, P. Venkatapuram, J. R. Garcia, V. N. Charushin, “A PASE-based approach towards 12-(1H-1,2,3-triazol-1-yl)-indolo[2,1-a]isoquinolines via the reaction of 3-(isoquinolin-1-yl)-1,2,4-triazines with benzyne”, Mendeleev Commun., 29:4 (2019), 369–371  mathnet  crossref
    7. 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  mathnet  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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