С. К. Петкевич

544 total citations
77 papers, 394 citations indexed

About

С. К. Петкевич is a scholar working on Organic Chemistry, Molecular Biology and Spectroscopy. According to data from OpenAlex, С. К. Петкевич has authored 77 papers receiving a total of 394 indexed citations (citations by other indexed papers that have themselves been cited), including 69 papers in Organic Chemistry, 17 papers in Molecular Biology and 9 papers in Spectroscopy. Recurrent topics in С. К. Петкевич's work include Synthesis and Biological Evaluation (22 papers), Synthesis and Characterization of Heterocyclic Compounds (19 papers) and Synthesis and Reactions of Organic Compounds (19 papers). С. К. Петкевич is often cited by papers focused on Synthesis and Biological Evaluation (22 papers), Synthesis and Characterization of Heterocyclic Compounds (19 papers) and Synthesis and Reactions of Organic Compounds (19 papers). С. К. Петкевич collaborates with scholars based in Belarus, Russia and China. С. К. Петкевич's co-authors include В. И. Поткин, Н. А. Бумагин, Alexey V. Kletskov, Е. А. Дикусар, Никита Е. Голанцов, М. В. Ливанцов, Alexander S. Lyakhov, Ludmila S. Ivashkevich, V. A. Kulchitsky and R. S. Alekseyev and has published in prestigious journals such as Scientific Reports, Inorganic Chemistry and Tetrahedron.

In The Last Decade

С. К. Петкевич

71 papers receiving 394 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
С. К. Петкевич Belarus 11 367 102 29 25 20 77 394
Takayuki Tsuritani Japan 15 505 1.4× 109 1.1× 52 1.8× 18 0.7× 11 0.6× 22 531
Wang‐Ge Shou China 8 405 1.1× 81 0.8× 41 1.4× 10 0.4× 10 0.5× 15 417
Bohdan Snovydovych Germany 8 473 1.3× 56 0.5× 48 1.7× 19 0.8× 17 0.8× 9 499
Vladimir Y. Vvedensky United States 13 408 1.1× 89 0.9× 16 0.6× 20 0.8× 10 0.5× 25 431
Yulia A. Khomutova Russia 14 379 1.0× 81 0.8× 35 1.2× 34 1.4× 4 0.2× 28 413
Manian Ramesh Canada 7 348 0.9× 89 0.9× 64 2.2× 12 0.5× 16 0.8× 12 382
И. Р. Рамазанов Russia 11 346 0.9× 73 0.7× 63 2.2× 35 1.4× 7 0.3× 82 382
Andrij Dreger Germany 6 442 1.2× 38 0.4× 25 0.9× 21 0.8× 10 0.5× 10 457
В. И. Станинец Ukraine 10 299 0.8× 47 0.5× 39 1.3× 44 1.8× 28 1.4× 54 327
B.O. Ashburn United States 11 358 1.0× 65 0.6× 55 1.9× 11 0.4× 4 0.2× 18 399

Countries citing papers authored by С. К. Петкевич

Since Specialization
Citations

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

Fields of papers citing papers by С. К. Петкевич

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by С. К. Петкевич. 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 С. К. Петкевич. The network helps show where С. К. Петкевич may publish in the future.

Co-authorship network of co-authors of С. К. Петкевич

This figure shows the co-authorship network connecting the top 25 collaborators of С. К. Петкевич. A scholar is included among the top collaborators of С. К. Петкевич 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 С. К. Петкевич. С. К. Петкевич 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.
Дикусар, Е. А., С. К. Петкевич, R. S. Alekseyev, et al.. (2022). Synthesis of Bisacridine Derivatives with Pyridine and 1,2-Azole Fragments. Russian Journal of General Chemistry. 92(1). 40–53. 1 indexed citations
2.
Петкевич, С. К., et al.. (2022). Synthesis of 5-Arylisoxazole and 4,5-Dichloroisothiazole Amino-Substituted Derivatives and Their Biological Activity. Russian Journal of General Chemistry. 92(1). 29–39. 1 indexed citations
3.
Нуркенов, О. А., et al.. (2022). Quinine Esters with 1,2-Azole, Pyridine and Adamantane Fragments. Molecules. 27(11). 3476–3476. 4 indexed citations
4.
Зубков, Федор И., С. К. Петкевич, В. И. Поткин, et al.. (2021). Cascade of the Hinsberg / IMDAF reactions in the synthesis 2-arylsulfonyl-3a,6-epoxyisoindoles and 4a,7-epoxyisoquinolines in water. Tetrahedron. 85. 132032–132032. 4 indexed citations
5.
Дикусар, Е. А., et al.. (2021). Methylamine Derivatives with 1,2-Azole Fragments: Synthesis, Palladium Complexes, Catalysis of the Suzuki Reaction. Russian Journal of General Chemistry. 91(8). 1512–1518. 4 indexed citations
6.
Shakirova, O.G., Dmitry Yu. Naumov, Л. Г. Лавренова, С. К. Петкевич, & В. И. Поткин. (2021). Structural identification of the new binuclear Cu(II) complex with unexpected nitration of a ligand. Inorganic Chemistry Communications. 133. 108957–108957. 1 indexed citations
7.
Kletskov, Alexey V., Н. А. Бумагин, С. К. Петкевич, et al.. (2020). Mimics of Pincer Ligands: An Accessible Phosphine-Free N-(Pyrimidin-2-yl)-1,2-azole-3-carboxamide Framework for Binuclear Pd(II) Complexes and High-Turnover Catalysis in Water. Inorganic Chemistry. 59(15). 10384–10388. 22 indexed citations
8.
Shаhаb, Siyamak, et al.. (2018). SYNTHESIS OF (E,E)-AZOAZOMETHINES BASED ON 4-AMINOAZOBENZENE. 54(1). 58–71. 1 indexed citations
9.
Levkovskaya, G. G., et al.. (2016). Reaction of polychloroacetaldehyde arylsulfonylimines with 2-amino-6H-1,3-thiazine-6-thiones and 2-amino-4-phenyl-6H-1,3-thiazin-6-one. Russian Journal of Organic Chemistry. 52(11). 1670–1673.
10.
Поткин, В. И., et al.. (2016). Synthesis of N’-substituted derivatives of 5-(4-methylphenyl)isoxazole-3-carbohydrazonamide. Russian Journal of General Chemistry. 86(9). 2059–2066. 1 indexed citations
11.
Поткин, В. И., et al.. (2015). Synthesis of functional isoxazole derivatives proceeding from (5-arylisoxazol-3-yl)chloromethanes. Russian Journal of Organic Chemistry. 51(8). 1119–1130. 10 indexed citations
12.
Дикусар, Е. А., et al.. (2014). Esters of benzoic, 5-arylisoxazole-3-carboxylic and 4,5-dichloroisothiazole-3-carboxylic acids. Russian Journal of General Chemistry. 84(6). 1179–1185. 1 indexed citations
13.
Поткин, В. И., et al.. (2013). Synthesis of functionally substituted isoxazole and isothiazole derivatives. Russian Journal of Organic Chemistry. 49(10). 1523–1533. 22 indexed citations
14.
Дикусар, Е. А., et al.. (2013). Catalytic synthesis of 2,2′-arylmethylenebis(3-hydroxy-5,5-dimethylcyclohex-2-en-1-ones) and 3,3,6,6-tetramethyl-9-aryl-3,4,5,6,7,9-hexahydro-1H-xanthene-1,8(2H)-diones. Russian Journal of Organic Chemistry. 49(2). 233–242. 5 indexed citations
15.
Дикусар, Е. А., et al.. (2013). Esters of isoxazole- and isothiazolecarboxylic acids and oximes of β-isatin, isoxazole- and ferrocene-containing ketones and carborane alcohols. Russian Journal of General Chemistry. 83(3). 542–544. 1 indexed citations
16.
Дикусар, Е. А., et al.. (2013). Synthesis of 2-R-1,3-dioxanes, derivatives of functionally substituted aldehydes of vanillin series. Russian Journal of Organic Chemistry. 49(2). 221–227.
17.
18.
Дикусар, Е. А., et al.. (2009). Synthesis of 1,1′-diacetylferrocene dioxime esters. Russian Journal of General Chemistry. 79(8). 1660–1662. 1 indexed citations
19.
Поткин, В. И., et al.. (2009). Synthesis of 5-substituted 3-[5-(2,5-dimethylphenyl)-1,2-oxazol-3-yl]-1,2,4-oxadiazoles. Russian Journal of Organic Chemistry. 45(4). 551–554. 2 indexed citations
20.
Поткин, В. И., et al.. (2002). N-Chloroacyl Derivatives of Valine Esters. Russian Journal of Organic Chemistry. 38(6). 915–916. 1 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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