Lushi Tan

2.2k total citations
50 papers, 1.4k citations indexed

About

Lushi Tan is a scholar working on Organic Chemistry, Molecular Biology and Inorganic Chemistry. According to data from OpenAlex, Lushi Tan has authored 50 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Organic Chemistry, 21 papers in Molecular Biology and 10 papers in Inorganic Chemistry. Recurrent topics in Lushi Tan's work include Chemical Synthesis and Analysis (13 papers), Asymmetric Synthesis and Catalysis (12 papers) and Asymmetric Hydrogenation and Catalysis (10 papers). Lushi Tan is often cited by papers focused on Chemical Synthesis and Analysis (13 papers), Asymmetric Synthesis and Catalysis (12 papers) and Asymmetric Hydrogenation and Catalysis (10 papers). Lushi Tan collaborates with scholars based in United States, China and Canada. Lushi Tan's co-authors include Dawei Ma, Lanting Xu, Paul J. Reider, Richard D. Tillyer, Edward J. J. Grabowski, Yu‐Peng He, Chao Zhang, Thomas R. Hoye, Cheng‐Yi Chen and Naoki Yoshikawa and has published in prestigious journals such as Angewandte Chemie International Edition, The Journal of Organic Chemistry and Tetrahedron.

In The Last Decade

Lushi Tan

49 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lushi Tan United States 22 1.0k 351 312 159 141 50 1.4k
Ana Bellomo United States 21 1.5k 1.4× 270 0.8× 246 0.8× 85 0.5× 76 0.5× 43 1.6k
Richard Desmond United States 17 916 0.9× 495 1.4× 247 0.8× 137 0.9× 51 0.4× 30 1.3k
Bryon Simmons United States 14 1.5k 1.5× 432 1.2× 320 1.0× 65 0.4× 41 0.3× 22 1.8k
Cheng‐yi Chen United States 27 2.1k 2.0× 694 2.0× 687 2.2× 208 1.3× 234 1.7× 70 2.5k
Edward G. Corley United States 20 1.4k 1.4× 423 1.2× 312 1.0× 57 0.4× 102 0.7× 39 1.6k
Radhe K. Vaid United States 16 1.1k 1.0× 229 0.7× 237 0.8× 91 0.6× 64 0.5× 48 1.3k
Mark A. Huffman United States 22 1.9k 1.9× 406 1.2× 387 1.2× 75 0.5× 147 1.0× 47 2.2k
John Limanto United States 15 560 0.5× 318 0.9× 192 0.6× 89 0.6× 46 0.3× 24 834
Roberta L. Dorow United States 20 1.8k 1.7× 664 1.9× 388 1.2× 58 0.4× 165 1.2× 31 2.0k
Felix Kopp Germany 13 1.6k 1.5× 306 0.9× 270 0.9× 50 0.3× 66 0.5× 22 1.8k

Countries citing papers authored by Lushi Tan

Since Specialization
Citations

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

Fields of papers citing papers by Lushi Tan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lushi Tan

This figure shows the co-authorship network connecting the top 25 collaborators of Lushi Tan. A scholar is included among the top collaborators of Lushi Tan 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 Lushi Tan. Lushi Tan 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.
Xiao, Kai‐Jiong, Qinghao Chen, Yingju Xu, et al.. (2025). Process Development toward a Key Fragment of the PCSK9 Inhibitor Enlicitide Decanoate. Organic Process Research & Development. 29(4). 1083–1092.
2.
Turnbull, Ben W. H., Feng Peng, Andrew J. Neel, et al.. (2023). Development of a Kilogram-Scale Synthesis of a Key Ulevostinag Subunit Part I: Accessing a Keto-Nucleoside Intermediate from Guanosine. Organic Process Research & Development. 27(3). 448–457. 2 indexed citations
3.
Neel, Andrew J., Ben W. H. Turnbull, William Carson, et al.. (2022). A Unified Strategy to Fluorinated Nucleoside Analogues Via an Electrophilic Manifold. Organic Letters. 24(41). 7701–7706. 5 indexed citations
4.
Bottecchia, Cecilia, François Lévesque, Jonathan P. McMullen, et al.. (2021). Manufacturing Process Development for Belzutifan, Part 2: A Continuous Flow Visible-Light-Induced Benzylic Bromination. Organic Process Research & Development. 26(3). 516–524. 68 indexed citations
5.
Zhong, Yong‐Li, Jeffrey C. Moore, Michael Shevlin, et al.. (2021). Scalable Asymmetric Synthesis of MK-8998, a T-Type Calcium Channel Antagonist. The Journal of Organic Chemistry. 87(4). 2120–2128. 2 indexed citations
6.
Martinot, Theodore A., Michael J. Ardolino, Lu Chen, et al.. (2019). Process Safety Considerations for the Supply of a High-Energy Oxadiazole IDO1-Selective Inhibitor. Organic Process Research & Development. 23(6). 1178–1190. 3 indexed citations
7.
Kuethe, Jeffrey T., et al.. (2017). Development of a stereoselective and scalable process for the preparation of a methylcyclobutanol-pyridyl ether. Bioorganic & Medicinal Chemistry. 26(4). 938–944. 2 indexed citations
8.
McLaughlin, Mark, Jongrock Kong, Kevin M. Belyk, et al.. (2017). Enantioselective Synthesis of 4′-Ethynyl-2-fluoro-2′-deoxyadenosine (EFdA) via Enzymatic Desymmetrization. Organic Letters. 19(4). 926–929. 43 indexed citations
9.
Xu, Lanting, Lushi Tan, & Dawei Ma. (2017). Rhodium-Catalyzed Regioselective C7-Functionalization of Indole Derivatives with Acrylates by Using an N-Imino Directing Group. Synlett. 28(20). 2839–2844. 5 indexed citations
10.
Campeau, Louis‐Charles, Qinghao Chen, Danny Gauvreau, et al.. (2016). A Robust Kilo-Scale Synthesis of Doravirine. Organic Process Research & Development. 20(8). 1476–1481. 51 indexed citations
11.
Song, Zhiguo J., et al.. (2016). Concise Cu (I) Catalyzed Synthesis of Substituted Benzofurans via a Tandem SNAr/C–O Coupling Process. Organic Process Research & Development. 20(6). 1088–1092. 6 indexed citations
12.
Xu, Lanting, Chao Zhang, Yu‐Peng He, Lushi Tan, & Dawei Ma. (2015). Rhodium‐Catalyzed Regioselective C7‐Functionalization of N‐Pivaloylindoles. Angewandte Chemie International Edition. 55(1). 321–325. 159 indexed citations
13.
14.
Yoshikawa, Naoki, Lushi Tan, Jerry A. Murry, et al.. (2007). An Efficient and Scalable Synthesis of Substituted Phenanthrenequinones by Intramolecular Friedel−Crafts Reaction of Imidazolides. Organic Letters. 9(21). 4103–4106. 7 indexed citations
15.
Yasuda, Nobuyoshi, Lushi Tan, Naoki Yoshikawa, & Frederick W. Hartner. (2005). Methods for the Preparation of Highly Functionalized Bicyclo[3.1.0]hexane mGluR2/3 Agonists. Journal of Synthetic Organic Chemistry Japan. 63(11). 1147–1156. 2 indexed citations
16.
Hartner, Frederick W., Yi Hsiao, Kan K. Eng, et al.. (2004). Methods for the Synthesis of 5,6,7,8-Tetrahydro-1,8-naphthyridine Fragments for αVβ3 Integrin Antagonists. The Journal of Organic Chemistry. 69(25). 8723–8730. 33 indexed citations
17.
Yasuda, Nobuyoshi, Yi Hsiao, Mark S. Jensen, et al.. (2004). An Efficient Synthesis of an αvβ3 Antagonist. The Journal of Organic Chemistry. 69(6). 1959–1966. 52 indexed citations
18.
Song, Zhiguo J., Lisa Frey, Jing Li, et al.. (2001). Practical Asymmetric Synthesis of a Selective Endothelin A Receptor (ETA) Antagonist. Organic Letters. 3(21). 3357–3360. 22 indexed citations
19.
Tan, Lushi, Cheng‐Yi Chen, Richard D. Tillyer, Edward J. J. Grabowski, & Paul J. Reider. (1999). A Novel, Highly Enantioselective Ketone Alkynylation Reaction Mediated by Chiral Zinc Aminoalkoxides. Angewandte Chemie International Edition. 38(5). 711–713. 158 indexed citations
20.
Tan, Lushi, Cheng‐yi Chen, Richard D. Tillyer, Edward J. J. Grabowski, & Paul J. Reider. (1999). Eine neue, hochenantioselektive Alkinylierung von Ketonen, die durch chirale Zinkaminoalkoxide gesteuert wird. Angewandte Chemie. 111(5). 724–727. 52 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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