E. I. Boreko

978 total citations
75 papers, 816 citations indexed

About

E. I. Boreko is a scholar working on Organic Chemistry, Molecular Biology and Biochemistry. According to data from OpenAlex, E. I. Boreko has authored 75 papers receiving a total of 816 indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Organic Chemistry, 28 papers in Molecular Biology and 10 papers in Biochemistry. Recurrent topics in E. I. Boreko's work include Natural product bioactivities and synthesis (26 papers), Synthesis and biological activity (21 papers) and Synthesis and Characterization of Heterocyclic Compounds (14 papers). E. I. Boreko is often cited by papers focused on Natural product bioactivities and synthesis (26 papers), Synthesis and biological activity (21 papers) and Synthesis and Characterization of Heterocyclic Compounds (14 papers). E. I. Boreko collaborates with scholars based in Russia, Belarus and Ukraine. E. I. Boreko's co-authors include О. В. Савинова, N. I. Pavlova, С. Н. Николаева, О. Б. Флехтер, Г. А. Толстиков, Л. А. Балтина, Ф. З. Галин, И. А. Толмачева, Victoria V. Grishko and И. К. Моисеев and has published in prestigious journals such as Tetrahedron, European Journal of Medicinal Chemistry and Bioorganic & Medicinal Chemistry Letters.

In The Last Decade

E. I. Boreko

70 papers receiving 791 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
E. I. Boreko Russia 15 527 245 110 107 105 75 816
Robert D. Sindelar United States 14 466 0.9× 203 0.8× 69 0.6× 67 0.6× 59 0.6× 35 797
О. Б. Флехтер Russia 16 782 1.5× 170 0.7× 177 1.6× 129 1.2× 111 1.1× 69 934
Gerald A. Wächter United States 15 405 0.8× 156 0.6× 158 1.4× 105 1.0× 29 0.3× 24 841
Lucie Heller Germany 18 656 1.2× 218 0.9× 70 0.6× 93 0.9× 35 0.3× 37 857
Tangai E. Chagwedera United States 9 793 1.5× 83 0.3× 211 1.9× 101 0.9× 67 0.6× 11 1.1k
Jack B. Jiang United States 11 587 1.1× 497 2.0× 98 0.9× 41 0.4× 42 0.4× 17 1.1k
Ф. З. Галин Russia 14 446 0.8× 249 1.0× 93 0.8× 93 0.9× 53 0.5× 134 667
Chung-Ren Su Taiwan 18 427 0.8× 244 1.0× 272 2.5× 158 1.5× 37 0.4× 21 1.0k
N. I. Pavlova Russia 13 374 0.7× 92 0.4× 86 0.8× 70 0.7× 73 0.7× 30 500
Miguel A. González Spain 22 855 1.6× 597 2.4× 154 1.4× 99 0.9× 33 0.3× 50 1.5k

Countries citing papers authored by E. I. Boreko

Since Specialization
Citations

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

Fields of papers citing papers by E. I. Boreko

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by E. I. Boreko. 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 E. I. Boreko. The network helps show where E. I. Boreko may publish in the future.

Co-authorship network of co-authors of E. I. Boreko

This figure shows the co-authorship network connecting the top 25 collaborators of E. I. Boreko. A scholar is included among the top collaborators of E. I. Boreko 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 E. I. Boreko. E. I. Boreko 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.
Шадыро, О. И., et al.. (2019). Comparative Evaluation of the Antiherpes Activity of Compounds with Different Mechanisms of Action. Pharmaceutical Chemistry Journal. 53(7). 646–649. 1 indexed citations
2.
Klimochkin, Yu. N., И. К. Моисеев, М. В. Леонова, С. Н. Николаева, & E. I. Boreko. (2017). Synthesis and Antiviral Properties of Ethyl(3-ethyladamant-1-yl)carbamate. Pharmaceutical Chemistry Journal. 51(1). 13–17. 10 indexed citations
3.
Шадыро, О. И., О. В. Савинова, Svetlana N. Samovich, et al.. (2016). Synthesis and Antiviral Activity of Hydroxy-Substituted Benzaldehydes and Related Compounds. Pharmaceutical Chemistry Journal. 50(3). 156–158. 6 indexed citations
4.
Бринкевич, С. Д., E. I. Boreko, О. В. Савинова, N. I. Pavlova, & О. И. Шадыро. (2012). Radical-regulating and antiviral properties of ascorbic acid and its derivatives. Bioorganic & Medicinal Chemistry Letters. 22(7). 2424–2427. 13 indexed citations
5.
Толмачева, И. А., et al.. (2012). Synthesis and biological activity of amides of 28-methoxy-28-oxo-1-cyano-2,3-seco-lup-20(29)-en-3-oic acid. Chemistry of Natural Compounds. 48(3). 426–431. 6 indexed citations
6.
Савинова, О. В., N. I. Pavlova, & E. I. Boreko. (2009). [New betulin derivatives in combination with rimantadine for inhibition of influenza virus reproduction].. PubMed. 54(5-6). 16–20. 6 indexed citations
7.
Флехтер, О. Б., И. Е. Смирнова, E. V. Tret’yakova, et al.. (2009). Synthesis of dihydroquinopimaric acid conjugates with amino acids. Russian Journal of Bioorganic Chemistry. 35(3). 385–390. 15 indexed citations
8.
Флехтер, О. Б., Н. И. Медведева, Г. А. Толстиков, et al.. (2009). Betulonic amides modified at cycle a by amino acids: Synthesis and inhibition of flu A virus reproduction. Russian Journal of Bioorganic Chemistry. 35(1). 118–122. 8 indexed citations
9.
Шадыро, О. И., et al.. (2008). Synthesis and study of antiviral and anti-radical properties of aminophenol derivatives. Bioorganic & Medicinal Chemistry Letters. 18(7). 2420–2423. 24 indexed citations
10.
Флехтер, О. Б., E. I. Boreko, E. V. Tret’yakova, et al.. (2004). Synthesis and Antiviral Activity of Betulonic Acid Amides and Conjugates with Amino Acids. Russian Journal of Bioorganic Chemistry. 30(1). 80–88. 23 indexed citations
11.
Флехтер, О. Б., E. I. Boreko, E. V. Tret’yakova, et al.. (2003). Synthesis and Antiviral Activity of Ureides and Carbamates of Betulinic Acid and Its Derivatives. Russian Journal of Bioorganic Chemistry. 29(6). 594–600. 16 indexed citations
12.
Балтина, Л. А., О. Б. Флехтер, E. I. Boreko, et al.. (2003). Lupane triterpenes and derivatives with antiviral activity. Bioorganic & Medicinal Chemistry Letters. 13(20). 3549–3552. 99 indexed citations
13.
Флехтер, О. Б., Л. А. Балтина, Ф. З. Галин, et al.. (2003). Preparation of Betulinic Acids from Betulin Extract. Antiviral and Antiulcer Activity of Some Related Terpenoids.. ChemInform. 34(4). 1 indexed citations
14.
Pavlova, N. I., О. В. Савинова, С. Н. Николаева, E. I. Boreko, & О. Б. Флехтер. (2003). Antiviral activity of betulin, betulinic and betulonic acids against some enveloped and non-enveloped viruses. Fitoterapia. 74(5). 489–492. 125 indexed citations
15.
Шадыро, О. И., Г. И. Полозов, С. Н. Николаева, et al.. (2003). Synthesis and Antiviral Activity of 4,6‐Di‐tert‐butyl‐2‐aminophenol Derivatives.. ChemInform. 34(52). 1 indexed citations
16.
Boreko, E. I., et al.. (2002). Antiviral Activity of Adamantane-Containing Heterocycles. Pharmaceutical Chemistry Journal. 36(1). 3–6. 13 indexed citations
17.
Озеров, А. А., et al.. (1991). Synthesis and antiviral activity of new unsaturated pyrimidine acyclonucleosides. Pharmaceutical Chemistry Journal. 25(8). 560–565. 4 indexed citations
18.
Гейн, В. Л., et al.. (1991). Synthesis of 4-substituted 1-methyl-5-aryl- and 1,5-diaryltetrahydropyrrole-2,3-diones and their antiviral action. Pharmaceutical Chemistry Journal. 25(12). 884–887. 11 indexed citations
19.
Русинов, В. Л., et al.. (1990). Synthesis of nitro derivatives of azolo[1,5-a]pyrimidine and their antiviral action. Pharmaceutical Chemistry Journal. 24(1). 55–58. 3 indexed citations
20.
Boreko, E. I., et al.. (1985). Synthesis and antiviral activity of N9-[β-D-arabinofuranosyl]guanine. Pharmaceutical Chemistry Journal. 19(4). 259–261.

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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