В. А. Глушков

789 total citations
92 papers, 636 citations indexed

About

В. А. Глушков is a scholar working on Organic Chemistry, Molecular Biology and Cancer Research. According to data from OpenAlex, В. А. Глушков has authored 92 papers receiving a total of 636 indexed citations (citations by other indexed papers that have themselves been cited), including 76 papers in Organic Chemistry, 16 papers in Molecular Biology and 15 papers in Cancer Research. Recurrent topics in В. А. Глушков's work include Synthesis and Reactions of Organic Compounds (15 papers), Synthesis and Biological Activity (14 papers) and Synthetic Organic Chemistry Methods (14 papers). В. А. Глушков is often cited by papers focused on Synthesis and Reactions of Organic Compounds (15 papers), Synthesis and Biological Activity (14 papers) and Synthetic Organic Chemistry Methods (14 papers). В. А. Глушков collaborates with scholars based in Russia, Israel and Bulgaria. В. А. Глушков's co-authors include А. Г. Толстиков, Yu. V. Shklyaev, Л. В. Аникина, М. В. Дмитриев, Павел А. Слепухин, В.С. Сергиенко, М. С. Котелев, Alexander S. Shashkov, Valery M. Dembitsky and Kyrill Yu. Suponitsky and has published in prestigious journals such as Tetrahedron, Russian Chemical Reviews and Russian Chemical Bulletin.

In The Last Decade

В. А. Глушков

81 papers receiving 622 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
В. А. Глушков Russia 11 586 127 70 64 46 92 636
Yasuyuki Kita Japan 17 810 1.4× 99 0.8× 66 0.9× 55 0.9× 52 1.1× 34 884
Yu. V. Shklyaev Russia 10 479 0.8× 59 0.5× 34 0.5× 79 1.2× 33 0.7× 133 522
В. Л. Гейн Russia 14 956 1.6× 142 1.1× 46 0.7× 25 0.4× 78 1.7× 238 1.0k
Štefan Marchalı́n Slovakia 16 624 1.1× 187 1.5× 55 0.8× 30 0.5× 33 0.7× 88 696
Jean‐Pierre Deprés France 15 533 0.9× 137 1.1× 61 0.9× 95 1.5× 64 1.4× 40 630
Yoshizumi Yasui Japan 16 997 1.7× 156 1.2× 145 2.1× 68 1.1× 61 1.3× 36 1.0k
Carolina Fernández-Rivas Spain 9 643 1.1× 113 0.9× 101 1.4× 137 2.1× 119 2.6× 9 807
Miklós Nyerges Hungary 21 1.0k 1.7× 188 1.5× 52 0.7× 52 0.8× 84 1.8× 84 1.1k
Guangzhong Wu United States 18 957 1.6× 80 0.6× 139 2.0× 54 0.8× 19 0.4× 19 1.0k
Eberhard Reimann Germany 11 353 0.6× 123 1.0× 38 0.5× 60 0.9× 67 1.5× 80 425

Countries citing papers authored by В. А. Глушков

Since Specialization
Citations

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

Fields of papers citing papers by В. А. Глушков

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of В. А. Глушков

This figure shows the co-authorship network connecting the top 25 collaborators of В. А. Глушков. A scholar is included among the top collaborators of В. А. Глушков 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 В. А. Глушков. В. А. Глушков 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.
Глушков, В. А., et al.. (2021). Quaternary 2-R-5,6-dihydro-1,2,4-triazolo[3,4-a]isoquinolin-2-ium salts and PEPPSI complexes based thereof. Russian Chemical Bulletin. 70(1). 122–127. 6 indexed citations
2.
Глушков, В. А., et al.. (2020). Pyridine imine palladium(ii) complex based on oleanane. Russian Chemical Bulletin. 69(10). 2013–2016. 7 indexed citations
3.
Дмитриев, М. В., et al.. (2019). Complexes of palladium(II) with N-heterocyclic carbenes from adamantylimidazole as precatalysts for thiophene and imidazole arylation. Russian Chemical Bulletin. 68(11). 2039–2047. 7 indexed citations
4.
Глушков, В. А., et al.. (2018). A THREE-COMPONENT SYNTHESIS OF N-SUBSTITUTED 6,7-DIMETHOXY-3,3-DIMETHYL3,4-DIHYDROISOQUINOLYL-1-ACETIC ACID AMIDES. 8(4). 451–462. 1 indexed citations
5.
Глушков, В. А., et al.. (2018). BIOLOGICAL ACTIVE COMPLEXES OF PALLADIUM(II) WITH AROMATIC N-HETEROCYCLES (Review). 8(4). 388–411. 3 indexed citations
6.
Дмитриев, М. В., et al.. (2016). Synthesis and Structure of Ferrocenol Esters. International Journal of Organic Chemistry. 6(2). 107–116. 1 indexed citations
7.
Глушков, В. А., et al.. (2012). Synthesis of ferrocenyl chalcones of the abietane series. Russian Journal of Organic Chemistry. 48(6). 836–839. 3 indexed citations
8.
Глушков, В. А., et al.. (2009). Chiral ionic liquids based on abietane. Russian Journal of Organic Chemistry. 45(3). 404–407. 6 indexed citations
9.
Глушков, В. А., et al.. (2008). The Povarov reaction of ethyl (18-carbomethoxyabieta-8,11,13-triene-12-imino)glyoxylate with electron-donating dienophiles. Mendeleev Communications. 18(4). 188–190. 9 indexed citations
10.
Глушков, В. А., et al.. (2008). Synthesis of 2-aryl-5,5-dimethyl-5,6-dihydro-1,2,4-triazolo-[3,4-a]isoquinolinium tetrafluoroborates. Russian Journal of Organic Chemistry. 44(7). 1091–1093. 1 indexed citations
11.
Толмачева, И. А., et al.. (2007). Reaction of 3-acetoxy-(2,3),(19β,28)-diepoxyoleanane with cyclic and linear amines. Chemistry of Natural Compounds. 43(2). 153–158. 3 indexed citations
12.
Глушков, В. А., et al.. (2005). 1-R-3,3-dialkyl-6,7-ethylenedioxy-3,4-dihydroisoquinolines. Chemistry of Heterocyclic Compounds. 41(8). 1022–1026. 1 indexed citations
13.
Глушков, В. А., et al.. (2002). Synthesis of substituted bis(3,3-dialkyl-3,4-dihydro-1-isoquinolyl)methanes. Russian Chemical Bulletin. 51(7). 1303–1307.
14.
Глушков, В. А., et al.. (2002). Spirocyclohexadienones. 5. Synthesis of 2-R-7a-methyl-3-(spirocyclohexa-2,5-dien-4-one)perhydro-1-indolines. Russian Chemical Bulletin. 51(4). 709–711. 4 indexed citations
15.
Глушков, В. А., et al.. (2002). Spirocyclohexadienones. 6. Three-component synthesis of 1-R-3,3-dimethyl-2-azaspiro[4.5]deca-1,6,9-trien-8-ones. Russian Chemical Bulletin. 51(5). 894–896. 4 indexed citations
16.
Глушков, В. А., et al.. (2001). Oxiranes in the Ritter Reaction. Synthesis of 6,7- and 5,8-Dimethoxy-3,3-dialkyl-3,4-dihydroisoquinolines by a Tandem Alkylation-Cyclization Reaction. Chemistry of Heterocyclic Compounds. 37(4). 444–452. 4 indexed citations
17.
Глушков, В. А., et al.. (2000). Investigation of paths for the synthesis of 5,5-dialkyl-3-perfluoroalkyl-5,6-dihydro-1,2,4-triazolo[3,4-a]isoquinolines. Chemistry of Heterocyclic Compounds. 36(3). 319–325. 1 indexed citations
18.
Глушков, В. А., et al.. (2000). An unusual 3,4-dihydroisoquinoline ring enlargement with the annulation of pyrazole. Mendeleev Communications. 10(1). 36–37. 3 indexed citations
19.
Глушков, В. А., et al.. (1998). Synthesis and study of antiinflammatory and analgesic activity of 1-hydrazino-3,3-dialkyl-3,4-dihydroisoquinoline derivatives. Pharmaceutical Chemistry Journal. 32(5). 258–261. 1 indexed citations
20.
Shklyaev, Yu. V., et al.. (1996). Reaction of 1-methylthio-3,4-dihydroisoquinolines with amines. Chemistry of Heterocyclic Compounds. 32(6). 689–695. 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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