Loading [MathJax]/jax/output/SVG/config.js
Mendeleev Communications
RUS  ENG    JOURNALS   PEOPLE   ORGANISATIONS   CONFERENCES   SEMINARS   VIDEO LIBRARY   PACKAGE AMSBIB  
General information
Latest issue
Archive

Search papers
Search references

RSS
Latest issue
Current issues
Archive issues
What is RSS



Mendeleev Commun.:
Year:
Volume:
Issue:
Page:
Find






Personal entry:
Login:
Password:
Save password
Enter
Forgotten password?
Register


Mendeleev Communications, 2017, Volume 27, Issue 2, Pages 134–136
DOI: https://doi.org/10.1016/j.mencom.2017.03.008
(Mi mendc1920)
 

This article is cited in 17 scientific papers (total in 17 papers)

Communications

Phosphonium salts with a dihydroxynaphthyl substituent: versatile synthesis and evaluation of antimicrobial activity

N. R. Khasiyatullinaa, A. M. Vazykhovaa, V. F. Mironovab, D. B. Krivolapova, J. K. Voroninaa, A. D. Voloshinaa, N. V. Kulika, A. S. Strobykinaa

a A.E. Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center of the Russian Academy of Sciences, Kazan, Russian Federation
b Kazan Federal University, Kazan, Russian Federation
Abstract: (1,4-Dihydroxynaphthalen-2-yl)phosphonium salts were obtained by reaction of P–H phosphonium salts with substituted 1,4-naphthoquinones. Some representatives of this series possess high activity against Gram-positive bacteria (Staphylococcus aureus ATCC 209p, Bacillus cereus ATCC 8035).
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (900.1 Kb)


Citation: N. R. Khasiyatullina, A. M. Vazykhova, V. F. Mironov, D. B. Krivolapov, J. K. Voronina, A. D. Voloshina, N. V. Kulik, A. S. Strobykina, “Phosphonium salts with a dihydroxynaphthyl substituent: versatile synthesis and evaluation of antimicrobial activity”, Mendeleev Commun., 27:2 (2017), 134–136
Linking options:
  • https://www.mathnet.ru/eng/mendc1920
  • https://www.mathnet.ru/eng/mendc/v27/i2/p134
  • This publication is cited in the following 17 articles:
    1. Joachim W. Heinicke, “o‐Hydroxyarylphosphanes: Strategies for Syntheses of Configurationally Stable, Electronically and Sterically Tunable Ambiphiles with Multiple Applications”, Chemistry A European J, 30:6 (2024)  crossref
    2. A. M. Shinkareva, A. V. Nemtarev, D. V. Chachkov, A. B. Dobrynin, I. A. Litvinov, V. F. Mironov, “Quaternary phosphonium salts based on quinopimaric acid”, Mendeleev Commun., 34:1 (2024), 113–115  mathnet  crossref
    3. Elleuch Haitham, Ferid Yaccoubi, “Spectral study of phosphonium salts synthesized from Michael acceptors”, Phosphorus, Sulfur, and Silicon and the Related Elements, 198:4 (2023), 354  crossref
    4. Andrey Belyaev, Pi‐Tai Chou, Igor O. Koshevoy, “Cationic Organophosphorus Chromophores: A Diamond in the Rough among Ionic Dyes”, Chemistry A European J, 27:2 (2021), 537  crossref
    5. Seyed Reza Nokhbeh, Mostafa Gholizadeh, Alireza Salimi, Behnaz Delaram, Faezeh Makari, “Synthesis, crystal and structural characterization, Hirshfeld surface analysis and DFT calculations of three symmetrical and asymmetrical phosphonium salts”, Journal of Molecular Structure, 1242 (2021), 130718  crossref
    6. S. R. Romanov, Ya. V. Dolgova, M. V. Morozov, K. A. Ivshin, D. A. Semenov, Yu. V. Bakhtiyarova, I. V. Galkina, O. N. Kataeva, V. I. Galkin, “New phosphonium salts based on 3-(diphenylphosphino)propanoic and ω-haloalkanoic acids”, Mendeleev Commun., 31:2 (2021), 242–243  mathnet  crossref
    7. N. R. Khasiyatullina, A. T. Gubaidullin, A. M. Shinkareva, D. R. Islamov, V. F. Mironov, “New bisphosphonium salt containing a 1,4-dihydroxynaphthalene moiety: molecular and supramolecular structure”, Russ Chem Bull, 69:11 (2020), 2140  crossref
    8. N. R. Khasiyatullina, V. F. Mironov, “Convenient Synthesis of Polyfunctional Diphosphonium Salts Based on 2-Methyl-1,4-naphthoquinone”, Russ J Org Chem, 55:1 (2019), 124  crossref
    9. Nadezhda R. Khasiyatullina, Vladimir F. Mironov, Alexandra D. Voloshina, Anastasiya S. Sapunova, “Synthesis and Antimicrobial Properties of Novel Phosphonium Salts Bearing 1,4‐Dihydroxyaryl Fragment”, Chemistry & Biodiversity, 16:5 (2019)  crossref
    10. M. Selva, A. Perosa, G. Fiorani, Organophosphorus Chemistry, 2019, 145  crossref
    11. N. R. Khasiyatullina, V. F. Mironov, S. K. Gumerova, A. D. Voloshina, A. S. Sapunova, “Versatile approach to naphthoquinone phosphonium salts and evaluation of their biological activity”, Mendeleev Commun., 29:4 (2019), 435–437  mathnet  crossref
    12. Elmira M. Gibadullina, Albert R. Kayupov, Yulia K. Voronina, Victor V. Syakaev, Michael A. Pudovik, Alexander R. Burilov, “Phosphorylation of oxyethylated resorcinol and calix[4]resorcinarene with P(III) acid amides”, Phosphorus, Sulfur, and Silicon and the Related Elements, 193:11 (2018), 787  crossref
    13. D. A. Tatarinov, N. V. Terekhova, A. D. Voloshina, A. S. Sapunova, A. P. Lyubina, V. F. Mironov, “Synthesis and Antimicrobial Activity of New Dialkyl(diaryl)-2-(5-chloro-2-hydroxyphenyl)-2-(phenylethenyl)pentylphosphonium Salts”, Russ J Gen Chem, 88:9 (2018), 1800  crossref
    14. N. R. Khasiyatullina, A. V. Bogdanov, V. F. Mironov, “Reaction of 6-Bromo-1,2-naphthoquinone with Tertiary ortho-Anisylphosphines as a Convenient Synthetic Approach to 1,2-Dihydroxynaphthylphosphonium Salts”, Russ J Gen Chem, 88:10 (2018), 2233  crossref
    15. Yu. M. Sadykova, L. M. Sadikova, A. V. Zalaltdinova, A. G. Strelnik, A. R. Burilov, M. A. Pudovik, “New bicyclic phosphonates of unsymmetrical structure”, Mendeleev Commun., 28:6 (2018), 655–656  mathnet  crossref
    16. L. I. Vagapova, J. K. Voronina, V. V. Syakaev, A. R. Burilov, A. R. Garyfzyanov, M. A. Pudovik, “Synthesis and structure of new 2-aryl-substituted pyrrolidines containing phosphine oxide group”, Mendeleev Commun., 28:4 (2018), 398–400  mathnet  crossref
    17. N. R. Khasiyatullina, A. M. Vazykhova, Yu. K. Voronina, V. F. Mironov, “Reaction of 1,4-benzoquinones with PH-phosphonium salts”, Russ J Gen Chem, 87:9 (2017), 1934  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
    Mendeleev Communications
    Statistics & downloads:
    Abstract page:25
    Full-text PDF :5
     
      Contact us:
    math-net2025_03@mi-ras.ru
     Terms of Use  Registration to the website  Logotypes © Steklov Mathematical Institute RAS, 2025