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Virág Zsoldos-Mády

Researcher at Hungarian Academy of Sciences

Publications -  20
Citations -  244

Virág Zsoldos-Mády is an academic researcher from Hungarian Academy of Sciences. The author has contributed to research in topics: Furanose & Moiety. The author has an hindex of 8, co-authored 20 publications receiving 235 citations.

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Synthesis, structure, and in vitro antitumor activity of some glycoside derivatives of ferrocenyl-chalcones and ferrocenyl-pyrazolines.

TL;DR: Some new glycosides of 3‐ferrocenyl‐1‐(4′‐hydroxyphenyl)‐prop‐2‐en‐ 1‐one were prepared and transformed into the corresponding pyrazoline and pyrazole derivatives, and some chalcone derivatives showed attractive in vitro antitumor effects on human leukemia cells.
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New ferrocene containing peptide conjugates: synthesis and effect on human leukemia (HL-60) cells.

TL;DR: It is demonstrated that ferrocenylacrylic acid possessing an enone (--CH==CH--CO--) moiety exhibited remarkable antiproliferative effect against human leukemia cells (HL-60) in vitro, but its effect was not improved by conjugation with hexa- or octaarginines, while highly increased water-solubility was observed.
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Ferrocenyl pyrazolines: Preparation, structure, redox properties and DFT study on regioselective ring-closure

TL;DR: In this paper, cyclocondensation of 1-phenyl-3-ferrocenyl-2-propen-1-one (1) with RNHNH2 hydrazines and the substituent-dependent product distribution were investigated.
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(E)-3-(2-Alkyl-10H-phenothiazin-3-yl)-1-arylprop-2-en-1-ones: Preparative, IR, NMR and DFT study on their substituent-dependent reactivity in hydrazinolysis and sonication-assisted oxidation with copper(II)nitrate.

TL;DR: A series of novel 3(5)-aryl/ferrocenyl-5(3)-phenothiazinylpyrazoles and pyrazolines were obtained by substituent-dependent regioselective condensation of the corresponding (E)-3-(2-alkyl-10H- phenothiazin-3-yl)-1-aryl/ ferrocene-2-en-1-one with hydrazine or methylhydrazine in acetic acid
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Synthesis, IR-, NMR- and X-ray investigations on some novel N-hetaryl-dihydro-pyrazolyl ferrocenes. Study on ferrocenes, part 16 ☆

TL;DR: The structure of the new compounds was established by IR, 1H and 13C NMR spectroscopy, including DNOE, HMQC, HMBC and DEPT methods.