Ming Wang

3.8k total citations · 2 hit papers
83 papers, 3.3k citations indexed

About

Ming Wang is a scholar working on Organic Chemistry, Molecular Biology and Pharmaceutical Science. According to data from OpenAlex, Ming Wang has authored 83 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 65 papers in Organic Chemistry, 6 papers in Molecular Biology and 6 papers in Pharmaceutical Science. Recurrent topics in Ming Wang's work include Sulfur-Based Synthesis Techniques (39 papers), Chemical Synthesis and Reactions (23 papers) and Synthesis and Catalytic Reactions (19 papers). Ming Wang is often cited by papers focused on Sulfur-Based Synthesis Techniques (39 papers), Chemical Synthesis and Reactions (23 papers) and Synthesis and Catalytic Reactions (19 papers). Ming Wang collaborates with scholars based in China, Poland and United Kingdom. Ming Wang's co-authors include Xuefeng Jiang, Shihao Chen, Qiaoling Fan, Yaping Li, Daming Zeng, Wei‐Ping Deng, Su Huang, Yiming Li, Zhijian Huang and Jianpeng Wei and has published in prestigious journals such as Journal of the American Chemical Society, Chemical Society Reviews and Angewandte Chemie International Edition.

In The Last Decade

Ming Wang

78 papers receiving 3.2k citations

Hit Papers

Ni-catalyzed C–S bond construction and cleavage 2022 2026 2023 2024 2022 2022 50 100 150

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ming Wang China 31 3.0k 237 173 141 104 83 3.3k
Georg Manolikakes Germany 36 3.5k 1.2× 422 1.8× 162 0.9× 341 2.4× 89 0.9× 95 3.8k
Bingqing Tang China 8 1.8k 0.6× 166 0.7× 83 0.5× 89 0.6× 69 0.7× 10 1.9k
Ri‐Yuan Tang China 32 3.7k 1.2× 271 1.1× 276 1.6× 404 2.9× 200 1.9× 121 3.9k
Guanyinsheng Qiu China 37 4.9k 1.6× 334 1.4× 359 2.1× 314 2.2× 85 0.8× 137 5.1k
Mieko Arisawa Japan 25 2.0k 0.7× 259 1.1× 175 1.0× 209 1.5× 91 0.9× 100 2.2k
Shun‐Yi Wang China 43 4.8k 1.6× 518 2.2× 243 1.4× 407 2.9× 429 4.1× 153 5.0k
Manuel A. Fernández‐Rodríguez Spain 32 3.2k 1.1× 167 0.7× 63 0.4× 314 2.2× 138 1.3× 78 3.3k
Lal Dhar S. Yadav India 36 4.3k 1.4× 583 2.5× 132 0.8× 281 2.0× 39 0.4× 231 4.5k
Biquan Xiong China 26 1.7k 0.5× 149 0.6× 106 0.6× 235 1.7× 47 0.5× 117 1.9k
Torben Rogge Germany 30 2.7k 0.9× 211 0.9× 248 1.4× 676 4.8× 99 1.0× 47 2.9k

Countries citing papers authored by Ming Wang

Since Specialization
Citations

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

Fields of papers citing papers by Ming Wang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ming Wang

This figure shows the co-authorship network connecting the top 25 collaborators of Ming Wang. A scholar is included among the top collaborators of Ming Wang 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 Ming Wang. Ming Wang 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.
Zeng, Daming, et al.. (2025). Construction of a Chiral Click Chemistry Platform via Enantioselective F/Cl Exchange at S(VI) Centers. Journal of the American Chemical Society. 147(33). 30380–30389. 6 indexed citations
2.
Zhang, Qianyu, Ziyu Huang, Mingxing Ren, et al.. (2025). Injectable cationic dynamic hydrogel with supramolecular drug loading reprograms neutrophil fate to alleviate diabetic periodontitis. Materials Today Bio. 35. 102557–102557.
3.
Huang, Su, Daming Zeng, Ming Wang, & Xuefeng Jiang. (2025). Ligand-controlled divergent sulfuration and disulfuration via Ni-catalysed reductive cross-coupling involving thiourea dioxide. Nature Synthesis. 5(3). 398–408. 1 indexed citations
5.
Yang, Heqing, Yanyan Liao, Hao Guo, & Ming Wang. (2025). Emerging Applications of Thiol-Based Catalysts in Hydrogen Atom Transfer Reactions: A Comprehensive Review. Molecules. 30(20). 4058–4058. 1 indexed citations
6.
Zeng, Daming, et al.. (2025). Cu‐catalyzed Bilateral Linkage of Sulfenamides for the Construction of Benzothiophene‐based Cyclic Sulfilimines. European Journal of Organic Chemistry. 28(16). 3 indexed citations
8.
Huang, Rui, et al.. (2024). Desulfonylative Functionalization of Organosulfones via Inert (Hetero)Aryl C(sp2)–SO2 Bond Cleavage. Molecules. 29(17). 4137–4137. 1 indexed citations
9.
Zeng, Daming, et al.. (2024). C-SuFEx linkage of sulfonimidoyl fluorides and organotrifluoroborates. Nature Communications. 15(1). 727–727. 23 indexed citations
10.
Ji, Lei, et al.. (2024). From Polyester Plastics to Diverse Monomers via Low‐Energy Upcycling. Advanced Science. 11(25). e2403002–e2403002. 28 indexed citations
11.
Liao, Yanyan, Ming Wang, & Xuefeng Jiang. (2023). Sulfur-containing peptides: Synthesis and application in the discovery of potential drug candidates. Current Opinion in Chemical Biology. 75. 102336–102336. 19 indexed citations
12.
Wu, Yunjun, Xiaoxia Gu, Zhijun Feng, et al.. (2022). Synthesis of pyrano[3,2-c]quinolones and furo[3,2-c]quinolonesviaacid-catalyzed tandem reaction of 4-hydroxy-1-methylquinolin-2(1H)-one and propargylic alcohols. RSC Advances. 12(33). 21066–21078. 6 indexed citations
13.
Ma, Qin, Yushan Wang, Xiaoxia Gu, et al.. (2021). Synthesis of tetrahydro-β-carbolines from 2-indolylmethyl azides and propargylic alcohols. RSC Advances. 11(32). 19639–19646. 7 indexed citations
14.
Wang, Ming & Xuefeng Jiang. (2020). Transition Metal-Catalyzed Cross-Coupling of Carbene from Ketones or Aldehydes via N-Tosylhydrazones. Chinese Journal of Organic Chemistry. 40(10). 3473–3473. 2 indexed citations
15.
Wang, Ming, et al.. (2019). Design and application of α-ketothioesters as 1,2-dicarbonyl-forming reagents. Nature Communications. 10(1). 2661–2661. 123 indexed citations
16.
Peng, Lifen, et al.. (2018). Phosphoryl Protecting Group Enabled Facile Synthesis of Unsymmetrical 1,3-Diynes by Selective Hay Coupling. Chinese Journal of Organic Chemistry. 38(11). 3048–3048. 5 indexed citations
17.
Wang, Ming & Xuefeng Jiang. (2018). Sulfur–Sulfur Bond Construction. Topics in Current Chemistry. 376(2). 14–14. 109 indexed citations
18.
Wang, Ming, et al.. (2011). An exo‐ and Enantioselective 1,3‐Dipolar Cycloaddition of Azomethine Ylides with Alkylidene Malonates Catalyzed by a N,O‐Ligand/Cu(OAc)2‐Derived Chiral Complex. Angewandte Chemie International Edition. 50(21). 4897–4900. 62 indexed citations
19.
Wang, Ming. (2005). Preparation of Miconazole and Econazole by PEG-400 Catalyzed Reactions of Tandem N- and O-Alkylation. Chinese Journal of Pharmaceuticals. 2 indexed citations
20.
Wilton‐Ely, James D. E. T., et al.. (2005). σ-Organyl complexes of ruthenium and osmium supported by a mixed-donor ligand. Dalton Transactions. 1930–1930. 29 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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