Вадим Э. Матулис

1.0k total citations
51 papers, 863 citations indexed

About

Вадим Э. Матулис is a scholar working on Organic Chemistry, Inorganic Chemistry and Oncology. According to data from OpenAlex, Вадим Э. Матулис has authored 51 papers receiving a total of 863 indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Organic Chemistry, 8 papers in Inorganic Chemistry and 6 papers in Oncology. Recurrent topics in Вадим Э. Матулис's work include Coordination Chemistry and Organometallics (15 papers), Synthesis and Characterization of Heterocyclic Compounds (13 papers) and Synthesis of Tetrazole Derivatives (13 papers). Вадим Э. Матулис is often cited by papers focused on Coordination Chemistry and Organometallics (15 papers), Synthesis and Characterization of Heterocyclic Compounds (13 papers) and Synthesis of Tetrazole Derivatives (13 papers). Вадим Э. Матулис collaborates with scholars based in Belarus, France and Algeria. Вадим Э. Матулис's co-authors include Олег А. Ивашкевич, Yury S. Halauko, P.N. Gaponik, Florence Mongin, Thierry Roisnel, Alexander S. Lyakhov, Сергей В. Войтехович, Floris Chevallier, Vincent Dorcet and William Erb and has published in prestigious journals such as SHILAP Revista de lepidopterología, Chemistry - A European Journal and Tetrahedron.

In The Last Decade

Вадим Э. Матулис

49 papers receiving 857 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Вадим Э. Матулис Belarus 19 763 128 117 85 76 51 863
Wojciech P. Ozimiński Poland 17 704 0.9× 157 1.2× 138 1.2× 20 0.2× 46 0.6× 53 897
Aida I. Samigullina Russia 13 345 0.5× 108 0.8× 188 1.6× 13 0.2× 60 0.8× 84 543
M. Ángeles García Spain 16 385 0.5× 111 0.9× 144 1.2× 13 0.2× 30 0.4× 43 680
Irina V. Sterkhova Russia 15 478 0.6× 201 1.6× 184 1.6× 13 0.2× 48 0.6× 125 763
V. K. Bel’skii Russia 11 197 0.3× 115 0.9× 114 1.0× 26 0.3× 54 0.7× 78 347
O.A. Egorova Russia 10 193 0.3× 87 0.7× 233 2.0× 24 0.3× 29 0.4× 21 478
Harald Brand Germany 11 230 0.3× 167 1.3× 64 0.5× 22 0.3× 13 0.2× 18 397
M. RIVIERE‐BAUDET France 15 790 1.0× 585 4.6× 105 0.9× 19 0.2× 24 0.3× 76 909
Б. И. Бузыкин Russia 13 467 0.6× 73 0.6× 127 1.1× 8 0.1× 58 0.8× 81 587
Lev R. Ryzhkov United States 9 377 0.5× 106 0.8× 47 0.4× 26 0.3× 14 0.2× 15 469

Countries citing papers authored by Вадим Э. Матулис

Since Specialization
Citations

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

Fields of papers citing papers by Вадим Э. Матулис

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Вадим Э. Матулис

This figure shows the co-authorship network connecting the top 25 collaborators of Вадим Э. Матулис. A scholar is included among the top collaborators of Вадим Э. Матулис 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 Э. Матулис. Вадим Э. Матулис 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.
Erb, William, Yury S. Halauko, Вадим Э. Матулис, et al.. (2024). Functionalisation of Chromane by Deprotonative Metallation. European Journal of Organic Chemistry. 27(34).
2.
Erb, William, Florence Mongin, Jean‐Pierre Hurvois, et al.. (2023). From ferrocene to decasubstituted enantiopure ferrocene-1,1′-disulfoxide derivatives. Dalton Transactions. 52(12). 3725–3737. 2 indexed citations
3.
Войтехович, Сергей В., Alexander S. Lyakhov, Ludmila S. Ivashkevich, et al.. (2022). 5‐Amino‐2‐isopropenyltetrazole and its Cupric Chloride Complex: Synthesis, Structure and Magnetism. Zeitschrift für anorganische und allgemeine Chemie. 648(22).
4.
Erb, William, Yury S. Halauko, Олег А. Ивашкевич, et al.. (2020). On the N ‐Arylation of Acetamide Using 2‐, 3‐ and 1’‐Substituted Iodoferrocenes**. European Journal of Inorganic Chemistry. 2021(4). 377–391. 5 indexed citations
5.
Demmer, Charles S., Floris Chevallier, Thierry Roisnel, et al.. (2018). Functionalization of Oxazolo[4,5‐b]pyrazines by Deprotometallation. European Journal of Organic Chemistry. 2018(29). 3904–3913. 4 indexed citations
6.
Erb, William, Yury S. Halauko, Олег А. Ивашкевич, et al.. (2018). Fluoro- and Chloroferrocene: From 2- to 3-Substituted Derivatives. Organometallics. 37(14). 2207–2211. 35 indexed citations
7.
Bentabed‐Ababsa, Ghenia, A. Derdour, Floris Chevallier, et al.. (2015). Deproto-metallation of N-arylated pyrroles and indoles using a mixed lithium–zinc base and regioselectivity-computed CH acidity relationship. Beilstein Journal of Organic Chemistry. 11. 1475–1485. 18 indexed citations
8.
Bentabed‐Ababsa, Ghenia, Floris Chevallier, Stéphanie Philippot, et al.. (2015). Deprotometalation–iodolysis and computed CH acidity of 1,2,3- and 1,2,4-triazoles. Application to the synthesis of resveratrol analogues. Bioorganic & Medicinal Chemistry. 23(19). 6355–6363. 26 indexed citations
9.
10.
Chevallier, Floris, Thierry Roisnel, Vincent Dorcet, et al.. (2013). Deproto-metallation using a mixed lithium–zinc base and computed CH acidity of 1-aryl 1H-benzotriazoles and 1-aryl 1H-indazoles. Organic & Biomolecular Chemistry. 12(9). 1475–1475. 31 indexed citations
11.
Chevallier, Floris, Thomas Blin, Thierry Roisnel, et al.. (2012). Deproto-metallation and computed CH acidity of 2-aryl-1,2,3-triazoles. Organic & Biomolecular Chemistry. 10(25). 4878–4878. 32 indexed citations
12.
13.
Chevallier, Floris, Yury S. Halauko, Ibrahim F. Nassar, et al.. (2011). N-aryl pyrazoles: DFT calculations of CH acidity and deprotonative metallation using a combination of lithium and zinc amides. Organic & Biomolecular Chemistry. 9(12). 4671–4671. 48 indexed citations
14.
15.
Halauko, Yury S., et al.. (2010). DFT calculations of CH acidity of substituted triazoles and experimental study of their ability to undergo mercuration. Tetrahedron. 66(19). 3415–3420. 17 indexed citations
16.
Ивашкевич, Олег А., et al.. (2009). Selective synthesis of 1,3-dialkyl-4-nitro-1,2,3-triazolium salts from 1-alkyl-4-nitro-1,2,3-triazoles and dialkyl sulfates. Chemistry of Heterocyclic Compounds. 45(10). 1218–1225. 3 indexed citations
17.
Матулис, Вадим Э., Yury S. Halauko, Олег А. Ивашкевич, & P.N. Gaponik. (2009). CH acidity of five-membered nitrogen-containing heterocycles: DFT investigation. Journal of Molecular Structure THEOCHEM. 909(1-3). 19–24. 42 indexed citations
18.
Lyakhov, Alexander S., Вадим Э. Матулис, P.N. Gaponik, Сергей В. Войтехович, & Олег А. Ивашкевич. (2007). 1-Vinyl-5-amino-1H-tetrazole: X-ray molecular and crystal structures and quantum-chemical DFT calculations. Journal of Molecular Structure. 876(1-3). 260–267. 20 indexed citations
19.
Матулис, Вадим Э., Alexander S. Lyakhov, P.N. Gaponik, Сергей В. Войтехович, & Олег А. Ивашкевич. (2003). 1,5-Diamino-1H-1,2,3,4-tetrazolium picrate: X-ray molecular and crystal structures and ab initio MO calculations. Journal of Molecular Structure. 649(3). 309–314. 46 indexed citations
20.
Lyakhov, Alexander S., et al.. (2003). Two derivatives of 5-aminotetrazole: 5-amino-1-phenyltetrazole and 5-amino-1-(1-naphthyl)tetrazole. Acta Crystallographica Section C Crystal Structure Communications. 59(12). o690–o693. 15 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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