Hong Geun Lee

1.4k total citations
29 papers, 1.1k citations indexed

About

Hong Geun Lee is a scholar working on Organic Chemistry, Pharmaceutical Science and Molecular Biology. According to data from OpenAlex, Hong Geun Lee has authored 29 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Organic Chemistry, 11 papers in Pharmaceutical Science and 9 papers in Molecular Biology. Recurrent topics in Hong Geun Lee's work include Catalytic C–H Functionalization Methods (14 papers), Catalytic Cross-Coupling Reactions (12 papers) and Fluorine in Organic Chemistry (10 papers). Hong Geun Lee is often cited by papers focused on Catalytic C–H Functionalization Methods (14 papers), Catalytic Cross-Coupling Reactions (12 papers) and Fluorine in Organic Chemistry (10 papers). Hong Geun Lee collaborates with scholars based in South Korea, United States and Germany. Hong Geun Lee's co-authors include Stephen L. Buchwald, Phillip J. Milner, Guillaume Lautrette, Bradley L. Pentelute, Jacob M. Hooker, Aaron C. Sather, Fayçal Touti, Peng Dai, Péter Müller and Yang Yang and has published in prestigious journals such as Nature, Journal of the American Chemical Society and Angewandte Chemie International Edition.

In The Last Decade

Hong Geun Lee

29 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
Hong Geun Lee South Korea 18 859 388 332 217 76 29 1.1k
Paul T. Nyffeler United States 7 799 0.9× 280 0.7× 443 1.3× 178 0.8× 22 0.3× 8 987
Suvajit Koley India 16 987 1.1× 211 0.5× 194 0.6× 117 0.5× 14 0.2× 39 1.1k
YU. G. GOLOLOBOV Russia 7 775 0.9× 256 0.7× 67 0.2× 148 0.7× 41 0.5× 74 882
Domitila Aparicio Spain 25 1.7k 2.0× 336 0.9× 212 0.6× 164 0.8× 20 0.3× 59 1.8k
Antoine Sallustrau France 14 417 0.5× 235 0.6× 104 0.3× 43 0.2× 52 0.7× 32 634
В. И. Поткин Belarus 15 815 0.9× 187 0.5× 78 0.2× 141 0.6× 66 0.9× 198 1.0k
Ana B. Cuenca Spain 23 1.6k 1.9× 288 0.7× 70 0.2× 335 1.5× 19 0.3× 48 1.8k
Kevin D. Hesp United States 25 2.3k 2.7× 182 0.5× 199 0.6× 861 4.0× 43 0.6× 46 2.4k
Yuri G. Gololobov Russia 9 771 0.9× 281 0.7× 52 0.2× 195 0.9× 44 0.6× 25 840
Alessandro Ruffoni United Kingdom 21 1.4k 1.7× 219 0.6× 337 1.0× 180 0.8× 15 0.2× 40 1.7k

Countries citing papers authored by Hong Geun Lee

Since Specialization
Citations

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

Fields of papers citing papers by Hong Geun Lee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hong Geun Lee. 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 Hong Geun Lee. The network helps show where Hong Geun Lee may publish in the future.

Co-authorship network of co-authors of Hong Geun Lee

This figure shows the co-authorship network connecting the top 25 collaborators of Hong Geun Lee. A scholar is included among the top collaborators of Hong Geun Lee 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 Hong Geun Lee. Hong Geun Lee 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.
Lee, Hong Geun, et al.. (2025). Employment of a C(sp3)-based nucleophile for photoinduced palladium-catalysed cross-coupling. Chemical Science. 16(27). 12343–12349. 1 indexed citations
2.
Kim, Soo Young, et al.. (2025). Dual Activation of Organoboron for the Ion-Pair-Mediated Synthesis of Hindered Alkyl Fluorides. Organic Letters. 27(17). 4559–4564. 1 indexed citations
3.
Lee, Hong Geun, et al.. (2024). Stereospecific Palladium-Catalyzed Cross-Coupling of Alkylboron Compounds: A Short Account. Synthesis. 56(17). 2614–2626. 3 indexed citations
4.
Chung, Taek Dong, et al.. (2023). Dual Function of N-Iodosuccinimide for C(sp3)–B Bond Activation. Organic Letters. 26(1). 198–203. 3 indexed citations
5.
Lee, Yujin, et al.. (2023). Mechanistic duality of indolyl 1,3-heteroatom transposition. Chemical Science. 14(28). 7688–7698. 3 indexed citations
6.
Chung, Taek Dong, et al.. (2022). A Unified Synthetic Strategy to Introduce Heteroatoms via Electrochemical Functionalization of Alkyl Organoboron Reagents. Journal of the American Chemical Society. 144(20). 9149–9160. 35 indexed citations
7.
8.
Song, In‐Seok, et al.. (2021). Molecular mechanism underlying substrate recognition of the peptide macrocyclase PsnB. Nature Chemical Biology. 17(11). 1123–1131. 17 indexed citations
9.
Cheong, Paul Ha‐Yeon, et al.. (2021). Modular Counter-Fischer–Indole Synthesis through Radical-Enolate Coupling. Organic Letters. 23(3). 1096–1102. 15 indexed citations
10.
Lee, Hong Geun, et al.. (2021). Formation of the Tertiary Sulfonamide C(sp3)–N Bond Using Alkyl Boronic Ester via Intramolecular and Intermolecular Copper-Catalyzed Oxidative Cross-Coupling. The Journal of Organic Chemistry. 86(23). 17380–17394. 4 indexed citations
11.
Seo, Minjee, et al.. (2021). Revisiting Thin-Layer Electrochemistry in a Chip-Type Cell for the Study of Electro-organic Reactions. Analytical Chemistry. 94(2). 1248–1255. 11 indexed citations
12.
Lee, Hong Geun, et al.. (2017). Direct 11CN-Labeling of Unprotected Peptides via Palladium-Mediated Sequential Cross-Coupling Reactions. Journal of the American Chemical Society. 139(21). 7152–7155. 62 indexed citations
13.
Lee, Hong Geun, Guillaume Lautrette, Bradley L. Pentelute, & Stephen L. Buchwald. (2017). Palladium‐Mediated Arylation of Lysine in Unprotected Peptides. Angewandte Chemie International Edition. 56(12). 3177–3181. 119 indexed citations
14.
Sather, Aaron C., et al.. (2015). A Fluorinated Ligand Enables Room-Temperature and Regioselective Pd-Catalyzed Fluorination of Aryl Triflates and Bromides. Journal of the American Chemical Society. 137(41). 13433–13438. 92 indexed citations
15.
Sather, Aaron C., et al.. (2015). Dosage delivery of sensitive reagents enables glove-box-free synthesis. Nature. 524(7564). 208–211. 68 indexed citations
16.
Lee, Hong Geun, Phillip J. Milner, Michael T. Colvin, Loren B. Andreas, & Stephen L. Buchwald. (2014). Structure and reactivity of [(L·Pd) ·(1,5-cyclooctadiene)] (n= 1–2) complexes bearing biaryl phosphine ligands. Inorganica Chimica Acta. 422. 188–192. 33 indexed citations
17.
Im, Jeongdae, et al.. (2014). 4-Methylphenol produced in freshwater sediment microcosms is not a bisphenol A metabolite. Chemosphere. 117. 521–526. 10 indexed citations
18.
Lee, Hong Geun, Phillip J. Milner, & Stephen L. Buchwald. (2013). An Improved Catalyst System for the Pd-Catalyzed Fluorination of (Hetero)Aryl Triflates. Organic Letters. 15(21). 5602–5605. 114 indexed citations
19.
Lee, Hong Geun, Jae Young Ahn, Amy S. Lee, & Matthew D. Shair. (2010). Enantioselective Synthesis of the Lomaiviticin Aglycon Full Carbon Skeleton Reveals Remarkable Remote Substituent Effects during the Dimerization Event. Chemistry - A European Journal. 16(44). 13058–13062. 33 indexed citations
20.

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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