Goran Benedeković

432 total citations
36 papers, 360 citations indexed

About

Goran Benedeković is a scholar working on Biochemistry, Organic Chemistry and Molecular Biology. According to data from OpenAlex, Goran Benedeković has authored 36 papers receiving a total of 360 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Biochemistry, 20 papers in Organic Chemistry and 18 papers in Molecular Biology. Recurrent topics in Goran Benedeković's work include Traditional and Medicinal Uses of Annonaceae (27 papers), Carbohydrate Chemistry and Synthesis (16 papers) and Cocoa and Sweet Potato Agronomy (11 papers). Goran Benedeković is often cited by papers focused on Traditional and Medicinal Uses of Annonaceae (27 papers), Carbohydrate Chemistry and Synthesis (16 papers) and Cocoa and Sweet Potato Agronomy (11 papers). Goran Benedeković collaborates with scholars based in Serbia and Switzerland. Goran Benedeković's co-authors include Velimir Popsavin, Mirjana Popsavin, Vesna Kojić, Gordana Bogdanović, Vladimir Divjaković, Tatjana Srdić‐Rajić, Marko V. Rodić, Dimitar Jakimov, Thomas Armbruster and Lidija R. Jevrić and has published in prestigious journals such as Tetrahedron, Organic Letters and Tetrahedron Letters.

In The Last Decade

Goran Benedeković

32 papers receiving 357 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Goran Benedeković Serbia 13 227 212 147 81 39 36 360
Ahmad Yazbak Israel 9 185 0.8× 244 1.2× 171 1.2× 113 1.4× 41 1.1× 9 362
Shivajirao L. Gholap India 14 325 1.4× 122 0.6× 144 1.0× 31 0.4× 68 1.7× 26 479
Jean‐Christophe Jullian France 12 138 0.6× 63 0.3× 180 1.2× 11 0.1× 34 0.9× 25 409
Bambang W. Nugroho Germany 14 146 0.6× 91 0.4× 486 3.3× 38 0.5× 13 0.3× 15 590
Santosh C. Sinha United States 9 215 0.9× 291 1.4× 140 1.0× 122 1.5× 49 1.3× 10 362
Reen-Yen Kuo Taiwan 10 78 0.3× 102 0.5× 228 1.6× 25 0.3× 10 0.3× 12 366
George R. Kriek United States 7 131 0.6× 57 0.3× 203 1.4× 31 0.4× 27 0.7× 12 343
Wei‐Shan Zhou China 17 493 2.2× 71 0.3× 282 1.9× 11 0.1× 103 2.6× 34 695
Ming-Jung Wu Taiwan 10 87 0.4× 232 1.1× 162 1.1× 123 1.5× 11 0.3× 13 331
Jin‐Biao Xu China 15 179 0.8× 97 0.5× 443 3.0× 6 0.1× 32 0.8× 25 614

Countries citing papers authored by Goran Benedeković

Since Specialization
Citations

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

Fields of papers citing papers by Goran Benedeković

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Goran Benedeković

This figure shows the co-authorship network connecting the top 25 collaborators of Goran Benedeković. A scholar is included among the top collaborators of Goran Benedeković 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 Goran Benedeković. Goran Benedeković 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.
Benedeković, Goran, et al.. (2024). First total synthesis of asperilactone B. Revision of absolute stereochemistry of asperilactones B and C. Organic & Biomolecular Chemistry. 22(24). 4864–4867.
2.
Farkas, Sándor, et al.. (2023). Synthesis and antiproliferative activity of (5R)-cleistenolide and analogues. Journal of the Serbian Chemical Society. 88(7-8). 705–713.
3.
Popsavin, Mirjana, et al.. (2022). The first total synthesis and revision of absolute stereochemistry of natural cytotoxic lactone cleistanolate. Bioorganic Chemistry. 128. 106073–106073.
4.
Benedeković, Goran, Mirjana Popsavin, Niko S. Radulović, et al.. (2020). Synthesis and antimicrobial activity of (−)-cleistenolide and analogues. Bioorganic Chemistry. 106. 104491–104491. 5 indexed citations
5.
Benedeković, Goran, et al.. (2020). Synthesis, antiproliferative activity and SAR analysis of (−)-cleistenolide and analogues. European Journal of Medicinal Chemistry. 202. 112597–112597. 6 indexed citations
6.
Vukić, Vladimir, et al.. (2019). In vitro antitumor activity, ADME-Tox and 3D-QSAR of synthesized and selected natural styryl lactones. Computational Biology and Chemistry. 83. 107112–107112. 7 indexed citations
7.
Popsavin, Mirjana, Goran Benedeković, Vesna Kojić, et al.. (2017). Synthesis and in vitro antitumour activity of crassalactone D, its stereoisomers and novel cinnamic ester derivatives. European Journal of Medicinal Chemistry. 134. 293–303. 8 indexed citations
8.
Benedeković, Goran, et al.. (2017). A comparative study of chromatographic behavior and lipophilicity of selected natural styryl lactones, their derivatives and analogues. European Journal of Pharmaceutical Sciences. 105. 99–107. 9 indexed citations
9.
Popsavin, Mirjana, Goran Benedeković, Vesna Kojić, et al.. (2017). Design, synthesis and in vitro antitumour activity of new goniofufurone and 7- epi -goniofufurone mimics with halogen or azido groups at the C-7 position. European Journal of Medicinal Chemistry. 128. 13–24. 17 indexed citations
10.
Benedeković, Goran, et al.. (2016). New antitumour agents with α,β-unsaturated δ-lactone scaffold: Synthesis and antiproliferative activity of (−)-cleistenolide and analogues. Bioorganic & Medicinal Chemistry Letters. 26(14). 3318–3321. 17 indexed citations
11.
Popsavin, Mirjana, Goran Benedeković, Vesna Kojić, et al.. (2015). Synthesis and antiproliferative activity of goniobutenolides A and B, 5-halogenated crassalactone D derivatives and the corresponding 7-epimers. European Journal of Medicinal Chemistry. 108. 594–604. 4 indexed citations
12.
Benedeković, Goran, et al.. (2015). Divergent total synthesis of crassalactones B and C and evaluation of their antiproliferative activity. Tetrahedron. 71(28). 4581–4589. 11 indexed citations
13.
Benedeković, Goran, Mirjana Popsavin, Vesna Kojić, et al.. (2014). Design, synthesis and SAR analysis of antitumour styryl lactones related to (+)-crassalactones B and C. European Journal of Medicinal Chemistry. 87. 237–247. 17 indexed citations
14.
Benedeković, Goran, Mirjana Popsavin, Vesna Kojić, et al.. (2014). Conformationally constrained goniofufurone mimics as inhibitors of tumour cells growth: Design, synthesis and SAR study. European Journal of Medicinal Chemistry. 82. 449–458. 20 indexed citations
15.
Popsavin, Velimir, et al.. (2013). Heteroannelated and 7-deoxygenated goniofufurone mimics with antitumour activity: Design, synthesis and preliminary SAR studies. Bioorganic & Medicinal Chemistry Letters. 23(20). 5507–5510. 8 indexed citations
16.
Popsavin, Velimir, et al.. (2010). Design, synthesis and antiproliferative activity of styryl lactones related to (+)-goniofufurone. European Journal of Medicinal Chemistry. 45(7). 2876–2883. 29 indexed citations
17.
Popsavin, Velimir, Goran Benedeković, Mirjana Popsavin, Vesna Kojić, & Gordana Bogdanović. (2010). Divergent synthesis of cytotoxic styryl lactones isolated from Polyalthia crassa. The first total synthesis of crassalactone B. Tetrahedron Letters. 51(26). 3426–3429. 15 indexed citations
18.
Popsavin, Velimir, et al.. (2008). Synthesis and antiproliferative activity of unnatural enantiomers of 7-epi-goniofufurone and crassalactone C. Bioorganic & Medicinal Chemistry Letters. 18(19). 5178–5181. 12 indexed citations
19.
Popsavin, Velimir, et al.. (2008). Design, synthesis and antiproliferative activity of two new heteroannelated (−)-muricatacin mimics. Bioorganic & Medicinal Chemistry Letters. 18(19). 5182–5185. 12 indexed citations
20.
Popsavin, Velimir, et al.. (2005). Regiochemistry of epoxide ring opening in methyl 2,3-anhydro-4-azido-4-deoxy-α- and β-l-lyxopyranosides. Carbohydrate Research. 340(11). 1866–1871. 2 indexed citations

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