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Mendeleev Communications, 2010, Volume 20, Issue 2, Pages 106–108
DOI: https://doi.org/10.1016/j.mencom.2010.03.014
(Mi mendc3005)
 

This article is cited in 4 scientific papers (total in 4 papers)

General regioselective synthesis and crystal structure of racemic 5-substituted 2,2-dimethyl-3-hydroxyimidazolidin-4-ones

I. V. Vystoropa, Yu. V. Nelyubinab, V. N. Voznesenskyc, W.-H. Sund, V. P. Lodyginaa, K. A. Lyssenkob, R. G. Kostyanovskyc

a Institute of Problems of Chemical Physics, Russian Academy of Sciences, Chernogolovka, Moscow Region, Russian Federation
b A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation
c N.N. Semenov Federal Research Center for Chemical Physics, Russian Academy of Sciences, Moscow, Russian Federation
d Institute of Chemistry, Chinese Academy of Sciences, Beijing, China
Full-text PDF (490 kB) Citations (4)
Abstract: The cyclocondensation of racemic valine, leucine and β-phenylalanine hydroxamic acids with acetone regioselectively affords corresponding cyclic hydroxamic acids; the crystal structure of the 5-isobutyl derivative was determined by X-ray diffraction analysis and compared with that of its 5-methyl homologue.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (31.6 Kb)


Citation: I. V. Vystorop, Yu. V. Nelyubina, V. N. Voznesensky, W.-H. Sun, V. P. Lodygina, K. A. Lyssenko, R. G. Kostyanovsky, “General regioselective synthesis and crystal structure of racemic 5-substituted 2,2-dimethyl-3-hydroxyimidazolidin-4-ones”, Mendeleev Commun., 20:2 (2010), 106–108
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  • https://www.mathnet.ru/eng/mendc3005
  • https://www.mathnet.ru/eng/mendc/v20/i2/p106
  • This publication is cited in the following 4 articles:
    1. I. V. Vystorop, G. V. Shilov, A. V. Chernyak, E. N. Klimanova, T. E. Sashenkova, S. G. Klochkov, M. E. Neganova, Yu. R. Aleksandrova, U. Yu. Allayarova, D. V. Mishchenko, “Regioselective Synthesis, Structure, and Chemosensitizing Antitumor Activity of Cyclic Hydroxamic Acid Based on DL-Valine”, Russ J Bioorg Chem, 47:3 (2021), 757  crossref
    2. N. P. Akentieva, A. R. Gizatullin, S. A. Goncharova, T. A. Raevskaya, N. S. Goryachev, N. I. Shkondina, T. R. Prichodchenko, I. V. Vystorop, S. S. Shushanov, “Anticancer Activity of Spirocyclic Hydroxamic Acids (Derivatives of 1-Hydroxy-1,4,8-Triazaspiro[4,5]Decan-2-One), Histone Deacetylase Inhibitors”, Biochem. Moscow Suppl. Ser. A, 13:1 (2019), 12  crossref
    3. I. V. Vystorop, N. P. Konovalova, Yu. V. Nelyubina, A. V. Chernyak, T. E. Sashenkova, E. N. Klimanova, A. N. Utienyshev, B. S. Fedorov, G. V. Shilov, R. G. Kostyanovsky, “Cyclic hydroxamic acids derived from α-amino acids 2. Regioselective synthesis, crystal structure, and antitumor activity of spiropiperidine-imidazolidine hydroxamic acids based on glycine and dl-alanine”, Russ Chem Bull, 62:5 (2013), 1272  crossref
    4. Igor V. Vystorop, Yulia V. Nelyubina, Vladimir N. Voznesensky, Wen‐Hua Sun, Vera P. Lodygina, Konstantin A. Lyssenko, Remir G. Kostyanovsky, “ChemInform Abstract: General Regioselective Synthesis and Crystal Structure of Racemic 5‐Substituted 2,2‐Dimethyl‐3‐hydroxyimidazolidin‐4‐ones.”, ChemInform, 41:49 (2010)  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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