В. Е. Катаев

1.5k total citations
140 papers, 1.3k citations indexed

About

В. Е. Катаев is a scholar working on Organic Chemistry, Molecular Biology and Nutrition and Dietetics. According to data from OpenAlex, В. Е. Катаев has authored 140 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 69 papers in Organic Chemistry, 59 papers in Molecular Biology and 57 papers in Nutrition and Dietetics. Recurrent topics in В. Е. Катаев's work include Biochemical Analysis and Sensing Techniques (57 papers), Natural product bioactivities and synthesis (26 papers) and Analytical Chemistry and Chromatography (23 papers). В. Е. Катаев is often cited by papers focused on Biochemical Analysis and Sensing Techniques (57 papers), Natural product bioactivities and synthesis (26 papers) and Analytical Chemistry and Chromatography (23 papers). В. Е. Катаев collaborates with scholars based in Russia, United States and Italy. В. Е. Катаев's co-authors include I. Yu. Strobykina, B. F. Garifullin, Р. Р. Шарипова, О. В. Андреева, В. Ф. Миронов, Vasily M. Babaev, Alexandra D. Voloshina, А.Т. Губайдуллин, V. A. Al’fonsov and Р. З. Мусин and has published in prestigious journals such as International Journal of Molecular Sciences, Journal of Colloid and Interface Science and Physical Chemistry Chemical Physics.

In The Last Decade

В. Е. Катаев

133 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
В. Е. Катаев Russia 20 631 604 401 235 95 140 1.3k
I. Yu. Strobykina Russia 17 470 0.7× 359 0.6× 385 1.0× 134 0.6× 89 0.9× 92 873
Petri Tähtinen Finland 16 373 0.6× 352 0.6× 76 0.2× 177 0.8× 60 0.6× 39 886
Suzanne Toppet Belgium 24 656 1.0× 1.9k 3.2× 138 0.3× 167 0.7× 96 1.0× 195 2.5k
András Neszmélyi Hungary 22 825 1.3× 765 1.3× 104 0.3× 201 0.9× 130 1.4× 97 1.5k
Vladimı́r Kováčik Slovakia 16 500 0.8× 372 0.6× 117 0.3× 302 1.3× 45 0.5× 91 1.0k
André De Bruyn Belgium 19 750 1.2× 423 0.7× 137 0.3× 98 0.4× 70 0.7× 84 1.3k
Rodrigo L.O.R. Cunha Brazil 22 313 0.5× 514 0.9× 149 0.4× 43 0.2× 50 0.5× 57 1.2k
Luca Sancineto Italy 27 466 0.7× 1.7k 2.8× 289 0.7× 74 0.3× 147 1.5× 77 2.6k
Silvana Raić‐Malić Croatia 23 564 0.9× 1.3k 2.1× 109 0.3× 30 0.1× 82 0.9× 92 1.8k
Laurent Legentil France 18 396 0.6× 411 0.7× 63 0.2× 81 0.3× 56 0.6× 55 896

Countries citing papers authored by В. Е. Катаев

Since Specialization
Citations

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

Fields of papers citing papers by В. Е. Катаев

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by В. Е. Катаев. 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 В. Е. Катаев. The network helps show where В. Е. Катаев may publish in the future.

Co-authorship network of co-authors of В. Е. Катаев

This figure shows the co-authorship network connecting the top 25 collaborators of В. Е. Катаев. A scholar is included among the top collaborators of В. Е. Катаев 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 В. Е. Катаев. В. Е. Катаев 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.
Андреева, О. В., Alexandra D. Voloshina, Anna P. Lyubina, et al.. (2025). Antimicrobial activity of triphenylphosphonium (TPP) conjugates of alkynyl−substituted nucleic bases and their analogues. The Journal of Antibiotics. 78(12). 731–756.
2.
Андреева, О. В., Liliya F. Saifina, B. F. Garifullin, et al.. (2024). Synthesis and Antiviral Activity of Homodimers of 1,2,3-Triazolyl Nucleoside Analogues Based on Quinazoline-2,4-dione. Russian Journal of General Chemistry. 94(5). 1127–1138.
3.
Kuznetsova, Darya A., Elmira A. Vasilieva, Denis M. Kuznetsov, et al.. (2024). Self-assembly and functional activity of amphiphilic conjugates of the diterpenoid isosteviol and triphenylphosphonium cation, with focusing on biotechnological potential. Colloids and Surfaces A Physicochemical and Engineering Aspects. 697. 134505–134505. 5 indexed citations
4.
Андреева, О. В., Liliya F. Saifina, B. F. Garifullin, et al.. (2024). Synthesis and antiviral activity of homodimers of 1,2,3-triazolyl nucleoside analogs. Russian Chemical Bulletin. 73(6). 1789–1800. 1 indexed citations
5.
Garifullin, B. F., D. A. Tatarinov, О. В. Андреева, et al.. (2023). Synthesis, antiviral evaluation, molecular docking study and cytotoxicity of 5′-phosphorylated 1,2,3-triazolyl nucleoside analogues with thymine and 6-methyl uracil moieties. Medicinal Chemistry Research. 32(8). 1770–1803. 1 indexed citations
6.
Андреева, О. В., Alexandra D. Voloshina, Anna P. Lyubina, et al.. (2023). Acetylenyl substituted nucleic bases and their triphenylphosphonium (TPP) conjugates. Unexpected surge in cytotoxicity. Bioorganic Chemistry. 142. 106959–106959. 2 indexed citations
7.
Tatarinov, D. A., B. F. Garifullin, О. В. Андреева, et al.. (2022). The First 5′-Phosphorylated 1,2,3-Triazolyl Nucleoside Analogues with Uracil and Quinazoline-2,4-Dione Moieties: A Synthesis and Antiviral Evaluation. Molecules. 27(19). 6214–6214. 14 indexed citations
8.
Strobykina, I. Yu., Alexandra D. Voloshina, О. В. Андреева, et al.. (2021). Synthesis, antimicrobial activity and cytotoxicity of triphenylphosphonium (TPP) conjugates of 1,2,3-triazolyl nucleoside analogues. Bioorganic Chemistry. 116. 105328–105328. 23 indexed citations
9.
Катаев, В. Е. & B. F. Garifullin. (2021). Antiviral nucleoside analogs. Chemistry of Heterocyclic Compounds. 57(4). 326–341. 48 indexed citations
10.
Voloshina, Alexandra D., Аnastasiia S. Sapunova, Natalia Kulik, et al.. (2020). Antimicrobial and cytotoxic effects of ammonium derivatives of diterpenoids steviol and isosteviol. Bioorganic & Medicinal Chemistry. 32. 115974–115974. 45 indexed citations
11.
Андреева, О. В., B. F. Garifullin, Владимир В. Зарубаев, et al.. (2020). Synthesis of 1,2,3-triazolyl nucleoside analogues and their antiviral activity. Molecular Diversity. 25(1). 473–490. 37 indexed citations
12.
Шарипова, Р. Р., B. F. Garifullin, Alexandra D. Voloshina, et al.. (2019). Synthesis and anti-cancer activities of glycosides and glycoconjugates of diterpenoid isosteviol. MedChemComm. 10(8). 1488–1498. 21 indexed citations
13.
Garifullin, B. F., Р. Р. Шарипова, A. D. Voloshina, М. А. Кравченко, & В. Е. Катаев. (2018). Synthesis and Antitubercular and Antibacterial Activities of Triethylammonium 2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy-D-glucopyranosyl Decyl Phosphate. Russian Journal of Organic Chemistry. 54(9). 1333–1336. 1 indexed citations
14.
Медведева, Н. И., О. Б. Казакова, И. Е. Смирнова, et al.. (2017). Synthesis and antimycobacterial activity of triterpenic A-ring azepanes. European Journal of Medicinal Chemistry. 143. 464–472. 39 indexed citations
15.
Катаев, В. Е., I. Yu. Strobykina, & L. Ya. Zakharova. (2014). Quaternary ammonium derivatives of natural terpenoids. Synthesis and properties. Russian Chemical Bulletin. 63(9). 1884–1900. 16 indexed citations
16.
Gabdrakhmanov, Dinar R., I. Yu. Strobykina, В. Е. Катаев, et al.. (2013). Novel biomimetic systems based on amphiphilic compounds with a diterpenoid fragment: Role of counterions in self-assembly. Journal of Colloid and Interface Science. 405. 125–133. 14 indexed citations
17.
Gabdrakhmanov, Dinar R., L. Ya. Zakharova, A. I. Konovalov, et al.. (2013). Supramolecular design of biocompatible nanocontainers based on amphiphilic derivatives of a natural compound isosteviol. Physical Chemistry Chemical Physics. 15(39). 16725–16725. 22 indexed citations
18.
Казакова, О. Б., G. V. Giniyatullina, Г. А. Толстиков, В. Е. Катаев, & Р. З. Мусин. (2009). Synthesis and modification of triterpenoids with two lupan backbones. Russian Journal of Bioorganic Chemistry. 35(5). 645–650. 1 indexed citations
19.
Казакова, Э. Х., et al.. (2002). A Watersoluble Sulfonatomethylated Calix[4]resorcinarene as Artificial Receptor of Metal Complexes. Journal of Inclusion Phenomena and Macrocyclic Chemistry. 42(1-2). 77–81. 19 indexed citations
20.
Mustafina, Asiya R., et al.. (2001). The Inclusion Properties of a New Watersoluble Sulfonated Calix[4]resorcinarene towards Alkylammonium and N-Methylpyridinium Cations. Journal of Inclusion Phenomena and Macrocyclic Chemistry. 40(1-2). 73–76. 30 indexed citations

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