Min‐Can Wang

2.2k total citations
105 papers, 1.9k citations indexed

About

Min‐Can Wang is a scholar working on Organic Chemistry, Inorganic Chemistry and Molecular Biology. According to data from OpenAlex, Min‐Can Wang has authored 105 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 97 papers in Organic Chemistry, 37 papers in Inorganic Chemistry and 17 papers in Molecular Biology. Recurrent topics in Min‐Can Wang's work include Asymmetric Synthesis and Catalysis (68 papers), Asymmetric Hydrogenation and Catalysis (33 papers) and Synthesis and Catalytic Reactions (31 papers). Min‐Can Wang is often cited by papers focused on Asymmetric Synthesis and Catalysis (68 papers), Asymmetric Hydrogenation and Catalysis (33 papers) and Synthesis and Catalytic Reactions (31 papers). Min‐Can Wang collaborates with scholars based in China, United States and Russia. Min‐Can Wang's co-authors include Yuan‐Zhao Hua, Junbiao Chang, Guang‐Jian Mei, Lantao Liu, Shi‐Kun Jia, Xixi Song, Mengmeng Liu, Huijie Lü, Dekun Wang and Yu‐Hang Miao and has published in prestigious journals such as Angewandte Chemie International Edition, Nature Communications and SHILAP Revista de lepidopterología.

In The Last Decade

Min‐Can Wang

104 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Min‐Can Wang China 25 1.7k 651 279 138 126 105 1.9k
Stephan J. Zuend United States 14 1.4k 0.8× 511 0.8× 387 1.4× 146 1.1× 58 0.5× 16 1.7k
Katsuhiko Moriyama Japan 30 2.4k 1.4× 618 0.9× 444 1.6× 77 0.6× 113 0.9× 97 2.6k
Anita E. Mattson United States 25 2.0k 1.2× 448 0.7× 265 0.9× 109 0.8× 80 0.6× 51 2.2k
Xueling Mi China 22 1.9k 1.1× 484 0.7× 392 1.4× 123 0.9× 100 0.8× 44 2.1k
Kohsuke Ohmatsu Japan 23 1.7k 1.0× 589 0.9× 301 1.1× 79 0.6× 78 0.6× 56 1.8k
Eugenia Marqués‐López Spain 26 2.1k 1.2× 683 1.0× 492 1.8× 151 1.1× 99 0.8× 60 2.3k
Patrick Y. Toullec France 29 3.4k 2.0× 920 1.4× 237 0.8× 93 0.7× 111 0.9× 61 3.6k
Floris Chevallier France 26 2.0k 1.2× 420 0.6× 229 0.8× 56 0.4× 51 0.4× 83 2.1k
Søren Bertelsen Denmark 15 2.6k 1.5× 659 1.0× 580 2.1× 100 0.7× 102 0.8× 21 2.7k
Eddie L. Myers United Kingdom 26 2.6k 1.6× 382 0.6× 357 1.3× 96 0.7× 195 1.5× 39 2.8k

Countries citing papers authored by Min‐Can Wang

Since Specialization
Citations

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

Fields of papers citing papers by Min‐Can Wang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Min‐Can Wang

This figure shows the co-authorship network connecting the top 25 collaborators of Min‐Can Wang. A scholar is included among the top collaborators of Min‐Can 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 Min‐Can Wang. Min‐Can 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.
Shi, Jian‐Wen, Tong Wang, Yuan‐Zhao Hua, et al.. (2024). Access to Tetrahydrothiopyrano[2,3‐b]Indole Derivatives via Zinc‐Catalyzed Asymmetric [3+3] Annulation of Indoline‐2‐Thiones with Yne–Enones. Advanced Synthesis & Catalysis. 366(8). 1770–1775. 8 indexed citations
2.
Zhang, Han, Beibei Li, Li‐Hua Huang, et al.. (2024). Azocarboxamide-enabled enantioselective regiodivergent unsymmetrical 1,2-diaminations. Nature Communications. 15(1). 10225–10225. 7 indexed citations
3.
Guan, Chun-Yan, Zhenyu Li, Ming-Jie Huang, et al.. (2024). Catalytic asymmetric synthesis of planar-chiral dianthranilides via (Dynamic) kinetic resolution. Nature Communications. 15(1). 4580–4580. 12 indexed citations
4.
Wang, Min‐Can, et al.. (2024). A Chemically Powered Rotary Molecular Motor Based on Reversible Oxazepine Formation. Angewandte Chemie International Edition. 64(5). e202418933–e202418933. 2 indexed citations
5.
Li, Na, Yu‐Hang Miao, Yuan‐Zhao Hua, et al.. (2024). Reversal of enantioselectivity by tuning the ring size of ProPhenol. Organic Chemistry Frontiers. 11(15). 4109–4118. 1 indexed citations
6.
Miao, Yu‐Hang, Yuan‐Zhao Hua, Shi‐Kun Jia, et al.. (2023). Catalytic asymmetric dearomative azo-Diels–Alder reaction of 2-vinlyindoles. Chinese Chemical Letters. 35(4). 108830–108830. 23 indexed citations
7.
Gao, Xiang, Beibei Li, Xiaoxiao Hou, et al.. (2023). Catalytic asymmetric dearomatization of phenols via divergent intermolecular (3 + 2) and alkylation reactions. Nature Communications. 14(1). 5189–5189. 22 indexed citations
8.
Han, Jiaojiao, Tao Jiang, Cui Zhang, et al.. (2023). Enantioselective access to spiro[2,3-dihydrofuran-2,2′-inden-1-ones]viazinc catalyzed [3 + 2] annulation of α-hydroxy-1-indanones with yne–enones. Organic Chemistry Frontiers. 10(16). 4061–4067. 4 indexed citations
9.
Xu, Zhihua, Na Li, Yuan‐Zhao Hua, et al.. (2023). Acyl transfer-enabled catalytic asymmetric Michael addition of α-hydroxy-1-indanones to nitroolefins. Chemical Synthesis. 3(2). 17–17. 1 indexed citations
10.
Guan, Chun-Yan, Na Li, Li‐Ping Xu, et al.. (2023). Catalytic atroposelective synthesis of heterobiaryls with vicinal C−C and N−N diaxes via dynamic kinetic resolution. iScience. 26(10). 107978–107978. 11 indexed citations
12.
Miao, Yu‐Hang, Rui Zhao, Xiao Xiao, et al.. (2023). Diversity‐Oriented Catalytic Asymmetric Dearomatization of Indoles with o‐Quinone Diimides. Advanced Science. 10(35). e2305101–e2305101. 16 indexed citations
13.
Liu, Tiantian, Yu Chen, Guang‐Jian Mei, et al.. (2023). Zinc-Catalyzed Enantioselective [3 + 3] Annulation for Synthesis of Chiral Spiro[indoline-3,4′-thiopyrano[2,3-b]indole] Derivatives. Molecules. 28(3). 1056–1056. 15 indexed citations
14.
Liu, Xinming, Lü Li, Jincan Zhao, et al.. (2020). Oxidative Halocyclization of N-Allylarylamides with KX/Oxone System: Green Synthesis of 5-Halomethyl-2-Oxazolines. Chinese Journal of Organic Chemistry. 40(12). 4298–4298. 1 indexed citations
15.
Liu, Shanshan, Wen‐Chao Gao, Yu‐Hang Miao, & Min‐Can Wang. (2019). Dinuclear Zinc-AzePhenol Catalyzed Asymmetric Aza-Henry Reaction of N-Boc Imines and Nitroalkanes under Ambient Conditions. The Journal of Organic Chemistry. 84(5). 2652–2659. 24 indexed citations
16.
Hou, Jingjing, et al.. (2018). Reactivity of sp2 Nitrogen and Phosphorus in a Stable Imidazolophosphinine. Organometallics. 37(3). 464–468. 10 indexed citations
17.
Hou, Jingjing, et al.. (2018). λ3‐Pyrroloazaphosphinines with Relatively Stable P=C Double Bonds. European Journal of Organic Chemistry. 2018(22). 2863–2869. 2 indexed citations
18.
Guo, Yifei, et al.. (2016). Well-defined podophyllotoxin polyprodrug brushes: preparation via RAFT polymerization and evaluation as drug carriers. Polymer Chemistry. 8(5). 901–909. 14 indexed citations
19.
Hua, Yuan‐Zhao, et al.. (2015). A New Strategy for Enantioselective Construction of Multisubstituted Five‐Membered Oxygen Heterocycles via a Domino Michael/Hemiketalization Reaction. Chemistry - A European Journal. 21(34). 11994–11998. 51 indexed citations
20.
Hua, Yuan‐Zhao, et al.. (2014). Highly Enantioselective Catalytic System for Asymmetric Copolymerization of Carbon Dioxide and Cyclohexene Oxide. Chemistry - A European Journal. 20(39). 12394–12398. 49 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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