Zhen‐Ting Du

1.8k total citations · 1 hit paper
65 papers, 1.6k citations indexed

About

Zhen‐Ting Du is a scholar working on Organic Chemistry, Molecular Biology and Insect Science. According to data from OpenAlex, Zhen‐Ting Du has authored 65 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Organic Chemistry, 12 papers in Molecular Biology and 9 papers in Insect Science. Recurrent topics in Zhen‐Ting Du's work include Synthetic Organic Chemistry Methods (19 papers), Catalytic C–H Functionalization Methods (15 papers) and Asymmetric Synthesis and Catalysis (12 papers). Zhen‐Ting Du is often cited by papers focused on Synthetic Organic Chemistry Methods (19 papers), Catalytic C–H Functionalization Methods (15 papers) and Asymmetric Synthesis and Catalysis (12 papers). Zhen‐Ting Du collaborates with scholars based in China, United States and Germany. Zhen‐Ting Du's co-authors include Zhihui Shao, Yin Wang, Jing Zhou, Congyang Wang, Yuying Zhang, Bang‐Guo Wei, Youqiang Li, Johannes H. J. Berthel, Udo Radius and Todd B. Marder and has published in prestigious journals such as Journal of the American Chemical Society, Chemical Society Reviews and ACS Catalysis.

In The Last Decade

Zhen‐Ting Du

63 papers receiving 1.6k citations

Hit Papers

Combining transition metal catalysis and organocatalysis ... 2012 2026 2016 2021 2012 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Zhen‐Ting Du China 15 1.5k 345 175 145 75 65 1.6k
Oleg G. Kulinkovich Belarus 21 1.9k 1.3× 226 0.7× 192 1.1× 172 1.2× 39 0.5× 70 2.0k
Asunción Barbero Spain 20 1.6k 1.1× 248 0.7× 187 1.1× 75 0.5× 63 0.8× 67 1.7k
Fredrik Cederbaum Switzerland 15 1.2k 0.8× 339 1.0× 188 1.1× 50 0.3× 42 0.6× 17 1.4k
Suk‐Ku Kang South Korea 29 2.3k 1.6× 330 1.0× 261 1.5× 59 0.4× 54 0.7× 138 2.5k
Jin‐Tao Liu China 21 1.1k 0.8× 234 0.7× 269 1.5× 671 4.6× 63 0.8× 122 1.5k
Xiao‐Feng Xia China 26 1.8k 1.3× 271 0.8× 153 0.9× 133 0.9× 65 0.9× 69 2.0k
Jianyou Mao China 24 1.6k 1.1× 384 1.1× 203 1.2× 127 0.9× 111 1.5× 73 1.9k
Michael E. Furrow United States 4 1.0k 0.7× 261 0.8× 285 1.6× 48 0.3× 96 1.3× 5 1.3k
Vito Fiandanese Italy 26 1.5k 1.1× 188 0.5× 285 1.6× 75 0.5× 96 1.3× 89 1.7k
Jun‐ichi Matsuo Japan 27 2.1k 1.4× 344 1.0× 348 2.0× 100 0.7× 101 1.3× 112 2.3k

Countries citing papers authored by Zhen‐Ting Du

Since Specialization
Citations

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

Fields of papers citing papers by Zhen‐Ting Du

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Zhen‐Ting Du. 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 Zhen‐Ting Du. The network helps show where Zhen‐Ting Du may publish in the future.

Co-authorship network of co-authors of Zhen‐Ting Du

This figure shows the co-authorship network connecting the top 25 collaborators of Zhen‐Ting Du. A scholar is included among the top collaborators of Zhen‐Ting Du 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 Zhen‐Ting Du. Zhen‐Ting Du 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.
Yang, Xuan, et al.. (2025). Design and synthesis of thiolutin derived PSMD14/HDAC dual-target inhibitors against esophageal squamous cell carcinoma. Bioorganic Chemistry. 161. 108500–108500. 1 indexed citations
2.
Chen, Dongdong, et al.. (2024). Design, Synthesis, and Antimicrobial Activity of Amide Derivatives Containing Cyclopropane. Molecules. 29(17). 4124–4124. 3 indexed citations
3.
He, Chun‐Ting, et al.. (2022). Asymmetric Synthesis of (S)-14-Methyl-1-Octadecene, the Sex Pheromone of the Peach Leafminer Moth. Chemistry of Natural Compounds. 58(2). 320–325. 1 indexed citations
4.
Liu, Sifan, et al.. (2021). A New Asymmetric Synthesis of (S)-14-Methyl-1-Octadecene, the Sex Pheromone of the Peach Leafminer Moth. Natural Product Communications. 16(5). 1 indexed citations
5.
Zhang, Tao, et al.. (2021). A Novel Synthesis of Sex Pheromone from the Longicorn Beetle(Psacothea hilaris). Russian Journal of Organic Chemistry. 57(3). 455–461. 2 indexed citations
6.
Shi, Jianmin, Liang Wei, Lu Liu, et al.. (2019). An efficient asymmetric synthesis of (4R,8R)‐4,8‐dimethyldecanal, the most active component of natural Tribolure. Journal of the Chinese Chemical Society. 66(7). 756–760. 4 indexed citations
7.
Chen, Ya‐Fang, et al.. (2017). Synthesis of Xanthones by Palladium‐Catalyzed Tandem Carbonylation/C–H Activation via 2‐Iodo Diaryl Ethers. Journal of the Chinese Chemical Society. 65(1). 28–32. 4 indexed citations
8.
Zhang, Tao, et al.. (2017). Concise asymmetric synthesis of the sex pheromone of the tea tussock moth. Tetrahedron Asymmetry. 28(11). 1562–1567. 11 indexed citations
9.
Zhang, Yuying, Yiwen Liu, Zhuo‐Ya Mao, et al.. (2016). Asymmetric synthesis of epohelmins A, B and 3-epi ent-epohelmin A. Tetrahedron. 72(49). 8091–8098. 10 indexed citations
10.
Zhang, Yuying, Zhuo‐Ya Mao, Zhu Zhou, Zhen‐Ting Du, & Bang‐Guo Wei. (2015). Divergent synthesis of L-685,458 and its analogues involving one-pot intramolecular tandem sequence reaction. Tetrahedron. 71(50). 9396–9402. 8 indexed citations
11.
Du, Zhen‐Ting, et al.. (2013). A Metal-Free Oxidation of Benzo[c]chromen to Benzo[c]chromen-6-ones by t-Butyl Hydroperoxide in the Presence of Potassium Iodide. Heterocycles. 87(9). 1889–1889. 5 indexed citations
12.
Zhang, Tao, et al.. (2013). A Facile Asymmetric Synthesis of (S)-14-Methyl-1-Octadecene, the Sex Pheromone of the Peach Leafminer Moth. Molecules. 18(5). 5201–5208. 12 indexed citations
13.
Du, Zhen‐Ting & Zhihui Shao. (2012). Combining transition metal catalysis and organocatalysis – an update. Chemical Society Reviews. 42(3). 1337–1378. 630 indexed citations breakdown →
14.
Du, Zhen‐Ting, et al.. (2012). Synthesis of Dibenzofurans by Palladium-Catalysed Tandem Denitrification/C-H Activation. Synlett. 23(14). 2146–2146. 4 indexed citations
15.
Yuan, Mao‐Sen, Tianbao Li, Wenji Wang, et al.. (2012). Thiophene-functionalized octupolar triindoles: Synthesis and photophysical properties. Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy. 96. 1020–1024. 7 indexed citations
16.
Shi, Baojun, et al.. (2011). 2-Methoxy-4-methyl-1-[1-(phenylsulfonyl)propan-2-yl]benzene. Acta Crystallographica Section E Structure Reports Online. 67(10). o2589–o2589.
17.
Du, Zhen‐Ting, et al.. (2010). Facile Syntheses of (±)-Curcuphenol, (±)-Curcudiol, (±)-Curcuhydroquinone, and (±)-Curcuquinone. Synthetic Communications. 40(13). 1920–1926. 3 indexed citations
18.
Du, Zhen‐Ting, et al.. (2010). 2,4-Dinitro-1-phenoxybenzene. Acta Crystallographica Section E Structure Reports Online. 66(2). o415–o415. 1 indexed citations
19.
Du, Zhen‐Ting, et al.. (2004). Enantioselective Synthesis of (+)-Nuciferal, (+)-(E)-Nuciferol and (+)α-Curcumene by Chiral Hydrogenesterification Reaction. Chinese Chemical Letters. 15(12). 1389–1391. 4 indexed citations
20.
Du, Zhen‐Ting, et al.. (2004). Enantioselective synthesis of (+)-nuciferal, (+)-(E)-nuciferol and (+)-α-curcumene by chiral hydrogenesterification reaction. Journal of Chemical Research. 2004(6). 427–429. 8 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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