Thomas Magauer

2.1k total citations
77 papers, 1.7k citations indexed

About

Thomas Magauer is a scholar working on Organic Chemistry, Pharmacology and Molecular Biology. According to data from OpenAlex, Thomas Magauer has authored 77 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 62 papers in Organic Chemistry, 31 papers in Pharmacology and 21 papers in Molecular Biology. Recurrent topics in Thomas Magauer's work include Synthetic Organic Chemistry Methods (38 papers), Microbial Natural Products and Biosynthesis (28 papers) and Marine Sponges and Natural Products (20 papers). Thomas Magauer is often cited by papers focused on Synthetic Organic Chemistry Methods (38 papers), Microbial Natural Products and Biosynthesis (28 papers) and Marine Sponges and Natural Products (20 papers). Thomas Magauer collaborates with scholars based in Austria, Germany and United States. Thomas Magauer's co-authors include Klaus Speck, Cedric L. Hugelshofer, Johann Mulzer, Harry J. Martin, Klaus Wurst, Andrew G. Myers, Konrad Tiefenbacher, Konstantin Karaghiosoff, Matthias Schmid and Péter Mayer and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Nature Communications.

In The Last Decade

Thomas Magauer

75 papers receiving 1.7k 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 Magauer Austria 24 1.4k 399 324 274 149 77 1.7k
Krishna P. Kaliappan India 24 2.1k 1.5× 447 1.1× 255 0.8× 263 1.0× 238 1.6× 85 2.2k
Hanfeng Ding China 26 1.6k 1.1× 472 1.2× 184 0.6× 301 1.1× 137 0.9× 86 1.9k
Dipakranjan Mal India 23 1.9k 1.3× 320 0.8× 259 0.8× 164 0.6× 160 1.1× 105 2.2k
Alexandros L. Zografos Greece 22 1.5k 1.0× 474 1.2× 254 0.8× 361 1.3× 115 0.8× 59 1.8k
Ken‐ichi Takao Japan 27 2.1k 1.5× 562 1.4× 422 1.3× 397 1.4× 99 0.7× 125 2.5k
Ian S. Young United States 14 1.9k 1.4× 428 1.1× 123 0.4× 205 0.7× 180 1.2× 24 2.1k
Jinghan Gui China 15 1.7k 1.2× 348 0.9× 168 0.5× 205 0.7× 374 2.5× 43 2.0k
Tanja Gaich Germany 23 1.9k 1.4× 371 0.9× 272 0.8× 223 0.8× 138 0.9× 59 2.2k
Masanori Nagatomo Japan 21 1.0k 0.7× 311 0.8× 136 0.4× 131 0.5× 86 0.6× 49 1.3k
Shuanhu Gao China 31 2.4k 1.7× 644 1.6× 434 1.3× 374 1.4× 180 1.2× 96 2.9k

Countries citing papers authored by Thomas Magauer

Since Specialization
Citations

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

Fields of papers citing papers by Thomas Magauer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas Magauer

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas Magauer. A scholar is included among the top collaborators of Thomas Magauer 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 Magauer. Thomas Magauer 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.
Kouklovsky, Cyrille, et al.. (2025). Total Synthesis of Dactyloquinone A and Spiroetherone A via a Metal‐Hydride Hydrogen Atom Transfer (MHAT) Process and a Quinol–Enedione Rearrangement. Angewandte Chemie International Edition. 64(25). e202505270–e202505270. 1 indexed citations
2.
Magauer, Thomas, Davide Mandelli, Jörg B. Schulz, et al.. (2025). Refining Ligand Poses in RNA/Ligand Complexes of Pharmaceutical Relevance: A Perspective by QM/MM Simulations and NMR Measurements. The Journal of Physical Chemistry Letters. 16(7). 1702–1708.
3.
4.
Wurst, Klaus, et al.. (2025). Non-enzymatic methylcyclization of alkenes. Nature Chemistry. 17(6). 904–910.
5.
Magauer, Thomas, et al.. (2024). Development of a Triethylborane-Mediated Giese Cyclization/Aldol Reaction Cascade for the Total Synthesis of Ganoapplanin. Synlett. 36(8). 915–920. 1 indexed citations
6.
Wurst, Klaus, et al.. (2024). Synthesis of C3-epi-virenose and anomerically activated derivatives. Tetrahedron Letters. 140. 155041–155041. 1 indexed citations
7.
Berger, J.M., et al.. (2024). Development of a Synthetic Platform for Ent‐Pimaranes Reveals their Potential as Novel Non‐Redox Active Ferroptosis Inhibitors. Chemistry - A European Journal. 31(7). e202403811–e202403811. 1 indexed citations
8.
Pinkert, Tobias, et al.. (2023). A Divergent Polyene Cyclization for the Total Synthesis of Greenwayodendrines, Greenwaylactams, Polysin and Polyveoline. Angewandte Chemie. 135(32). 1 indexed citations
9.
Pinkert, Tobias, et al.. (2023). A Divergent Polyene Cyclization for the Total Synthesis of Greenwayodendrines, Greenwaylactams, Polysin and Polyveoline. Angewandte Chemie International Edition. 62(32). e202307719–e202307719. 9 indexed citations
10.
Wurst, Klaus, et al.. (2023). Total Syntheses of (+)-Waixenicin A, (+)-9-Deacetoxy-14,15-deepoxyxeniculin, and (−)-Xeniafaraunol A. Journal of the American Chemical Society. 145(21). 11811–11817. 8 indexed citations
11.
Magauer, Thomas, et al.. (2021). Total Synthesis of Oxepin and Dihydrooxepin Containing Natural Products. Synthesis. 53(22). 4187–4202. 7 indexed citations
12.
Schmid, Matthias, et al.. (2019). Ring-expansion approaches for the total synthesis of salimabromide. Tetrahedron. 75(24). 3195–3215. 13 indexed citations
13.
Speck, Klaus, et al.. (2017). A modular synthesis of tetracyclic meroterpenoid antibiotics. Nature Communications. 8(1). 2083–2083. 32 indexed citations
14.
Magauer, Thomas & Cedric L. Hugelshofer. (2015). Strategies for the Synthesis of Antifeedant Leucosceptroid Natural Products. Synlett. 26(5). 572–579. 6 indexed citations
15.
Magauer, Thomas, et al.. (2015). Ring Opening of Bicyclo[3.1.0]hexan‐2‐ones: A Versatile Synthetic Platform for the Construction of Substituted Benzoates. Angewandte Chemie International Edition. 54(40). 11835–11838. 29 indexed citations
16.
Magauer, Thomas, et al.. (2015). Synthesis of Xenia diterpenoids and related metabolites isolated from marine organisms. Beilstein Journal of Organic Chemistry. 11. 2521–2539. 22 indexed citations
17.
Pröpper, Kevin, et al.. (2014). Crystalline guanine adducts of natural and synthetic trioxacarcins suggest a common biological mechanism and reveal a basis for the instability of trioxacarcin A. Bioorganic & Medicinal Chemistry Letters. 24(18). 4410–4413. 6 indexed citations
18.
Hammann, Jeffrey M., et al.. (2014). A Transition‐Metal‐Free Synthesis of Fluorinated Naphthols. Chemistry - A European Journal. 20(22). 6733–6738. 17 indexed citations
19.
Martin, Harry J., Thomas Magauer, & Johann Mulzer. (2010). In Pursuit of a Competitive Target: Total Synthesis of the Antibiotic Kendomycin. Angewandte Chemie International Edition. 49(33). 5614–5626. 49 indexed citations
20.
Magauer, Thomas, Harry J. Martin, & Johann Mulzer. (2009). Total Synthesis of the Antibiotic Kendomycin by Macrocyclization using Photo‐Fries Rearrangement and Ring‐Closing Metathesis. Angewandte Chemie International Edition. 48(33). 6032–6036. 67 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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