С. А. Рубцова

644 total citations
88 papers, 491 citations indexed

About

С. А. Рубцова is a scholar working on Organic Chemistry, Molecular Biology and Pharmacology. According to data from OpenAlex, С. А. Рубцова has authored 88 papers receiving a total of 491 indexed citations (citations by other indexed papers that have themselves been cited), including 77 papers in Organic Chemistry, 23 papers in Molecular Biology and 10 papers in Pharmacology. Recurrent topics in С. А. Рубцова's work include Sulfur-Based Synthesis Techniques (25 papers), Chemical Synthesis and Reactions (22 papers) and Synthesis and biological activity (17 papers). С. А. Рубцова is often cited by papers focused on Sulfur-Based Synthesis Techniques (25 papers), Chemical Synthesis and Reactions (22 papers) and Synthesis and biological activity (17 papers). С. А. Рубцова collaborates with scholars based in Russia, France and Belarus. С. А. Рубцова's co-authors include A. V. Kutchin, А. В. Кучин, Павел А. Слепухин, О. Г. Шевченко, А. В. Кучин, I. V. Loginova, Л. Л. Фролова, Marina Ya. Demakova, Konstantin S. Rodygin and Л. Е. Никитина and has published in prestigious journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and Molecules.

In The Last Decade

С. А. Рубцова

81 papers receiving 488 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. А. Рубцова Russia 12 373 102 42 41 33 88 491
Li‐Jun Wu China 17 485 1.3× 138 1.4× 56 1.3× 34 0.8× 29 0.9× 39 672
Jianwei Bian United States 12 303 0.8× 155 1.5× 31 0.7× 28 0.7× 44 1.3× 22 532
Ljubinka Joksović Serbia 14 270 0.7× 117 1.1× 30 0.7× 30 0.7× 20 0.6× 34 490
Eva Veverková Slovakia 14 313 0.8× 111 1.1× 29 0.7× 54 1.3× 15 0.5× 32 484
Yaşar Dürüst Türkiye 16 509 1.4× 105 1.0× 56 1.3× 47 1.1× 19 0.6× 55 672
Theeraphan Machan Thailand 10 192 0.5× 97 1.0× 59 1.4× 60 1.5× 20 0.6× 14 374
Narsimha Reddy Yellu India 16 222 0.6× 109 1.1× 46 1.1× 30 0.7× 13 0.4× 50 540
Ana N. Santiago Argentina 16 401 1.1× 77 0.8× 56 1.3× 41 1.0× 63 1.9× 44 596
Tian Cai China 13 319 0.9× 103 1.0× 22 0.5× 77 1.9× 26 0.8× 48 520
Biagia Musio Italy 19 539 1.4× 181 1.8× 27 0.6× 30 0.7× 29 0.9× 40 783

Countries citing papers authored by С. А. Рубцова

Since Specialization
Citations

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

Fields of papers citing papers by С. А. Рубцова

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of С. А. Рубцова

This figure shows the co-authorship network connecting the top 25 collaborators of С. А. Рубцова. A scholar is included among the top collaborators of С. А. Рубцова 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. А. Рубцова. С. А. Рубцова 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.
Pavelyev, Roman S., С. А. Рубцова, Svetlana А. Lisovskaya, et al.. (2025). Novel Fluoroquinolones With Pinane Moiety: Synthesis and Antimicrobial Activity. Chemistry & Biodiversity. 22(5). e202402601–e202402601.
2.
3.
Lodochnikova, О.А., et al.. (2024). Synthesis of New Sulfonic Acid Derivatives by the Reaction of S-(1S,2R,3S,5R)-2-Formyl-6,6-dimethylnorpinan-3-yl Thioacetate with Chlorine Dioxide. Russian Journal of Organic Chemistry. 60(4). 611–619. 1 indexed citations
4.
Baidamshina, Diana R., et al.. (2024). Synthesis and antimicrobial activity of new thiomonoterpene carboxylic acids. Russian Chemical Bulletin. 73(2). 449–457.
5.
Рубцова, С. А., et al.. (2024). New Polyfunctional N-Terpenyl-4-aminobenzenesulfonamides. Журнал Общей Химии. 94(3). 395–409. 1 indexed citations
6.
Baidamshina, Diana R., et al.. (2024). Synthesis of new chiral arylsulfonamides based on carane amino alcohols. Russian Chemical Bulletin. 73(8). 2238–2247. 1 indexed citations
7.
Никитина, Л. Е., Alexander A. Ksenofontov, Е. В. Антина, et al.. (2023). Unraveling the Mechanism of Platelet Aggregation Suppression by Thioterpenoids: Molecular Docking and In Vivo Antiaggregant Activity. Biomimetics. 8(8). 570–570.
8.
Lodochnikova, О.А., et al.. (2023). Ethyl 12-Sulfamoyl-abieta-8,11,13-trien-18-oate. SHILAP Revista de lepidopterología. 2023(1). M1584–M1584.
9.
Никитина, Л. Е., et al.. (2023). Monoterpene Thiols: Synthesis and Modifications for Obtaining Biologically Active Substances. International Journal of Molecular Sciences. 24(21). 15884–15884. 1 indexed citations
10.
Rumyantcev, Roman V., et al.. (2022). New trifluoromethylated sesquiterpenoids: synthesis, rearrangement, and biological activity. New Journal of Chemistry. 46(48). 23165–23172. 1 indexed citations
11.
Ksenofontov, Alexander A., Е. В. Антина, О. Г. Шевченко, et al.. (2022). Thioterpenoids as Potential Antithrombotic Drugs: Molecular Docking, Antiaggregant, Anticoagulant and Antioxidant Activities. Biomolecules. 12(11). 1599–1599. 8 indexed citations
12.
Рубцова, С. А., et al.. (2021). Caryophyllene and caryophyllene oxide: a variety of chemical transformations and biological activities. Chemical Papers. 76(1). 1–39. 46 indexed citations
13.
Гусева, Г. Б., Е. В. Антина, М. Б. Березин, et al.. (2021). Conjugate of meso-carboxysubstituted-BODIPY with thioterpenoid as an effective fluorescent probe: Synthesis, structure, spectral characteristics, and molecular docking. Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy. 268. 120638–120638. 8 indexed citations
14.
Рубцова, С. А., et al.. (2017). Oxidative transformations of alkyl caryophyllanyl sulfides. Russian Journal of Organic Chemistry. 53(6). 853–859. 4 indexed citations
15.
Kutchin, A. V., et al.. (2017). Studies on oxidative transformations of thiols, sulfides and alcohols in the presence of chlorine dioxide. Pure and Applied Chemistry. 89(10). 1379–1401. 4 indexed citations
16.
Шевченко, О. Г., et al.. (2016). Synthesis and Membranе-Protective Properties of Sulfur-Containing Monoterpenoids with Monosaccharide Fragments. 13–17. 2 indexed citations
17.
Рубцова, С. А., et al.. (2015). Reaction of monoterpene hydroxy thiols with chlorine dioxide. Russian Journal of Organic Chemistry. 51(10). 1359–1367. 10 indexed citations
18.
Рубцова, С. А., et al.. (2013). Synthesis and asymmetric oxidation of thioglycosides derived from neomenthanethiol and α-d-galactose. Russian Journal of Organic Chemistry. 49(3). 366–373. 7 indexed citations
19.
Demakova, Marina Ya., et al.. (2012). Reaction of 1-methyl-2-terpenylsulfanylimidazoles with chlorine dioxide. Russian Journal of Organic Chemistry. 48(11). 1490–1492. 1 indexed citations
20.
Rodygin, Konstantin S., С. А. Рубцова, A. V. Kutchin, & Павел А. Слепухин. (2011). One-Pot Synthesis and Asymmetric Oxidation of 2-Nitro-4-(Trifluoromethyl)Benzene Containing Sulfides. Phosphorus, sulfur, and silicon and the related elements. 186(9). 1885–1894. 8 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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