Guangxun Li

2.7k total citations
86 papers, 2.2k citations indexed

About

Guangxun Li is a scholar working on Organic Chemistry, Molecular Biology and Inorganic Chemistry. According to data from OpenAlex, Guangxun Li has authored 86 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 56 papers in Organic Chemistry, 24 papers in Molecular Biology and 18 papers in Inorganic Chemistry. Recurrent topics in Guangxun Li's work include Synthesis and Catalytic Reactions (21 papers), Asymmetric Synthesis and Catalysis (21 papers) and Asymmetric Hydrogenation and Catalysis (16 papers). Guangxun Li is often cited by papers focused on Synthesis and Catalytic Reactions (21 papers), Asymmetric Synthesis and Catalysis (21 papers) and Asymmetric Hydrogenation and Catalysis (16 papers). Guangxun Li collaborates with scholars based in China, United States and Taiwan. Guangxun Li's co-authors include Zhuo Tang, Junxuan Lü, Hongbo Hu, Zhuo Tang, Qingquan Fu, Shiqi Zhang, Xin Cui, Chung S. Yang, Kyung‐Sun Kang and Xiaomei Zhang 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

Guangxun Li

85 papers receiving 2.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Guangxun Li China 29 1.1k 648 314 266 229 86 2.2k
Aristi P. Fernandes Sweden 28 471 0.4× 1.7k 2.7× 1.3k 4.0× 151 0.6× 306 1.3× 42 3.3k
Qiuzhi Cindy Cui United States 20 431 0.4× 1.4k 2.1× 290 0.9× 300 1.1× 75 0.3× 27 2.8k
Howard D. Beall United States 26 783 0.7× 1.4k 2.1× 112 0.4× 143 0.5× 172 0.8× 52 2.4k
Daniel Plano Spain 30 1.3k 1.2× 559 0.9× 823 2.6× 63 0.2× 79 0.3× 103 2.7k
Yum‐Shing Wong Hong Kong 20 323 0.3× 692 1.1× 567 1.8× 63 0.2× 87 0.4× 48 2.1k
Mümtaz İşcan Türkiye 24 490 0.5× 558 0.9× 81 0.3× 151 0.6× 174 0.8× 69 1.6k
Juan Antonio Palop Spain 32 1.6k 1.5× 604 0.9× 696 2.2× 69 0.3× 80 0.3× 97 2.9k
Vesna Milacic United States 18 694 0.7× 837 1.3× 127 0.4× 136 0.5× 32 0.1× 21 2.1k
Jorge Gaspar Portugal 29 189 0.2× 792 1.2× 62 0.2× 616 2.3× 370 1.6× 78 2.1k
Mamdouh M. Ali Egypt 33 2.0k 1.9× 980 1.5× 114 0.4× 74 0.3× 27 0.1× 120 3.1k

Countries citing papers authored by Guangxun Li

Since Specialization
Citations

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

Fields of papers citing papers by Guangxun Li

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Guangxun Li

This figure shows the co-authorship network connecting the top 25 collaborators of Guangxun Li. A scholar is included among the top collaborators of Guangxun 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 Guangxun Li. Guangxun 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.
Zhang, Shiqi, Xuyang Wang, Wanting Yang, et al.. (2025). Catalytic Enantioselective Nucleophilic Desymmetrization at Phosphorus(V): A Three-Phase Strategy for Modular Preparation of Phosphoramidates. Journal of the American Chemical Society. 147(13). 11010–11018. 14 indexed citations
2.
Li, Guangxun, et al.. (2025). One-Pot Efficient Synthesis of Sulfonimidamides from Sulfonyl Chloride. Synlett. 36(11). 1502–1507. 2 indexed citations
3.
Yan, Ming, Jiawei Zou, Dongmei Fang, et al.. (2025). Enantioselective Desymmetrization of Phosphinic Acids via Cu-Catalyzed O-Arylation. ACS Catalysis. 15(6). 4719–4725. 7 indexed citations
4.
Yuan, Yi, Yi Fu, Shan Zhou, et al.. (2023). The aptamer-based RNA-PROTAC. Bioorganic & Medicinal Chemistry. 86. 117299–117299. 16 indexed citations
5.
Yan, Ming, et al.. (2023). Synthesis of sulfinamides via photocatalytic alkylation or arylation of sulfinylamine. Organic & Biomolecular Chemistry. 22(2). 348–352. 17 indexed citations
6.
Zhang, Shiqi, et al.. (2023). Quinoxaline-specific enantioselective sulfa-michael reaction catalyzed by chiral phosphoric acid. Chinese Chemical Letters. 34(12). 108145–108145. 4 indexed citations
7.
Chen, Jinfang, Congcong Yin, Xin Cui, et al.. (2022). Synthesis of axially chiral N-aryl benzimidazoles via chiral phosphoric acid catalyzed enantioselective oxidative aromatization. New Journal of Chemistry. 46(14). 6398–6402. 3 indexed citations
8.
Huang, Jin, Jinfang Chen, Xin Cui, et al.. (2022). Preparation of Dihydronaphthofurans from α-Hydroxyl Ketones via a One-Pot Multicomponent Reaction Based on Heyns Rearrangement. The Journal of Organic Chemistry. 87(5). 3311–3318. 8 indexed citations
9.
10.
Guo, Dongdong, et al.. (2020). Pictet–Spengler reaction based on in situ generated α-amino iminium ions through the Heyns rearrangement. Organic Chemistry Frontiers. 7(20). 3242–3246. 11 indexed citations
11.
12.
Li, Guangxun, Zhuo Tang, Hongxin Liu, Yingwei Wang, & Shiqi Zhang. (2017). Bioinspired Catalysis: Self-Assembly of a Protein and DNA as a Catalyst for the Aldol Reaction in Aqueous Media. Synlett. 29(5). 560–565. 3 indexed citations
13.
14.
Li, Guangxun, et al.. (2016). Investigation and Application of Amphoteric α-Amino Aldehyde: An in Situ Generated Species Based on Heyns Rearrangement. Organic Letters. 18(18). 4526–4529. 32 indexed citations
15.
Li, Guangxun, Hongxin Liu, Gang Lv, et al.. (2015). Enantioselective Organocatalytic Transfer Hydrogenation of 1,2-Dihydroquinoline through Formation of Aza-o-xylylene. Organic Letters. 17(17). 4125–4127. 55 indexed citations
16.
Sakamori, Ryotaro, Shiyan Yu, Xiao Zhang, et al.. (2014). CDC42 Inhibition Suppresses Progression of Incipient Intestinal Tumors. Cancer Research. 74(19). 5480–5492. 44 indexed citations
17.
Smolarek, Amanda K., Jae Young So, Ah‐Ng Tony Kong, et al.. (2012). Dietary Administration of δ- and γ-Tocopherol Inhibits Tumorigenesis in the Animal Model of Estrogen Receptor–Positive, but not HER-2 Breast Cancer. Cancer Prevention Research. 5(11). 1310–1320. 41 indexed citations
18.
Wu, Lei, Guangxun Li, Qingquan Fu, Luoting Yu, & Zhuo Tang. (2012). Organocatalytic asymmetric Michael reaction with acylsilane donors. Organic & Biomolecular Chemistry. 11(3). 443–447. 19 indexed citations
19.
Li, Guangxun, Zhizhong Wang, Runhua Lu, & Zhuo Tang. (2011). Enantiodifferentiating photoisomerization of cyclooctene included and sensitized by benzoate modified β-cyclodextrin derivatives: switching of product chirality by solvent. Tetrahedron Letters. 52(24). 3097–3101. 6 indexed citations
20.
Wang, Lei, Melissa J.L. Bonorden, Guangxun Li, et al.. (2009). Methyl-Selenium Compounds Inhibit Prostate Carcinogenesis in the Transgenic Adenocarcinoma of Mouse Prostate Model with Survival Benefit. Cancer Prevention Research. 2(5). 484–495. 99 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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