Thomas Oeser

1.4k total citations
65 papers, 1.2k citations indexed

About

Thomas Oeser is a scholar working on Organic Chemistry, Materials Chemistry and Inorganic Chemistry. According to data from OpenAlex, Thomas Oeser has authored 65 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Organic Chemistry, 9 papers in Materials Chemistry and 7 papers in Inorganic Chemistry. Recurrent topics in Thomas Oeser's work include Synthesis and Properties of Aromatic Compounds (13 papers), Catalytic Alkyne Reactions (9 papers) and Organometallic Complex Synthesis and Catalysis (7 papers). Thomas Oeser is often cited by papers focused on Synthesis and Properties of Aromatic Compounds (13 papers), Catalytic Alkyne Reactions (9 papers) and Organometallic Complex Synthesis and Catalysis (7 papers). Thomas Oeser collaborates with scholars based in Germany, Saudi Arabia and China. Thomas Oeser's co-authors include Thomas J. J. Müller, Frank Röminger, A. Stephen K. Hashmi, Matthias Rudolph, Hermann Irngartinger, Alexei S. Karpov, Xianhai Tian, Lina Song, Alexandru Rotaru and Rolf Gleiter and has published in prestigious journals such as Angewandte Chemie International Edition, Chemical Communications and Nature Chemistry.

In The Last Decade

Thomas Oeser

63 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thomas Oeser Germany 17 977 156 155 144 73 65 1.2k
Jürgen Voß Germany 17 859 0.9× 151 1.0× 144 0.9× 105 0.7× 83 1.1× 133 1.1k
S. Shaun Murphree United States 18 1.1k 1.1× 156 1.0× 84 0.5× 110 0.8× 47 0.6× 36 1.3k
Yoshiaki Sugihara Japan 18 962 1.0× 78 0.5× 167 1.1× 81 0.6× 36 0.5× 96 1.1k
Zoia Voïtenko Ukraine 16 632 0.6× 158 1.0× 180 1.2× 85 0.6× 37 0.5× 112 829
Susana Rojas‐Lima Mexico 16 484 0.5× 120 0.8× 124 0.8× 167 1.2× 87 1.2× 56 682
Bipin Pandey India 18 600 0.6× 107 0.7× 215 1.4× 134 0.9× 48 0.7× 59 853
Shi‐Hui Wu China 18 984 1.0× 221 1.4× 250 1.6× 207 1.4× 31 0.4× 50 1.2k
Junes Ipaktschi Germany 22 1.1k 1.1× 171 1.1× 151 1.0× 224 1.6× 106 1.5× 81 1.2k
Toshio Itahara Japan 19 870 0.9× 184 1.2× 137 0.9× 118 0.8× 82 1.1× 89 1.1k
Zhihai Ke Hong Kong 20 985 1.0× 155 1.0× 220 1.4× 406 2.8× 61 0.8× 48 1.4k

Countries citing papers authored by Thomas Oeser

Since Specialization
Citations

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

Fields of papers citing papers by Thomas Oeser

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas Oeser

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas Oeser. A scholar is included among the top collaborators of Thomas Oeser 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 Thomas Oeser. Thomas Oeser 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.
Shi, Hongwei, Matthias Rudolph, Jun Li, et al.. (2025). Bidentate N-ligand-assisted gold redox catalysis with hydrogen peroxide. Nature Chemistry. 17(6). 822–834. 1 indexed citations
2.
3.
Rudolph, Matthias, et al.. (2023). Cascade Reactions of Aryl‐Substituted Terminal Alkynes Involving in Situ‐Generated α‐Imino Gold Carbenes. Angewandte Chemie International Edition. 63(5). e202313738–e202313738. 18 indexed citations
4.
Röminger, Frank, et al.. (2021). Quinoxalinophenanthrophenazine Based Cruciforms. European Journal of Organic Chemistry. 2021(34). 4816–4823. 6 indexed citations
5.
Nie, Yong, Jinling Miao, Hubert Wadepohl, et al.. (2013). Syntheses and Characterization of o‐Carboranes Containing Fused exo‐Polyhedral Di‐ and Triboraheterocycles. Zeitschrift für anorganische und allgemeine Chemie. 639(7). 1188–1193. 12 indexed citations
6.
Müller, Thomas J. J., et al.. (2008). Rapid One-Pot Synthesis of Antiparasitic Quinolines Based upon the Microwave-Assisted Coupling-Isomerization Reaction (MACIR). Synlett. 2008(3). 359–362. 6 indexed citations
7.
8.
Oeser, Thomas, et al.. (2008). Phenothiazinophanes: Synthesis, Structure, and Intramolecular Electronic Communication. Organic Letters. 10(13). 2797–2800. 34 indexed citations
9.
10.
Kovbasyuk, Larisa, et al.. (2006). Zn2+ dependent DNA binders based on terminally modified peptide nucleic acids. Bioorganic & Medicinal Chemistry Letters. 16(10). 2781–2785. 7 indexed citations
11.
Piestert, Frederik, et al.. (2005). Easy one-pot synthesis of new dppm-type linkers for immobilizations. Chemical Communications. 1481–1483. 30 indexed citations
12.
Pritzkow, Hans, et al.. (2005). Biphenyl derived oxovanadium(IV) and copper(II) salen-type complexes – structure and redox tuning. Journal of Inorganic Biochemistry. 99(5). 1230–1237. 19 indexed citations
13.
Karpov, Alexei S., Eugen Merkul, Thomas Oeser, & Thomas J. J. Müller. (2005). A novel one-pot three-component synthesis of 3-halofurans and sequential Suzuki coupling. Chemical Communications. 2581–2581. 65 indexed citations
14.
Karpov, Alexei S., Thomas Oeser, & Thomas J. J. Müller. (2004). A novel one-pot four-component access to tetrahydro-β-carbolines by a coupling-amination-aza-annulation-Pictet–Spengler sequence (CAAPS). Chemical Communications. 1502–1503. 49 indexed citations
15.
Balalaie, Saeed, et al.. (2003). Inside Protonation of 1,8‐Diazabicyclo[6.6.n]alka‐4,11‐diynes. European Journal of Organic Chemistry. 2003(17). 3378–3381. 5 indexed citations
16.
Werz, Daniel B., et al.. (2003). Modes of Reactivity of Cyclic Diynes: Probing the syn/anti Selectivity of Tetrathiacycloalkadiynes and Mono(alkyne)cobalt Complexes. European Journal of Inorganic Chemistry. 2003(6). 1099–1112. 12 indexed citations
17.
Schmitt, H., H. Zimmermann, U. Haeberlen, et al.. (2002). Location of the H atoms in ammonium persulphate by deuteron NMR. Verification by X-ray diffraction. Acta Crystallographica Section B Structural Science. 58(5). 760–769. 5 indexed citations
18.
Irngartinger, Hermann, et al.. (1999). Determination of the Electron Density Distribution in the Bonds of a Fullerene Derivative by High-Resolution X-Ray Structure Analysis. Angewandte Chemie International Edition. 38(9). 1279–1281. 12 indexed citations
19.
Gleiter, Rolf, et al.. (1998). Synthesis and Structural Properties of Bridged 1,8-Diazacyclotetradeca-4,11-diynes. European Journal of Organic Chemistry. 1998(12). 2803–2809. 8 indexed citations
20.
Weinges, Klaus, et al.. (1990). Synthese von enantiomerenreinem (−)‐Hypnophilin. Angewandte Chemie. 102(6). 685–687. 6 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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