Chi‐Sing Lee

2.1k total citations
77 papers, 1.7k citations indexed

About

Chi‐Sing Lee is a scholar working on Organic Chemistry, Molecular Biology and Materials Chemistry. According to data from OpenAlex, Chi‐Sing Lee has authored 77 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Organic Chemistry, 20 papers in Molecular Biology and 15 papers in Materials Chemistry. Recurrent topics in Chi‐Sing Lee's work include Synthetic Organic Chemistry Methods (26 papers), Microbial Natural Products and Biosynthesis (10 papers) and Oxidative Organic Chemistry Reactions (10 papers). Chi‐Sing Lee is often cited by papers focused on Synthetic Organic Chemistry Methods (26 papers), Microbial Natural Products and Biosynthesis (10 papers) and Oxidative Organic Chemistry Reactions (10 papers). Chi‐Sing Lee collaborates with scholars based in China, Hong Kong and United Kingdom. Chi‐Sing Lee's co-authors include Craig J. Forsyth, Hoi‐Lun Kwong, Lizhi Zhu, Wung‐Wai Tso, Wing‐Leung Wong, Feryan Ahmed, Russell D. Cink, Guangyan Du, Xiaozu Liu and Pang‐Fei Teng 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

Chi‐Sing Lee

77 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chi‐Sing Lee China 27 942 471 222 219 205 77 1.7k
Kei Takeda Japan 26 1.7k 1.8× 502 1.1× 366 1.6× 234 1.1× 155 0.8× 122 2.3k
Takumi Furuta Japan 27 1.5k 1.6× 765 1.6× 253 1.1× 134 0.6× 99 0.5× 115 2.1k
Willi M. Amberg Switzerland 16 1.6k 1.7× 658 1.4× 207 0.9× 98 0.4× 180 0.9× 27 2.2k
A. Venkateswarlu India 17 1.9k 2.0× 896 1.9× 202 0.9× 130 0.6× 119 0.6× 30 2.4k
Hiroko Masamune United States 10 1.5k 1.6× 673 1.4× 172 0.8× 129 0.6× 259 1.3× 18 2.1k
Gerard A. Crispino United States 13 1.6k 1.7× 639 1.4× 178 0.8× 109 0.5× 204 1.0× 18 2.0k
Joaquı́n Tamariz Mexico 27 1.8k 1.9× 422 0.9× 97 0.4× 113 0.5× 94 0.5× 174 2.5k
Jacek W. Morzycki Poland 23 701 0.7× 964 2.0× 102 0.5× 128 0.6× 323 1.6× 154 1.8k
Jadwiga Frelek Poland 25 1.0k 1.1× 839 1.8× 634 2.9× 135 0.6× 175 0.9× 124 2.2k

Countries citing papers authored by Chi‐Sing Lee

Since Specialization
Citations

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

Fields of papers citing papers by Chi‐Sing Lee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Chi‐Sing 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 Chi‐Sing Lee. The network helps show where Chi‐Sing Lee may publish in the future.

Co-authorship network of co-authors of Chi‐Sing Lee

This figure shows the co-authorship network connecting the top 25 collaborators of Chi‐Sing Lee. A scholar is included among the top collaborators of Chi‐Sing 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 Chi‐Sing Lee. Chi‐Sing 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.
Liu, Jiqiang, Qihang Ding, Jinxin Zhang, et al.. (2025). 808 nm Light-Triggered Cyanine-Decorated Iridium(III) Complexes for Antibacterial Photodynamic Therapy in Deep-Tissue. Inorganic Chemistry. 64(16). 8135–8142. 1 indexed citations
2.
Li, Yuling, et al.. (2024). Discovery of α-hexyl cinnamaldehyde and its derivatives as novel larvicides against Aedes albopictus. Arabian Journal of Chemistry. 17(9). 105873–105873. 1 indexed citations
3.
Ge, Si-Yuan, Wenjiao Li, Xiaole Chen, et al.. (2024). Novel antimalarial 3-substituted quinolones isosteres with improved pharmacokinetic properties. European Journal of Medicinal Chemistry. 284. 117228–117228. 1 indexed citations
4.
Liu, Jiqiang, Xing Yang, Ping Gong, et al.. (2024). Iridium(iii) complexes decorated with silicane-modified rhodamine: near-infrared light-initiated photosensitizers for efficient deep-tissue penetration photodynamic therapy. Journal of Materials Chemistry B. 12(15). 3710–3718. 11 indexed citations
5.
Huang, Junrong, et al.. (2023). Formal Synthesis of (+)‐Phomactin A via a Prins/Conia‐ene Cascade and γ‐Hydroxylation Strategy. ChemistrySelect. 8(42). 1 indexed citations
6.
Shi, Hua‐Tian, et al.. (2021). Room Temperature Aerobic Peroxidation of Organic Substrates Catalyzed by Cobalt(III) Alkylperoxo Complexes. Journal of the American Chemical Society. 143(36). 14445–14450. 12 indexed citations
7.
Lee, Chi‐Sing, et al.. (2020). Total Synthesis of (－)-Glaucocalyxin A. Chinese Journal of Organic Chemistry. 40(10). 3487–3487. 1 indexed citations
8.
Zhu, Lizhi, Wenjing Ma, Magnolia Muk‐Lan Lee, et al.. (2018). Scalable synthesis enabling multilevel bio-evaluations of natural products for discovery of lead compounds. Nature Communications. 9(1). 1283–1283. 43 indexed citations
9.
Min, Long, et al.. (2014). A Biomimetic Synthesis of (±)‐Basiliolide B. Angewandte Chemie International Edition. 53(42). 11294–11297. 20 indexed citations
10.
Li, Hongguang, Rongfeng Lan, Chi‐Fai Chan, et al.. (2013). Real time detection of cell cycle regulator cyclin A on living tumor cells with europium emission. Dalton Transactions. 42(37). 13495–13495. 9 indexed citations
11.
Law, Ga‐Lai, Hongguang Li, Hoi Lam Tam, et al.. (2011). Two-photon induced responsive f–f emissive detection of Cyclin A with a europium-chelating peptide. Chemical Communications. 47(28). 8052–8052. 20 indexed citations
12.
Wu, Wanqing, Long Min, Lizhi Zhu, & Chi‐Sing Lee. (2011). A New Class of Enantioselective Catalytic 2‐Pyrone Diels–Alder Cycloadditions. Advanced Synthesis & Catalysis. 353(7). 1135–1145. 14 indexed citations
13.
14.
Wang, Bo, Terkel Hansen, Ting Wang, et al.. (2010). Total Synthesis of Phorboxazole A via de Novo Oxazole Formation: Strategy and Component Assembly. Journal of the American Chemical Society. 133(5). 1484–1505. 46 indexed citations
15.
Wu, Wanqing, et al.. (2008). Base-Catalyzed Diels−Alder Reactions of 2H-Pyran-2,5-diones: A Mild Approach to Basiliolide B. Organic Letters. 10(24). 5525–5528. 49 indexed citations
16.
Lee, Chi‐Sing, et al.. (2007). InCl3-Mediated Cascade Reactions for the Construction of Highly Functionalized 1-Oxadecalins. Synlett. 2008(1). 142–146. 4 indexed citations
17.
Wong, Wing‐Leung, et al.. (2004). The first series of chiral 2,2′:6′,2″-terpyridine tri-N-oxide ligands for Lewis base-catalyzed asymmetric allylation of aldehydes. Organic & Biomolecular Chemistry. 2(14). 1967–1969. 37 indexed citations
18.
19.
Ciske, Fred L., Michael R. Barbachyn, Michaël Génin, et al.. (2003). The effect of remote chirality on the antibacterial activity of indolinyl, tetrahydroquinolyl and dihydrobenzoxazinyl oxazolidinones. Bioorganic & Medicinal Chemistry Letters. 13(23). 4235–4239. 22 indexed citations
20.
Tso, Wung‐Wai & Chi‐Sing Lee. (1981). Variations of gossypol sensitivity in boar spermatozoal electron transport chain segments. Contraception. 24(5). 569–576. 14 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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