Chuan‐Ying Li

2.9k total citations
74 papers, 2.5k citations indexed

About

Chuan‐Ying Li is a scholar working on Organic Chemistry, Inorganic Chemistry and Pharmaceutical Science. According to data from OpenAlex, Chuan‐Ying Li has authored 74 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 70 papers in Organic Chemistry, 6 papers in Inorganic Chemistry and 3 papers in Pharmaceutical Science. Recurrent topics in Chuan‐Ying Li's work include Cyclopropane Reaction Mechanisms (51 papers), Catalytic C–H Functionalization Methods (45 papers) and Catalytic Alkyne Reactions (19 papers). Chuan‐Ying Li is often cited by papers focused on Cyclopropane Reaction Mechanisms (51 papers), Catalytic C–H Functionalization Methods (45 papers) and Catalytic Alkyne Reactions (19 papers). Chuan‐Ying Li collaborates with scholars based in China, United States and Germany. Chuan‐Ying Li's co-authors include Aaron Aponick, Mei Xu, Ze‐Feng Xu, Yong Tang, Xiu‐Li Sun, Yi‐Xia Jia, Chengfu Xu, Emerson Finco Marques, Jun He and Wanli Cheng and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and SHILAP Revista de lepidopterología.

In The Last Decade

Chuan‐Ying Li

71 papers receiving 2.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chuan‐Ying Li China 28 2.5k 302 120 108 66 74 2.5k
Chao Shu China 32 3.1k 1.3× 269 0.9× 141 1.2× 174 1.6× 67 1.0× 72 3.2k
Minqiang Jia China 20 1.9k 0.8× 394 1.3× 79 0.7× 59 0.5× 54 0.8× 29 2.0k
Deyun Qian China 23 2.5k 1.0× 484 1.6× 128 1.1× 119 1.1× 46 0.7× 34 2.5k
Ke‐Gong Ji China 34 3.0k 1.2× 415 1.4× 146 1.2× 44 0.4× 100 1.5× 75 3.0k
William E. Brenzovich United States 10 1.2k 0.5× 258 0.9× 84 0.7× 61 0.6× 53 0.8× 16 1.3k
Amandine Guérinot France 23 1.7k 0.7× 424 1.4× 251 2.1× 81 0.8× 23 0.3× 50 1.8k
Yoshikazu Horino Japan 21 1.4k 0.6× 437 1.4× 203 1.7× 35 0.3× 39 0.6× 74 1.5k
Yunkui Liu China 25 1.8k 0.7× 294 1.0× 142 1.2× 230 2.1× 24 0.4× 109 1.9k
Jonathan P. Brand Switzerland 17 2.5k 1.0× 293 1.0× 157 1.3× 156 1.4× 18 0.3× 20 2.5k
Marc Presset France 21 1.2k 0.5× 191 0.6× 178 1.5× 112 1.0× 15 0.2× 59 1.3k

Countries citing papers authored by Chuan‐Ying Li

Since Specialization
Citations

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

Fields of papers citing papers by Chuan‐Ying Li

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Chuan‐Ying Li. 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 Chuan‐Ying Li. The network helps show where Chuan‐Ying Li may publish in the future.

Co-authorship network of co-authors of Chuan‐Ying Li

This figure shows the co-authorship network connecting the top 25 collaborators of Chuan‐Ying Li. A scholar is included among the top collaborators of Chuan‐Ying Li 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 Chuan‐Ying Li. Chuan‐Ying Li 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.
Meng, Hui, Zehua Wang, Ze‐Feng Xu, & Chuan‐Ying Li. (2025). Synthesis of Tetrahydroisoquinolin‐4‐Ones via Rh(II)‐Catalyzed One‐Pot Reaction of Aldehyde‐Tethered N‐Sulfonyl‐1,2,3‐Triazoles with Indoles. Advanced Synthesis & Catalysis. 367(8).
2.
Wang, Han, et al.. (2025). Intramolecular nitrogen insertion of oxime ester to access aminated N-heterocycles. Green Chemistry. 27(31). 9445–9451.
3.
Wang, Yunxiao, Ze‐Feng Xu, Jing Chen, et al.. (2024). Rhodium-catalyzed intramolecular cyclization for synthesizing thiodihydropyrans. Organic & Biomolecular Chemistry. 22(33). 6695–6698. 1 indexed citations
4.
Yang, Mingqi, Tao Chen, Ze‐Feng Xu, Mingming Yu, & Chuan‐Ying Li. (2024). Copper-catalyzed deborodeuteration of arylboronic acids/borates using D2O as the deuterium source. Organic & Biomolecular Chemistry. 22(37). 7596–7600. 2 indexed citations
5.
Zhang, Wenzheng, et al.. (2024). Thermal‐Induced Synthesis of Cyclobute[b]indolines via Intramolecular Formal [2+2] Cycloaddition of Enamines and Triazole‐Derived Ketenimines. Advanced Synthesis & Catalysis. 366(18). 3790–3795. 1 indexed citations
6.
Chen, Jing, et al.. (2024). Rhodium‐Catalyzed Synthesis of Polycyclic Spiroindolines via Intramolecular 1,2‐Acyloxy Migration‐Cyclization Cascade. European Journal of Organic Chemistry. 27(48). 4 indexed citations
7.
Xu, Ze‐Feng, et al.. (2023). Synthesis of 3‐Methylidene‐2,3‐dihydropyrroles via Formal 1,2‐Enamine Migration/Cyclization Cascade of Rhodium Carbenes. Advanced Synthesis & Catalysis. 365(2). 161–166. 5 indexed citations
9.
Xu, Ze‐Feng, et al.. (2022). Synthesis of Azepane Derivatives via Formal 1,3-Migration of Hydroxy and Acyloxy Groups and Selective Annulation. Organic Letters. 24(29). 5254–5259. 10 indexed citations
10.
Li, Chuan‐Ying, et al.. (2021). A2 adenosine receptor contributes to the development of cow’s milk protein allergy via regulating regulatory T cells. SHILAP Revista de lepidopterología. 1 indexed citations
11.
Duan, Shengguo, et al.. (2021). Rhodium(II)‐Catalyzed [4+3] Cyclization of Triazoles with Indole Derivatives and Its Application in the Total Synthesis of (±)‐Aurantioclavine. Chinese Journal of Chemistry. 39(5). 1145–1152. 16 indexed citations
12.
Duan, Shengguo, et al.. (2020). Synthesis of Cyclopenta[b]indoles via a Formal [3+2] Cyclization of N‐Sulfonyl‐1,2,3‐triazoles and Indoles. Advanced Synthesis & Catalysis. 362(17). 3570–3575. 14 indexed citations
13.
Wang, Wenlin, et al.. (2018). Synthesis of Piperidine Derivatives by Rhodium‐ Catalyzed Tandem Reaction of N‐Sulfonyl‐1,2,3‐Triazole and Vinyl Ether. Advanced Synthesis & Catalysis. 360(11). 2125–2130. 22 indexed citations
14.
Shan, Lihong, et al.. (2018). Metal-free synthesis of imidazole by BF3·Et2O promoted denitrogenative transannulation of N-sulfonyl-1,2,3-triazole. Organic & Biomolecular Chemistry. 16(9). 1461–1464. 27 indexed citations
15.
Xu, Ze‐Feng, et al.. (2017). Metal-free synthesis of 2-aminonaphthalenes by intramolecular transannulation of 1-sulfonyl-4-(2-alkenylphenyl)-1,2,3-triazoles. Organic & Biomolecular Chemistry. 15(15). 3161–3164. 16 indexed citations
16.
Cheng, Wanli, Yanhua Tang, Ze‐Feng Xu, & Chuan‐Ying Li. (2016). Synthesis of Multifunctionalized 2-Carbonylpyrrole by Rhodium-Catalyzed Transannulation of 1-Sulfonyl-1,2,3-triazole with β-Diketone. Organic Letters. 18(23). 6168–6171. 49 indexed citations
17.
Zhang, Wenbiao, et al.. (2014). Rhodium-catalyzed synthesis of multi-substituted furans from N-sulfonyl-1,2,3-triazoles bearing a tethered carbonyl group. Organic Chemistry Frontiers. 2(1). 47–50. 32 indexed citations
18.
Wu, Hao, et al.. (2011). Nickel‐Catalyzed Intramolecular Nucleophilic Addition of Aryl or Vinyl Chlorides to α‐Ketoamides Through CCl Bond Activation. Chemistry - A European Journal. 17(19). 5234–5237. 69 indexed citations
19.
Aponick, Aaron, et al.. (2009). An Extremely Facile Synthesis of Furans, Pyrroles, and Thiophenes by the Dehydrative Cyclization of Propargyl Alcohols. Organic Letters. 11(20). 4624–4627. 210 indexed citations
20.
Aponick, Aaron, Chuan‐Ying Li, & Bérenger Biannic. (2008). Au-Catalyzed Cyclization of Monoallylic Diols. Organic Letters. 10(4). 669–671. 97 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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