V. Štěrba

782 total citations
140 papers, 553 citations indexed

About

V. Štěrba is a scholar working on Organic Chemistry, Physical and Theoretical Chemistry and Molecular Biology. According to data from OpenAlex, V. Štěrba has authored 140 papers receiving a total of 553 indexed citations (citations by other indexed papers that have themselves been cited), including 129 papers in Organic Chemistry, 39 papers in Physical and Theoretical Chemistry and 23 papers in Molecular Biology. Recurrent topics in V. Štěrba's work include Chemical Reaction Mechanisms (84 papers), Synthesis and Characterization of Heterocyclic Compounds (38 papers) and Chemical Reactions and Mechanisms (36 papers). V. Štěrba is often cited by papers focused on Chemical Reaction Mechanisms (84 papers), Synthesis and Characterization of Heterocyclic Compounds (38 papers) and Chemical Reactions and Mechanisms (36 papers). V. Štěrba collaborates with scholars based in India, Czechia and Slovakia. V. Štěrba's co-authors include Jaromír Kaválek, V. Macháček, Jiří Hanusek, Miloš Sedlák, Antonı́n Lyčka, M. Večeřa, Krisztina Valter, Josef Jirman, Norbert Hoffmann and P. Šimůnek and has published in prestigious journals such as Journal of Applied Polymer Science, Organic & Biomolecular Chemistry and European Journal of Organic Chemistry.

In The Last Decade

V. Štěrba

122 papers receiving 478 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
V. Štěrba India 11 482 117 114 76 39 140 553
A. J. Waring United Kingdom 10 299 0.6× 138 1.2× 52 0.5× 69 0.9× 38 1.0× 41 456
Toshikazu Nagai Japan 13 593 1.2× 52 0.4× 124 1.1× 74 1.0× 62 1.6× 115 682
Andrew Streitwieser United States 8 449 0.9× 86 0.7× 93 0.8× 101 1.3× 43 1.1× 9 586
ALJ Beckwith 14 507 1.1× 100 0.9× 71 0.6× 66 0.9× 34 0.9× 36 623
Manfred Schulz Germany 13 548 1.1× 100 0.9× 83 0.7× 66 0.9× 40 1.0× 91 655
H. G. O. Becker Germany 14 478 1.0× 93 0.8× 169 1.5× 43 0.6× 37 0.9× 84 602
G. C. Robinson Slovenia 6 393 0.8× 94 0.8× 161 1.4× 145 1.9× 30 0.8× 6 546
Peter A. Wriede United States 8 322 0.7× 71 0.6× 58 0.5× 51 0.7× 52 1.3× 8 388
Claude Marzin France 12 436 0.9× 64 0.5× 62 0.5× 76 1.0× 22 0.6× 18 552
Koji Aigami Japan 11 301 0.6× 92 0.8× 61 0.5× 87 1.1× 27 0.7× 40 462

Countries citing papers authored by V. Štěrba

Since Specialization
Citations

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

Fields of papers citing papers by V. Štěrba

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of V. Štěrba

This figure shows the co-authorship network connecting the top 25 collaborators of V. Štěrba. A scholar is included among the top collaborators of V. Štěrba 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 V. Štěrba. V. Štěrba 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.
Hanusek, Jiří, et al.. (2004). Influence of substitution on kinetics and mechanism of ring transformation of substituted S-[1-phenylpyrrolidin-2-on-3-yl]isothiuronium salts. Organic & Biomolecular Chemistry. 2(12). 1756–1763. 14 indexed citations
2.
Beier, Petr, et al.. (2004). Kinetics and mechanism of base-catalysed degradations of substituted aryl-N-hydroxycarbamates, their N-methyl and N-phenyl analogues. Organic & Biomolecular Chemistry. 2(4). 562–569. 8 indexed citations
3.
Štěrba, V., et al.. (2002). The base-catalysed cyclisation of phenyl N-(2-hydroxybenzyl)-N-methylcarbamates is concerted. Organic & Biomolecular Chemistry. 1(2). 415–421. 4 indexed citations
4.
Štěrba, V., et al.. (2000). Cyclization of Substituted Phenyl N-(2-Hydroxybenzyl)carbamates in Aprotic Solvents. Synthesis of 4H-1,3-Benzoxazin-2(3H)-ones. Collection of Czechoslovak Chemical Communications. 65(8). 1262–1272. 27 indexed citations
5.
Kaválek, Jaromír, et al.. (1999). Kinetics and mechanism of the reaction of substitutedO-benzoylbenzamidoximes with sodium methoxide in methanol. Journal of Physical Organic Chemistry. 12(8). 626–634. 3 indexed citations
6.
7.
Kaválek, Jaromír, V. Macháček, & V. Štěrba. (1994). Coupling Kinetics of 4-Sulfobenzenediazonium Ion with 2,4-Thiazolidinedione, Its 3-Methyl Derivative and 3-Methyl-5-isoxazolone. Collection of Czechoslovak Chemical Communications. 59(9). 2022–2028. 1 indexed citations
8.
Kaválek, Jaromír, V. Macháček, Miloš Sedlák, & V. Štěrba. (1992). Kinetics and Mechanism of Cyclization of N-(2-Methoxycarbonylphenyl)-N-methylsulfonamide to 1-Methyl-(1H)-2,1,3-benzothiadiazine-4(3H)-one-2,2-dioxide. Collection of Czechoslovak Chemical Communications. 57(6). 1282–1290. 1 indexed citations
9.
Macháček, V., et al.. (1986). Formation of the Meisenheimer spiro adduct of N-(2,4,6-trinitrophenyl)alanine methylamide and its rearrangement to 2-amino-N-methyl-N-(2,4,6-trinitrophenyl)propanamide. Collection of Czechoslovak Chemical Communications. 51(9). 1972–1985. 1 indexed citations
10.
Kaválek, Jaromír, et al.. (1986). Solvolysis kinetics of ethyl 3-ethoxy-3-iminopropanoate. Collection of Czechoslovak Chemical Communications. 51(3). 677–683. 2 indexed citations
11.
Kaválek, Jaromír, et al.. (1978). Hydrolysis kinetics of 4-amino-3-pentene-2-one and its N-substituted derivatives. Collection of Czechoslovak Chemical Communications. 43(10). 2732–2739. 4 indexed citations
12.
Kaválek, Jaromír, et al.. (1977). Kinetics and mechanism of formation of Meisenheimer complexes from methyl malonate and 2,4,6-trinitroanisole. Collection of Czechoslovak Chemical Communications. 42(10). 2928–2937. 3 indexed citations
13.
Kaválek, Jaromír, et al.. (1973). Kinetics and mechanism of reaction of 2-anilino-4,6-dichloro- and -difluoro-1,3,5-triazine with substituted anilines. Collection of Czechoslovak Chemical Communications. 38(7). 1935–1939.
14.
Hoffmann, Norbert & V. Štěrba. (1973). Kinetics and mechanism of hydrolysis of substituted N-(5-methylsalicylidene)anilines in acidity range H0 -4 to 4.5. Collection of Czechoslovak Chemical Communications. 38(7). 2091–2097. 2 indexed citations
15.
Štěrba, V., et al.. (1972). Rate and equilibrium constants of the system diazonium ion, syn, anti-diazohydroxide, syn, anti-diazotate. Collection of Czechoslovak Chemical Communications. 37(10). 3313–3327. 10 indexed citations
16.
Štěrba, V. & Krisztina Valter. (1972). Kinetics and mechanism of diazo coupling. XXI. Kinetics of diazo coupling with 1-naphthol and 1-methoxynaphthalene. Collection of Czechoslovak Chemical Communications. 37(1). 270–281. 1 indexed citations
17.
Hoffmann, Norbert, et al.. (1970). Kinetics of hydrolysis of substituted salicylideneanilines. Collection of Czechoslovak Chemical Communications. 35(5). 1387–1398. 8 indexed citations
18.
Štěrba, V., et al.. (1968). Kupplungskinetik der Benzoldiazoniumsalze mit 2-Naphthol-6-sulfonsäure. Collection of Czechoslovak Chemical Communications. 33(3). 894–900. 3 indexed citations
19.
Štěrba, V., et al.. (1967). Über die Bildung von Azoverbindungen bei der Zersetzungsreaktion aromatischer Diazoverbindungen in wässrigem Medium. Collection of Czechoslovak Chemical Communications. 32(4). 1462–1471. 4 indexed citations
20.
Štěrba, V., et al.. (1965). Oxydation von para-ständig substituierten Dimethylanilinderivaten. Collection of Czechoslovak Chemical Communications. 30(7). 2475–2477. 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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