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Mendeleev Communications, 2022, Volume 32, Issue 4, Pages 537–539
DOI: https://doi.org/10.1016/j.mencom.2022.07.034
(Mi mendc718)
 

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

Communications

Synthesis and crystal structures of novel glycoluril carboxylic acids conglomerates

V. V. Baranova, T. N. Vol'khinabc, N. G. Kolotyrkinaa, A. N. Kravchenkoa

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 D.Mendeleev University of Chemical Technology of Russia, Moscow, Russian Federation
Full-text PDF (426 kB) Citations (6)
Abstract: The two novel conglomerates were obtained by crystallization of racemic (2'S,3aS,6aR)/(2'R,3aR,6aS) (glycoluril-1-yl)-3-methylbutanoic acid and (2'R,3aR,6aR)/(2'S,3aS,6aS) (4,6-dimethylglycoluril-1-yl)pentanoic acid synthesized by highly diastereoselective condensation of 4,5-dihydroxy- imidazolidin-2-ones with racemic ureido acids. The differences in the molecular geometry of synthesized racemates were studied by X-ray diffraction that showed them to crystallize as conglomerates in non-centrosymmetric space groups Pna21 and P212121, respectively
Keywords: conglomerats, glycolurils, carboxylic acids, racemates, ureido acids, 45-dihydroxyimidazolidin-2-ones, crystallization, crystal structures.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (1.8 Mb)


Citation: 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
Linking options:
  • https://www.mathnet.ru/eng/mendc718
  • https://www.mathnet.ru/eng/mendc/v32/i4/p537
  • This publication is cited in the following 6 articles:
    1. V. V. Baranov, M. M. Antonova, S. A. Aksenova, N. G. Kolotyrkina, A. N. Kravchenko, Mendeleev Commun., 35:1 (2025), 27–30  mathnet  crossref
    2. V. V. Baranov, P. D. Prakhov, N. G. Kolotyrkina, A. N. Kravchenko, “An efficient synthesis of substituted 4,5-dihydroxyimidazolidin-2-ones by oxidation of imidazolin-2-ones with HNO3”, Mendeleev Commun., 34:1 (2024), 116–118  mathnet  crossref
    3. V. V. Baranov, M. M. Antonova, S. A. Aksenova, N. G. Kolotyrkina, A. N. Kravchenko, “Novel synthesis of 1,6- and 1,4-dialkyl glycolurils and their supramolecular organization”, Mendeleev Commun., 34:6 (2024), 871–874  mathnet  crossref
    4. Sergey I. Gorbin, Abdigali A. Bakibaev, Vera P. Tuguldurova, Andrey V. Kotov, Gleb O. Sysoev, Andrei S. Potapov, Dmitry I. Pavlov, Victor S. Malkov, Alexey S. Knyazev, Dmitriy A. Kurgachev, Mark V. Michalchenkov, “Synthesis of Novel Phosphorus-Containing Derivatives of 1,3,4-Trimethylglycoluril via the Birum–Oleksyszyn Reaction”, IJMS, 24:23 (2023), 17082  crossref
    5. S. I. Gorbin, A. A. Bakibaev, D. A. Kurgachev, V. S. Malkov, K. Yu. Novolokov, G. O. Sysoev, “Synthesis of 1-[1-(diphenoxyphosphoryl)alkyl]-3,4,6-trimethylglycolurils”, Mendeleev Commun., 33:5 (2023), 638–639  mathnet  crossref
    6. 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
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