Elvira E. Shults

2.2k total citations
290 papers, 1.8k citations indexed

About

Elvira E. Shults is a scholar working on Organic Chemistry, Molecular Biology and Pharmacology. According to data from OpenAlex, Elvira E. Shults has authored 290 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 158 papers in Organic Chemistry, 123 papers in Molecular Biology and 72 papers in Pharmacology. Recurrent topics in Elvira E. Shults's work include Natural product bioactivities and synthesis (49 papers), Synthesis and biological activity (42 papers) and Biological Activity of Diterpenoids and Biflavonoids (42 papers). Elvira E. Shults is often cited by papers focused on Natural product bioactivities and synthesis (49 papers), Synthesis and biological activity (42 papers) and Biological Activity of Diterpenoids and Biflavonoids (42 papers). Elvira E. Shults collaborates with scholars based in Russia, Kazakhstan and Mongolia. Elvira E. Shults's co-authors include М. М. Шакиров, Г. А. Толстиков, Dmitry S. Baev, Irina Yu. Bagryanskaya, Аndrey G. Pokrovsky, Yu. V. Gatilov, Tatyana V. Rybalova, Sergey A. Popov, Т. Г. Толстикова and Г. А. Толстиков and has published in prestigious journals such as Blood, Polymer and Tetrahedron.

In The Last Decade

Elvira E. Shults

263 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elvira E. Shults Russia 19 873 859 365 244 235 290 1.8k
Kyoko Nakagawa‐Goto United States 27 949 1.1× 1.1k 1.2× 457 1.3× 240 1.0× 223 0.9× 141 2.2k
Jiang‐Jiang Tang China 24 627 0.7× 681 0.8× 414 1.1× 127 0.5× 302 1.3× 68 1.9k
Midori A. Arai Japan 27 877 1.0× 1.3k 1.6× 373 1.0× 168 0.7× 174 0.7× 138 2.5k
Masuo Goto United States 26 958 1.1× 1.1k 1.3× 320 0.9× 338 1.4× 218 0.9× 112 2.3k
Lo‐Ti Tsao Taiwan 26 823 0.9× 769 0.9× 343 0.9× 156 0.6× 306 1.3× 48 1.8k
Jean‐Charles Chapuis United States 24 650 0.7× 642 0.7× 406 1.1× 110 0.5× 224 1.0× 54 1.5k
Ming‐Jaw Don Taiwan 24 398 0.5× 688 0.8× 258 0.7× 230 0.9× 262 1.1× 44 1.4k
Masayoshi Ando Japan 25 1.0k 1.2× 771 0.9× 231 0.6× 224 0.9× 248 1.1× 93 2.0k
Mangalam S. Nair India 23 491 0.6× 822 1.0× 126 0.3× 200 0.8× 244 1.0× 70 1.6k
Fan‐Dong Kong China 28 785 0.9× 774 0.9× 1.0k 2.8× 165 0.7× 216 0.9× 103 2.2k

Countries citing papers authored by Elvira E. Shults

Since Specialization
Citations

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

Fields of papers citing papers by Elvira E. Shults

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Elvira E. Shults. 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 Elvira E. Shults. The network helps show where Elvira E. Shults may publish in the future.

Co-authorship network of co-authors of Elvira E. Shults

This figure shows the co-authorship network connecting the top 25 collaborators of Elvira E. Shults. A scholar is included among the top collaborators of Elvira E. Shults 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 Elvira E. Shults. Elvira E. Shults 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.
Rybalova, Tatyana V., et al.. (2025). Synthesis and exploration of anticancer potential of spirocyclic 1,2,3-triazoline and aziridine derivatives of natural eudesmanolide isoalantolactone. Bioorganic Chemistry. 155. 108124–108124. 1 indexed citations
2.
3.
Shults, Elvira E., et al.. (2025). Investigation of N-(2-oxo-2H-chromen-3-carbonyl)cytisine’s Crystal Structure and Optical Properties. Materials. 18(13). 3153–3153. 1 indexed citations
4.
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Rybalova, Tatyana V., et al.. (2024). Synthesis and spectroscopic studies of triazole-based macroheterocycles containing eudesmane-type sesquiterpenoid moieties. Journal of Molecular Structure. 1321. 140236–140236. 1 indexed citations
6.
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Нуркенов, О. А., et al.. (2024). Antiviral Activity of (1S,9aR)-1-[(1,2,3-Triazol-1-yl)methyl]octahydro-1H-quinolizines from the Alkaloid Lupinine. Molecules. 29(23). 5742–5742. 1 indexed citations
8.
Shults, Elvira E., et al.. (2023). Synthesis and evaluation of antibacterial activity of bis-eudesmanolides connected by nitrogen-containing linkers. Russian Chemical Bulletin. 72(10). 2513–2524. 5 indexed citations
9.
Baev, Dmitry S., et al.. (2023). Synthesis, Pharmacological Evaluation, and Molecular Modeling of Lappaconitine–1,5-Benzodiazepine Hybrids. Molecules. 28(10). 4234–4234. 6 indexed citations
10.
11.
Шакиров, М. М., et al.. (2017). Synthesis of Novel Labdanoid-Based Macroheterocycles Using Click-Cycloaddition Reaction Protocol. Macroheterocycles. 10(1). 117–122. 1 indexed citations
12.
Толстикова, Т. Г., et al.. (2017). THE STRUCTURE-ANTIBACTERIAL ACTIVITY RELATIONSHIPS IN A SERIES OF ISOALANTOLACTONE DERIVATIVES. Fundamental and Clinical Medicine. 2(1). 28–34.
13.
Толстикова, Т. Г., et al.. (2014). Lappaconitine: Influence of Halogen Substituent on the Antiarrhythmic Activity. Cardiovascular & Hematological Agents in Medicinal Chemistry. 11(3). 211–217. 13 indexed citations
14.
Шакиров, М. М., et al.. (2013). Synthetic transformations of sesquiterpene lactones: VII. Palladium-catalyzed cross-coupling of isoalantolactone with 5-halouracils. Russian Journal of Organic Chemistry. 49(12). 1783–1797. 8 indexed citations
15.
Shults, Elvira E., et al.. (2012). Synthesis of (Z)-styrylfurocoumarins as the heterocyclic analogues of combretastatins. Doklady Chemistry. 447(2). 282–285. 3 indexed citations
16.
Govdi, Anastasia I., et al.. (2009). Synthesis of the first acetylene derivatives of betulonic acid. Doklady Chemistry. 424(2). 39–42. 2 indexed citations
17.
Martemyanov, Vyacheslav V., et al.. (2009). The response of gypsy moth (Lymantria dispar L.) larvae infected with nuclear polyhedrosis virus to induced resistance in birch (Betula pendula Roth.). Russian Journal of Ecology. 40(6). 434–439. 5 indexed citations
18.
Shults, Elvira E., et al.. (2008). Plant Coumarins. 3. (+)-PTeryxin from Peucedanum terebinthaceum. Chemistry of Natural Compounds. 44(5). 578–581. 5 indexed citations
19.
Толстикова, Т. Г., et al.. (2007). Formation of salts with hydrobromic acid determines the antiarrhythmic effect of lappaconitine derivatives. Doklady Biological Sciences. 415(1). 265–266. 5 indexed citations
20.
Shults, Elvira E., et al.. (2002). Study of alkaloids of the Siberian and Altai flora. 9. Synthesis of amino derivatives of elatidine. Russian Chemical Bulletin. 51(12). 2290–2294. 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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