Tibor Liptaj

2.8k total citations
137 papers, 2.3k citations indexed

About

Tibor Liptaj is a scholar working on Organic Chemistry, Molecular Biology and Spectroscopy. According to data from OpenAlex, Tibor Liptaj has authored 137 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Organic Chemistry, 36 papers in Molecular Biology and 21 papers in Spectroscopy. Recurrent topics in Tibor Liptaj's work include Molecular spectroscopy and chirality (11 papers), Synthesis and biological activity (8 papers) and Catalysis for Biomass Conversion (7 papers). Tibor Liptaj is often cited by papers focused on Molecular spectroscopy and chirality (11 papers), Synthesis and biological activity (8 papers) and Catalysis for Biomass Conversion (7 papers). Tibor Liptaj collaborates with scholars based in Slovakia, Czechia and France. Tibor Liptaj's co-authors include Milan Hronec, Katarína Fulajtárová, Dušan Uhrı́n, Naďa Prónayová, Ernest Šturdı́k, Vladı́mir Mlynárik, Ľubica Pospíšilová, M. Šturdíková, Tomáš Soták and Jana Viskupičová and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Applied and Environmental Microbiology.

In The Last Decade

Tibor Liptaj

133 papers receiving 2.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tibor Liptaj Slovakia 25 615 570 449 295 210 137 2.3k
Zhen Yang China 34 1.7k 2.8× 463 0.8× 882 2.0× 186 0.6× 373 1.8× 99 4.1k
Hideki Kanda Japan 32 429 0.7× 400 0.7× 1.2k 2.6× 185 0.6× 182 0.9× 188 3.2k
Valdemar Lacerda Brazil 26 304 0.5× 480 0.8× 363 0.8× 121 0.4× 198 0.9× 145 2.2k
Shizhong Chen China 33 971 1.6× 200 0.4× 150 0.3× 150 0.5× 322 1.5× 183 4.0k
Lin Zhu China 27 253 0.4× 269 0.5× 351 0.8× 172 0.6× 122 0.6× 94 1.8k
Kaixun Huang China 38 1.0k 1.6× 464 0.8× 359 0.8× 184 0.6× 380 1.8× 154 4.5k
John H. P. Tyman United Kingdom 23 476 0.8× 887 1.6× 417 0.9× 122 0.4× 228 1.1× 95 2.5k
Jike Lu China 26 1.3k 2.1× 152 0.3× 740 1.6× 195 0.7× 419 2.0× 96 2.7k
Marina Scarpa Italy 25 686 1.1× 307 0.5× 373 0.8× 62 0.2× 272 1.3× 107 2.4k
John L. Gainer United States 28 912 1.5× 191 0.3× 452 1.0× 176 0.6× 80 0.4× 101 2.3k

Countries citing papers authored by Tibor Liptaj

Since Specialization
Citations

This map shows the geographic impact of Tibor Liptaj'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 Tibor Liptaj with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tibor Liptaj more than expected).

Fields of papers citing papers by Tibor Liptaj

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tibor Liptaj. 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 Tibor Liptaj. The network helps show where Tibor Liptaj may publish in the future.

Co-authorship network of co-authors of Tibor Liptaj

This figure shows the co-authorship network connecting the top 25 collaborators of Tibor Liptaj. A scholar is included among the top collaborators of Tibor Liptaj 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 Tibor Liptaj. Tibor Liptaj 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.
Hudec, Jozef, Ján Mojžíš, Marta Habánová, et al.. (2021). In Vitro Cytotoxic Effects of Secondary Metabolites Present in Sarcopoterium Spinosum L.. Applied Sciences. 11(11). 5300–5300. 3 indexed citations
2.
Renda, Gülin, et al.. (2017). Bioassay Guided Isolation of Active Compounds from Alchemilla barbatiflora Juz.. Records of Natural Products. 12(1). 76–85. 18 indexed citations
3.
4.
Kollár, Jozef, Miroslav Mrlík, Zuzana Kroneková, et al.. (2016). Tulips: A Renewable Source of Monomer for Superabsorbent Hydrogels. Macromolecules. 49(11). 4047–4056. 48 indexed citations
5.
Kos, Jiří, Iveta Zadražilová, Michal Šoral, et al.. (2015). Ring-substituted 8-hydroxyquinoline-2-carboxanilides as potential antimycobacterial agents. Bioorganic & Medicinal Chemistry. 23(15). 4188–4196. 31 indexed citations
6.
Karakaş, Fatma Pehlivan, Didem Şöhretoğlu, Tibor Liptaj, et al.. (2014). Isolation of an oleanane-type saponin active fromBellis perennisthrough antitumor bioassay-guided procedures. Pharmaceutical Biology. 52(8). 951–955. 11 indexed citations
7.
Fodran, Peter, Vladimı́r Lukeš, Adam Vagánek, et al.. (2014). Physicochemical and biological properties of luteolin-7-O-β-d-glucoside (cynaroside) isolated from Anthriscus sylvestris (L.) Hoffm.. Monatshefte für Chemie - Chemical Monthly. 145(8). 1307–1318. 28 indexed citations
8.
Jampílek, Josef, Jiří Kos, Matúš Peško, et al.. (2013). Preparation and Herbicidal Activity of Halogenated 8-Hydroxyquinoline-2-carboxanilides. ASEP. b013–b013.
9.
Janega, Pavol, et al.. (2012). Middle-aged rat hippocampus and some early changes accompanying aging. Open Life Sciences. 7(5). 810–816. 3 indexed citations
10.
Mučaji, Pavel, Milan Nagy, Tibor Liptaj, Nadežda Prónayová, & Emil Švajdlenka. (2009). Separation of a mixture of luteolin-7-rutinoside and luteolin-7-neohesperidoside isolated fromLigustrum vulgareL.. Journal of Planar Chromatography – Modern TLC. 22(4). 301–304. 3 indexed citations
11.
Brezová, Vlasta, Marián Valko, J Horecký, et al.. (2005). Study of the oxidative stress in a rat model of chronic brain hypoperfusion. Neurochemistry International. 46(8). 601–611. 89 indexed citations
12.
Sulová, Zdena, B Uhrík, Tibor Liptaj, et al.. (2003). P-glycoprotein-mediated multidrug resistance phenotype of L1210/VCR cells is associated with decreases of oligo- and/or polysaccharide contents. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1639(3). 213–224. 23 indexed citations
13.
14.
Solladié‐Cavallo, Arlette, Tibor Liptaj, Michel Schmitt, & Audrey Solgadi. (2002). iso-Propyl phenylacetate: formation of a single enolate with tBuP4 as base. Tetrahedron Letters. 43(3). 415–418. 14 indexed citations
15.
16.
Liptaj, Tibor, et al.. (2001). Identification of the configuration of neosartorin by long‐range nuclear Overhauser effect measurements. Chirality. 13(9). 545–547. 4 indexed citations
17.
Šturdíková, M., et al.. (2001). OR-1—a mixture of esters of glyceric acid produced byPenicillium funiculosum and its antitrypsin activity. Folia Microbiologica. 46(1). 21–23. 17 indexed citations
18.
Uhrı́n, Dušan & Tibor Liptaj. (1989). Determination and assignment of heteronuclear long-range coupling constants. Methods based on semiselective INEPT. Journal of Magnetic Resonance (1969). 81(1). 82–91. 14 indexed citations
19.
Lyčka, Antonı́n, Tibor Liptaj, & Josef Jirman. (1987). 13C and 15N NMR spectra of 3-methyl-1-phenylpyrazole-4,5-dione 4-(4'-substituted phenyl)hydrazones. Collection of Czechoslovak Chemical Communications. 52(3). 727–735. 8 indexed citations
20.
Kellö, Vladimı́r, et al.. (1974). 1H NMR spectra and electronic structure of 3‐arylmethyl‐idenephthalide and 3‐arylthiomethylidenephthalide derivatives. Organic Magnetic Resonance. 6(7). 400–403. 1 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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