Zhanchao Meng

465 total citations
8 papers, 386 citations indexed

About

Zhanchao Meng is a scholar working on Organic Chemistry, Molecular Biology and Pharmacology. According to data from OpenAlex, Zhanchao Meng has authored 8 papers receiving a total of 386 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Organic Chemistry, 3 papers in Molecular Biology and 3 papers in Pharmacology. Recurrent topics in Zhanchao Meng's work include Synthetic Organic Chemistry Methods (4 papers), Marine Sponges and Natural Products (3 papers) and Microbial Natural Products and Biosynthesis (3 papers). Zhanchao Meng is often cited by papers focused on Synthetic Organic Chemistry Methods (4 papers), Marine Sponges and Natural Products (3 papers) and Microbial Natural Products and Biosynthesis (3 papers). Zhanchao Meng collaborates with scholars based in Germany, China and United States. Zhanchao Meng's co-authors include Alois Fürstner, Ang Li, Peng Yang, Wanyin Tao, Jin Zhong, David J. Edmonds, Ming Wan, Li Li, Hao Chen and Rolf Müller and has published in prestigious journals such as Journal of the American Chemical Society, Nature Communications and The Journal of Organic Chemistry.

In The Last Decade

Zhanchao Meng

8 papers receiving 380 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Zhanchao Meng Germany 8 330 109 108 65 52 8 386
Janick Ardisson France 12 371 1.1× 94 0.9× 81 0.8× 58 0.9× 28 0.5× 32 424
Matthew J. Palframan United Kingdom 13 296 0.9× 160 1.5× 65 0.6× 45 0.7× 25 0.5× 22 410
Gangarajula Sudhakar India 12 313 0.9× 114 1.0× 49 0.5× 56 0.9× 30 0.6× 40 377
Day‐Shin Hsu Taiwan 13 365 1.1× 51 0.5× 68 0.6× 73 1.1× 24 0.5× 31 414
Jesse D. More United States 5 325 1.0× 111 1.0× 58 0.5× 43 0.7× 29 0.6× 8 383
Lujiang Deng China 9 375 1.1× 141 1.3× 72 0.7× 37 0.6× 60 1.2× 14 457
Sotirios Totokotsopoulos United States 8 319 1.0× 73 0.7× 45 0.4× 44 0.7× 25 0.5× 9 385
Chris Sfouggatakis United States 12 462 1.4× 133 1.2× 130 1.2× 74 1.1× 36 0.7× 20 542
Yosuke Kaburagi Japan 9 450 1.4× 110 1.0× 47 0.4× 73 1.1× 76 1.5× 10 518
Yian Guo China 12 307 0.9× 90 0.8× 64 0.6× 88 1.4× 33 0.6× 29 390

Countries citing papers authored by Zhanchao Meng

Since Specialization
Citations

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

Fields of papers citing papers by Zhanchao Meng

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Zhanchao Meng

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

All Works

8 of 8 papers shown
1.
Meng, Zhanchao, et al.. (2024). Total Synthesis of the Norcembranoid Scabrolide B and Its Transformation into Sinuscalide C, Ineleganolide, and Horiolide. Journal of the American Chemical Society. 146(35). 24250–24256. 13 indexed citations
2.
Meng, Zhanchao & Alois Fürstner. (2022). Total Syntheses of Scabrolide A and Nominal Scabrolide B. Journal of the American Chemical Society. 144(4). 1528–1533. 25 indexed citations
3.
Meng, Zhanchao, et al.. (2021). A Unified Approach to Polycyclic Alkaloids of the Ingenamine Estate: Total Syntheses of Keramaphidin B, Ingenamine, and Nominal Njaoamine I. Journal of the American Chemical Society. 143(35). 14402–14414. 34 indexed citations
4.
Meng, Zhanchao & Alois Fürstner. (2020). Total Synthesis Provides Strong Evidence: Xestocyclamine A is the Enantiomer of Ingenamine. Journal of the American Chemical Society. 142(27). 11703–11708. 39 indexed citations
5.
Meng, Zhanchao & Alois Fürstner. (2018). Total Synthesis of (−)-Sinulariadiolide. A Transannular Approach. Journal of the American Chemical Society. 141(2). 805–809. 56 indexed citations
6.
Meng, Zhanchao, Laetitia Souillart, Brendan M. Monks, et al.. (2017). A “Motif-Oriented” Total Synthesis of Nannocystin Ax. Preparation and Biological Assessment of Analogues. The Journal of Organic Chemistry. 83(13). 6977–6994. 67 indexed citations
7.
Sun, Yu, Zhanchao Meng, Deliang Zhang, et al.. (2016). A concise total synthesis of sespenine, a structurally unusual indole terpenoid from Streptomyces. Organic Chemistry Frontiers. 3(3). 368–374. 27 indexed citations
8.
Meng, Zhanchao, Li Li, Wanyin Tao, et al.. (2015). Total synthesis and antiviral activity of indolosesquiterpenoids from the xiamycin and oridamycin families. Nature Communications. 6(1). 6096–6096. 125 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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