Вадим М. Тимошенко

819 total citations
63 papers, 590 citations indexed

About

Вадим М. Тимошенко is a scholar working on Organic Chemistry, Pharmaceutical Science and Spectroscopy. According to data from OpenAlex, Вадим М. Тимошенко has authored 63 papers receiving a total of 590 indexed citations (citations by other indexed papers that have themselves been cited), including 55 papers in Organic Chemistry, 41 papers in Pharmaceutical Science and 7 papers in Spectroscopy. Recurrent topics in Вадим М. Тимошенко's work include Fluorine in Organic Chemistry (41 papers), Synthesis and Reactions of Organic Compounds (31 papers) and Organic Chemistry Cycloaddition Reactions (14 papers). Вадим М. Тимошенко is often cited by papers focused on Fluorine in Organic Chemistry (41 papers), Synthesis and Reactions of Organic Compounds (31 papers) and Organic Chemistry Cycloaddition Reactions (14 papers). Вадим М. Тимошенко collaborates with scholars based in Ukraine, France and Germany. Вадим М. Тимошенко's co-authors include Yuriy G. Shermolovich, Charles Portella, Paolo Passaniti, Paul D. Beer, Mauro Maestri, Vincenzo Balzani, Fabienne Grellepois, Alexander B. Rozhenko, Эдуард Б. Русанов and Alexander N. Chernega and has published in prestigious journals such as SHILAP Revista de lepidopterología, Chemical Communications and The Journal of Organic Chemistry.

In The Last Decade

Вадим М. Тимошенко

56 papers receiving 583 citations

Peers

Вадим М. Тимошенко
N. А. Nedolya Russia
Hans‐Ulrich Reißig Germany
Stefania Fioravanti Italy
Américo Lemos Portugal
Evgeniy V. Kondrashov Russia
Olesya V. Khoroshilova Russia
Shiro Matsukawa Japan
А. И. Албанов Russia
Alexandre R. Meyer Brazil
M. Perseghini Switzerland
N. А. Nedolya Russia
Вадим М. Тимошенко
Citations per year, relative to Вадим М. Тимошенко Вадим М. Тимошенко (= 1×) peers N. А. Nedolya

Countries citing papers authored by Вадим М. Тимошенко

Since Specialization
Citations

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

Fields of papers citing papers by Вадим М. Тимошенко

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Вадим М. Тимошенко. 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 Вадим М. Тимошенко. The network helps show where Вадим М. Тимошенко may publish in the future.

Co-authorship network of co-authors of Вадим М. Тимошенко

This figure shows the co-authorship network connecting the top 25 collaborators of Вадим М. Тимошенко. A scholar is included among the top collaborators of Вадим М. Тимошенко 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 Вадим М. Тимошенко. Вадим М. Тимошенко 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.
Тимошенко, Вадим М., et al.. (2023). The Synthesis of the Hydrogenated Thiophenes by [3+2] Cycloaddition Reaction of Thiocarbonyl Ylide. SHILAP Revista de lepidopterología. 21(2). 53–63.
3.
Тимошенко, Вадим М., et al.. (2021). Synthesis of five-membered heterocycles by [3+2] cycloaddition reactions of sulfur-containing 3,3,3-trifluoropropene derivatives. Chemistry of Heterocyclic Compounds. 57(12). 1149–1154. 9 indexed citations
4.
Тимошенко, Вадим М., et al.. (2021). [3+2] Cycloaddition reactions of 1-substituted 3,3,3-trifluoropropenes with diazo compounds and nitrilimines – synthesis of pyrazolines and pyrazoles. Chemistry of Heterocyclic Compounds. 57(11). 1107–1115. 3 indexed citations
5.
Тимошенко, Вадим М., et al.. (2019). 3-Functional substituted 4-trifluoromethyl tetrahydrothiophenes via [3 + 2]-cycloaddition reactions. Journal of Sulfur Chemistry. 40(6). 629–640. 5 indexed citations
6.
Shermolovich, Yuriy G., et al.. (2018). Trifluoromethylated Thiopyranoid Glycals: Synthesis and Ferrier (I) Type Reactions. European Journal of Organic Chemistry. 2018(40). 5570–5584. 3 indexed citations
7.
Тимошенко, Вадим М., et al.. (2014). 2-Oxo-2-polyfluoroalkylethane-1-sulfones and -sulfamides in the three-component reactions leading to pyrimidine derivatives. ARKIVOC. 2014(6). 86–107. 1 indexed citations
8.
Тимошенко, Вадим М., et al.. (2013). β-Keto sulfones: preparation and application in organic synthesis. Journal of Sulfur Chemistry. 35(2). 188–236. 95 indexed citations
9.
Тимошенко, Вадим М., et al.. (2013). Synthesis of Fluorinated Cyclobutenes Based on β‑Polyfluoroalkyl β‐Keto Sulfones, Sulfamides, and Phosphonates. Heteroatom Chemistry. 24(5). 437–441.
10.
Тимошенко, Вадим М., et al.. (2012). Synthesis of polyfluoroalkyl containing thiopyran derivatives and their applications in fluoroorganic chemistry. Journal of Fluorine Chemistry. 137. 6–21. 16 indexed citations
11.
Тимошенко, Вадим М., et al.. (2011). Thiophilic nucleophilic trifluoromethylation of α-substituted dithioesters. Access to S-trifluoromethyl ketene dithioacetals and their reactivity with electrophilic species. Journal of Fluorine Chemistry. 134. 164–171. 12 indexed citations
12.
Тимошенко, Вадим М., et al.. (2010). 2-Polyfluoroalkyl thiopyrylium salts: synthesis and reactions with nucleophiles. Tetrahedron Letters. 51(49). 6406–6409. 7 indexed citations
13.
Тимошенко, Вадим М. & Charles Portella. (2009). Domino nucleophilic trifluoromethylations of alkyl perfluorodithioesters. Journal of Fluorine Chemistry. 130(6). 586–590. 11 indexed citations
14.
Тимошенко, Вадим М., et al.. (2007). Multi-step reactions of N-monosubstituted (polyfluoroalkane)thioamides with alkyllithium reagents. Journal of Fluorine Chemistry. 128(7). 703–709. 7 indexed citations
15.
Grellepois, Fabienne, Вадим М. Тимошенко, Yuriy G. Shermolovich, & Charles Portella. (2006). New Three-Step Domino Reaction, “Thiophilic Addition−β-Elimination of Fluoride−[3,3] Sigmatropic Rearrangement”:  Synthesis of α-Allylic and α,α-Bis(allylic) α-Trifluoromethyl Dithioesters. Organic Letters. 8(19). 4323–4326. 15 indexed citations
16.
Тимошенко, Вадим М., et al.. (2006). Chlorination and Oxidation of 4‐Fluoro‐5‐tetrafluoroethyl‐1,2‐dithiole‐3‐thione.. ChemInform. 37(40). 1 indexed citations
17.
Тимошенко, Вадим М., Jean‐Philippe Bouillon, Alexander N. Chernega, Yuriy G. Shermolovich, & Charles Portella. (2003). Synthesis of a New Polyfluorinated Vinylogue of Tetrathiafulvalene through 1,3‐Dipolar Cycloaddition of Ethyl β‐Bromoperfluorodithiocrotonate with Dimethyl Acetylenedicarboxylate. Chemistry - A European Journal. 9(18). 4324–4329. 6 indexed citations
18.
Тимошенко, Вадим М., et al.. (2003). Synthesis and some chemical properties of the 6-arylsulfonyl-6-polyfluoroalkanoyl-5,6-dihydro-2H-thiins—new fluorine-containing ketones. Journal of Fluorine Chemistry. 123(2). 197–205. 3 indexed citations
19.
Тимошенко, Вадим М., et al.. (2002). Reaction of 1H,1H,ωH-Perfluoroalkyl Sulfones with α-Phenylglycine Methyl Ester. Russian Journal of Organic Chemistry. 38(5). 756–758. 1 indexed citations
20.
Roesky, Herbert W., et al.. (1995). N‐alkyl‐C‐polyfluoroalkyl‐C‐chlorosulfinimides RFC(Cl)SNR. Heteroatom Chemistry. 6(1). 9–13. 4 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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