Andriy V. Tymtsunik

498 total citations
26 papers, 397 citations indexed

About

Andriy V. Tymtsunik is a scholar working on Organic Chemistry, Molecular Biology and Pharmaceutical Science. According to data from OpenAlex, Andriy V. Tymtsunik has authored 26 papers receiving a total of 397 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Organic Chemistry, 14 papers in Molecular Biology and 5 papers in Pharmaceutical Science. Recurrent topics in Andriy V. Tymtsunik's work include Chemical Synthesis and Analysis (14 papers), Asymmetric Synthesis and Catalysis (9 papers) and Synthetic Organic Chemistry Methods (7 papers). Andriy V. Tymtsunik is often cited by papers focused on Chemical Synthesis and Analysis (14 papers), Asymmetric Synthesis and Catalysis (9 papers) and Synthetic Organic Chemistry Methods (7 papers). Andriy V. Tymtsunik collaborates with scholars based in Ukraine, Germany and United States. Andriy V. Tymtsunik's co-authors include Oleksandr O. Grygorenko, Igor V. Komarov, Ilija Čorić, Markus Leutzsch, Philip S. J. Kaib, Manuel van Gemmeren, Subhas Chandra Pan, Benjamin List, Anna Lee and Pavel K. Mykhailiuk and has published in prestigious journals such as Angewandte Chemie International Edition, The Journal of Organic Chemistry and RSC Advances.

In The Last Decade

Andriy V. Tymtsunik

26 papers receiving 393 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Andriy V. Tymtsunik Ukraine 12 360 92 74 68 18 26 397
Christopher A. Reiher United States 6 338 0.9× 95 1.0× 52 0.7× 67 1.0× 11 0.6× 9 405
Marcos Escolano Spain 11 371 1.0× 51 0.6× 40 0.5× 56 0.8× 19 1.1× 20 402
Janice E. Sieser United States 12 520 1.4× 100 1.1× 80 1.1× 102 1.5× 26 1.4× 16 574
Deidre L. Sandrock United States 10 785 2.2× 114 1.2× 49 0.7× 96 1.4× 21 1.2× 11 832
Patrick Q Kelly United States 6 367 1.0× 95 1.0× 36 0.5× 47 0.7× 23 1.3× 6 423
Matthew M. Zhao United States 11 449 1.2× 168 1.8× 77 1.0× 71 1.0× 23 1.3× 15 554
Aleksandr Denisenko Ukraine 10 526 1.5× 70 0.8× 121 1.6× 34 0.5× 25 1.4× 13 574
John M. Ovian United States 9 326 0.9× 64 0.7× 42 0.6× 60 0.9× 12 0.7× 9 346
Julien Brioche France 11 414 1.1× 84 0.9× 56 0.8× 60 0.9× 22 1.2× 17 469
Hyelee Lee United States 6 437 1.2× 131 1.4× 20 0.3× 72 1.1× 33 1.8× 10 491

Countries citing papers authored by Andriy V. Tymtsunik

Since Specialization
Citations

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

Fields of papers citing papers by Andriy V. Tymtsunik

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Andriy V. Tymtsunik. 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 Andriy V. Tymtsunik. The network helps show where Andriy V. Tymtsunik may publish in the future.

Co-authorship network of co-authors of Andriy V. Tymtsunik

This figure shows the co-authorship network connecting the top 25 collaborators of Andriy V. Tymtsunik. A scholar is included among the top collaborators of Andriy V. Tymtsunik 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 Andriy V. Tymtsunik. Andriy V. Tymtsunik 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.
Radchenko, Dmytro S., et al.. (2020). Cyclopropyl boronic derivatives in parallel synthesis of sp3-enriched compound libraries. Monatshefte für Chemie - Chemical Monthly. 151(6). 953–962. 5 indexed citations
2.
Tymtsunik, Andriy V., et al.. (2020). 3‐Carboxy‐/3‐Aminobicyclo[1.1.1]pentane‐Derived Sulfonamides and Sulfonyl Fluorides – Advanced Bifunctional Reagents for Organic Synthesis and Drug Discovery. European Journal of Organic Chemistry. 2020(15). 2210–2216. 12 indexed citations
3.
Tymtsunik, Andriy V., et al.. (2020). Multigram Synthesis of Heterabicyclo[n.1.0]alkan‐1‐yl Trifluoroborates. European Journal of Organic Chemistry. 2021(47). 6551–6560. 10 indexed citations
4.
Vashchenko, Bohdan V., et al.. (2020). Photochemical [2 + 2] Cycloaddition of Alkenyl Boronic Derivatives: An Entry into 3-Azabicyclo[3.2.0]heptane Scaffold. The Journal of Organic Chemistry. 85(9). 5927–5940. 32 indexed citations
5.
Grygorenko, Oleksandr O., et al.. (2020). Cycloadditions of Alkenylboronic Derivatives. Synthesis. 52(19). 2761–2780. 22 indexed citations
6.
Tymtsunik, Andriy V., et al.. (2019). Multigram Synthesis and C−C/C−N Couplings of Functionalized 1,2‐Disubstituted Cyclopropyltrifluoroborates. Advanced Synthesis & Catalysis. 361(23). 5428–5439. 13 indexed citations
7.
Serhiichuk, Dmytro, et al.. (2019). The Boron‐Wittig Olefination of Aldehydes and Ketones with Bis[(pinacolato)boryl]methane: an Extended Reaction Scope. European Journal of Organic Chemistry. 2019(33). 5624–5635. 17 indexed citations
8.
Tymtsunik, Andriy V., et al.. (2018). Preparation of 5-Fluoropyrazoles from Pyrazoles and N-Fluorobenzenesulfonimide (NFSI). The Journal of Organic Chemistry. 83(6). 3265–3274. 9 indexed citations
9.
Grygorenko, Oleksandr O., et al.. (2018). Synthesis of 2-Azabicyclo[n.2.0]alkane-Derived Building Blocks. Synthesis. 50(10). 1973–1978. 4 indexed citations
10.
Tymtsunik, Andriy V., et al.. (2017). O-(α-Phenylethyl)hydroxylamine as a ‘chiral ammonia equivalent’: synthesis and resolution of 5-oxopyrrolidine- and 6-oxopiperidine-3-carboxylic acids. Tetrahedron Asymmetry. 28(12). 1817–1822. 2 indexed citations
11.
Tymtsunik, Andriy V., et al.. (2017). Bicyclo[1.1.1]pentane‐Derived Building Blocks for Click Chemistry. European Journal of Organic Chemistry. 2017(43). 6450–6456. 19 indexed citations
12.
Mikhalyova, Elena A., Sergey V. Kolotilov, Mat­thias Zeller, et al.. (2016). Sorption discrimination between secondary alcohol enantiomers by chiral alkyl-dicarboxylate MOFs. RSC Advances. 6(96). 93707–93714. 9 indexed citations
13.
Tymtsunik, Andriy V., et al.. (2016). Intramolecular functional group differentiation as a strategy for the synthesis of bridged bicyclic β-amino acids. RSC Advances. 6(27). 22737–22748. 12 indexed citations
14.
Tymtsunik, Andriy V., et al.. (2015). Synthesis of racemic and enantiopure 3,4-methanonipecotic acid. Tetrahedron Asymmetry. 26(21-22). 1268–1272. 2 indexed citations
15.
Grygorenko, Oleksandr O., et al.. (2015). Synthesis of a 2,5-Diazabicyclo[2.2.1]heptane-Derived α,β-Diamino Acid. Synthesis. 47(8). 1123–1130. 6 indexed citations
16.
Artamonov, Oleksiy S., et al.. (2014). The synthesis of a 2-azabicyclo[3.1.0]hexane by rearrangement of a spirocyclic epoxide. Tetrahedron Letters. 55(43). 5970–5972. 6 indexed citations
17.
List, Benjamin, Ilija Čorić, Oleksandr O. Grygorenko, et al.. (2013). The Catalytic Asymmetric α‐Benzylation of Aldehydes. Angewandte Chemie International Edition. 53(1). 282–285. 72 indexed citations
18.
Grygorenko, Oleksandr O., et al.. (2013). Gram-Scale Synthesis of 3,5-Methanonipecotic Acid, a Nonchiral Bicyclic β-Amino Acid. Synlett. 25(3). 355–358. 8 indexed citations
19.
List, Benjamin, Ilija Čorić, Oleksandr O. Grygorenko, et al.. (2013). Die katalytische asymmetrische α‐Benzylierung von Aldehyden. Angewandte Chemie. 126(1). 286–289. 24 indexed citations
20.
Tymtsunik, Andriy V., et al.. (2012). Synthesis of a novel Boc-protected cyclopropane-modified proline analogue. Tetrahedron Letters. 53(30). 3847–3849. 11 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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