Владимир С. Мошкин

1.1k total citations
67 papers, 768 citations indexed

About

Владимир С. Мошкин is a scholar working on Organic Chemistry, Pharmacology and Molecular Biology. According to data from OpenAlex, Владимир С. Мошкин has authored 67 papers receiving a total of 768 indexed citations (citations by other indexed papers that have themselves been cited), including 67 papers in Organic Chemistry, 28 papers in Pharmacology and 12 papers in Molecular Biology. Recurrent topics in Владимир С. Мошкин's work include Synthesis of Organic Compounds (28 papers), Asymmetric Synthesis and Catalysis (19 papers) and Synthesis and Catalytic Reactions (17 papers). Владимир С. Мошкин is often cited by papers focused on Synthesis of Organic Compounds (28 papers), Asymmetric Synthesis and Catalysis (19 papers) and Synthesis and Catalytic Reactions (17 papers). Владимир С. Мошкин collaborates with scholars based in Russia, Germany and North Korea. Владимир С. Мошкин's co-authors include Vyacheslav Ya. Sosnovskikh, М. И. Кодесс, Evgeny M. Buev, Alexey Yu. Barkov, Vladislav Yu. Korotaev, Роман А. Иргашев, Gerd‐Volker Röschenthaler, Igor B. Kutyashev, Oleg S. Eltsov and Павел А. Слепухин and has published in prestigious journals such as The Journal of Organic Chemistry, Tetrahedron and Organic Letters.

In The Last Decade

Владимир С. Мошкин

64 papers receiving 738 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Владимир С. Мошкин Russia 20 749 271 109 79 31 67 768
А. М. Шестопалов Russia 17 1.2k 1.6× 278 1.0× 124 1.1× 33 0.4× 9 0.3× 101 1.2k
Andrey S. Plaskon Ukraine 16 681 0.9× 182 0.7× 152 1.4× 30 0.4× 14 0.5× 47 730
В. Л. Гейн Russia 14 956 1.3× 78 0.3× 142 1.3× 25 0.3× 25 0.8× 238 1.0k
Alexey А. Festa Russia 13 670 0.9× 47 0.2× 65 0.6× 42 0.5× 15 0.5× 46 721
R. Raghunathan India 12 429 0.6× 94 0.3× 89 0.8× 35 0.4× 8 0.3× 46 441
L. A. Rodinovskaya Russia 17 1.1k 1.4× 225 0.8× 113 1.0× 25 0.3× 5 0.2× 75 1.1k
Andrey N. Komogortsev Russia 14 590 0.8× 145 0.5× 84 0.8× 19 0.2× 8 0.3× 94 628
Antoinette E. Nibbs United States 10 426 0.6× 68 0.3× 117 1.1× 31 0.4× 17 0.5× 11 502
Jayadevan Jayashankaran India 11 436 0.6× 82 0.3× 62 0.6× 13 0.2× 13 0.4× 32 460
Boris I. Usachev Russia 16 671 0.9× 308 1.1× 37 0.3× 373 4.7× 21 0.7× 73 737

Countries citing papers authored by Владимир С. Мошкин

Since Specialization
Citations

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

Fields of papers citing papers by Владимир С. Мошкин

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Владимир С. Мошкин

This figure shows the co-authorship network connecting the top 25 collaborators of Владимир С. Мошкин. A scholar is included among the top collaborators of Владимир С. Мошкин 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 Владимир С. Мошкин. Владимир С. Мошкин 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.
2.
Buev, Evgeny M., et al.. (2024). Novel synthesis of 2,3-dihydrobenzofuran-3-amines from salicylic aldehydes: Trimethylsilyl as traceless activating group. Tetrahedron Letters. 139. 154992–154992. 1 indexed citations
3.
Buev, Evgeny M., et al.. (2024). 3,4,5,6-Tetrahydro-2H-3,6-epoxybenzo[g][1,4]oxazocine – A new bridged heterocyclic system. Tetrahedron Letters. 155. 155405–155405.
4.
Buev, Evgeny M., et al.. (2023). Arylethanolamines in Ritter reaction: Synthesis of 2,4‐Diarylimidazole Core. Asian Journal of Organic Chemistry. 12(2).
5.
Обыденнов, Дмитрий Л., et al.. (2021). Reactions of 4-Pyrones with Azomethine Ylides as a Chemoselective Method for the Construction of Multisubstituted Pyrano[2,3-c]pyrrolidines. Synthesis. 53(15). 2621–2631. 4 indexed citations
6.
Buev, Evgeny M., et al.. (2021). 5-Aryloxazolidines as Reagents for Double Alkylation of Arenes: A Novel Synthesis of 4-Aryltetrahydroisoquinolines. The Journal of Organic Chemistry. 86(21). 15307–15317. 5 indexed citations
7.
Buev, Evgeny M., et al.. (2019). Synthesis of 6,12-Methanodibenzo[c,f]azocines and 4-Aryltetrahydroisoquinolines from Aromatic Aldehydes. Organic Letters. 22(2). 631–635. 11 indexed citations
8.
Buev, Evgeny M., et al.. (2019). Reactions of 5-aryloxazolidines with CH-acidic compounds. Tetrahedron Letters. 60(24). 1620–1623. 4 indexed citations
9.
Buev, Evgeny M., Владимир С. Мошкин, & Vyacheslav Ya. Sosnovskikh. (2018). Reactivity of spiroanthraceneoxazolidines with cyclopropanes: An approach to the oxindole alkaloid scaffold. Tetrahedron Letters. 59(37). 3409–3412. 11 indexed citations
10.
11.
Мошкин, Владимир С., et al.. (2016). Reactions of chromone-3-carboxylic acid and chromone-3-carboxamides with cyanoacetic acid hydrazide. Mendeleev Communications. 26(1). 72–74. 20 indexed citations
12.
Buev, Evgeny M., Владимир С. Мошкин, & Vyacheslav Ya. Sosnovskikh. (2016). Reagents for Storage and Regeneration of Nonstabilized Azomethine Ylides: Spiroanthraceneoxazolidines. Organic Letters. 18(8). 1764–1767. 32 indexed citations
13.
Мошкин, Владимир С., et al.. (2015). Synthesis of 4-aryl-6-methyl-7a-(trifluoromethyl)-2,4a,5,6,7,7a-hexahydropyrano[2,3-c]pyrrol-2-ones from 4-aryl-6-(trifluoromethyl)-2-pyrones, sarcosine, and formaldehyde. Chemistry of Heterocyclic Compounds. 51(10). 913–917. 6 indexed citations
14.
15.
Мошкин, Владимир С. & Vyacheslav Ya. Sosnovskikh. (2013). A simple two-step synthesis of 2-(alkylamino)-1-arylethanols, including racemic adrenaline, from aromatic aldehydes via 5-aryloxazolidines. Tetrahedron Letters. 54(44). 5869–5872. 22 indexed citations
16.
Пестов, А. В., et al.. (2012). Structure and absorption spectra of substituted 2-hydroxy-2-trifluoromethylchroman-4-ones. Journal of Applied Spectroscopy. 79(4). 509–514. 1 indexed citations
17.
Sosnovskikh, Vyacheslav Ya. & Владимир С. Мошкин. (2012). Novel data for the reaction of 3-cyano-(thio)chromones with N-nucleophiles. Chemistry of Heterocyclic Compounds. 48(1). 139–146. 21 indexed citations
18.
Sosnovskikh, Vyacheslav Ya. & Владимир С. Мошкин. (2010). Direct synthesis of 3-(diaminomethylidene)chromane-2,4-diones from 3-formylchromones and hydroxylamine. Russian Chemical Bulletin. 59(5). 1056–1058. 5 indexed citations
19.
Sosnovskikh, Vyacheslav Ya., et al.. (2006). Reactions of 3-polyfluoroacylchromones with primary amines. Russian Chemical Bulletin. 55(3). 593–594. 1 indexed citations
20.
Sosnovskikh, Vyacheslav Ya., et al.. (2005). Synthesis and some properties of 6-di(tri)fluoromethyl-and 5-di(tri)fluoroacetyl-3-methyl-1-phenylpyrano[2,3-c]pyrazol-4(1H)-ones. Russian Chemical Bulletin. 54(12). 2846–2850. 21 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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