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Mendeleev Communications, 2024, Volume 34, Issue 1, Pages 116–118
DOI: https://doi.org/10.1016/j.mencom.2024.01.035
(Mi mendc60)
 

This article is cited in 2 scientific papers (total in 2 papers)

Communications

An efficient synthesis of substituted 4,5-dihydroxyimidazolidin-2-ones by oxidation of imidazolin-2-ones with HNO3

V. V. Baranova, P. D. Prakhovab, N. G. Kolotyrkinaa, A. N. Kravchenkoa

a N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
b D.Mendeleev University of Chemical Technology of Russia, Moscow, Russian Federation
Abstract: Previously unavailable 1,3-dialkyl-4,5-diaryl-4,5-dihydroxyimidazolidin-2-ones were obtained by the oxidation of 1,3-dialkyl-4,5-diaryl-4-imidazolin-2-ones with HNO3 (65 or 84% aq.). The scope of required 4-imidazolin-2-ones obtained from acyloins has been expanded, which provided preparation of new representatives of the title compounds.
Keywords: 4,5-dihydroxyimidazolidin-2-ones, nitric acid, oxidation, 4-imidazolin-2-ones, diastereomers, acyloins, ureas.
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (3.0 Mb)


Citation: 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
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  • https://www.mathnet.ru/eng/mendc/v34/i1/p116
  • This publication is cited in the following 2 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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