Hao Ding

1.2k total citations
45 papers, 952 citations indexed

About

Hao Ding is a scholar working on Organic Chemistry, Inorganic Chemistry and Molecular Biology. According to data from OpenAlex, Hao Ding has authored 45 papers receiving a total of 952 indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Organic Chemistry, 15 papers in Inorganic Chemistry and 9 papers in Molecular Biology. Recurrent topics in Hao Ding's work include Asymmetric Hydrogenation and Catalysis (10 papers), Catalytic C–H Functionalization Methods (9 papers) and Organometallic Complex Synthesis and Catalysis (9 papers). Hao Ding is often cited by papers focused on Asymmetric Hydrogenation and Catalysis (10 papers), Catalytic C–H Functionalization Methods (9 papers) and Organometallic Complex Synthesis and Catalysis (9 papers). Hao Ding collaborates with scholars based in China, United States and Japan. Hao Ding's co-authors include Brian E. Hanson, Berit Bartik, Tamás Bartik, Christian W. Kohlpaintner, Panyi Huang, Bin Sun, Can Jin, Akira Shigenaga, Akira Otaka and Kohei Sato and has published in prestigious journals such as Angewandte Chemie International Edition, SHILAP Revista de lepidopterología and Macromolecules.

In The Last Decade

Hao Ding

41 papers receiving 925 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hao Ding China 18 742 310 217 123 94 45 952
Martin Lersch Norway 8 630 0.8× 341 1.1× 117 0.5× 129 1.0× 44 0.5× 9 1.0k
J.-C. Wasilke United States 6 1.4k 1.8× 462 1.5× 257 1.2× 150 1.2× 112 1.2× 8 1.5k
Julien Monot France 21 1.1k 1.5× 452 1.5× 121 0.6× 102 0.8× 197 2.1× 42 1.4k
Philip L. Osburn United States 10 804 1.1× 250 0.8× 157 0.7× 156 1.3× 43 0.5× 11 941
Wubing Yao China 16 693 0.9× 542 1.7× 128 0.6× 159 1.3× 152 1.6× 25 947
César A. Urbina‐Blanco United Kingdom 21 991 1.3× 209 0.7× 295 1.4× 104 0.8× 93 1.0× 32 1.2k
Amy H. Roy United States 9 1.5k 2.1× 575 1.9× 105 0.5× 102 0.8× 108 1.1× 10 1.7k
Shun‐ya Onozawa Japan 20 1.0k 1.4× 363 1.2× 114 0.5× 79 0.6× 132 1.4× 44 1.2k
Isabelle Suisse France 19 756 1.0× 545 1.8× 213 1.0× 85 0.7× 142 1.5× 55 1.1k
Simone Manzini United Kingdom 25 1.2k 1.6× 491 1.6× 291 1.3× 63 0.5× 223 2.4× 30 1.4k

Countries citing papers authored by Hao Ding

Since Specialization
Citations

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

Fields of papers citing papers by Hao Ding

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hao Ding

This figure shows the co-authorship network connecting the top 25 collaborators of Hao Ding. A scholar is included among the top collaborators of Hao Ding 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 Hao Ding. Hao Ding 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.
Gao, Pengfei, Boxing Yin, Yang Cao, et al.. (2025). An optimized SPE ‐ UPLC – MS / MS method for simultaneous quantification of 11 tetracyclines in dairy products. Journal of the Science of Food and Agriculture. 105(15). 8525–8539. 1 indexed citations
2.
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Xu, Junjie, Shuyu Liu, Pengfei Gao, et al.. (2025). Confirmation of enrofloxacin, ofloxacin, sarafloxacin and danofloxacin residues in poultry meat and pork via LLE-SPE-GC–MS/MS coupled with derivatization treatment. Food Chemistry X. 27. 102393–102393. 1 indexed citations
4.
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Neumann, Constanze N., et al.. (2025). Rh(II)-Catalyzed Synthesis of 1,3-Diols via 5-endo-trig Cyclization of Silyl Radicals. Synthesis. 57(15). 2320–2330. 1 indexed citations
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8.
Wang, Xiaokun, Hao Ding, Yanling Ma, et al.. (2024). CRISPR/HCR-powered ratiometric fluorescence aptasensor for ochratoxin A detection. Food Chemistry. 468. 142437–142437. 7 indexed citations
9.
Hu, Miao, et al.. (2023). The Construction of Highly Substituted Piperidines via Dearomative Functionalization Reaction. Angewandte Chemie International Edition. 62(49). e202315108–e202315108. 11 indexed citations
10.
Ding, Hao, et al.. (2021). Gelation Based on Host–Guest Interactions Induced by Multi-Functionalized Nanosheets. Gels. 7(3). 106–106. 10 indexed citations
11.
Ding, Hao, et al.. (2019). Synthesis of bioactive 2-(2-(difluoromethoxy)aryl)benzo[d]thiazole derivatives via base-promoted one-pot process. Tetrahedron. 75(35). 130472–130472. 2 indexed citations
12.
Gong, Chao, Hao Ding, Chengrong Lu, Bei Zhao, & Yingming Yao. (2017). An amidato divalent ytterbium cluster: synthesis and molecular structure, its reactivity to carbodiimides and application in the guanylation reaction. Dalton Transactions. 46(18). 6031–6038. 12 indexed citations
13.
Lei, Xiao‐Wu, Cheng‐Yang Yue, Jian-Qiang Zhao, et al.. (2015). Low-Dimensional Hybrid Cuprous Halides Directed by Transition Metal Complex: Syntheses, Crystal Structures, and Photocatalytic Properties. Crystal Growth & Design. 15(11). 5416–5426. 71 indexed citations
14.
Qin, Jie, et al.. (2015). Syntheses, Crystal Structures, and Fluorescence Properties of Cd(II), Ag(I) Complexes Based on 3,5-bis(pyridin-2-yl)-4-amino-1,2,4-triazole. Synthesis and Reactivity in Inorganic Metal-Organic and Nano-Metal Chemistry. 46(7). 968–974. 2 indexed citations
15.
Otaka, Akira, Kohei Sato, Hao Ding, & Akira Shigenaga. (2012). One‐Pot/Sequential Native Chemical Ligation Using N‐Sulfanylethylanilide Peptide. The Chemical Record. 12(5). 479–490. 37 indexed citations
16.
Ding, Hao, Brian E. Hanson, & József Bakos. (1995). Preparation of a Surface‐Active Chiral Diphosphane and Its Use in the Hydrogenation of Prochiral Olefins. Angewandte Chemie International Edition in English. 34(15). 1645–1647. 43 indexed citations
17.
Ding, Hao, et al.. (1995). Synthese eines oberflächenaktiven chiralen Diphosphans und seine Verwendung zur Hydrierung von prochiralen Olefinen. Angewandte Chemie. 107(15). 1728–1730. 19 indexed citations
18.
Bartik, Tamás, Hao Ding, Berit Bartik, & Brian E. Hanson. (1995). Surface active phosphines for catalysis under two-phase reaction conditions. P(menthyl) [(CH2)8C6H4-p-SO3Na]2 and the hydroformylation of styrene. Journal of Molecular Catalysis A Chemical. 98(3). 117–122. 48 indexed citations
19.
Ding, Hao & Brian E. Hanson. (1995). Spectator cations and catalysis with sulfonated phosphines. The role of cations in determining reaction selectivity in the aqueous phase hydroformylation of olefins. Journal of Molecular Catalysis A Chemical. 99(3). 131–137. 29 indexed citations
20.
Ding, Hao & Brian E. Hanson. (1994). Reaction activity and selectivity as a function of solution ionic strength in oct-1-ene hydroformylation with sulfonated phosphines. Journal of the Chemical Society Chemical Communications. 2747–2747. 25 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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