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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Mendeleev Communications, 2018, Volume 28, Issue 3, Pages 320–322
DOI: https://doi.org/10.1016/j.mencom.2018.05.031 (Mi mendc1752)

This article is cited in 6 scientific papers (total in 6 papers)

Communications

Synthesis of phenanthro[1,2-d]azepine derivatives containing a new heterocyclic system from the aporphine alkaloid glaucine

A. A. Zubenko^a, A. S. Morkovnik^b, L. N. Divaeva^b, V. G. Kartsev^c, K. Yu. Suponitsky^d, A. I. Klimenko^e

^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 A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation
^e Don State Agrarian University, Novocherkassk, Russian Federation

Full-text PDF (295 kB) Citations (6)

DOI: https://doi.org/10.1016/j.mencom.2018.05.031

Graphic abstract: Synthesis of phenanthro[1,2-<i>d</i>]azepine derivatives containing a new heterocyclic system from the aporphine alkaloid glaucine

Abstract: Derivatives of phenanthro[1,2-d]azepine, a previously unknown heterocyclic system, can be easily obtained from aporphine alkaloids by successive pyridine–pyridine and pyridine–azepine recyclizations. The starting glaucine was used as an illustrative example.

Document Type: Article

Language: English

Citation: 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

Linking options:

https://www.mathnet.ru/eng/mendc1752

https://www.mathnet.ru/eng/mendc/v28/i3/p320

This publication is cited in the following 6 articles:

Kanika Patel, Dinesh Kumar Patel, “Biological importance and therapeutic effectiveness of thaliporphine in medicine: An aporphine alkaloid from natural sources”, Pharmacological Research - Natural Products, 2 (2024), 100019
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, 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
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. 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
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

Citing articles in Google Scholar: Russian citations, English citations
Related articles in Google Scholar: Russian articles, English articles

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