Lu-Tai Pan

684 total citations
35 papers, 578 citations indexed

About

Lu-Tai Pan is a scholar working on Molecular Biology, Plant Science and Pharmacology. According to data from OpenAlex, Lu-Tai Pan has authored 35 papers receiving a total of 578 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 13 papers in Plant Science and 10 papers in Pharmacology. Recurrent topics in Lu-Tai Pan's work include Bioactive Natural Diterpenoids Research (14 papers), Phytochemistry and Biological Activities (10 papers) and Plant-based Medicinal Research (9 papers). Lu-Tai Pan is often cited by papers focused on Bioactive Natural Diterpenoids Research (14 papers), Phytochemistry and Biological Activities (10 papers) and Plant-based Medicinal Research (9 papers). Lu-Tai Pan collaborates with scholars based in China, Hong Kong and Singapore. Lu-Tai Pan's co-authors include Chengli Mou, Yonggui Robin, Liejin Zhou, Zhichao Jin, Xingxing Wu, Huifang Chai, Yunpeng Lu, Rakesh Maiti, Hongjie Zhang and Runjiang Song and has published in prestigious journals such as Angewandte Chemie International Edition, Nature Communications and SHILAP Revista de lepidopterología.

In The Last Decade

Lu-Tai Pan

31 papers receiving 570 citations

Peers

Lu-Tai Pan

OC

MB

PS

PHARM

IC

Ren‐Qiang Mei China

Nadiah Mad Nasir Malaysia

Rong Long China

Mariola Zielińska‐Błajet Poland

Stéphane Lebrun France

Kathlia A. De Castro-Cruz Philippines

Kazutada Ikeuchi Japan

Tomohiro Asakawa Japan

Rosimeire C. Barcelos Brazil

Li‐Jun Wu China

Ren‐Qiang Mei China

Lu-Tai Pan

209 ×0.6

OC

157 ×0.9

MB

78 ×0.9

PS

50 ×0.6

PHARM

48 ×0.7

IC

Citations per year, relative to Lu-Tai Pan Lu-Tai Pan (= 1×) peers Ren‐Qiang Mei

Countries citing papers authored by Lu-Tai Pan

Since Specialization

Citations

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

Fields of papers citing papers by Lu-Tai Pan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lu-Tai Pan. 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 Lu-Tai Pan. The network helps show where Lu-Tai Pan may publish in the future.

Co-authorship network of co-authors of Lu-Tai Pan

This figure shows the co-authorship network connecting the top 25 collaborators of Lu-Tai Pan. A scholar is included among the top collaborators of Lu-Tai Pan 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 Lu-Tai Pan. Lu-Tai Pan is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

1.

Yang, Yaxin, Abdullah Al Mamun, Lei Wang, et al.. (2025). Cytotoxic and anticoagulative diterpenoid glycosides from Pteris decrescens. Phytochemistry. 240. 114643–114643.

2.

Pan, Lu-Tai, et al.. (2024). Abietane diterpenoids from Isodon amethystoides and their biological activities. Phytochemistry. 225. 114171–114171.

3.

Luo, Guoyong, et al.. (2023). Flavidanolides A and B from Isodon flavidus. Chinese Chemical Letters. 34(9). 108621–108621. 1 indexed citations

4.

Zou, Juan, et al.. (2023). Guidongnins I–J: Two New 6,7-seco-7,20-Olide-ent-kaurene Diterpenes with Unusual Structures from Isodon rubescens. International Journal of Molecular Sciences. 24(17). 13451–13451. 1 indexed citations

5.

Zhang, Chiyuan, et al.. (2023). Design and synthesis of oridonin derivatives as cytotoxic agents. Natural Product Research. 39(3). 550–558.

6.

Zhang, Chiyuan, et al.. (2022). Bioactive isopimarane and 3,4-seco isopimarane diterpenoids from Isodon amethystoides. BMC Chemistry. 16(1). 96–96. 3 indexed citations

7.

Zhu, Xun, et al.. (2020). Green and Facile Synthesis of Spirocyclopentanes Through NaOH-Promoted Chemo- and Diastereo-Selective (3 + 2) Cycloaddition Reactions of Activated Cyclopropanes and Enamides. Frontiers in Chemistry. 8. 542–542. 3 indexed citations

8.

Ke, Jie, Hongling Wang, Liejin Zhou, et al.. (2019). Hydrodehalogenation of Aryl Halides through Direct Electrolysis. Chemistry - A European Journal. 25(28). 6911–6914. 43 indexed citations

9.

Zhou, Liejin, Xingxing Wu, Xing Yang, et al.. (2019). Gold and Carbene Relay Catalytic Enantioselective Cycloisomerization/Cyclization Reactions of Ynamides and Enals. Angewandte Chemie. 132(4). 1573–1577. 18 indexed citations

10.

Zhou, Liejin, Xingxing Wu, Xing Yang, et al.. (2019). Gold and Carbene Relay Catalytic Enantioselective Cycloisomerization/Cyclization Reactions of Ynamides and Enals. Angewandte Chemie International Edition. 59(4). 1557–1561. 80 indexed citations

11.

Wu, Xingxing, Liejin Zhou, Rakesh Maiti, et al.. (2018). Sulfinate and Carbene Co‐catalyzed Rauhut–Currier Reaction for Enantioselective Access to Azepino[1,2‐a]indoles. Angewandte Chemie. 131(2). 487–491. 15 indexed citations

12.

Zhu, Tingshun, Liejin Zhou, Chengli Mou, et al.. (2018). Access to All‐Carbon Spirocycles through a Carbene and Thiourea Cocatalytic Desymmetrization Cascade Reaction. Angewandte Chemie. 131(6). 1798–1802. 14 indexed citations

13.

Zhu, Tingshun, Liejin Zhou, Chengli Mou, et al.. (2018). Access to All‐Carbon Spirocycles through a Carbene and Thiourea Cocatalytic Desymmetrization Cascade Reaction. Angewandte Chemie International Edition. 58(6). 1784–1788. 64 indexed citations

14.

Wu, Xingxing, Liejin Zhou, Rakesh Maiti, et al.. (2018). Sulfinate and Carbene Co‐catalyzed Rauhut–Currier Reaction for Enantioselective Access to Azepino[1,2‐a]indoles. Angewandte Chemie International Edition. 58(2). 477–481. 65 indexed citations

15.

Liu, Yuchen, Zhijun Zhang, Jia Su, et al.. (2017). Lycodine-Type Lycopodium Alkaloids from the Whole Plants of Huperzia serrata. Natural Products and Bioprospecting. 7(5). 405–411. 12 indexed citations

16.

Luo, Guoyong, et al.. (2017). Two cytotoxic 6,7-seco-spiro-lacton-ent-kauranoids from Isodon rubescens. Journal of Asian Natural Products Research. 20(3). 227–233. 8 indexed citations

17.

Zou, Juan, Lu-Tai Pan, Qi‐Ji Li, et al.. (2012). Rubesanolides C–E: abietane diterpenoids isolated from Isodon rubescens and evaluation of their anti-biofilm activity. Organic & Biomolecular Chemistry. 10(26). 5039–5039. 33 indexed citations

18.

Pan, Lu-Tai, et al.. (2009). Resource distribution and exploitation of edible ferns in Guizhou.. Anhui nongye kexue. 10(5). 102–139. 3 indexed citations

19.

Pan, Lu-Tai, et al.. (2002). [Studies on chemical constituents in the leaf of Ligustrum delavayanum].. PubMed. 27(10). 754–6. 1 indexed citations

20.

Sun, Han-Dong, et al.. (1995). Diterpenoids from Isodon eriocalyx var. laxiflora. Phytochemistry. 38(6). 1451–1455. 27 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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