Yeon‐Hee Lim

1.3k total citations
19 papers, 1.1k citations indexed

About

Yeon‐Hee Lim is a scholar working on Organic Chemistry, Molecular Biology and Physiology. According to data from OpenAlex, Yeon‐Hee Lim has authored 19 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Organic Chemistry, 8 papers in Molecular Biology and 2 papers in Physiology. Recurrent topics in Yeon‐Hee Lim's work include Asymmetric Synthesis and Catalysis (5 papers), Chemical Synthesis and Analysis (3 papers) and Click Chemistry and Applications (3 papers). Yeon‐Hee Lim is often cited by papers focused on Asymmetric Synthesis and Catalysis (5 papers), Chemical Synthesis and Analysis (3 papers) and Click Chemistry and Applications (3 papers). Yeon‐Hee Lim collaborates with scholars based in United States, China and South Korea. Yeon‐Hee Lim's co-authors include M. G. Finn, Manuel de Lera Ruiz, Junying Zheng, Stanislav I. Presolski, Valentin O. Rodionov, Kathlyn A. Parker, Jeffrey T. Koberstein, Nicholas J. Turro, David A. Tirrell and Jeremiah A. Johnson and has published in prestigious journals such as Journal of the American Chemical Society, Journal of Medicinal Chemistry and The Journal of Organic Chemistry.

In The Last Decade

Yeon‐Hee Lim

17 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yeon‐Hee Lim United States 10 703 451 150 111 105 19 1.1k
Danny Hung‐Chieh Chou United States 18 460 0.7× 862 1.9× 19 0.1× 78 0.7× 11 0.1× 45 1.5k
Yun Hak Lee South Korea 9 223 0.3× 346 0.8× 23 0.2× 238 2.1× 29 0.3× 12 1.2k
Hongping Deng China 23 270 0.4× 439 1.0× 12 0.1× 319 2.9× 40 0.4× 46 1.3k
Craig A. Aspinwall United States 23 53 0.1× 828 1.8× 47 0.3× 54 0.5× 28 0.3× 66 1.7k
Neta Pessah Israel 10 241 0.3× 325 0.7× 5 0.0× 89 0.8× 35 0.3× 12 605
Judith A. Stolwijk Germany 15 77 0.1× 416 0.9× 23 0.2× 98 0.9× 11 0.1× 23 1.1k
Vasiliy N. Goral United States 14 125 0.2× 401 0.9× 19 0.1× 35 0.3× 18 0.2× 20 1.2k
Hans Schupp Germany 11 337 0.5× 375 0.8× 4 0.0× 179 1.6× 57 0.5× 15 743
Christian Grunwald Germany 19 194 0.3× 620 1.4× 7 0.0× 37 0.3× 110 1.0× 32 1.1k
Shaojia Zhu China 13 218 0.3× 468 1.0× 15 0.1× 234 2.1× 22 0.2× 13 1.9k

Countries citing papers authored by Yeon‐Hee Lim

Since Specialization
Citations

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

Fields of papers citing papers by Yeon‐Hee Lim

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yeon‐Hee Lim. 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 Yeon‐Hee Lim. The network helps show where Yeon‐Hee Lim may publish in the future.

Co-authorship network of co-authors of Yeon‐Hee Lim

This figure shows the co-authorship network connecting the top 25 collaborators of Yeon‐Hee Lim. A scholar is included among the top collaborators of Yeon‐Hee Lim 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 Yeon‐Hee Lim. Yeon‐Hee Lim is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Lei, Zhiyu, Lianyun Zhao, Tao Ji, et al.. (2025). CuOTf(Tol)1/2-Catalyzed O-Trifluoroethylation of Alcohols with 2,2,2-Trifluorodiazoethane. Organic Letters. 27(17). 4485–4490.
2.
Mak, Victor, Aileen Soriano, M. Zebisch, et al.. (2023). Structural insights into selective small molecule activation of PKG1α. Communications Biology. 6(1). 798–798.
3.
Beshore, Douglas C., Andrew M. Haidle, Ashok Arasappan, et al.. (2022). Building a Culture of Medicinal Chemistry Knowledge Sharing. Journal of Medicinal Chemistry. 65(5). 3776–3785. 1 indexed citations
4.
Satapati, Santhosh, Daniel Metzger, Harish Shankaran, et al.. (2022). Using measures of metabolic flux to align screening and clinical development: Avoiding pitfalls to enable translational studies. SLAS DISCOVERY. 27(1). 20–28. 4 indexed citations
5.
Hugelshofer, Cedric L., Jianming Bao, Juana Du, et al.. (2021). Scalable Preparation of 4,4-Disubstituted Six-Membered Cyclic Sulfones. Organic Letters. 23(3). 943–947. 9 indexed citations
6.
Deng, Qiaolin, Yeon‐Hee Lim, Rajan Anand, et al.. (2015). Use of molecular modeling aided design to dial out hERG liability in adenosine A2A receptor antagonists. Bioorganic & Medicinal Chemistry Letters. 25(15). 2958–2962. 9 indexed citations
7.
Lim, Yeon‐Hee, et al.. (2014). Synthesis of novel anti-inflammatory steroidal macrocycles using ring closing metathesis reaction. Tetrahedron Letters. 56(4). 636–638. 4 indexed citations
8.
Ruiz, Manuel de Lera, Yeon‐Hee Lim, & Junying Zheng. (2013). Adenosine A 2A Receptor as a Drug Discovery Target. Journal of Medicinal Chemistry. 57(9). 3623–3650. 220 indexed citations
9.
Rodionov, Valentin O., et al.. (2013). Benzimidazole and Related Ligands for Cu-Catalyzed Azide–Alkyne Cycloaddition. Journal of the American Chemical Society. 135(4). 1626–1626. 6 indexed citations
10.
Wang, Hongwu, John C. Anthes, Kevin D. McCormick, et al.. (2012). Steroidal C-21 heteroaryl thioethers. Part 3: Pregn-4-eno-[3,2-c]pyrazole fused A ring modified steroids as selective glucocorticoid receptor modulators (dissociated steroids). Bioorganic & Medicinal Chemistry Letters. 22(9). 3291–3295. 4 indexed citations
11.
Bonham, Kevin S., et al.. (2010). Effects of a novel arginine methyltransferase inhibitor on T‐helper cell cytokine production. FEBS Journal. 277(9). 2096–2108. 53 indexed citations
12.
Johnson, Jeremiah A., Ying Y. Lu, Alan O. Burts, et al.. (2010). Core-Clickable PEG-Branch-Azide Bivalent-Bottle-Brush Polymers by ROMP: Grafting-Through and Clicking-To. Journal of the American Chemical Society. 133(3). 559–566. 313 indexed citations
13.
Lim, Yeon‐Hee, et al.. (2008). Cycloaddition reactions of trimethylenemethane diyls generated from alkynyl iodonium salts. Tetrahedron Letters. 49(39). 5693–5696. 11 indexed citations
14.
Rodionov, Valentin O., et al.. (2007). Benzimidazole and Related Ligands for Cu-Catalyzed Azide−Alkyne Cycloaddition. Journal of the American Chemical Society. 129(42). 12696–12704. 351 indexed citations
15.
Lim, Yeon‐Hee, et al.. (2005). Asymmetry by Electrophilic Rearrangement of Symmetric 2-Pyridone Photodimers. Organic Letters. 7(24). 5413–5415. 7 indexed citations
16.
Parker, Kathlyn A. & Yeon‐Hee Lim. (2004). The Total Synthesis of (−)-SNF4435 C and (+)-SNF4435 D. Journal of the American Chemical Society. 126(49). 15968–15969. 67 indexed citations
18.
Lim, Yeon‐Hee, Kevin F. McGee, & Scott McN. Sieburth. (2002). Studies in Bicyclo[3.1.0]hexane Methanolysis. Ring Opening of Activated Cyclopropanes under Acidic and Basic Conditions. The Journal of Organic Chemistry. 67(18). 6535–6538. 21 indexed citations
19.
Lim, Yeon‐Hee, et al.. (2001). Polyquinanes by [4 + 4] Cycloaddition−Transannular Cyclization. Organic Letters. 3(14). 2165–2167. 16 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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