Taotao Ling

2.5k total citations
47 papers, 2.0k citations indexed

About

Taotao Ling is a scholar working on Organic Chemistry, Molecular Biology and Biotechnology. According to data from OpenAlex, Taotao Ling has authored 47 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Organic Chemistry, 22 papers in Molecular Biology and 13 papers in Biotechnology. Recurrent topics in Taotao Ling's work include Synthetic Organic Chemistry Methods (14 papers), Marine Sponges and Natural Products (12 papers) and Marine Toxins and Detection Methods (9 papers). Taotao Ling is often cited by papers focused on Synthetic Organic Chemistry Methods (14 papers), Marine Sponges and Natural Products (12 papers) and Marine Toxins and Detection Methods (9 papers). Taotao Ling collaborates with scholars based in United States, Puerto Rico and Japan. Taotao Ling's co-authors include Fatima Rivas, David Y.‐K. Chen, K. C. Nicolaou, Emmanuel A. Theodorakis, Scott A. Snyder, Marco Bella, Theocharis V. Koftis, Xianhai Huang, Štěpán Vyskočil and Goran Petrović and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and International Journal of Molecular Sciences.

In The Last Decade

Taotao Ling

46 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Taotao Ling United States 24 1.3k 576 334 330 324 47 2.0k
Seijiro Hosokawa Japan 30 2.2k 1.6× 607 1.1× 212 0.6× 576 1.7× 525 1.6× 101 2.6k
Chihiro Tsukano Japan 26 1.4k 1.1× 366 0.6× 248 0.7× 172 0.5× 202 0.6× 81 1.7k
Haruaki Ishiyama Japan 26 1.1k 0.8× 406 0.7× 98 0.3× 398 1.2× 382 1.2× 57 1.6k
Paul R. Blakemore United States 24 2.2k 1.6× 523 0.9× 126 0.4× 410 1.2× 290 0.9× 59 2.6k
Daisuke Urabe Japan 31 1.3k 1.0× 924 1.6× 199 0.6× 447 1.4× 336 1.0× 110 2.4k
Jun Ishihara Japan 28 1.8k 1.3× 666 1.2× 160 0.5× 298 0.9× 306 0.9× 145 2.4k
Deukjoon Kim South Korea 29 1.7k 1.3× 537 0.9× 75 0.2× 355 1.1× 347 1.1× 108 2.3k
Yoshiki Morimoto Japan 24 1.2k 0.9× 381 0.7× 84 0.3× 463 1.4× 323 1.0× 111 1.6k
Atsuo Nakazaki Japan 24 1.4k 1.1× 424 0.7× 64 0.2× 345 1.0× 338 1.0× 110 1.8k
Fuyuhiko Matsuda Japan 25 1.3k 1.0× 465 0.8× 66 0.2× 298 0.9× 291 0.9× 101 1.8k

Countries citing papers authored by Taotao Ling

Since Specialization
Citations

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

Fields of papers citing papers by Taotao Ling

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Taotao Ling

This figure shows the co-authorship network connecting the top 25 collaborators of Taotao Ling. A scholar is included among the top collaborators of Taotao Ling 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 Taotao Ling. Taotao Ling 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.
Ling, Taotao, et al.. (2024). Recent Advances in Chemistry and Antioxidant/Anticancer Biology of Monoterpene and Meroterpenoid Natural Product. Molecules. 29(1). 279–279. 14 indexed citations
2.
Martínez, Michelle, et al.. (2019). Identification of Biologically Active Ganoderma lucidum Compounds and Synthesis of Improved Derivatives That Confer Anti-cancer Activities in vitro. Frontiers in Pharmacology. 10. 115–115. 75 indexed citations
3.
Ling, Taotao, Darcie J. Miller, Walter H. Lang, et al.. (2019). Mechanistic Insight on the Mode of Action of Colletoic Acid. Journal of Medicinal Chemistry. 62(15). 6925–6940. 3 indexed citations
4.
Ling, Taotao, Walter H. Lang, Sourav Das, et al.. (2018). Novel vitexin-inspired scaffold against leukemia. European Journal of Medicinal Chemistry. 146. 501–510. 16 indexed citations
5.
Ling, Taotao, Julie Maier, Sourav Das, et al.. (2018). Identification of substituted 5-membered heterocyclic compounds as potential anti-leukemic agents. European Journal of Medicinal Chemistry. 164. 391–398. 6 indexed citations
6.
Gautam, Lekh Nath S., Taotao Ling, Walter H. Lang, & Fatima Rivas. (2016). Anti-proliferative evaluation of monoterpene derivatives against leukemia. European Journal of Medicinal Chemistry. 113. 75–80. 18 indexed citations
7.
Ling, Taotao, Lekh Nath S. Gautam, Elizabeth C. Griffith, et al.. (2016). Synthesis and evaluation of colletoic acid core derivatives. European Journal of Medicinal Chemistry. 110. 126–132. 6 indexed citations
8.
Ling, Taotao, My Tran, Miguel A. González, et al.. (2015). (+)-Dehydroabietylamine derivatives target triple-negative breast cancer. European Journal of Medicinal Chemistry. 102. 9–13. 27 indexed citations
9.
Ling, Taotao, et al.. (2013). Evaluation of Jatropha isabelli natural products and their synthetic analogs as potential antimalarial therapeutic agents. European Journal of Medicinal Chemistry. 65. 376–380. 22 indexed citations
10.
Mitachi, Katsuhiko, et al.. (2012). Synthesis and structure–activity relationship of disubstituted benzamides as a novel class of antimalarial agents. Bioorganic & Medicinal Chemistry Letters. 22(14). 4536–4539. 13 indexed citations
11.
Ling, Taotao, et al.. (2011). Synthesis of (−)-callicarpenal, a potent arthropod repellent. Tetrahedron. 67(17). 3023–3029. 21 indexed citations
12.
Nicolaou, K. C., Theocharis V. Koftis, Štěpán Vyskočil, et al.. (2004). Structural Revision and Total Synthesis of Azaspiracid‐1, Part 2: Definition of the ABCD Domain and Total Synthesis. Angewandte Chemie International Edition. 43(33). 4318–4324. 127 indexed citations
13.
Nicolaou, K. C., Štěpán Vyskočil, Theocharis V. Koftis, et al.. (2004). Structural Revision and Total Synthesis of Azaspiracid‐1, Part 1: Intelligence Gathering and Tentative Proposal. Angewandte Chemie International Edition. 43(33). 4312–4318. 84 indexed citations
14.
Nicolaou, K. C., Štěpán Vyskočil, Theocharis V. Koftis, et al.. (2004). Titelbild: Structural Revision and Total Synthesis of Azaspiracid‐1, Part 1: Intelligence Gathering and Tentative Proposal (Angew. Chem. 33/2004). Angewandte Chemie. 116(33). 4335–4335. 1 indexed citations
15.
Nicolaou, K. C., David Y.‐K. Chen, Yiwei Li, et al.. (2003). Total Synthesis of the Proposed Azaspiracid‐1 Structure, Part 2: Coupling of the C1–C20, C21–C27, and C28–C40 Fragments and Completion of the Synthesis. Angewandte Chemie International Edition. 42(31). 3649–3653. 72 indexed citations
16.
Lam, Thanh, Taotao Ling, Chinmay Chowdhury, et al.. (2003). Synthesis of a novel family of diterpenes and their evaluation as anti-inflammatory agents. Bioorganic & Medicinal Chemistry Letters. 13(19). 3217–3221. 13 indexed citations
17.
Nicolaou, K. C., Yiwei Li, Noriaki Uesaka, et al.. (2003). Total Synthesis of the Proposed Azaspiracid‐1 Structure, Part 1: Construction of the Enantiomerically Pure C1–C20, C21–C27, and C28–C40 Fragments. Angewandte Chemie International Edition. 42(31). 3643–3648. 83 indexed citations
18.
Nicolaou, K. C., Marco Bella, David Y.‐K. Chen, et al.. (2002). Total Synthesis of Diazonamide A. Angewandte Chemie International Edition. 41(18). 3495–3499. 150 indexed citations
19.
Ling, Taotao, et al.. (2001). Enantioselective Synthesis of the Antiinflammatory Agent (−)-Acanthoic Acid. The Journal of Organic Chemistry. 66(26). 8843–8853. 63 indexed citations
20.
Ling, Taotao, Alan X. Xiang, & Emmanuel A. Theodorakis. (1999). Enantioselektive Totalsynthese von Avarol und Avaron. Angewandte Chemie. 111(20). 3277–3279. 6 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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