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

Nadezhda R Khasiyatullina 1
Nadezhda R Khasiyatullina
, 
Albina M Vazykhova 1
Albina M Vazykhova
, 
Vladimir Fedorovich Mironov 1, 2
Vladimir Fedorovich Mironov
, 
Dmitry Borisovich Krivolapov 1
Dmitry Borisovich Krivolapov
, 
Julia Konstantinovna Voronina 1
Julia Konstantinovna Voronina
, 
Alexandra Dmitrievna Voloshina 1
Alexandra Dmitrievna Voloshina
, 
Natalia Vladimirovna Kulik 1
Natalia Vladimirovna Kulik
, 
Anastasia S Strobykina 1
Anastasia S Strobykina
10.1016/j.mencom.2017.03.008
Published 2017-02-27
Communication , Volume 27, Issue 2, 134-136
17
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Khasiyatullina N. R. et al. Phosphonium salts with a dihydroxynaphthyl substituent: versatile synthesis and evaluation of antimicrobial activity // Mendeleev Communications. 2017. Vol. 27. No. 2. pp. 134-136.
GOST all authors (up to 50) Copy
Khasiyatullina N. R., Vazykhova A. M., Mironov V. F., Krivolapov D. B., Voronina J. K., Voloshina A. D., Kulik N. V., Strobykina A. S. Phosphonium salts with a dihydroxynaphthyl substituent: versatile synthesis and evaluation of antimicrobial activity // Mendeleev Communications. 2017. Vol. 27. No. 2. pp. 134-136.
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TY - JOUR
DO - 10.1016/j.mencom.2017.03.008
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2017.03.008
TI - Phosphonium salts with a dihydroxynaphthyl substituent: versatile synthesis and evaluation of antimicrobial activity
T2 - Mendeleev Communications
AU - Khasiyatullina, Nadezhda R
AU - Vazykhova, Albina M
AU - Mironov, Vladimir Fedorovich
AU - Krivolapov, Dmitry Borisovich
AU - Voronina, Julia Konstantinovna
AU - Voloshina, Alexandra Dmitrievna
AU - Kulik, Natalia Vladimirovna
AU - Strobykina, Anastasia S
PY - 2017
DA - 2017/02/27
PB - Mendeleev Communications
SP - 134-136
IS - 2
VL - 27
ER -
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@article{2017_Khasiyatullina,
author = {Nadezhda R Khasiyatullina and Albina M Vazykhova and Vladimir Fedorovich Mironov and Dmitry Borisovich Krivolapov and Julia Konstantinovna Voronina and Alexandra Dmitrievna Voloshina and Natalia Vladimirovna Kulik and Anastasia S Strobykina},
title = {Phosphonium salts with a dihydroxynaphthyl substituent: versatile synthesis and evaluation of antimicrobial activity},
journal = {Mendeleev Communications},
year = {2017},
volume = {27},
publisher = {Mendeleev Communications},
month = {Feb},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2017.03.008},
number = {2},
pages = {134--136},
doi = {10.1016/j.mencom.2017.03.008}
}
MLA
Cite this
MLA Copy
Khasiyatullina, Nadezhda R., et al. “Phosphonium salts with a dihydroxynaphthyl substituent: versatile synthesis and evaluation of antimicrobial activity.” Mendeleev Communications, vol. 27, no. 2, Feb. 2017, pp. 134-136. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2017.03.008.

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).

References

1.
Cationic π-electron systems with high quadratic hyperpolarisability
Lambert C., Gaschler W., Nöll G., Weber M., Schmälzlin E., Bräuchle C., Meerholz K.
Journal of the Chemical Society Perkin Transactions 2, 2001
2.
10.1016/j.mencom.2017.03.008_bib0010
He
Synthesis, 2009
4.
Mitochondrial targeting of electron scavenging antioxidants: Regulation of selective oxidation vs random chain reactions☆
Kagan V.E., Wipf P., Stoyanovsky D., Greenberger J.S., Borisenko G., Belikova N.A., Yanamala N., Samhan Arias A.K., Tungekar M.A., Jiang J.
Advanced Drug Delivery Reviews, 2009
6.
Antimicrobial Polymeric Materials with Quaternary Ammonium and Phosphonium Salts
Xue Y., Xiao H., Zhang Y.
International Journal of Molecular Sciences, 2015
7.
Synthesis and antibacterial and antifungal properties of some phosphorus-containing 1,2-dihydroxynaphthalenes
Khasiyatullina N.R., Mironov V.F., Bogdanov A.V., Zobov V.V., Voloshina A.D., Kulik N.V., Konovalov A.I.
Pharmaceutical Chemistry Journal, 2009
8.
Triphenylphosphonium Cations of the Diterpenoid Isosteviol: Synthesis and Antimitotic Activity in a Sea Urchin Embryo Model
Strobykina I.Y., Belenok M.G., Semenova M.N., Semenov V.V., Babaev V.M., Rizvanov I.K., Mironov V.F., Kataev V.E.
Journal of Natural Products, 2015
9.
Preclinical Evaluation of Novel Triphenylphosphonium Salts with Broad-Spectrum Activity
Millard M., Pathania D., Shabaik Y., Taheri L., Deng J., Neamati N.
PLoS ONE, 2010
10.
Synthesis of lupane triterpenoids with triphenylphosphonium substituents and studies of their antitumor activity
Spivak A.Y., Nedopekina D.A., Shakurova E.R., Khalitova R.R., Gubaidullin R.R., Odinokov V.N., Dzhemilev U.M., Bel’skii Y.P., Bel’skaya N.V., Stankevich S.A., Korotkaya E.V., Khazanov V.A.
Russian Chemical Bulletin, 2013
13.
Catalytic methods for building up phosphorus-carbon bond
Beletskaya I.P., Kazankova M.A.
Russian Journal of Organic Chemistry, 2002
14.
Odinets I.L.
Organophosphorus Chemistry, 2010
16.
Khasiyatullina N.R., Mironov V.F., Bogdanov A.V., Krivolapov D.B., Litvinov I.A.
Mendeleev Communications, 2011
17.
Reaction of 6-bromo-1,2-naphthoquinone with diethylphosphine
Khasiyatullina N.R., Mironov V.F.
Russian Journal of Organic Chemistry, 2015
20.
Tables of bond lengths determined by X-ray and neutron diffraction. Part 1. Bond lengths in organic compounds
Allen F.H., Kennard O., Watson D.G., Brammer L., Orpen A.G., Taylor R.
Journal of the Chemical Society Perkin Transactions 2, 1987
21.
Self-assembling systems based on quaternized derivatives of 1,4-diazabicyclo[2.2.2]octane in nutrient broth as antimicrobial agents and carriers for hydrophobic drugs
Pashirova T.N., Lukashenko S.S., Zakharov S.V., Voloshina A.D., Zhiltsova E.P., Zobov V.V., Souto E.B., Zakharova L.Y.
Colloids and Surfaces B: Biointerfaces, 2015
22.
A short history of SHELX
Sheldrick G.M.
Acta Crystallographica Section A Foundations of Crystallography, 2007
23.
10.1016/j.mencom.2017.03.008_bib0070
Sheldrick
SHELXL, Version 2014/7, 2014
24.
WinGXsuite for small-molecule single-crystal crystallography
Farrugia L.J.
Journal of Applied Crystallography, 1999
25.
10.1016/j.mencom.2017.03.008_bib0080
APEX (Version 2.1), SAINTPlus (Version 7.31A), Bruker Advanced X-ray Solutions, 2006
26.
Single-crystal structure validation with the programPLATON
Spek A.L.
Journal of Applied Crystallography, 2003
27.
Mercury CSD 2.0– new features for the visualization and investigation of crystal structures
Macrae C.F., Bruno I.J., Chisholm J.A., Edgington P.R., McCabe P., Pidcock E., Rodriguez-Monge L., Taylor R., van de Streek J., Wood P.A.
Journal of Applied Crystallography, 2008
28.
10.1016/j.mencom.2017.03.008_sbref0095a
Methods for Dilution Antimicrobial Susceptibility. Tests for Bacteria that Grow Aerobically. Approved Standard M7-A5, 2000
29.
10.1016/j.mencom.2017.03.008_sbref0095b
Reference Method for Broth Dilution Antifungal Susceptibility Testing of Conidium-Forming Filamentous Fungi. Proposed Standard M38-P, 1998
30.
Antimicrobial activity of pyrimidinophanes with thiocytosine and uracil moieties
Semenov V.E., Mikhailov A.S., Voloshina A.D., Kulik N.V., Nikitashina A.D., Zobov V.V., Kharlamov S.V., Latypov S.K., Reznik V.S.
European Journal of Medicinal Chemistry, 2011