Tanja Gaich

2.8k total citations · 2 hit papers
59 papers, 2.2k citations indexed

About

Tanja Gaich is a scholar working on Organic Chemistry, Pharmacology and Pharmacology. According to data from OpenAlex, Tanja Gaich has authored 59 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Organic Chemistry, 23 papers in Pharmacology and 14 papers in Pharmacology. Recurrent topics in Tanja Gaich's work include Synthetic Organic Chemistry Methods (25 papers), Alkaloids: synthesis and pharmacology (22 papers) and Chemical synthesis and alkaloids (20 papers). Tanja Gaich is often cited by papers focused on Synthetic Organic Chemistry Methods (25 papers), Alkaloids: synthesis and pharmacology (22 papers) and Chemical synthesis and alkaloids (20 papers). Tanja Gaich collaborates with scholars based in Germany, Austria and United States. Tanja Gaich's co-authors include Phil S. Baran, Johann Mulzer, Philipp J. Gritsch, Peter Siengalewicz, Christian Leitner, Harald Weinstabl, A. Nakamura, Ian B. Seiple, Ian S. Young and Junichiro Yamaguchi and has published in prestigious journals such as Nature, Science and Journal of the American Chemical Society.

In The Last Decade

Tanja Gaich

55 papers receiving 2.2k citations

Hit Papers

Aiming for the Ideal Synthesis 2010 2026 2015 2020 2010 2016 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tanja Gaich Germany 23 1.9k 418 371 272 223 59 2.2k
Ken‐ichi Takao Japan 27 2.1k 1.1× 130 0.3× 562 1.5× 422 1.6× 397 1.8× 125 2.5k
Kavirayani R. Prasad India 22 1.5k 0.8× 126 0.3× 399 1.1× 175 0.6× 237 1.1× 114 1.7k
Xingang Xie China 27 1.7k 0.9× 218 0.5× 301 0.8× 217 0.8× 172 0.8× 119 2.0k
Glenn C. Micalizio United States 33 2.2k 1.1× 129 0.3× 558 1.5× 237 0.9× 213 1.0× 111 2.5k
Hanfeng Ding China 26 1.6k 0.8× 224 0.5× 472 1.3× 184 0.7× 301 1.3× 86 1.9k
Takayuki Yakura Japan 25 1.9k 1.0× 202 0.5× 283 0.8× 123 0.5× 181 0.8× 93 2.1k
Rodney A. Fernandes India 28 2.2k 1.1× 155 0.4× 538 1.5× 219 0.8× 286 1.3× 155 2.5k
Sakae Aoyagi Japan 29 1.8k 1.0× 125 0.3× 445 1.2× 229 0.8× 229 1.0× 78 2.1k
Miyoji Hanaoka Japan 27 1.9k 1.0× 340 0.8× 504 1.4× 313 1.2× 198 0.9× 211 2.3k
Marco Santagostino Italy 15 1.5k 0.8× 115 0.3× 449 1.2× 177 0.7× 212 1.0× 32 1.8k

Countries citing papers authored by Tanja Gaich

Since Specialization
Citations

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

Fields of papers citing papers by Tanja Gaich

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tanja Gaich

This figure shows the co-authorship network connecting the top 25 collaborators of Tanja Gaich. A scholar is included among the top collaborators of Tanja Gaich 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 Tanja Gaich. Tanja Gaich 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.
Pan, Lu, et al.. (2025). Gram‐Scale Access to (3,11)‐Cyclotaxanes—Synthesis of 1‐Hydroxytaxuspine C. Angewandte Chemie International Edition. 64(35). e202506245–e202506245.
2.
Gaich, Tanja, et al.. (2025). Total Synthesis and Structural Revision of (−)‐Sodagnitin E. Angewandte Chemie International Edition. 64(35). e202506247–e202506247.
3.
Pan, Lu, et al.. (2024). A general strategy for the synthesis of taxane diterpenes. Nature. 632(8025). 543–549. 16 indexed citations
4.
Pan, Lu, et al.. (2021). The Chemistry of Nonclassical Taxane Diterpene. Accounts of Chemical Research. 54(10). 2347–2360. 21 indexed citations
5.
Gaich, Tanja, et al.. (2020). Total synthesis of the complex taxane diterpene canataxpropellane. Science. 367(6478). 676–681. 76 indexed citations
6.
Gaich, Tanja, et al.. (2019). Structure‐Pattern‐Based Total Synthesis. Chemistry - A European Journal. 25(46). 10782–10791. 8 indexed citations
7.
Gaich, Tanja, et al.. (2017). Methoxatin as a Target in Total Synthesis. Synthesis. 49(8). 1746–1756. 3 indexed citations
8.
Gaich, Tanja, et al.. (2016). The Rhazinilam-Leuconoxine-Mersicarpine Triad of Monoterpenoid Indole Alkaloids. PubMed. 77. 1–84. 11 indexed citations
9.
Gaich, Tanja, et al.. (2015). A Photoinduced Cyclization Cascade—Total Synthesis of (−)‐Leuconoxine. Chemistry - A European Journal. 21(17). 6355–6357. 23 indexed citations
10.
Weinstabl, Harald, et al.. (2014). Light‐Mediated Total Synthesis of 17‐Deoxyprovidencin. Angewandte Chemie International Edition. 53(15). 3859–3862. 26 indexed citations
11.
Gaich, Tanja, et al.. (2014). Recent applications of the divinylcyclopropane–cycloheptadiene rearrangement in organic synthesis. Beilstein Journal of Organic Chemistry. 10. 163–193. 82 indexed citations
12.
Gaich, Tanja, et al.. (2014). Enantioselective, Protecting‐Group‐Free Total Synthesis of Sarpagine Alkaloids—A Generalized Approach. Angewandte Chemie International Edition. 54(1). 315–317. 58 indexed citations
13.
Weinstabl, Harald, et al.. (2014). Lichtinduzierte Totalsynthese von 17‐Desoxyprovidencin. Angewandte Chemie. 126(15). 3940–3943. 8 indexed citations
14.
Gritsch, Philipp J., et al.. (2013). The Witkop Cyclization: A Photoinduced CH Activation of the Indole System. Angewandte Chemie International Edition. 53(5). 1208–1217. 50 indexed citations
15.
Gritsch, Philipp J., et al.. (2013). Enantioselective Synthesis of Cyclohepta[b]indoles: Gram-Scale Synthesis of (S)-SIRT1-Inhibitor IV. Organic Letters. 15(21). 5472–5475. 43 indexed citations
16.
Gritsch, Philipp J., et al.. (2012). Mimicking Dimethylallyltryptophan Synthase: Experimental Evidence for a Biosynthetic Cope Rearrangement Process. Angewandte Chemie International Edition. 51(46). 11514–11516. 44 indexed citations
17.
Weinstabl, Harald, Tanja Gaich, & Johann Mulzer. (2012). Application of the Rodriguez–Pattenden Photo-Ring Contraction: Total Synthesis and Configurational Reassignment of 11-Gorgiacerol and 11-Epigorgiacerol. Organic Letters. 14(11). 2834–2837. 32 indexed citations
18.
Siengalewicz, Peter, Tanja Gaich, & Johann Mulzer. (2008). It All Began with an Error: The Nomofungin/Communesin Story. Angewandte Chemie International Edition. 47(43). 8170–8176. 104 indexed citations
19.
Gaich, Tanja & Johann Mulzer. (2005). Recent Applications of Olefin Ring-Closing Metathesis (RCM) in the Synthesis of Biologically Important Alkaloids, Terpenoids, Polyketides and Other Secondary Metabolites. Current Topics in Medicinal Chemistry. 5(15). 1473–1494. 35 indexed citations
20.
Gaich, Tanja & Johann Mulzer. (2005). Synthesis of Epothilones via a Silicon-Tethered RCM Reaction. Organic Letters. 7(7). 1311–1313. 30 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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