Zoia Voïtenko

1.0k total citations
112 papers, 829 citations indexed

About

Zoia Voïtenko is a scholar working on Organic Chemistry, Molecular Biology and Materials Chemistry. According to data from OpenAlex, Zoia Voïtenko has authored 112 papers receiving a total of 829 indexed citations (citations by other indexed papers that have themselves been cited), including 97 papers in Organic Chemistry, 24 papers in Molecular Biology and 17 papers in Materials Chemistry. Recurrent topics in Zoia Voïtenko's work include Synthesis and pharmacology of benzodiazepine derivatives (31 papers), Synthesis and Reactivity of Heterocycles (19 papers) and Supramolecular Chemistry and Complexes (19 papers). Zoia Voïtenko is often cited by papers focused on Synthesis and pharmacology of benzodiazepine derivatives (31 papers), Synthesis and Reactivity of Heterocycles (19 papers) and Supramolecular Chemistry and Complexes (19 papers). Zoia Voïtenko collaborates with scholars based in Ukraine, France and Italy. Zoia Voïtenko's co-authors include В. А. Ковтуненко, Sonia Mallet‐Ladeira, Marian V. Gorichko, Oleksandr O. Grygorenko, Marc Sallé, Sébastien Goeb, Rémi Chauvin, Vincent Carré, Magali Allain and Michel Baltas and has published in prestigious journals such as Angewandte Chemie International Edition, Macromolecules and Chemical Communications.

In The Last Decade

Zoia Voïtenko

106 papers receiving 806 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Zoia Voïtenko Ukraine 16 632 180 158 88 85 112 829
Barbara Wicher Poland 18 463 0.7× 223 1.2× 364 2.3× 95 1.1× 64 0.8× 68 858
Luiz Antônio S. Costa Brazil 17 321 0.5× 157 0.9× 178 1.1× 33 0.4× 125 1.5× 52 694
Satyajit Saha India 21 1.3k 2.0× 231 1.3× 162 1.0× 80 0.9× 53 0.6× 50 1.6k
Ana M. Cuadro Spain 19 675 1.1× 174 1.0× 194 1.2× 63 0.7× 112 1.3× 51 901
Toshio Itahara Japan 19 870 1.4× 137 0.8× 184 1.2× 96 1.1× 116 1.4× 89 1.1k
Damian Trzybiński Poland 17 549 0.9× 229 1.3× 255 1.6× 99 1.1× 74 0.9× 115 964
Alain Marsura France 18 429 0.7× 168 0.9× 350 2.2× 195 2.2× 77 0.9× 77 885
Marek L. Główka Poland 14 578 0.9× 198 1.1× 311 2.0× 83 0.9× 62 0.7× 125 946
Carmela Bonaccorso Italy 20 387 0.6× 276 1.5× 162 1.0× 159 1.8× 80 0.9× 56 807
G. N. Lipunova Russia 17 831 1.3× 321 1.8× 269 1.7× 59 0.7× 56 0.7× 125 1.1k

Countries citing papers authored by Zoia Voïtenko

Since Specialization
Citations

This map shows the geographic impact of Zoia Voïtenko's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Zoia Voïtenko with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Zoia Voïtenko more than expected).

Fields of papers citing papers by Zoia Voïtenko

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Zoia Voïtenko. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Zoia Voïtenko. The network helps show where Zoia Voïtenko may publish in the future.

Co-authorship network of co-authors of Zoia Voïtenko

This figure shows the co-authorship network connecting the top 25 collaborators of Zoia Voïtenko. A scholar is included among the top collaborators of Zoia Voïtenko based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Zoia Voïtenko. Zoia Voïtenko is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Karpus, Andrii, et al.. (2024). Synthesis and organocatalytical evaluation of optically pure inherently chiral calix[4]arene phosphoric acids. Journal of Inclusion Phenomena and Macrocyclic Chemistry. 105(1-2). 75–86.
2.
Voïtenko, Zoia, et al.. (2020). Aliphatic α‐Boryl‐α‐bromoketones: Synthesis and Reactivity. European Journal of Organic Chemistry. 2020(23). 3367–3377. 9 indexed citations
3.
Dyakonenko, Viktoriya V., et al.. (2019). Azido-tetrazole isomerism in 2,2-dimethyl-1-(1-methyl-1H-tetrazolo[5,1-a]isoindol-5-yl)propan-1-one. Journal of Molecular Structure. 1203. 127469–127469. 9 indexed citations
4.
Allain, Magali, Vincent Carré, Frédéric Aubriet, et al.. (2018). A M2L2 Redox-Active Metalla-Macrocycle Based on Electron-Rich 9-(1,3-Dithiol-2-ylidene)Fluorene. Inorganics. 6(2). 44–44. 10 indexed citations
5.
Maraval, Valérie, et al.. (2014). First Evidence of 1,3-Bis-indolylallenes: Generation by a Sequential Double Nucleophilic Process from Ynones. Synthetic Communications. 45(2). 253–261. 2 indexed citations
6.
Шишкин, Олег В., et al.. (2014). Structure of adducts of isoindolo[2,1-a]benzimidazole derivatives with maleimides. Journal of Molecular Structure. 1084. 177–181. 1 indexed citations
7.
Vybornyi, Oleh, et al.. (2013). Michael addition of heteronucleophilic substances to N – Ar substituted maleimides: green approach. 1 indexed citations
8.
Gorichko, Marian V., Christian Lherbet, Frédéric Rodriguez, et al.. (2013). Synthesis of Potential Inhibitors of InhA with Pyrrolidine-2,5-dione Core Fragment and Evaluation of their Biological Activity. 1(1). 15–22. 1 indexed citations
9.
Voïtenko, Zoia, et al.. (2013). Hydantoins Derived from Ketopinic and 4-camphorcarboxylic Acids. 1(1). 23–26. 1 indexed citations
10.
Mori, Giorgia, Christian Lherbet, Frédéric Rodriguez, et al.. (2013). Synthesis of 3-heteryl substituted pyrrolidine-2,5-diones via catalytic Michael reaction and evaluation of their inhibitory activity against InhA and Mycobacterium tuberculosis. European Journal of Medicinal Chemistry. 71. 46–52. 41 indexed citations
11.
Rodriguez, Frédéric, N. Saffon, Sonia Mallet‐Ladeira, et al.. (2013). Design, chemical synthesis of 3-(9H-fluoren-9-yl)pyrrolidine-2,5-dione derivatives and biological activity against enoyl-ACP reductase (InhA) and Mycobacterium tuberculosis. European Journal of Medicinal Chemistry. 70. 37–48. 38 indexed citations
12.
Maraval, Valérie, et al.. (2013). Enhanced π-frustration in carbo-benzenic chromophores. Chemical Communications. 49(75). 8374–8374. 20 indexed citations
13.
Cassel, Stéphanie, et al.. (2013). Synthesis, Autoorganization and Reactivity of Amphiphilic Derivatives of 1‐Aminoisoindole in Water and Formamide. Journal of Surfactants and Detergents. 17(1). 101–109. 1 indexed citations
14.
Voïtenko, Zoia, et al.. (2013). MethylN-(3-cyanopicolinoyl)-L-tryptophanate. Acta Crystallographica Section E Structure Reports Online. 69(12). o1810–o1810. 2 indexed citations
15.
Rives, Arnaud, et al.. (2012). Highly π electron-rich macro-aromatics: bis(p-aminophenyl)-carbo-benzenes and their DBA acyclic references. Chemical Communications. 48(70). 8763–8763. 26 indexed citations
16.
Voïtenko, Zoia, Stéphanie Cassel, Олег В. Шишкин, et al.. (2012). Reaction of 1-Ethoxyisoindole with Maleimide and Its Derivatives. Heterocycles. 85(7). 1671–1671. 5 indexed citations
17.
Rodik, R. V., et al.. (2012). Synthesis, fluorescent properties and aggregation of 2,3-dihydroisoindolenylcalix[4]arenes. Journal of Inclusion Phenomena and Macrocyclic Chemistry. 77(1-4). 343–350. 3 indexed citations
18.
Voïtenko, Zoia, et al.. (2006). Benzo[f]isoindole derivatives from cycloaddition reaction of 2,4-dimethylpyrimido[2,1-a]isoindole and maleimides. Comptes Rendus Chimie. 9(11-12). 1482–1487. 7 indexed citations
19.
Voïtenko, Zoia, et al.. (2002). Cycloaddition in Condensed Isoindoles. 2. Method for Obtaining New Derivatives of 2-Phenylpyridine. Chemistry of Heterocyclic Compounds. 38(2). 190–196. 6 indexed citations
20.
Voïtenko, Zoia, et al.. (1999). Cycloaddition in condensed isoindoles 1. Preparation of 2-aryl-3-methyl-4-oxo-3,4-dihydroquinazoline. Chemistry of Heterocyclic Compounds. 35(5). 600–607. 8 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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