Algirdas Šačkus

1.5k total citations
126 papers, 1.2k citations indexed

About

Algirdas Šačkus is a scholar working on Organic Chemistry, Materials Chemistry and Molecular Biology. According to data from OpenAlex, Algirdas Šačkus has authored 126 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 99 papers in Organic Chemistry, 29 papers in Materials Chemistry and 28 papers in Molecular Biology. Recurrent topics in Algirdas Šačkus's work include Synthesis and Biological Evaluation (24 papers), Synthesis and biological activity (16 papers) and Synthesis and Reactivity of Heterocycles (13 papers). Algirdas Šačkus is often cited by papers focused on Synthesis and Biological Evaluation (24 papers), Synthesis and biological activity (16 papers) and Synthesis and Reactivity of Heterocycles (13 papers). Algirdas Šačkus collaborates with scholars based in Lithuania, Austria and Czechia. Algirdas Šačkus's co-authors include Wolfgang Hölzer, Eglė Arbačiauskienė, Arnaud Tatibouët, Patrick Rollin, Jolanta Rousseau, Asta Žukauskaitė, Sven Mangelinckx, Norbert De Kimpe, Vytautas Getautis and Cyril Rousseau and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Physical Chemistry C and Physical Chemistry Chemical Physics.

In The Last Decade

Algirdas Šačkus

117 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Algirdas Šačkus Lithuania 19 847 239 195 96 91 126 1.2k
Stéphane Massip France 23 1.2k 1.4× 414 1.7× 219 1.1× 56 0.6× 105 1.2× 93 1.6k
Mohammad Rahimizadeh Iran 23 1.3k 1.5× 362 1.5× 194 1.0× 104 1.1× 23 0.3× 124 1.6k
Hyunseok Kim South Korea 25 1.2k 1.5× 334 1.4× 119 0.6× 65 0.7× 72 0.8× 50 1.6k
Annamaria Deagostino Italy 24 976 1.2× 166 0.7× 260 1.3× 101 1.1× 37 0.4× 94 1.6k
Jean‐Paul Quintard France 24 1.3k 1.5× 299 1.3× 171 0.9× 46 0.5× 40 0.4× 95 1.5k
Cheol‐Hong Cheon South Korea 22 1.1k 1.3× 318 1.3× 107 0.5× 62 0.6× 39 0.4× 67 1.4k
Kentaro Okano Japan 24 1.6k 1.9× 283 1.2× 94 0.5× 118 1.2× 24 0.3× 120 1.9k
Toshiyuki Iwai Japan 17 625 0.7× 131 0.5× 91 0.5× 38 0.4× 121 1.3× 45 799
Alba Díaz‐Rodríguez United Kingdom 18 621 0.7× 581 2.4× 109 0.6× 200 2.1× 36 0.4× 32 1.2k
Cyrille Sabot France 21 1.1k 1.3× 472 2.0× 82 0.4× 61 0.6× 33 0.4× 57 1.5k

Countries citing papers authored by Algirdas Šačkus

Since Specialization
Citations

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

Fields of papers citing papers by Algirdas Šačkus

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Algirdas Šačkus. 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 Algirdas Šačkus. The network helps show where Algirdas Šačkus may publish in the future.

Co-authorship network of co-authors of Algirdas Šačkus

This figure shows the co-authorship network connecting the top 25 collaborators of Algirdas Šačkus. A scholar is included among the top collaborators of Algirdas Šačkus 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 Algirdas Šačkus. Algirdas Šačkus 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.
Řezníčková, Eva, et al.. (2024). Synthesis and photodynamic activity of new 5‐[(E)‐2‐(3‐alkoxy‐1‐phenyl‐1H‐pyrazol‐4‐yl)ethenyl]‐2‐phenyl‐3H‐indoles. Archiv der Pharmazie. 357(10). e2400282–e2400282. 2 indexed citations
3.
Belyakov, Sergey, et al.. (2024). Multicomponent Synthesis of New Fluorescent Boron Complexes Derived from 3-Hydroxy-1-phenyl-1H-pyrazole-4-carbaldehyde. Molecules. 29(14). 3432–3432. 1 indexed citations
4.
Belyakov, Sergey, et al.. (2024). Synthesis and characterization of novel biheterocyclic compounds from 3‐alkoxy‐1H‐pyrazole‐4‐carbaldehydes via multicomponent reactions. Journal of Heterocyclic Chemistry. 61(6). 927–947. 3 indexed citations
5.
Žukauskaitė, Asta, et al.. (2024). 3-(2-Chloroethoxy)-1-(4-methoxyphenyl)-1H-pyrazole-4-carbaldehyde. SHILAP Revista de lepidopterología. 2024(1). M1782–M1782. 1 indexed citations
6.
Pukalskienė, Milda, et al.. (2023). Glycerol‐1,2‐carbonate: A mild reagent for the N‐glycerylation of pyrazolecarboxylates. Journal of Heterocyclic Chemistry. 61(2). 305–323. 3 indexed citations
7.
Žukauskaitė, Asta, Iñigo Saiz‐Fernández, Chao Zhang, et al.. (2023). New PEO-IAA-Inspired Anti-Auxins: Synthesis, Biological Activity, and Possible Application in Hemp (Cannabis Sativa L.) Micropropagation. Journal of Plant Growth Regulation. 42(12). 7547–7563. 8 indexed citations
8.
Žukauskaitė, Asta, et al.. (2023). Synthesis and Characterization of New Pyrano[2,3-c]pyrazole Derivatives as 3-Hydroxyflavone Analogues. Molecules. 28(18). 6599–6599. 2 indexed citations
9.
Šačkus, Algirdas, et al.. (2023). Total synthesis of lamellarin G trimethyl ether through enaminone cyclocondensation. Organic & Biomolecular Chemistry. 21(29). 5997–6007. 6 indexed citations
10.
González, Gabriel, Šárka Štěpánková, Marek Zatloukal, et al.. (2023). Synthesis and neuroprotective activity of 3‐aryl‐3‐azetidinyl acetic acid methyl ester derivatives. Archiv der Pharmazie. 356(12). e2300378–e2300378.
11.
12.
Sløk, Frank A., et al.. (2022). Regioselective synthesis of methyl 5-(N-Boc-cycloaminyl)-1,2-oxazole-4-carboxylates as new amino acid-like building blocks. Beilstein Journal of Organic Chemistry. 18. 102–109. 4 indexed citations
13.
Luisi, Renzo, et al.. (2022). Synthesis and Characterization of Novel Heterocyclic Chalcones from 1-Phenyl-1H-pyrazol-3-ol. Molecules. 27(12). 3752–3752. 12 indexed citations
14.
Arbačiauskienė, Eglė, et al.. (2021). Convenient Synthesis of Pyrazolo[4′,3′:5,6]pyrano[4,3-c][1,2]oxazoles via Intramolecular Nitrile Oxide Cycloaddition. Molecules. 26(18). 5604–5604. 7 indexed citations
15.
Voller, Jiří, et al.. (2021). Synthesis of 5‐[(1H‐indol‐3‐yl)methyl]‐1,3,4‐oxadiazole‐2(3H)‐thiones and their protective activity against oxidative stress. Archiv der Pharmazie. 354(6). e2100001–e2100001. 4 indexed citations
16.
Sløk, Frank A., et al.. (2021). Methyl 2-Amino-4-[1-(tert-butoxycarbonyl)azetidin-3-yl]-1,3-selenazole-5-carboxylate. SHILAP Revista de lepidopterología. 2021(2). M1207–M1207. 4 indexed citations
17.
Arbačiauskienė, Eglė, et al.. (2021). Synthesis and Characterization of Novel Methyl (3)5-(N-Boc-piperidinyl)-1H-pyrazole-4-carboxylates. Molecules. 26(13). 3808–3808. 6 indexed citations
18.
Žukauskaitė, Asta, et al.. (2020). 3,3,3′,3′-Tetramethyl-2,2′-diphenyl-3H,3′H-5,5′-biindole. SHILAP Revista de lepidopterología. 2020(3). M1146–M1146.
19.
Žukauskaitė, Asta, Karel Doležal, Miroslav Strnad, et al.. (2019). Synthesis and anthelmintic activity of benzopyrano[2,3-c]pyrazol-4(2H)-one derivatives. Molecular Diversity. 24(4). 1025–1042. 16 indexed citations
20.
Arbačiauskienė, Eglė, et al.. (2018). On the Tautomerism of N-Substituted Pyrazolones: 1,2-Dihydro-3H-pyrazol-3-ones versus 1H-Pyrazol-3-ols. Molecules. 23(1). 129–129. 18 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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