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
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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
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
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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
K. A. Lyssenko, “Analysis of supramolecular architectures: beyond molecular packing diagrams”, Mendeleev Commun., 22:1 (2012), 1–7
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
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
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
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
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
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
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
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
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
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
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
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
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