Ming Yu Jin

784 total citations
31 papers, 603 citations indexed

About

Ming Yu Jin is a scholar working on Organic Chemistry, Inorganic Chemistry and Biomedical Engineering. According to data from OpenAlex, Ming Yu Jin has authored 31 papers receiving a total of 603 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Organic Chemistry, 9 papers in Inorganic Chemistry and 7 papers in Biomedical Engineering. Recurrent topics in Ming Yu Jin's work include Catalytic C–H Functionalization Methods (8 papers), Asymmetric Synthesis and Catalysis (6 papers) and Fluorine in Organic Chemistry (6 papers). Ming Yu Jin is often cited by papers focused on Catalytic C–H Functionalization Methods (8 papers), Asymmetric Synthesis and Catalysis (6 papers) and Fluorine in Organic Chemistry (6 papers). Ming Yu Jin collaborates with scholars based in China, South Korea and Hong Kong. Ming Yu Jin's co-authors include Do Hyun Ryu, Jun Wang, Xiangyou Xing, Jung Woon Yang, Sun Min Kim, Jun Wu, Chen Xu, Hogyu Han, Chengbing Wang and Qianqian Zhen and has published in prestigious journals such as Angewandte Chemie International Edition, Nature Communications and Advanced Functional Materials.

In The Last Decade

Ming Yu Jin

31 papers receiving 593 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ming Yu Jin China 14 354 169 107 102 80 31 603
Wenying Ai China 10 631 1.8× 360 2.1× 160 1.5× 132 1.3× 88 1.1× 26 927
Takafumi Yatabe Japan 14 468 1.3× 213 1.3× 60 0.6× 206 2.0× 57 0.7× 45 661
Graziano Di Carmine Italy 17 598 1.7× 135 0.8× 234 2.2× 160 1.6× 100 1.3× 49 923
M. Becker United States 16 763 2.2× 234 1.4× 65 0.6× 134 1.3× 81 1.0× 27 1.0k
Bilal Nişancı Türkiye 13 335 0.9× 129 0.8× 62 0.6× 143 1.4× 40 0.5× 26 450
Heng Li China 19 1.2k 3.4× 166 1.0× 88 0.8× 131 1.3× 96 1.2× 50 1.4k
Rui M. B. Carrilho Portugal 16 516 1.5× 246 1.5× 57 0.5× 144 1.4× 89 1.1× 37 700
Konstantin Yu. Koltunov Russia 19 588 1.7× 125 0.7× 76 0.7× 415 4.1× 88 1.1× 71 974
Amrita Das India 9 745 2.1× 122 0.7× 67 0.6× 125 1.2× 126 1.6× 17 973

Countries citing papers authored by Ming Yu Jin

Since Specialization
Citations

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

Fields of papers citing papers by Ming Yu Jin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ming Yu Jin

This figure shows the co-authorship network connecting the top 25 collaborators of Ming Yu Jin. A scholar is included among the top collaborators of Ming Yu Jin 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 Yu Jin. Ming Yu Jin 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.
Jin, Ming Yu, et al.. (2025). Copper-Catalyzed Regio- and Enantioselective Hydroamination of gem-Difluoroalkenes to Access Chiral Difluoromethyl Amines. Organic Letters. 27(22). 5835–5839. 2 indexed citations
2.
Jin, Ming Yu, et al.. (2024). Triethyl amine as an effective reducing agent for sulfoxide deoxygenation. Organic & Biomolecular Chemistry. 22(16). 3215–3219. 4 indexed citations
3.
Liu, Chao, Yu Chen, Donghao Wang, et al.. (2024). Highly Enantioselective Dihydroxylation of 1,1-Disubstituted Aliphatic Alkenes Enabled by Orchestrated Noncovalent π-Interactions. Organic Letters. 26(7). 1399–1404. 2 indexed citations
4.
Jin, Ming Yu, et al.. (2024). Synthesis of Axially Chiral Monofluoroalkenes via Nickel-Catalyzed Reductive Cross-Coupling of gem-Difluoroalkenes. Organic Letters. 26(38). 8194–8199. 2 indexed citations
5.
Xu, Dongdong, et al.. (2024). Indium-Catalyzed Reductive Coupling Enabled Efficient Synthesis of Acylphosphine Oxides and Diphosphines. ACS Catalysis. 14(5). 3241–3247. 6 indexed citations
6.
Wu, Jun, Ming Yu Jin, Yong Li, et al.. (2023). Earth-abundant Co nanoparticles encapsulated in N-doped hollow carbon sphere for highly selective hydrodeoxygenation of biomass-derived vanillin. Chemical Engineering Journal. 463. 142472–142472. 52 indexed citations
7.
Wu, Jun, Yuhang Xie, Yong Li, et al.. (2023). Layered double hydroxides-based metal nanocatalysts: Confinement engineering, microenvironment effect and applications in catalytic conversion of biomass. Coordination Chemistry Reviews. 497. 215437–215437. 29 indexed citations
8.
Zhen, Qianqian, et al.. (2023). Asymmetric Dihydroxylation-Based Desymmetrization Enabled by Lone-Pair−π Interaction. ACS Catalysis. 13(14). 9745–9752. 4 indexed citations
9.
Jin, Ming Yu, et al.. (2023). Pincer Ru with a single stereogenic identity for highly efficient asymmetric transfer hydrogenation of ketones. Science China Chemistry. 66(5). 1443–1449. 6 indexed citations
10.
Wei-feng, Shi, et al.. (2023). Efficient enzymatic synthesis of chiral 2,3-dihydro-1,4-benzodioxane motif using engineered Candida antarctica lipase B. RSC Advances. 13(27). 18953–18959. 3 indexed citations
11.
Jin, Ming Yu, et al.. (2022). Engineered non-covalent π interactions as key elements for chiral recognition. Nature Communications. 13(1). 3276–3276. 65 indexed citations
13.
14.
Yang, Zhiping, et al.. (2018). Atom‐Economical and Stereoselective Difunctionalization of Electron‐Withdrawing Alkynes with N‐Trifluoromethylthiophthalimide. Asian Journal of Organic Chemistry. 7(9). 1784–1787. 10 indexed citations
15.
Jin, Ming Yu, et al.. (2016). Indoline‐Based Molecular Engineering for Optimizing the Performance of Photoactive Thin Films. Advanced Functional Materials. 26(38). 6876–6887. 17 indexed citations
16.
Meng, Ling, Ming Yu Jin, & Jun Wang. (2016). Rh-Catalyzed Conjugate Addition of Arylzinc Chlorides to Thiochromones: A Highly Enantioselective Pathway for Accessing Chiral Thioflavanones. Organic Letters. 18(19). 4986–4989. 37 indexed citations
17.
Jin, Ming Yu, Sun Min Kim, Hui Mao, et al.. (2014). Chemoselective and repetitive intermolecular cross-acyloin condensation reactions between a variety of aromatic and aliphatic aldehydes using a robust N-heterocyclic carbene catalyst. Organic & Biomolecular Chemistry. 12(10). 1547–1550. 31 indexed citations
18.
Jin, Ming Yu, et al.. (2012). Synthesis of an Environmentally Friendly Phenol-Free Resin for Printing Ink. Bulletin of the Korean Chemical Society. 33(10). 3413–3416. 13 indexed citations
19.
Kim, Sun Min, Ming Yu Jin, Mi Jin Kim, et al.. (2011). N-Heterocyclic carbene-catalysed intermolecular Stetter reactions of acetaldehyde. Organic & Biomolecular Chemistry. 9(7). 2069–2069. 25 indexed citations
20.
Jin, Ming Yu, et al.. (2010). Highly Efficient Synthesis of (+)-Bromoxone, (+)-Epiepoxydon and (+)-Epiepoformin. Bulletin of the Korean Chemical Society. 31(3). 727–730. 13 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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