Su Zhou

560 total citations
20 papers, 445 citations indexed

About

Su Zhou is a scholar working on Organic Chemistry, Surgery and Neurology. According to data from OpenAlex, Su Zhou has authored 20 papers receiving a total of 445 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Organic Chemistry, 3 papers in Surgery and 2 papers in Neurology. Recurrent topics in Su Zhou's work include Catalytic C–H Functionalization Methods (9 papers), Catalytic Alkyne Reactions (9 papers) and Cyclopropane Reaction Mechanisms (7 papers). Su Zhou is often cited by papers focused on Catalytic C–H Functionalization Methods (9 papers), Catalytic Alkyne Reactions (9 papers) and Cyclopropane Reaction Mechanisms (7 papers). Su Zhou collaborates with scholars based in China, India and Germany. Su Zhou's co-authors include Xinfang Xu, Wenhao Hu, Kemiao Hong, Ming Bao, Yinwu Li, Zhuofeng Ke, Xiangrong Liu, Jiasheng Dong, Kaixiang Cheng and A. Stephen K. Hashmi and has published in prestigious journals such as Journal of the American Chemical Society, Nature Communications and Chemical Communications.

In The Last Decade

Su Zhou

18 papers receiving 429 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Su Zhou China 14 288 84 60 26 26 20 445
Álex Flores United States 7 218 0.8× 181 2.2× 48 0.8× 28 1.1× 10 0.4× 22 500
Jean‐Christophe Prost Switzerland 9 46 0.2× 73 0.9× 35 0.6× 124 4.8× 51 2.0× 18 322
Takashi Andou Japan 8 273 0.9× 20 0.2× 80 1.3× 44 1.7× 19 419
Naoto Yamada Japan 7 317 1.1× 18 0.2× 134 2.2× 44 1.7× 13 442
Xing‐Wang Wang China 13 307 1.1× 28 0.3× 66 1.1× 51 2.0× 21 479
Lei‐Lei Sun China 9 239 0.8× 46 0.5× 14 0.2× 24 0.9× 16 346
Christopher J. Simmons United States 11 160 0.6× 135 1.6× 13 0.2× 83 3.2× 2 0.1× 21 340
Bing Tu China 10 37 0.1× 82 1.0× 47 0.8× 30 1.2× 23 352

Countries citing papers authored by Su Zhou

Since Specialization
Citations

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

Fields of papers citing papers by Su Zhou

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Su Zhou. 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 Su Zhou. The network helps show where Su Zhou may publish in the future.

Co-authorship network of co-authors of Su Zhou

This figure shows the co-authorship network connecting the top 25 collaborators of Su Zhou. A scholar is included among the top collaborators of Su Zhou 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 Su Zhou. Su Zhou 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.
Chen, Nianhang, Su Zhou, Tao Zeng, et al.. (2025). An Effective Computational Strategy for UGTs Catalytic Function Prediction. ACS Synthetic Biology. 14(6). 2064–2080. 2 indexed citations
2.
Chen, Ke-Wei, Su Zhou, Chao Li, et al.. (2024). Enantioselective Construction of Quaternary Stereocenters via A Chiral Spiro Phosphoric Acid-Assisted Formal Gold Carbene gem-Dialkylation Reaction. Journal of the American Chemical Society. 146(28). 19261–19270. 14 indexed citations
3.
4.
Zhou, Su, Xinke Zhang, Jingyu Zhao, et al.. (2023). Gold-Catalyzed Alkyne Multifunctionalization through an Oxidation–Oxyalkylation–Aryloxylation Sequence. Organic Letters. 25(2). 405–409. 7 indexed citations
5.
Hong, Kemiao, Sujie Zhang, Zhijing Zhang, et al.. (2022). Asymmetric Three-Component Reaction of Two Diazo Compounds and Hyrdroxylamine Derivatives for the Access to Chiral α-Alkoxy-β-amino-carboxylates. ACS Catalysis. 12(19). 12302–12309. 13 indexed citations
6.
Bao, Ming, Su Zhou, Wenhao Hu, & Xinfang Xu. (2022). Recent advances in gold-complex and chiral organocatalyst cooperative catalysis for asymmetric alkyne functionalization. Chinese Chemical Letters. 33(12). 4969–4979. 39 indexed citations
7.
Zhou, Su, et al.. (2021). An asymmetric oxidative cyclization/Mannich-type addition cascade reaction for direct access to chiral pyrrolidin-3-ones. Chemical Communications. 57(91). 12171–12174. 6 indexed citations
8.
Zhou, Su, Yinwu Li, Xiangrong Liu, et al.. (2021). Enantioselective Oxidative Multi-Functionalization of Terminal Alkynes with Nitrones and Alcohols for Expeditious Assembly of Chiral α-Alkoxy-β-amino-ketones. Journal of the American Chemical Society. 143(36). 14703–14711. 61 indexed citations
9.
Zhang, Cheng, Kemiao Hong, Chao Pei, et al.. (2021). Gold(I)-catalyzed intramolecular cyclization/intermolecular cycloaddition cascade as a fast track to polycarbocycles and mechanistic insights. Nature Communications. 12(1). 1182–1182. 56 indexed citations
10.
Li, Yongqi, et al.. (2021). Serial dependence in biological motion perception. Journal of Vision. 21(9). 2962–2962. 1 indexed citations
11.
Zhou, Su, Qianqian Liu, Ming Bao, et al.. (2021). Gold(i)-catalyzed redox transformation of o-nitroalkynes with indoles for the synthesis of 2,3′-biindole derivatives. Organic Chemistry Frontiers. 8(8). 1808–1816. 18 indexed citations
12.
Zeng, Qian, et al.. (2020). Dirhodium(II)‐Catalyzed Cyclopropanation of Alkyne‐Containing α‐Diazoacetates for the Synthesis of Cycloalkynes. Advanced Synthesis & Catalysis. 362(15). 3137–3141. 1 indexed citations
13.
Lv, Xinxin, Shuhao Liu, Su Zhou, et al.. (2020). Asymmetric Three-Component Propargyloxylation for Direct Assembly of Polyfunctionalized Chiral Succinate Derivatives. CCS Chemistry. 3(7). 1903–1912. 21 indexed citations
14.
Hong, Kemiao, Su Zhou, Wenhao Hu, & Xinfang Xu. (2020). Rh-Catalyzed nitrene alkyne metathesis/formal C–N bond insertion cascade: synthesis of 3-iminoindolines. Organic Chemistry Frontiers. 7(11). 1327–1333. 19 indexed citations
15.
Reddy, Alavala Gopi Krishna, Su Zhou, Shi‐Kun Jia, et al.. (2020). Brønsted Acid Catalyzed Enantioselective Assembly of Spirochroman-3,3-oxindoles. Organic Letters. 22(8). 2925–2930. 29 indexed citations
16.
Zhang, Yan, Bin Chen, Su Zhou, et al.. (2019). A polyethylenimine-based diazeniumdiolate nitric oxide donor accelerates wound healing. Biomaterials Science. 7(4). 1607–1616. 52 indexed citations
17.
Wei, Hanlin, Su Zhou, Lihua Qiu, et al.. (2019). Gold‐Catalyzed Dual Annulation of Homopropargyl Alcohols with Nitrones: Synthesis of Tetrahydropyrano[4,3‐b]indole Scaffolds. Advanced Synthesis & Catalysis. 361(15). 3569–3574. 17 indexed citations
18.
Zhang, Ruhong, et al.. (1997). Cheng's Method for Reconstruction of a Functionally Sensitive Penis. Plastic & Reconstructive Surgery. 99(1). 87–91. 14 indexed citations
19.
Cheng, Kaixiang, et al.. (1996). Microsurgical Replantation of the Avulsed Scalp: Report of 20 Cases. Plastic & Reconstructive Surgery. 97(6). 1099–1106. 60 indexed citations
20.
Zhou, Su, et al.. (1993). Microsurgical Replantation of the Avulsed Scalp: Report of Six Cases. Journal of Reconstructive Microsurgery. 9(2). 121–125. 15 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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