R
Rastko D. Vukićević
Researcher at University of Kragujevac
Publications - 81
Citations - 979
Rastko D. Vukićević is an academic researcher from University of Kragujevac. The author has contributed to research in topics: Acylation & Catalysis. The author has an hindex of 15, co-authored 81 publications receiving 901 citations.
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Journal ArticleDOI
Synthesis and antimicrobial activity of some new pyrazole derivatives containing a ferrocene unit.
Ivan Damljanović,Mirjana Vukićević,Niko S. Radulović,Radosav Palić,Ernst P. Ellmerer,Zoran Ratković,Milan D. Joksović,Rastko D. Vukićević +7 more
TL;DR: A series of new imines and amines have been synthesized by condensation of 1H-3-ferrocenyl-1-phenylpyrazole-4-carboxaldehyde with the corresponding amines, followed by reduction with sodium borohydride, showing a wide range of activities.
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Synthesis, characterization, electrochemical studies and antitumor activity of some new chalcone analogues containing ferrocenyl pyrazole moiety
Zoran Ratković,Zorica Juranić,Tatjana Stanojković,Dragan Manojlović,Rastko D. Vukićević,Niko S. Radulović,Milan D. Joksović +6 more
TL;DR: A series of new alpha,beta-unsaturated conjugated ketones containing ferrocenyl pyrazole unit were synthesized and fully characterized by IR and NMR spectroscopy and exhibited a better cytotoxic activity in the cell growth inhibition of K562 cell lines in comparison with cisplatin as a reference compound.
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Synthesis, characterization and antitumor activity of novel N-substituted α-amino acids containing ferrocenyl pyrazole-moiety
Milan D. Joksović,Violeta Marković,Zorica Juranić,Tatjana Stanojković,Ljiljana S. Jovanović,Ivan Damljanović,Katalin Mészáros Szécsényi,Nina Todorović,Snežana Trifunović,Rastko D. Vukićević +9 more
TL;DR: Tryptophan derivative 1l exhibited the highest cytotoxic activity in the cell growth inhibition of all three types of cell lines and in the in vitro antitumor activity of all synthesized compounds.
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A Simple Synthesis of Oximes
TL;DR: In this paper, the conversion of alicyclic and aliphatic carbonyl compounds as well as aromatic aldehydes into the corresponding oximes (up to quantitative yields) was achieved by simply grinding these reactants, hydroxylamine hydrochloride and sodium hydroxide without solvent.
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Synthesis and Antimicrobial Activity of New 4-Heteroarylamino Coumarin Derivatives Containing Nitrogen and Sulfur as Heteroatoms
TL;DR: Eight new coumarin derivatives were synthesized in moderate to good yields by condensation of 4-chloro-3-nitrocoumarin and the corresponding heteroarylamine and have shown a wide range of activity - from one completely inactive compound to medium active ones.