Shu‐Li You

40.4k total citations · 17 hit papers
490 papers, 34.9k citations indexed

About

Shu‐Li You is a scholar working on Organic Chemistry, Inorganic Chemistry and Molecular Biology. According to data from OpenAlex, Shu‐Li You has authored 490 papers receiving a total of 34.9k indexed citations (citations by other indexed papers that have themselves been cited), including 471 papers in Organic Chemistry, 172 papers in Inorganic Chemistry and 48 papers in Molecular Biology. Recurrent topics in Shu‐Li You's work include Catalytic C–H Functionalization Methods (250 papers), Asymmetric Synthesis and Catalysis (217 papers) and Asymmetric Hydrogenation and Catalysis (161 papers). Shu‐Li You is often cited by papers focused on Catalytic C–H Functionalization Methods (250 papers), Asymmetric Synthesis and Catalysis (217 papers) and Asymmetric Hydrogenation and Catalysis (161 papers). Shu‐Li You collaborates with scholars based in China, United States and Russia. Shu‐Li You's co-authors include Chao Zheng, Qing Gu, Chun‐Xiang Zhuo, Li‐Xin Dai, Xiǎo Zhang, Wei Zhang, Jun Zheng, Qing‐Feng Wu, Quan Cai and Zhuo‐An Zhao and has published in prestigious journals such as Science, Chemical Reviews and Journal of the American Chemical Society.

In The Last Decade

Shu‐Li You

480 papers receiving 34.5k citations

Hit Papers

Catalytic Asymmetric Dearomatization Reactions 2003 2026 2010 2018 2012 2014 2009 2016 2018 250 500 750 1000

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shu‐Li You China 100 33.5k 9.1k 3.3k 1.9k 1.5k 490 34.9k
Karl Anker Jørgensen Denmark 111 40.3k 1.2× 9.9k 1.1× 7.5k 2.2× 701 0.4× 1.7k 1.1× 502 42.3k
Keiji Maruoka Japan 86 26.6k 0.8× 7.8k 0.9× 6.4k 1.9× 610 0.3× 2.3k 1.5× 680 28.7k
Benjamin List Germany 96 35.2k 1.0× 12.4k 1.4× 8.9k 2.6× 779 0.4× 2.6k 1.7× 414 38.7k
Dieter Enders Germany 86 35.8k 1.1× 6.5k 0.7× 6.7k 2.0× 450 0.2× 1.5k 1.0× 697 37.6k
Tamio Hayashi Japan 105 36.9k 1.1× 15.6k 1.7× 4.8k 1.4× 395 0.2× 2.0k 1.3× 523 38.8k
Jin‐Quan Yu United States 130 57.5k 1.7× 14.5k 1.6× 2.7k 0.8× 740 0.4× 651 0.4× 428 59.7k
Paul Knochel Germany 97 38.7k 1.2× 8.3k 0.9× 4.9k 1.5× 441 0.2× 850 0.6× 975 42.4k
Gregory C. Fu United States 120 41.3k 1.2× 10.4k 1.1× 5.6k 1.7× 394 0.2× 750 0.5× 319 43.5k
Mark Lautens Canada 90 31.8k 0.9× 7.1k 0.8× 2.5k 0.8× 400 0.2× 410 0.3× 526 33.2k
Liu‐Zhu Gong China 75 16.5k 0.5× 4.8k 0.5× 2.3k 0.7× 568 0.3× 844 0.5× 259 17.1k

Countries citing papers authored by Shu‐Li You

Since Specialization
Citations

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

Fields of papers citing papers by Shu‐Li You

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shu‐Li You

This figure shows the co-authorship network connecting the top 25 collaborators of Shu‐Li You. A scholar is included among the top collaborators of Shu‐Li You 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 Shu‐Li You. Shu‐Li You 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.
Zhang, Ruixue, et al.. (2025). Effective Coordination Promoted Carbene N─H Bond Insertion on Heterogeneous Cu Catalyst. Angewandte Chemie International Edition. 64(51). e17764–e17764.
2.
Zhao, Fangnuo, et al.. (2024). Rh(iii)-catalyzed atroposelective C–H alkynylation of 1-aryl isoquinolines with hypervalent iodine–alkyne reagents. Chemical Communications. 60(53). 6753–6756. 3 indexed citations
3.
Cui, Hao, Chao Zheng, Ji‐Lin Chen, et al.. (2024). Tunable C–H functionalization and dearomatization enabled by an organic photocatalyst. Chemical Science. 15(11). 4114–4120. 8 indexed citations
4.
Yu, Xuan, Chao Zheng, & Shu‐Li You. (2024). Chiral Brønsted Acid-Catalyzed Intramolecular Asymmetric Dearomatization Reaction of Indoles with Cyclobutanones via Cascade Friedel–Crafts/Semipinacol Rearrangement. Journal of the American Chemical Society. 146(37). 25878–25887. 17 indexed citations
5.
Šarlah, David & Shu‐Li You. (2024). The Current State of the Art of Dearomatization Chemistry. Advanced Synthesis & Catalysis. 366(20). 4186–4186. 1 indexed citations
6.
Xie, Pei‐Pei, Yunzhi Lin, Liwei Hu, et al.. (2024). Chiral Bis(binaphthyl) Cyclopentadienyl Ligands for Rhodium-Catalyzed Desymmetrization of Diarylmethanes via Selective Arene Coordination. Journal of the American Chemical Society. 146(39). 26630–26638. 3 indexed citations
7.
Zhang, Suzhen, Wenwen Zhang, Hui Yang, Qing Gu, & Shu‐Li You. (2023). Rhodium-Catalyzed Enantioselective Spiroannulation of 2-Alkenylphenols with Alkynes. Chinese Journal of Organic Chemistry. 43(8). 2926–2926. 7 indexed citations
8.
Xie, Pei‐Pei, et al.. (2023). Asymmetric Dearomatization of Indoles with Azodicarboxylates via Cascade Electrophilic Amination/Aza-Prins Cyclization/Phenonium-like Rearrangement. Journal of the American Chemical Society. 145(21). 11745–11753. 33 indexed citations
9.
Zhu, Min, Xiǎo Zhang, Chao Zheng, & Shu‐Li You. (2022). Energy-Transfer-Enabled Dearomative Cycloaddition Reactions of Indoles/Pyrroles via Excited-State Aromatics. Accounts of Chemical Research. 55(17). 2510–2525. 162 indexed citations breakdown →
10.
Yang, Ping, et al.. (2022). Pd-Catalyzed Asymmetric Dearomative Arylation of Indoles via a Desymmetrization Strategy. Organic Letters. 24(7). 1481–1485. 20 indexed citations
11.
Zhu, Min, Hao Xu, Xiǎo Zhang, Chao Zheng, & Shu‐Li You. (2021). Visible‐Light‐Induced Intramolecular Double Dearomative Cycloaddition of Arenes. Angewandte Chemie International Edition. 60(13). 7036–7040. 75 indexed citations
13.
Gao, Pei‐Sen, Zhen‐Hua Wang, Chao Zheng, et al.. (2020). CuII/TEMPO‐Catalyzed Enantioselective C(sp3)–H Alkynylation of Tertiary Cyclic Amines through Shono‐Type Oxidation. Angewandte Chemie International Edition. 59(35). 15254–15259. 142 indexed citations
14.
Liu, Xi‐Jia, et al.. (2019). Sequence‐Dependent Stereodivergent Allylic Alkylation/Fluorination of Acyclic Ketones. Angewandte Chemie International Edition. 59(5). 2039–2043. 98 indexed citations
15.
Tu, Hang‐Fei, Xiǎo Zhang, Chao Zheng, Min Zhu, & Shu‐Li You. (2018). Enantioselective dearomative prenylation of indole derivatives. Nature Catalysis. 1(8). 601–608. 110 indexed citations
16.
Xia, Zilei, Chao Zheng, Xiao‐Wei Liang, Yue Cai, & Shu‐Li You. (2018). Manipulation of Spiroindolenine Intermediates for Enantioselective Synthesis of 3‐(Indol‐3‐yl)‐Pyrrolidines. Angewandte Chemie International Edition. 58(4). 1158–1162. 11 indexed citations
17.
Yang, Ze‐Peng, et al.. (2018). Iridium‐Catalyzed Intramolecular Asymmetric Allylic Dearomatization of Benzene Derivatives. Angewandte Chemie. 130(49). 16422–16425. 2 indexed citations
18.
You, Shu‐Li. (2015). Asymmetric Functionalization of C–H Bonds. 75 indexed citations
19.
Shao, Wen, et al.. (2015). Copper‐Catalyzed Intermolecular Asymmetric Propargylic Dearomatization of Indoles. Angewandte Chemie International Edition. 54(26). 7684–7687. 162 indexed citations
20.
Han, Long, et al.. (2013). Dearomatization of tryptophols via a vanadium-catalyzed asymmetric epoxidation and ring-opening cascade. Chemical Communications. 50(10). 1231–1233. 76 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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