Е. П. Леванова

730 total citations
93 papers, 534 citations indexed

About

Е. П. Леванова is a scholar working on Organic Chemistry, Toxicology and Spectroscopy. According to data from OpenAlex, Е. П. Леванова has authored 93 papers receiving a total of 534 indexed citations (citations by other indexed papers that have themselves been cited), including 84 papers in Organic Chemistry, 44 papers in Toxicology and 8 papers in Spectroscopy. Recurrent topics in Е. П. Леванова's work include Organoselenium and organotellurium chemistry (44 papers), Organic Chemistry Cycloaddition Reactions (41 papers) and Sulfur-Based Synthesis Techniques (22 papers). Е. П. Леванова is often cited by papers focused on Organoselenium and organotellurium chemistry (44 papers), Organic Chemistry Cycloaddition Reactions (41 papers) and Sulfur-Based Synthesis Techniques (22 papers). Е. П. Леванова collaborates with scholars based in Russia, Denmark and Germany. Е. П. Леванова's co-authors include N. V. Russavskaya, Н. А. Корчевин, V. А. Grabel’nykh, G. G. Levkovskaya, Л. В. Клыба, Leonid B. Krivdin, Yury Yu. Rusakov, É. N. Deryagina, A. I. Albanov and И. Б. Розенцвейг and has published in prestigious journals such as Chemistry - A European Journal, Journal of Molecular Structure and Australian Journal of Chemistry.

In The Last Decade

Е. П. Леванова

87 papers receiving 523 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Е. П. Леванова Russia 11 408 222 101 54 48 93 534
A. I. Albanov Russia 13 463 1.1× 155 0.7× 53 0.5× 19 0.4× 54 1.1× 102 554
Vitalij D. Shteingarts Russia 15 448 1.1× 55 0.2× 29 0.3× 25 0.5× 23 0.5× 43 546
Dominic J. Pascoe United Kingdom 6 394 1.0× 83 0.4× 89 0.9× 56 1.0× 117 2.4× 6 693
Thomas M. Klapoetke Germany 12 258 0.6× 100 0.5× 37 0.4× 42 0.8× 80 1.7× 40 433
James X. Mao United States 13 104 0.3× 31 0.1× 163 1.6× 17 0.3× 39 0.8× 18 401
W. Lau United States 7 331 0.8× 53 0.2× 26 0.3× 28 0.5× 50 1.0× 12 443
Robin Panisch Germany 12 398 1.0× 43 0.2× 34 0.3× 29 0.5× 53 1.1× 15 545
Vijay Narayan India 10 302 0.7× 22 0.1× 38 0.4× 14 0.3× 73 1.5× 22 457
H. Lumbroso France 13 351 0.9× 27 0.1× 179 1.8× 112 2.1× 70 1.5× 64 534

Countries citing papers authored by Е. П. Леванова

Since Specialization
Citations

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

Fields of papers citing papers by Е. П. Леванова

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Е. П. Леванова

This figure shows the co-authorship network connecting the top 25 collaborators of Е. П. Леванова. A scholar is included among the top collaborators of Е. П. Леванова 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 Е. П. Леванова. Е. П. Леванова 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.
Чернышева, Е. А., et al.. (2018). REGRESSION ANALYSIS OF ZINC AND CADMIUM ION EXTRACTION FROM AQUEOUS SOLUTIONS USING A LIGNIN-BASED SULPHUR-CONTAINING SORBENT. Proceedings of universities Applied chemistry and biotechnology. 8(4). 174–183. 3 indexed citations
2.
Чернышева, Е. А., V. А. Grabel’nykh, Е. П. Леванова, & Н. А. Корчевин. (2017). THE USING OF SULFUR-CONTAINING LIGNIN BASED SORBENT FOR EXTRACTION OF MERCURY FROM AQUEOUS SOLUTIONS. Proceedings of universities Applied chemistry and biotechnology. 7(3). 169–177. 3 indexed citations
3.
Леванова, Е. П., et al.. (2017). THE USE OF ISOTHIURONIC SALTS AS BRIGHTENING ADDITIVES IN THE TECHNOLOGY OF BRIGHT NICKEL ELECTROCHEMICAL PLATING. Proceedings of universities Applied chemistry and biotechnology. 7(4). 136–141. 1 indexed citations
4.
Леванова, Е. П., V. А. Grabel’nykh, И. Б. Розенцвейг, et al.. (2015). Features of the synthesis of unsaturated sulfides proceeding from (2-chloroprop-2-en-1-yl)isothiouronium chloride. Russian Journal of Organic Chemistry. 51(2). 161–166. 14 indexed citations
5.
Sinegovskaya, L. M., et al.. (2014). Spectral and Quantum-Chemical Study of Acid-Catalyzed Heterocyclization of S-(2-Chloroprop-2-EN-1-YL)Isothiuronium Chloride with Acetylacetone. Chemistry of Heterocyclic Compounds. 50(3). 404–414. 1 indexed citations
6.
Леванова, Е. П., V. А. Grabel’nykh, N. V. Russavskaya, et al.. (2014). Effect of the chalcogen nature on the reaction of propane-1,3-dichalcogenolates with 2,3-dichloroprop-1-ene. Russian Journal of Organic Chemistry. 50(1). 6–12. 2 indexed citations
7.
Леванова, Е. П., V. А. Grabel’nykh, N. V. Russavskaya, et al.. (2012). Novel route to the synthesis of chalcogenolanes, chalcogenanes, and 1,2-dichalcogenaepanes*. Chemistry of Heterocyclic Compounds. 47(11). 1345–1352. 5 indexed citations
8.
Трофимов, Б. А., Elena Yu. Schmidt, А. Й. Михалева, et al.. (2009). Synthesis of 2‐(Selenophen‐2‐yl)pyrroles and Their Electropolymerization to Electrochromic Nanofilms. Chemistry - A European Journal. 15(26). 6435–6445. 18 indexed citations
9.
Rusakov, Yury Yu., et al.. (2009). Conformational Analysis of 2-Formylselenophene by Means of 13C–1H, 13C–13C, and 77Se–1H Spin–Spin Coupling Constants. Australian Journal of Chemistry. 62(7). 734–738. 19 indexed citations
10.
Rusakov, Yury Yu., Leonid B. Krivdin, Stephan P. A. Sauer, Е. П. Леванова, & G. G. Levkovskaya. (2009). Structural trends of 77Se1H spin–spin coupling constants and conformational behavior of 2‐substituted selenophenes. Magnetic Resonance in Chemistry. 48(1). 44–52. 72 indexed citations
11.
Леванова, Е. П., V. А. Grabel’nykh, N. V. Russavskaya, et al.. (2009). Reaction of tellurium with dichloromethane in the system hydrazine hydrate-alkali. Russian Journal of General Chemistry. 79(11). 2321–2327. 5 indexed citations
12.
Леванова, Е. П., V. А. Grabel’nykh, N. V. Russavskaya, et al.. (2008). Selective synthesis of isomeric dithioglycerols. Russian Journal of Organic Chemistry. 44(10). 1428–1433. 5 indexed citations
13.
Леванова, Е. П., T. I. Vakul’skaya, V. А. Grabel’nykh, et al.. (2008). Synthesis and paramagnetic properties of polytelluride oligomers. Russian Journal of Organic Chemistry. 44(10). 1422–1427. 5 indexed citations
14.
Russavskaya, N. V., et al.. (2006). Synthesis and oxidative cleavage of poly(trimethylene diselenides). Russian Journal of General Chemistry. 76(2). 229–234. 16 indexed citations
15.
Russavskaya, N. V., et al.. (2006). 1,2-Ditellurolane: A new synthetic method, structure and chemical reactions. Chemistry of Heterocyclic Compounds. 42(11). 1464–1471. 2 indexed citations
16.
Deryagina, É. N., et al.. (2005). Synthesis of organochalcogen compounds in basic reducing systems. Russian Chemical Bulletin. 54(11). 2473–2483. 28 indexed citations
17.
Воронков, М. Г., et al.. (2005). High-Temperature Synthesis of Thiophene from Bis(2-chloroethyl) Sulfide. Russian Journal of Organic Chemistry. 41(6). 891–893. 1 indexed citations
18.
Russavskaya, N. V., et al.. (2002). Reaction of Aldehydes with Hydrazine in the System Sulfur-Alkali. Russian Journal of Organic Chemistry. 38(10). 1498–1500. 8 indexed citations
19.
Леванова, Е. П., et al.. (1983). Nucleophilic addition of thiols to acetylenes in liquid ammonia. Russian Chemical Bulletin. 32(1). 186–189.
20.
NIKOL'SKAYA, A. N., et al.. (1979). Substituted dienic 1,3-dioxolan-2-ones and bis(1,3-dioxolan-2-ones). Chemistry of Heterocyclic Compounds. 15(12). 1296–1298. 1 indexed citations

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