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Mendeleev Communications, 2020, Volume 30, Issue 4, Pages 479–481
DOI: https://doi.org/10.1016/j.mencom.2020.07.024 (Mi mendc1229) 		 
This article is cited in 6 scientific papers (total in 6 papers)

Communications

New cage-fused polyaza polycyclic systems based on thioglycolurils and alkanediamines

V. V. Baranova, Ya. A. Barsegyana, Yu. A. Strelenkoa, V. A. Karnoukhovab, A. N. Kravchenkoac

a N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
b A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation
c G.V. Plekhanov Russian University of Economics, Moscow, Russian Federation
Full-text PDF (231 kB) Citations (6)
DOI: https://doi.org/10.1016/j.mencom.2020.07.024
Abstract: New aspects of multicomponent condensation reactions of ethylene/propylenediamine, formaldehyde and unsubstituted and 1-methyl substituted semithio- and dithioglycolurils have been examined. Ethylene-linked 2,3a,4a,6,9,10a,11aheptaaza-6,9-methanobenzo[cd]cyclonona[gh]pentalene and 2,6:10,14-dimethano-2,6,7a,8a,10,14,15a,16a-octaazadicyclodeca[cd,gh]pentalene as well as their simpler analogues were synthesized, and their structures were proved by 1D and 2D NMR spectroscopy, HRMS and X-ray analysis.
Keywords: thioglycolurils, multicomponent reactions, diamines, polyheterocycles, formaldehyde, aminals.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (3.3 Mb)


Citation: V. V. Baranov, Ya. A. Barsegyan, Yu. A. Strelenko, V. A. Karnoukhova, A. N. Kravchenko, “New cage-fused polyaza polycyclic systems based on thioglycolurils and alkanediamines”, Mendeleev Commun., 30:4 (2020), 479–481
Linking options:
  • https://www.mathnet.ru/eng/mendc1229
  • https://www.mathnet.ru/eng/mendc/v30/i4/p479
    • This publication is cited in the following 6 articles:
    1. Anton A. Galochkin, Vladimir V. Baranov, Karl A. Hansford, Louise I. M. Friberg, Elena D. Strel'tzova, Egor S. Lipatov, Yulia V. Nelyubina, Angelina N. Kravchenko, “Synthesis, Structures and Antifungal Activity of Selenoglycolurils”, ChemistrySelect, 8:14 (2023)  crossref
    2. Cheng Geng, “Modelling of mixed thermodynamic model based on new materials”, Therm sci, 27:2 Part A (2023), 1067  crossref
    3. V. V. Baranov, T. N. Vol'khina, N. G. Kolotyrkina, A. N. Kravchenko, “Synthesis and crystal structures of novel glycoluril carboxylic acids conglomerates”, Mendeleev Commun., 32:4 (2022), 537–539  mathnet  crossref
    4. A. A. Galochkin, V. V. Baranov, N. G. Kolotyrkina, A. N. Kravchenko, “Synthesis of trialkyl semithioglycolurils from alkylthiourea-glyoxal cyclic adducts and dialkylureas”, Mendeleev Commun., 32:6 (2022), 771–773  mathnet  crossref
    5. Elena A. Mamaeva, Anastasiya V. Leppa, Abdigali A. Bakibayev, “Selective synthesis of a novel glycoluril-based hybrid compound with high application potential”, Chem Heterocycl Comp, 57:6 (2021), 700  crossref
    6. I. Yu. Titov, V. S. Stroylov, P. V. Rusina, I. Svitanko, “Preliminary modelling as the first stage of targeted organic synthesis”, Russian Chem. Reviews, 90:7 (2021), 831–867  mathnet  mathnet  crossref  isi  scopus
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