С. А. Шевелев

2.6k total citations
201 papers, 1.9k citations indexed

About

С. А. Шевелев is a scholar working on Organic Chemistry, Physical and Theoretical Chemistry and Mechanics of Materials. According to data from OpenAlex, С. А. Шевелев has authored 201 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 173 papers in Organic Chemistry, 76 papers in Physical and Theoretical Chemistry and 51 papers in Mechanics of Materials. Recurrent topics in С. А. Шевелев's work include Chemical Reaction Mechanisms (114 papers), Chemical Reactions and Mechanisms (69 papers) and Energetic Materials and Combustion (51 papers). С. А. Шевелев is often cited by papers focused on Chemical Reaction Mechanisms (114 papers), Chemical Reactions and Mechanisms (69 papers) and Energetic Materials and Combustion (51 papers). С. А. Шевелев collaborates with scholars based in Russia, France and Czechia. С. А. Шевелев's co-authors include Igor L. Dalinger, Alexey M. Starosotnikov, Ирина А. Вацадзе, Tatyana K. Shkineva, Maxim A. Bastrakov, Вадим В. Качала, М. Д. Дутов, А. А. Зайцев, Б. И. Уграк and Ivan V. Fedyanin and has published in prestigious journals such as The Journal of Organic Chemistry, Tetrahedron and Journal of Applied Crystallography.

In The Last Decade

С. А. Шевелев

188 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
С. А. Шевелев Russia 21 1.5k 756 537 443 170 201 1.9k
Леонид Л. Ферштат Russia 26 1.6k 1.1× 1.1k 1.4× 511 1.0× 863 1.9× 118 0.7× 127 2.3k
Igor L. Dalinger Russia 24 1.7k 1.1× 1.6k 2.1× 648 1.2× 1.1k 2.5× 139 0.8× 160 2.5k
Jesse J. Sabatini United States 26 544 0.4× 1.0k 1.4× 208 0.4× 782 1.8× 74 0.4× 65 1.5k
Алексей Б. Шереметев Russia 32 2.1k 1.4× 2.2k 2.9× 815 1.5× 1.5k 3.5× 166 1.0× 219 3.4k
Л. И. Хмельницкий Russia 15 680 0.5× 386 0.5× 261 0.5× 215 0.5× 65 0.4× 123 870
Klaus Banert Germany 25 1.9k 1.3× 152 0.2× 430 0.8× 192 0.4× 361 2.1× 157 2.3k
Vikas D. Ghule India 28 929 0.6× 1.5k 2.0× 419 0.8× 1.4k 3.1× 193 1.1× 138 2.3k
Keerthi Jayasuriya United States 11 680 0.5× 142 0.2× 334 0.6× 243 0.5× 90 0.5× 23 1.2k
Rodney L. Willer United States 15 518 0.3× 159 0.2× 120 0.2× 157 0.4× 116 0.7× 42 744
Gregory H. Imler United States 37 1.2k 0.8× 3.0k 4.0× 845 1.6× 2.5k 5.6× 119 0.7× 100 3.7k

Countries citing papers authored by С. А. Шевелев

Since Specialization
Citations

This map shows the geographic impact of С. А. Шевелев'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. Шевелев 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. Шевелев more than expected).

Fields of papers citing papers by С. А. Шевелев

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

This figure shows the co-authorship network connecting the top 25 collaborators of С. А. Шевелев. A scholar is included among the top collaborators of С. А. Шевелев 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. Шевелев. С. А. Шевелев 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.
Bastrakov, Maxim A., et al.. (2019). Reactions of 3-R-5-nitropyridines with nucleophiles: Nucleophilic substitution vs conjugate addition. Tetrahedron. 75(47). 130659–130659. 5 indexed citations
2.
Starosotnikov, Alexey M., et al.. (2017). Nucleophilic dearomatization of 4-aza-6-nitrobenzofuroxan by CH acids in the synthesis of pharmacology-oriented compounds. Beilstein Journal of Organic Chemistry. 13. 2854–2861. 14 indexed citations
3.
Дутов, М. Д., et al.. (2017). Dual reactivity of 1-chloro- and 1-bromo-3,5-dinitrobenzenes in aromatic nucleophilic substitution. Mendeleev Communications. 27(2). 160–162. 1 indexed citations
4.
Bastrakov, Maxim A., et al.. (2017). Dearomatization of 3,5-dinitropyridines – an atom-efficient approach to fused 3-nitropyrrolidines. ARKIVOC. 2017(3). 181–190. 15 indexed citations
5.
Вацадзе, Ирина А., et al.. (2012). Nitropyrazoles 22. On reactivity of 3,5-dinitro-4-(phenylsulfonyl)pyrazole and its N-methyl derivative. Russian Chemical Bulletin. 61(2). 469–471. 1 indexed citations
6.
Дутов, М. Д., et al.. (2011). Synthesis, antifungal activity and QSAR study of 2-arylhydroxynitroindoles. European Journal of Medicinal Chemistry. 46(9). 4374–4382. 29 indexed citations
7.
Зайцев, А. А., Ирина А. Вацадзе, Igor L. Dalinger, et al.. (2009). Nitropyrazoles 15. Synthesis and some transformations of 1-(2,4-dinitrophenyl)-4-methyl-3,5-dinitropyrazole. Russian Chemical Bulletin. 58(10). 2109–2117. 8 indexed citations
8.
Cottyn, Betty, et al.. (2009). The versatile electrophilic reactivity of 4,6-dinitrobenzo[d]isoxazole-3-carbonitrile. Organic & Biomolecular Chemistry. 7(6). 1137–1137. 6 indexed citations
9.
Шевелев, С. А., et al.. (2006). Selective reduction of one, two, or three nitro groups in 1,3,5-trinitrobenzene with hydrazine hydrate. Russian Chemical Bulletin. 55(5). 938–939. 6 indexed citations
10.
Starosotnikov, Alexey M., et al.. (2004). Regiospecificity of nucleophilic substitution in 4,6-dinitro-1-phenyl-1H-indazole. Russian Chemical Bulletin. 53(3). 584–587. 13 indexed citations
11.
Rozhkov, Vladimir V., С. А. Шевелев, И. И. Червин, Alexander R. Mitchell, & Robert D. Schmidt. (2003). Direct Amination of 1-Substituted 3,5-Dinitrobenzenes by 1,1,1-Trimethylhydrazinium Iodide. The Journal of Organic Chemistry. 68(6). 2498–2501. 11 indexed citations
12.
Rozhkov, Vladimir V., et al.. (2002). SYNTHESIS OF 1-ARYL-4,6-DINITRO-1 H -INDAZOYL-3-METHYLCARBOXYLATES. Synthetic Communications. 32(3). 467–472. 1 indexed citations
13.
Шевелев, С. А., Ирина А. Вацадзе, & М. Д. Дутов. (2002). Substitution for a nitro group in 1,3,5-trinitrobenzene and meta-substituted 1,3-dinitrobenzenes under the action of oximes. Mendeleev Communications. 12(5). 196–197. 6 indexed citations
14.
Chiou, George C.Y., et al.. (2001). Effects of N-Nitropyrazoles on Ocular Blood Flow of Rabbits and Retinal Function Recovery of Rat Eyes after Ischemic Insults. Journal of Ocular Pharmacology and Therapeutics. 17(6). 505–515. 9 indexed citations
15.
Шевелев, С. А., et al.. (2001). Synthesis of Methyl 3-arylamino-4,6-Dinitrobenzo[b]thiophene-2-carboxylates. Smooth Dehydrogenation of 2,3-Dihydrobenzo[b]thiophene Derivatives.. Heterocyclic Communications. 7(3). 283–288. 3 indexed citations
16.
Rozhkov, Vladimir V., et al.. (2000). TRANSFORMATIONS OF 2-ARYL-4,6-DINITROINDOLES. Heterocyclic Communications. 6(6). 525–528. 7 indexed citations
17.
Dalinger, Igor L., et al.. (2000). Synthesis and transformations of picrylacetaldehyde. Mendeleev Communications. 10(4). 140–141. 9 indexed citations
18.
19.
Dalinger, Igor L., et al.. (1993). Nitropyrazoles. Russian Chemical Bulletin. 42(8). 1369–1371. 10 indexed citations
20.

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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