Olga V. Serdyuk

903 total citations
27 papers, 682 citations indexed

About

Olga V. Serdyuk is a scholar working on Organic Chemistry, Molecular Biology and Pharmacology. According to data from OpenAlex, Olga V. Serdyuk has authored 27 papers receiving a total of 682 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Organic Chemistry, 4 papers in Molecular Biology and 4 papers in Pharmacology. Recurrent topics in Olga V. Serdyuk's work include Synthesis and pharmacology of benzodiazepine derivatives (6 papers), Synthesis and Characterization of Pyrroles (5 papers) and Synthesis and Biological Evaluation (5 papers). Olga V. Serdyuk is often cited by papers focused on Synthesis and pharmacology of benzodiazepine derivatives (6 papers), Synthesis and Characterization of Pyrroles (5 papers) and Synthesis and Biological Evaluation (5 papers). Olga V. Serdyuk collaborates with scholars based in Russia, Germany and United Kingdom. Olga V. Serdyuk's co-authors include Svetlana B. Tsogoeva, Anja Fingerhut, А. В. Бутин, Владимир Т. Абаев, Igor V. Trushkov, Maxim G. Uchuskin, Valentine G. Nenajdenko, Frank Hampel, Alexandra A. Kolodina and Vasiliy M. Muzalevskiy and has published in prestigious journals such as SHILAP Revista de lepidopterología, Green Chemistry and Tetrahedron Letters.

In The Last Decade

Olga V. Serdyuk

27 papers receiving 670 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Olga V. Serdyuk Russia 12 617 137 137 73 67 27 682
Jian Lei China 15 678 1.1× 92 0.7× 117 0.9× 41 0.6× 69 1.0× 33 763
Zhilong Chen China 13 621 1.0× 110 0.8× 150 1.1× 38 0.5× 34 0.5× 30 704
Ramakrishna G. Bhat India 17 653 1.1× 167 1.2× 101 0.7× 30 0.4× 50 0.7× 56 720
Shaoxia Lin China 19 804 1.3× 115 0.8× 210 1.5× 54 0.7× 33 0.5× 34 874
Taiga Yurino Japan 15 708 1.1× 133 1.0× 226 1.6× 56 0.8× 31 0.5× 30 773
Tao Miao China 22 1.3k 2.1× 92 0.7× 101 0.7× 58 0.8× 61 0.9× 52 1.3k
Govind Goroba Pawar India 12 1.1k 1.7× 73 0.5× 162 1.2× 39 0.5× 66 1.0× 15 1.1k
Morgan Donnard France 14 924 1.5× 110 0.8× 148 1.1× 30 0.4× 92 1.4× 44 1.0k
Michael J. Zacuto United States 18 856 1.4× 168 1.2× 151 1.1× 37 0.5× 68 1.0× 29 946

Countries citing papers authored by Olga V. Serdyuk

Since Specialization
Citations

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

Fields of papers citing papers by Olga V. Serdyuk

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Olga V. Serdyuk. 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 Olga V. Serdyuk. The network helps show where Olga V. Serdyuk may publish in the future.

Co-authorship network of co-authors of Olga V. Serdyuk

This figure shows the co-authorship network connecting the top 25 collaborators of Olga V. Serdyuk. A scholar is included among the top collaborators of Olga V. Serdyuk 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 Olga V. Serdyuk. Olga V. Serdyuk 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.
Hampel, Frank, et al.. (2019). Synthesis of pyrazolylvinyl ketones from furan derivatives. Organic & Biomolecular Chemistry. 17(19). 4850–4855. 10 indexed citations
2.
Serdyuk, Olga V., Igor V. Trushkov, Maxim G. Uchuskin, & Владимир Т. Абаев. (2019). Indolylvinyl Ketones: Building Blocks for the Synthesis of Natural Products and Bioactive Compounds. Synthesis. 51(4). 787–815. 20 indexed citations
3.
Kolodina, Alexandra A., et al.. (2019). (E)-4-(3-Phenylisoxazol-5-yl)but-3-en-2-one. SHILAP Revista de lepidopterología. 2019(3). M1081–M1081. 2 indexed citations
4.
Абаев, Владимир Т., et al.. (2018). Facile Synthesis of β-Keto Sulfones Employing Fenton’s Reagent in DMSO. Synlett. 29(5). 571–575. 6 indexed citations
5.
Serdyuk, Olga V. & Alexandra A. Kolodina. (2018). Eudistomin U, Isoeudistomin U, and Related Indole Compounds: Synthesis and Biological Activity. Heterocycles. 96(7). 1171–1171. 14 indexed citations
6.
Fingerhut, Anja, Olga V. Serdyuk, & Svetlana B. Tsogoeva. (2015). Non-heme iron catalysts for epoxidation and aziridination reactions of challenging terminal alkenes: towards sustainability. Green Chemistry. 17(4). 2042–2058. 106 indexed citations
7.
Serdyuk, Olga V., et al.. (2013). Bifunctional primary amine-thioureas in asymmetric organocatalysis. Organic & Biomolecular Chemistry. 11(41). 7051–7051. 281 indexed citations
8.
Uchuskin, Maxim G., et al.. (2012). From biomass to medicines. A simple synthesis of indolo[3,2-c]quinolines, antimalarial alkaloid isocryptolepine, and its derivatives. Organic & Biomolecular Chemistry. 10(36). 7262–7262. 56 indexed citations
9.
Serdyuk, Olga V., Alexandru Zamfir, Frank Hampel, & Svetlana B. Tsogoeva. (2012). Combining in situ Generated Chiral Silicon Lewis Acid and Chiral Brønsted Acid Catalysts for [3+2] Cycloadditions: Cooperative Catalysis as a Convenient Enantioselective Route to Pyrazolidines. Advanced Synthesis & Catalysis. 354(16). 3115–3121. 23 indexed citations
10.
Nenajdenko, Valentine G., Olga V. Serdyuk, & Vasiliy M. Muzalevskiy. (2012). Synthesis and Properties of Fluoropyrroles and Their Analogues. Synthesis. 44(14). 2115–2137. 19 indexed citations
11.
Serdyuk, Olga V., et al.. (2012). Furfuryl aryl(alkyl) ketones: preparation and synthetic potential (review). Chemistry of Heterocyclic Compounds. 48(9). 1281–1296. 4 indexed citations
13.
Бутин, А. В., et al.. (2011). Unusual reactivity of β-(3-indolyl)-α,β-unsaturated ketones. 2-Acetylvinyl group removal by phenylhydrazine hydrochloride. Tetrahedron Letters. 52(41). 5255–5258. 7 indexed citations
14.
Serdyuk, Olga V., Владимир Т. Абаев, & А. В. Бутин. (2011). Synthesis of new cyclopentenones from phenacylfurans. Chemistry of Heterocyclic Compounds. 47(7). 906–908. 1 indexed citations
15.
Serdyuk, Olga V., Valentine G. Nenajdenko, Владимир Т. Абаев, & А. В. Бутин. (2011). Synthesis of Fluorinated Thiophenes and Their Analogues. Synthesis. 2011(16). 2505–2529. 31 indexed citations
16.
Serdyuk, Olga V., Владимир Т. Абаев, Alexandra A. Kolodina, & А. В. Бутин. (2011). First example of the synthesis of indoles on a heterocyclic matrix. Chemistry of Heterocyclic Compounds. 47(3). 381–383. 2 indexed citations
17.
Абаев, Владимир Т., et al.. (2009). Radical alkylation in the synthesis of phenacylfurans. Chemistry of Heterocyclic Compounds. 45(5). 611–612. 5 indexed citations
18.
Serdyuk, Olga V., А. В. Бутин, & Владимир Т. Абаев. (2009). Synthesis of fluorofurans and perfluoroalkylfurans. Journal of Fluorine Chemistry. 131(3). 296–319. 19 indexed citations
19.
Абаев, Владимир Т. & Olga V. Serdyuk. (2008). Catalysis by palladium complexes: new prospects in amination of aryl and hetaryl chlorides. Russian Chemical Reviews. 77(2). 177–192. 17 indexed citations
20.
Serdyuk, Olga V., et al.. (2008). Benzobis(pyrrolopyrimidopiridazines): Molecular structure and properties of the first π‐electronic analogues of dibenzo[a,o]picene. Journal of Heterocyclic Chemistry. 45(1). 195–199. 4 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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