Vesna Čaplar

562 total citations
27 papers, 426 citations indexed

About

Vesna Čaplar is a scholar working on Organic Chemistry, Molecular Biology and Biomaterials. According to data from OpenAlex, Vesna Čaplar has authored 27 papers receiving a total of 426 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Organic Chemistry, 13 papers in Molecular Biology and 7 papers in Biomaterials. Recurrent topics in Vesna Čaplar's work include Supramolecular Self-Assembly in Materials (7 papers), Lipid Membrane Structure and Behavior (6 papers) and HIV/AIDS drug development and treatment (5 papers). Vesna Čaplar is often cited by papers focused on Supramolecular Self-Assembly in Materials (7 papers), Lipid Membrane Structure and Behavior (6 papers) and HIV/AIDS drug development and treatment (5 papers). Vesna Čaplar collaborates with scholars based in Croatia, Germany and France. Vesna Čaplar's co-authors include Mladen Žinić, Vitomir Šunjić, Fritz Vögtle, Jean‐Luc Pozzo, Fréderic Fagès, Leo Frkanec, Marc Schmutz, François Diederich, Ivo Piantanida and Anthony D’Aléo and has published in prestigious journals such as Chemical Communications, The Journal of Organic Chemistry and Chemistry - A European Journal.

In The Last Decade

Vesna Čaplar

27 papers receiving 411 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Vesna Čaplar Croatia 12 282 170 168 97 84 27 426
Markus P. Isler United States 4 296 1.0× 238 1.4× 200 1.2× 62 0.6× 81 1.0× 4 455
Erwin Snip Netherlands 9 331 1.2× 269 1.6× 404 2.4× 202 2.1× 56 0.7× 9 616
Tatsuo Oshikawa Japan 14 466 1.7× 255 1.5× 77 0.5× 64 0.7× 122 1.5× 66 633
Ana López‐Pérez Spain 14 595 2.1× 153 0.9× 129 0.8× 98 1.0× 83 1.0× 16 724
Jolly Deb India 11 184 0.7× 119 0.7× 166 1.0× 72 0.7× 64 0.8× 12 385
Claire Troufflard France 12 267 0.9× 71 0.4× 105 0.6× 77 0.8× 74 0.9× 27 374
赵新 2 305 1.1× 286 1.7× 140 0.8× 68 0.7× 31 0.4× 4 419
V. Noponen Finland 8 174 0.6× 120 0.7× 278 1.7× 142 1.5× 45 0.5× 9 367
Yeonhwan Jeong Japan 6 218 0.8× 111 0.7× 300 1.8× 136 1.4× 22 0.3× 12 360
Cristina Geiger United States 10 366 1.3× 165 1.0× 330 2.0× 250 2.6× 49 0.6× 15 594

Countries citing papers authored by Vesna Čaplar

Since Specialization
Citations

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

Fields of papers citing papers by Vesna Čaplar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vesna Čaplar

This figure shows the co-authorship network connecting the top 25 collaborators of Vesna Čaplar. A scholar is included among the top collaborators of Vesna Čaplar 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 Vesna Čaplar. Vesna Čaplar 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.
Molčanov, Krešimir, Vesna Čaplar, Milan Jokić, et al.. (2012). Hydrogen bonding topology influences gelating properties of malonamides. Structural Chemistry. 24(2). 597–609. 5 indexed citations
2.
Baretić, Domagoj, et al.. (2010). Novel bis-phenanthridine derivatives with easily tunable linkers, study of their interactions with DNA and screening of antiproliferative activity. European Journal of Medicinal Chemistry. 45(6). 2671–2676. 22 indexed citations
3.
Čaplar, Vesna, et al.. (2010). Positionally Isomeric Organic Gelators: Structure–Gelation Study, Racemic versus Enantiomeric Gelators, and Solvation Effects. Chemistry - A European Journal. 16(10). 3066–3082. 40 indexed citations
4.
Makarević, Janja, et al.. (2010). Oxalyl retro-peptide gelators. Synthesis, gelation properties and stereochemical effects. Beilstein Journal of Organic Chemistry. 6. 945–959. 14 indexed citations
5.
Jokić, Milan, et al.. (2008). Stereoisomeric bis(phenylglycinol)malonamide gelators: rare examples of gelling meso-compounds. Tetrahedron Letters. 50(5). 509–513. 14 indexed citations
6.
Makarević, Janja, Milan Jokić, Vesna Čaplar, et al.. (2004). Chiral bis(tyrosinol) and bis(p-hydroxyphenylglycinol) oxalamide gelators. influence of aromatic groups and hydrogen bonding on gelation properties. Croatica Chemica Acta. 77. 403–414. 9 indexed citations
7.
D’Aléo, Anthony, Jean‐Luc Pozzo, Fréderic Fagès, et al.. (2004). 11-Aminoundecanoic acid: a versatile unit for the generation of low molecular weight gelators for water and organic solvents. Chemical Communications. 190–191. 58 indexed citations
8.
9.
Čaplar, Vesna, et al.. (2003). Syntheses of Amino Alcohols and Chiral C 2 -Symmetric Bisoxazolines Derived from O -Alkylated R -4-Hydroxyphenylglycine and S -Tyrosine. Croatica Chemica Acta. 76(1). 23–36. 12 indexed citations
10.
Roje, Marin, et al.. (2000). Remarkable cumulative stereoselectivity in cyclopropanation with supramolecular Cu(i) catalytic complexes. Chemical Communications. 1993–1994. 11 indexed citations
11.
Vrček, Valerije, et al.. (1998). First Hydroxamic Seconucleoside Derivatives. Institutional Repository of the Ruđer Bošković Institute (Ruđer Bošković Institute). 1 indexed citations
12.
Čaplar, Vesna, et al.. (1996). A Novel Type of Rigid Macrocycle with Bis(3-uracilyl)methane and Hexadiyne Units. The Uracilophane. Croatica Chemica Acta. 69(4). 1617–1631. 2 indexed citations
13.
Čaplar, Vesna & Mladen Žinić. (1995). Bis-adeninyl and bis-uracilyl hexadiyne derivatives of nucleobases. Tetrahedron Letters. 36(25). 4455–4458. 7 indexed citations
14.
Vrček, Valerije & Vesna Čaplar. (1994). A novel type of unsaturated seconucleoside analogues. Tetrahedron Letters. 35(23). 3987–3990. 1 indexed citations
15.
SKARIC, V., et al.. (1991). From nucleosides, their acyclo- and anhydro-analogues to chiral complementary lariat ethers. Tetrahedron Letters. 32(15). 1821–1824. 2 indexed citations
16.
Staab, Heinz A., François Diederich, & Vesna Čaplar. (1983). Cycloarenes, a New Class of Aromatic Compounds, III. Studies towards the Synthesis of Cyclo[d.e.d.e.e.d.e.d.e.e]decakisbenzene. Liebigs Annalen der Chemie. 1983(12). 2262–2273. 21 indexed citations
17.
Čaplar, Vesna, et al.. (1981). Homogeneous Asymmetric Hydrogenation. Synthesis. 1981(2). 85–116. 75 indexed citations
18.
19.
Čaplar, Vesna, A. Lisini, F. KAJFEŽ, D. Kolbah, & Vitomir Šunjić. (1978). Synthesis of the 2,3-dihydro-6H-1,4-oxazin-2-ones chiral at C(3) and asymmetric induction in hydrogenation of the azomethine bond. The Journal of Organic Chemistry. 43(7). 1355–1360. 25 indexed citations
20.
Čaplar, Vesna, et al.. (1974). N1‐Substitution in 2‐methyl‐4(5)nitroimidazole. III. New syntheses of 1‐(2′‐(ethylsulfonyl)ethyl)‐2‐methyl‐5‐nitroimidazole. Journal of Heterocyclic Chemistry. 11(6). 1055–1060. 6 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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