Константин В. Саватеев

461 total citations
39 papers, 326 citations indexed

About

Константин В. Саватеев is a scholar working on Organic Chemistry, Molecular Biology and Physiology. According to data from OpenAlex, Константин В. Саватеев has authored 39 papers receiving a total of 326 indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Organic Chemistry, 11 papers in Molecular Biology and 6 papers in Physiology. Recurrent topics in Константин В. Саватеев's work include Synthesis and Biological Evaluation (20 papers), Synthesis and Characterization of Heterocyclic Compounds (16 papers) and Quinazolinone synthesis and applications (8 papers). Константин В. Саватеев is often cited by papers focused on Synthesis and Biological Evaluation (20 papers), Synthesis and Characterization of Heterocyclic Compounds (16 papers) and Quinazolinone synthesis and applications (8 papers). Константин В. Саватеев collaborates with scholars based in Russia and China. Константин В. Саватеев's co-authors include В. Л. Русинов, Victor V. Fedotov, Олег Н. Чупахин, А. А. Спасов, Valery N. Charushin, Павел А. Слепухин, Denis A. Babkov, Oleg S. Eltsov, S. K. Kotovskaya and Evgeny B. Gorbunov and has published in prestigious journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and The Journal of Organic Chemistry.

In The Last Decade

Константин В. Саватеев

36 papers receiving 312 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Константин В. Саватеев Russia 12 255 58 24 18 16 39 326
Victor V. Fedotov Russia 12 244 1.0× 52 0.9× 14 0.6× 17 0.9× 27 1.7× 34 308
Christian Glover United Kingdom 8 270 1.1× 119 2.1× 35 1.5× 6 0.3× 8 0.5× 11 383
Syed Jawad Ali Shah Pakistan 13 161 0.6× 164 2.8× 61 2.5× 3 0.2× 14 0.9× 35 379
Yaning Xu China 12 205 0.8× 110 1.9× 5 0.2× 2 0.1× 10 0.6× 36 349
Olivier Mirguet France 12 202 0.8× 142 2.4× 3 0.1× 4 0.2× 21 1.3× 18 334
Asim Kumar India 11 249 1.0× 71 1.2× 2 0.1× 4 0.2× 13 0.8× 18 325
Raghu Prasad Mailavaram India 15 324 1.3× 185 3.2× 61 2.5× 8 0.5× 41 492
Roger L. Xie United States 7 162 0.6× 83 1.4× 17 0.7× 1 0.1× 11 0.7× 8 252
Swapna Varghese Australia 8 82 0.3× 135 2.3× 11 0.5× 1 0.1× 7 0.4× 12 259
Parul Chauhan India 10 226 0.9× 43 0.7× 3 0.1× 17 1.1× 16 349

Countries citing papers authored by Константин В. Саватеев

Since Specialization
Citations

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

Fields of papers citing papers by Константин В. Саватеев

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Константин В. Саватеев

This figure shows the co-authorship network connecting the top 25 collaborators of Константин В. Саватеев. A scholar is included among the top collaborators of Константин В. Саватеев 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 Константин В. Саватеев. Константин В. Саватеев 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.
Саватеев, Константин В., et al.. (2025). Azolo[5′,1′,2,3]pyrimido[5,4-e]tetrazolo[1,5-c]pyrimidines as dual-action antiglycators and α-glucosidase inhibitors. Bioorganic & Medicinal Chemistry Letters. 128. 130333–130333. 1 indexed citations
2.
Саватеев, Константин В., et al.. (2024). Unexpected transformations of 3-bromo-5,7-dimethylpyrazolo[1,5-a]pyrimidine in reactions with BunLi. Russian Chemical Bulletin. 73(6). 1640–1646.
3.
Fedotov, Victor V., Константин В. Саватеев, Grigory А. Кim, et al.. (2024). Multi-component synthesis and enhanced photophysical study of novel azolo[1,5-a]pyrimidine based dyes. Dyes and Pigments. 232. 112447–112447. 6 indexed citations
4.
Саватеев, Константин В., et al.. (2023). 3-Halopyrazolo[1,5-a]pyrimidines as promising precursors of novel C-nucleosides. Russian Chemical Bulletin. 72(8). 1821–1836. 2 indexed citations
5.
Fedotov, Victor V., et al.. (2023). 2-Furyl-6-nitro-1,2,4-triazolo [1,5-a]pyrimidin-7-one. SHILAP Revista de lepidopterología. 2023(1). M1563–M1563. 1 indexed citations
6.
Саватеев, Константин В., et al.. (2023). Approaches to the synthesis of heterocyclic C-nucleosides. Russian Chemical Bulletin. 72(2). 425–481. 5 indexed citations
7.
Саватеев, Константин В., et al.. (2022). The Effects of Nitroazolopyrimidines on the A1 Adenosine Receptor and Intraocular Pressure in Rats. Russian Journal of Bioorganic Chemistry. 48(4). 777–782. 4 indexed citations
8.
Чупахин, Олег Н., В. Л. Русинов, Михаил В. Вараксин, et al.. (2022). Triazavirin—A Novel Effective Antiviral Drug. International Journal of Molecular Sciences. 23(23). 14537–14537. 17 indexed citations
9.
Саватеев, Константин В., S. K. Kotovskaya, В. Л. Русинов, et al.. (2022). 6-(Tetrazol-5-yl)-7-aminoazolo[1,5-a]pyrimidines as Novel Potent CK2 Inhibitors. Molecules. 27(24). 8697–8697. 4 indexed citations
10.
Спасов, А. А., Denis A. Babkov, E. V. Sokolova, et al.. (2022). Discovery of Nitro-azolo[1,5-a]pyrimidines with Anti-Inflammatory and Protective Activity against LPS-Induced Acute Lung Injury. Pharmaceuticals. 15(5). 537–537. 7 indexed citations
11.
Fedotov, Victor V., Константин В. Саватеев, Evgeny B. Gorbunov, et al.. (2022). Azolo[5,1‐ c ][1,2,4]triazines and Azoloazapurines: Synthesis, Antimicrobial activity and in silico Studies. ChemistrySelect. 7(5). 7 indexed citations
12.
Саватеев, Константин В., et al.. (2022). A Versatile Method for the Synthesis of 7-Aminoazolo[1,5-a]pyrimidine-6-carbonitriles. Doklady Chemistry. 505(2). 168–176. 4 indexed citations
13.
Саватеев, Константин В., et al.. (2022). Azolo[1,5-a]pyrimidines and Their Condensed Analogs with Anticoagulant Activity. Molecules. 27(1). 274–274. 12 indexed citations
14.
Саватеев, Константин В., Павел А. Слепухин, S. K. Kotovskaya, et al.. (2021). Atom-efficient synthesis of hybrid molecules combining fragments of triazolopyrimidines and 3-ethoxycarbonyl-1-ethyl-6-fluoroquinolin-4(1H)-one through 1,2,3-triazole linker. Chemistry of Heterocyclic Compounds. 57(2). 143–153. 5 indexed citations
15.
Саватеев, Константин В., Victor V. Fedotov, Oleg S. Eltsov, et al.. (2019). Nitrothiadiazolo[3,2-a]pyrimidines as promising antiglycating agents. European Journal of Medicinal Chemistry. 185. 111808–111808. 26 indexed citations
16.
Fedotov, Victor V., Константин В. Саватеев, Oleg S. Eltsov, et al.. (2018). ANRORC process in 1-alkylazolo[5,1-c][1,2,4]triazin-4(1H)-ones. Chemistry of Heterocyclic Compounds. 54(1). 63–69. 3 indexed citations
17.
Русинов, В. Л., et al.. (2016). New stable form of nitroacetonitrile. Mendeleev Communications. 26(2). 172–173. 16 indexed citations
18.
Саватеев, Константин В., et al.. (2015). Structural analogs of adenosine receptor inhibitors in the series of 1,2,4-triazolo[1,5-a]pyrimidines. Russian Chemical Bulletin. 64(6). 1378–1384. 9 indexed citations
19.
Eltsov, Oleg S., et al.. (2014). Halogen-Containing 2-methylpyrimido[1,2-a]-benzimidazol-4(10Н)-ones. Chemistry of Heterocyclic Compounds. 50(7). 1005–1013. 6 indexed citations
20.
Саватеев, Константин В., et al.. (2014). 8-Alkyl[1,2,4]Triazolo[5,1-b]Purines. Chemistry of Heterocyclic Compounds. 50(6). 880–887. 20 indexed citations

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