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Mendeleev Communications, 2018, Volume 28, Issue 1, Pages 58–60
DOI: https://doi.org/10.1016/j.mencom.2018.01.019
(Mi mendc1663)
 

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

Communications

Recyclization of glaucine as a new route to litebamine derivatives

A. A. Zubenkoa, A. S. Morkovnikb, L. N. Divaevab, V. G. Kartsevc, L. G. Kuz'minad, G. S. Borodkinb, A. I. Klimenkoe

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 N.S. Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
e Don State Agrarian University, Novocherkassk, Russian Federation
Full-text PDF (311 kB) Citations (8)
Abstract: Using glaucine as an example, a convenient access to naphtho[2,1-f]isoquinoline (litebamine) derivatives is proposed. The synthetic scheme involves a stepwise pyridine–pyridine recyclization of the intermediate N-acylsecoaporphine analogues.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (2.4 Mb)


Citation: 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
Linking options:
  • https://www.mathnet.ru/eng/mendc1663
  • https://www.mathnet.ru/eng/mendc/v28/i1/p58
  • This publication is cited in the following 8 articles:
    1. S. S. Khizrieva, S. N. Borisenko, E. V. Maksimenko, E. V. Vetrova, N. I. Borisenko, V. I. Minkin, “Antioxidant Properties and Effects of Aporphine Alkaloids and Their Phenanthrene Seco-Isomers on Acetylcholinesterase Activity”, Russ J Bioorg Chem, 48:7 (2022), 1433  crossref
    2. 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
    3. Salima Salimovna Khizrieva, Sergey Nikolaevich Borisenko, Elena Vladimirovna Maksimenko, Elena Vladimirovna Vetrova, Nikolay Ivanovich Borisenko, Vladimir Isaakovich Minkin, “ANTIOXIDANT PROPERTIES AND EFFECTS OF APORPHINE ALKALOIDS AND THEIR PHENANTHRENE SECO-ISOMERS ON ACETYLCHOLINESTERASE ACTIVITY”, JCPRM, 2021, no. 2, 237  crossref
    4. 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
    5. 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
    6. 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
    7. A. A. Zubenko, L. N. Divaeva, A. S. Morkovnik, V. G. Kartsev, Y. D. Drobin, N. M. Serbinovskaya, L. N. Fetisov, A. N. Bodryakov, M. A. Bodryakova, L. A. Lyashenko, A. I. Klimenko, “Synthesis and Anti-Infective Activity of 2-Heteroaryl(Acyl)-9,10,12,13-Tetramethoxy-3-Methyl-4,5-Dihydro-3H-Phenanthro[1,2-d]Azepines”, Russ J Bioorg Chem, 44:4 (2018), 461  crossref
    8. 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
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