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Mendeleev Communications, 2019, Volume 29, Issue 2, Pages 198–199
DOI: https://doi.org/10.1016/j.mencom.2019.03.028 (Mi mendc1470) 		 
This article is cited in 2 scientific papers (total in 2 papers)

Communications

Effective synthesis of non-racemic prenalterol based on spontaneous resolution of 3-(4-hydroxyphenoxy)propane-1,2-diol

Z. A. Bredikhina, A. V. Kurenkov, A. A. Bredikhin

A.E. Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center of the Russian Academy of Sciences, Kazan, Russian Federation
Full-text PDF (268 kB) Citations (2)
DOI: https://doi.org/10.1016/j.mencom.2019.03.028
Abstract: Spontaneous resolution of rac-3-(4-hydroxyphenoxy)propane-1,2-diol has been successfully used in the synthesis of both enantiomers of chiral drug prenalterol.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (1.2 Mb)


Citation: Z. A. Bredikhina, A. V. Kurenkov, A. A. Bredikhin, “Effective synthesis of non-racemic prenalterol based on spontaneous resolution of 3-(4-hydroxyphenoxy)propane-1,2-diol”, Mendeleev Commun., 29:2 (2019), 198–199
Linking options:
  • https://www.mathnet.ru/eng/mendc1470
  • https://www.mathnet.ru/eng/mendc/v29/i2/p198
    • This publication is cited in the following 2 articles:
    1. Alexander A. Bredikhin, Robert R. Fayzullin, Zemfira A. Bredikhina, “Crystal Structure of Chiral Drug Prenalterol and Its Precursor Prone to Spontaneous Resolution”, Symmetry, 14:6 (2022), 1150  crossref
    2. Alexander A. Bredikhin, Dmitry V. Zakharychev, Aidar T. Gubaidullin, Aida I. Samigullina, Zemfira A. Bredikhina, “Crystal Landscape of Chiral Drug Chlorphenesin and Its Structural Analogues: Polymorphism of Racemic and Enantiopure Samples, Metastable and Stable Racemic Conglomerates, Diverse in Unity Crystal Motifs”, Crystal Growth & Design, 21:6 (2021), 3211  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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