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Mendeleev Communications, 2004, Volume 14, Issue 3, Pages 105–107
DOI: https://doi.org/10.1070/MC2004v014n03ABEH001886
(Mi mendc3827)
 

This article is cited in 22 scientific papers (total in 22 papers)

New conglomerate in the series of glycoluriles

K. A. Lyssenkoa, D. G. Golovanova, A. N. Kravchenkob, I. E. Chikunovb, O. V. Lebedevb, N. N. Makhovab

a A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation
b N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Abstract: Three new chiral glycoluriles with a 2-(3-carboxypropyl) substituent were synthesised and characterised by X-ray diffraction analysis; one of them, 4-{3,7-dioxo-2-(3-carboxypropyl)-6,8-dimethyl-2,4,6,8-tetraazabicyclo[3.3.0]oct-2-yl}butanoic acid, was found to crystallise as a conglomerate
Document Type: Article
Language: English


Citation: K. A. Lyssenko, D. G. Golovanov, A. N. Kravchenko, I. E. Chikunov, O. V. Lebedev, N. N. Makhova, “New conglomerate in the series of glycoluriles”, Mendeleev Commun., 14:3 (2004), 105–107
Linking options:
  • https://www.mathnet.ru/eng/mendc3827
  • https://www.mathnet.ru/eng/mendc/v14/i3/p105
  • This publication is cited in the following 22 articles:
    1. Evgeniy V. Ivanov, Elena Yu. Lebedeva, Vladimir V. Baranov, Angelina N. Kravchenko, “Volume properties of bioactive glycoluril-derivatives of gamma-aminobutyric acid in aqueous solutions between 278.15 and 318.15 K”, Journal of Molecular Liquids, 384 (2023), 122234  crossref
    2. 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
    3. Vladimir V. Baranov, Anastasiya A. Baganova, Ilya E. Chikunov, Valentina A. Karnoukhova, Angelina N. Kravchenko, “Unexpected formation of novel two-component gels comprising of glycoluril carboxylic acid amides and imidazole: Synthesis and morphology”, Tetrahedron Letters, 60:17 (2019), 1174  crossref
    4. Ivan V. Fedyanin, Valentina A. Karnoukhova, Konstantin A. Lyssenko, “Conformational analysis of a supramolecular synthon: a case study of 8-hydroxyquinoline”, CrystEngComm, 20:5 (2018), 652  crossref
    5. Zhiguang Xu, Haiyang Liu, Mian HR Mahmood, Yuepeng Cai, Xuan Xu, Youwen Tang, “Spontaneous resolution of chiral bis-sulfoxides with asymmetric atropisomerism”, CrystEngComm, 16:19 (2014), 3839  crossref
    6. A. N. Kravchenko, V. V. Baranov, L. V. Anikina, Yu. B. Vikharev, I. S. Bushmarinov, Yu. V. Nelyubina, “Neuroprotective Activity of (+)-(S)-2-[(1S,5R)-(3,7-Dioxo-2,4,6,8-Tetraazabicyclo[3.3.0]oct-2-yl)]-4-methylthiobutanoic acid”, Russ J Bioorg Chem, 38:5 (2012), 550  crossref
    7. K. A. Lyssenko, “Analysis of supramolecular architectures: beyond molecular packing diagrams”, Mendeleev Commun., 22:1 (2012), 1–7  mathnet  crossref
    8. V. V. Baranov, G. A. Gazieva, Yu. V. Nelyubina, A. N. Kravchenko, N. N. Makhova, “α-Thioureidoalkylation of functionally substituted ureas: I. Tandem cyclization and esterification in reactions of N-(carboxyalkyl)ureas with 1,3-dialkyl-4,5-dihydroxy-4,5-diphenylimidazolidine-2-thiones in alcohols”, Russ J Org Chem, 47:10 (2011), 1564  crossref
    9. Cornelia Uncuţa, Emeric Bartha, Dragoş Gherase, Ioan Andrei Loas, Florina Teodorescu, Richard A. Varga, Nicolas Vanthuyne, Christian Roussel, Ulf Berg, “Chiral bicyclo[3.3.1]-3,7-dioxanonane derivatives: Study of crystallization mode and conformational dynamics in solution”, Journal of Molecular Structure, 989:1-3 (2011), 20  crossref
    10. V. V. Baranov, Yu. V. Nelyubina, A. N. Kravchenko, N. N. Makhova, “4,5-Dihydroxyimidazolidin-2-ones in the reaction of α-ureidoalkylation of N-(carboxyalkyl)-, N-(hydroxyalkyl)-, and N-(aminoalkyl)ureas”, Russ Chem Bull, 59:7 (2010), 1427  crossref
    11. Emiliana D'Oria, Panagiotis G. Karamertzanis, Sarah L. Price, “Spontaneous Resolution of Enantiomers by Crystallization: Insights from Computed Crystal Energy Landscapes”, Crystal Growth & Design, 10:4 (2010), 1749  crossref
    12. A. N. Kravchenko, A. S. Sigachev, P. A. Belyakov, M. M. Ilyin, K. A. Lyssenko, V. A. Davankov, O. V. Lebedev, N. N. Makhova, V. A. Tartakovsky, “4,5-Dihydroxyimidazolidin-2-ones in α-ureidoalkylation of N-carboxy-, N-hydroxy-, and N-aminoalkylureas 2. α-Ureidoalkylation of N-(hydroxyalkyl)ureas”, Russ Chem Bull, 58:6 (2009), 1264  crossref
    13. G. A. Gazieva, P. V. Lozhkin, V. V. Baranov, Yu. V. Nelyubina, A. N. Kravchenko, N. N. Makhova, “4,5-Dihydroxyimidazolidin-2-ones in an α-ureidoalkylation reaction of N-(carboxyalkyl)-, N-(hydroxyalkyl)-, and N-(aminoalkyl)ureas 3. α-Ureidoalkylation of N-[2-(dimethylamino)ethyl]urea”, Russ Chem Bull, 58:12 (2009), 2488  crossref
    14. A. N. Kravchenko, K. A. Lyssenko, I. E. Chikunov, P. A. Belyakov, M. M. Il'in, V. V. Baranov, Yu. V. Nelyubina, V. A. Davankov, T. S. Pivina, N. N. Makhova, M. Yu. Antipin, “4,5-Dihydroxyimidazolidin-2-ones in the α-ureidoalkylation reaction of N-(carboxyalkyl)-, N-(hydroxyalkyl)-, and N-(aminoalkyl)ureas 1. α-Ureidoalkylation of N-(carboxyalkyl)ureas”, Russ Chem Bull, 58:2 (2009), 395  crossref
    15. A. N. Kravchenko, E. Yu. Maksareva, S. V. Vasilevskii, O. V. Lebedev, K. A. Lyssenko, “A new approach to the synthesis of 1,3-dimethyl-4,5-disubstituted imidazolidin-2-ones”, Mendeleev Commun., 18:1 (2008), 45–47  mathnet  crossref
    16. Lluïsa Pérez-García, David B. Amabilino, “Spontaneous resolution, whence and whither: from enantiomorphic solids to chiral liquid crystals, monolayers and macro- and supra-molecular polymers and assemblies”, Chem. Soc. Rev., 36:6 (2007), 941  crossref
    17. B. V. Lozhkin, A. S. Sigachev, A. N. Kravchenko, K. A. Lyssenko, N. G. Kolotyrkina, N. N. Makhova, “The first conglomerate in the series of 2,4,6,8,10-pentaazatricyclo[5.3.1.03.11]undecane-1,5-diones”, Mendeleev Commun., 17:2 (2007), 85–87  mathnet  crossref
    18. I. E. Chikunov, A. N. Kravchenko, N. N. Makhova, “Synthesis of enantiomerically pure fused polyheterocyclic glycolurils based on (S)- α-amino acids”, Mendeleev Commun., 17:6 (2007), 321–322  mathnet  crossref
    19. A. N. Kravchenko, A. S. Sigachev, G. A. Gazieva, E. Yu. Maksareva, N. S. Trunova, K. A. Chegaev, K. A. Lyssenko, D. V. Lyubetsky, M. I. Struchkova, M. M. Il'in, V. A. Davankov, O. V. Lebedev, N. N. Makhova, V. A. Tartakovsky, “Reaction of N-alkylglycolurils with electrophilic reagents”, Chem Heterocycl Compd, 42:3 (2006), 365  crossref
    20. Andrey S. Sigachev, Angelina N. Kravchenko, Galina A. Gazieva, Pavel A. Belyakov, Natal'Ya G. Kolotyrkina, Oleg V. Lebedev, Nina N. Makhova, Konstantin A. Lyssenko, “Synthesis of first representatives of 3,3′-bi(6,8-dialkyl-2,4-dioxa-6,8-diazabicyclo[3.3.0]octan-7-ones)”, Journal of Heterocyclic Chemistry, 43:5 (2006), 1295  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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