Eva Solčániová

674 total citations
42 papers, 521 citations indexed

About

Eva Solčániová is a scholar working on Organic Chemistry, Molecular Biology and Oncology. According to data from OpenAlex, Eva Solčániová has authored 42 papers receiving a total of 521 indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Organic Chemistry, 6 papers in Molecular Biology and 6 papers in Oncology. Recurrent topics in Eva Solčániová's work include Ferrocene Chemistry and Applications (19 papers), Asymmetric Synthesis and Catalysis (8 papers) and Molecular Junctions and Nanostructures (6 papers). Eva Solčániová is often cited by papers focused on Ferrocene Chemistry and Applications (19 papers), Asymmetric Synthesis and Catalysis (8 papers) and Molecular Junctions and Nanostructures (6 papers). Eva Solčániová collaborates with scholars based in Slovakia, Hungary and France. Eva Solčániová's co-authors include Štefan Tomá, Battsengel Gotov, Iveta Kmentová, Peter Kotrusz, G. R. Knox, Marta Sališová, Peter L. Pauson, Debra Willison, Tibor Liptaj and Agnesa Fiedlerová and has published in prestigious journals such as Chemical Communications, Green Chemistry and The Journal of Organic Chemistry.

In The Last Decade

Eva Solčániová

38 papers receiving 505 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eva Solčániová Slovakia 11 451 116 102 64 57 42 521
Nicholas M. Leonard United States 8 594 1.3× 82 0.7× 183 1.8× 169 2.6× 28 0.5× 11 754
David Thompson United States 11 258 0.6× 33 0.3× 108 1.1× 26 0.4× 32 0.6× 17 422
W. E. Walker Belgium 11 418 0.9× 55 0.5× 249 2.4× 73 1.1× 20 0.4× 14 561
Cedric W. McCleland South Africa 11 369 0.8× 24 0.2× 103 1.0× 51 0.8× 57 1.0× 58 500
Paul Heimbach Germany 13 549 1.2× 37 0.3× 263 2.6× 47 0.7× 24 0.4× 45 624
Masuhiko Tamura Japan 11 866 1.9× 44 0.4× 311 3.0× 55 0.9× 18 0.3× 22 953
Mark E. Vol’pin Russia 18 519 1.2× 49 0.4× 169 1.7× 54 0.8× 173 3.0× 35 683
M. SCHROEDER United Kingdom 4 384 0.9× 39 0.3× 108 1.1× 102 1.6× 26 0.5× 7 508
Brandon R. Galan United States 14 792 1.8× 44 0.4× 186 1.8× 142 2.2× 18 0.3× 15 949
G. PARRINELLO United States 6 539 1.2× 18 0.2× 316 3.1× 93 1.5× 38 0.7× 6 652

Countries citing papers authored by Eva Solčániová

Since Specialization
Citations

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

Fields of papers citing papers by Eva Solčániová

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eva Solčániová

This figure shows the co-authorship network connecting the top 25 collaborators of Eva Solčániová. A scholar is included among the top collaborators of Eva Solčániová 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 Eva Solčániová. Eva Solčániová 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.
Fischer, Róbert, et al.. (2005). 1,3-Dipolar cycloaddition of mesitonitrile oxide to chirala,ß-unsaturated enones catalyzed by Lewis acids. ARKIVOC. 2005(5). 103–115. 1 indexed citations
2.
Kotrusz, Peter, Iveta Kmentová, Battsengel Gotov, Štefan Tomá, & Eva Solčániová. (2003). Proline‐Catalyzed Asymmetric Aldol Reaction in the Room Temperature Ionic Liquid [bmim]PF6.. ChemInform. 34(11).
3.
Kotrusz, Peter, Iveta Kmentová, Battsengel Gotov, Štefan Tomá, & Eva Solčániová. (2002). Proline-catalysed asymmetric aldol reaction in the room temperature ionic liquid [bmim]PF6. Chemical Communications. 2510–2511. 118 indexed citations
5.
Szemes, Fridrich, et al.. (1991). 6-(ω-Guanidinoalkyl)- and 6-(ω-imidazolinaminoalkyl)-5,6,7,8-tetrahydrodibenz[c,e]azocines. Collection of Czechoslovak Chemical Communications. 56(12). 2986–2990. 2 indexed citations
6.
Szemes, Fridrich, et al.. (1991). 6-(6-Substituted amino-2-hydroxypropyl)-5,6,7,8-tetrahydrodibenz[c, e]azocines. Collection of Czechoslovak Chemical Communications. 56(8). 1725–1731.
7.
Knox, G. R., Peter L. Pauson, Debra Willison, Eva Solčániová, & Štefan Tomá. (1990). Ferrocene derivatives. 23. Isocyanoferrocene and isothiocyanatoferrocene. Organometallics. 9(2). 301–306. 52 indexed citations
8.
Tomá, Štefan, et al.. (1987). Diels-Alder reaction of acryloylferrocene with 1-phenyl-1,3-butadiene catalysed by homoionic forms of montmorillonite. Collection of Czechoslovak Chemical Communications. 52(2). 391–394. 4 indexed citations
9.
Sališová, Marta, Štefan Tomá, & Eva Solčániová. (1987). Friedel—Crafts alkylations of ferrocene with unsaturated lactones. Some unusual reactions caused by the β-ferrocenylcarbenium ion. Journal of Organometallic Chemistry. 327(1). 77–83. 7 indexed citations
10.
Tomá, Štefan, et al.. (1986). Reactivity of [m]ferrocenophanones: The aldol condensation. Collection of Czechoslovak Chemical Communications. 51(5). 1112–1118. 3 indexed citations
11.
Tomá, Štefan, et al.. (1985). Cyclic voltammetry, 13C NMR and Mössbauer study of [m]-ferrocenophane-1,n-diones. Journal of Organometallic Chemistry. 288(3). 331–339. 11 indexed citations
12.
Sališová, Marta, Štefan Tomá, & Eva Solčániová. (1980). 2-Benzylidene[3]ferrocenophane-1,3-diones and their spectral properties. Collection of Czechoslovak Chemical Communications. 45(4). 1290–1298. 7 indexed citations
13.
Solčániová, Eva & Štefan Tomá. (1980). Investigation of substituent effects on the 1H NMR spectra of chalcones. Organic Magnetic Resonance. 14(2). 138–140. 20 indexed citations
14.
Tomá, Štefan, et al.. (1978). Condensation reactions of some homoannular diacylferrocenes. Collection of Czechoslovak Chemical Communications. 43(1). 295–303. 2 indexed citations
15.
Tomá, Štefan, et al.. (1977). Acetylation and formylation of substituted phenylferrocenes. Collection of Czechoslovak Chemical Communications. 42(3). 1013–1026. 3 indexed citations
16.
Gronowitz, Salo, et al.. (1975). Carbon‐13 NMR Spectra of some aryl substituted ferrocenes. Organic Magnetic Resonance. 7(8). 372–375. 20 indexed citations
17.
Solčániová, Eva, et al.. (1974). Acid-catalysed intramolecular Michael addition of 1-acyl-1'-cinnamoylferrocenes. Proof of the structure of 2-substituted 3-phenyl[5]ferrocenophane-1,5-diones. Collection of Czechoslovak Chemical Communications. 39(12). 3684–3688. 3 indexed citations
18.
Solčániová, Eva, et al.. (1973). Hydrogen bonding in 3,4-disubstituted 5-hydroxyfuran-2(5H)-ones. Journal of the Chemical Society Perkin Transactions 2. 105–105.
19.
Exner, Otto, Štefan Kováč, & Eva Solčániová. (1972). Substituent effects in infrared spectroscopy. II. Characteristic frequencies of the nitro group in meta- and para-substituted nitrobenzenes. Collection of Czechoslovak Chemical Communications. 37(7). 2156–2168. 22 indexed citations
20.
Solčániová, Eva, et al.. (1971). Hydrogen bonding in phenols—V. Tetrahedron. 27(13). 2823–2830. 10 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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