Hongbo Dong

536 total citations
52 papers, 402 citations indexed

About

Hongbo Dong is a scholar working on Molecular Biology, Organic Chemistry and Pharmacology. According to data from OpenAlex, Hongbo Dong has authored 52 papers receiving a total of 402 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 26 papers in Organic Chemistry and 10 papers in Pharmacology. Recurrent topics in Hongbo Dong's work include Bioactive natural compounds (12 papers), Natural product bioactivities and synthesis (10 papers) and Synthesis of Organic Compounds (7 papers). Hongbo Dong is often cited by papers focused on Bioactive natural compounds (12 papers), Natural product bioactivities and synthesis (10 papers) and Synthesis of Organic Compounds (7 papers). Hongbo Dong collaborates with scholars based in China, Taiwan and Singapore. Hongbo Dong's co-authors include Mingan Wang, Wenbo Ma, Lutz Ackermann, Yujiao He, Min Wu, Zheng Shi, Mingyan Yang, Zhi-Hong Xu, Weihong Du and Jinmin Wang and has published in prestigious journals such as Cancer Research, International Journal of Molecular Sciences and The Journal of Organic Chemistry.

In The Last Decade

Hongbo Dong

48 papers receiving 394 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Hongbo Dong China	13	218	143	54	48	38	52	402
M. B. M. DE AZEVEDO Brazil	11	245 1.1×	148 1.0×	69 1.3×	50 1.0×	31 0.8×	15	477
Thomas Gaslonde France	12	155 0.7×	180 1.3×	54 1.0×	122 2.5×	17 0.4×	32	374
K. K. Turgunov Uzbekistan	8	208 1.0×	124 0.9×	60 1.1×	83 1.7×	11 0.3×	106	363
Atef G. Hanna Egypt	12	107 0.5×	172 1.2×	78 1.4×	77 1.6×	22 0.6×	37	431
Stéphane Poigny France	13	249 1.1×	124 0.9×	56 1.0×	21 0.4×	18 0.5×	29	397
Kazuhito Ogihara Japan	12	139 0.6×	216 1.5×	27 0.5×	88 1.8×	22 0.6×	37	371
Juan M. Amaro‐Luis Venezuela	12	186 0.9×	234 1.6×	39 0.7×	106 2.2×	20 0.5×	58	457
Shurong Ban China	13	315 1.4×	138 1.0×	37 0.7×	36 0.8×	24 0.6×	52	481
Francine Libot France	12	130 0.6×	142 1.0×	42 0.8×	99 2.1×	49 1.3×	20	341
V. L. Niranjan Reddy India	11	300 1.4×	180 1.3×	68 1.3×	95 2.0×	12 0.3×	23	585

Countries citing papers authored by Hongbo Dong

Since Specialization

Citations

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

Fields of papers citing papers by Hongbo Dong

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hongbo Dong

This figure shows the co-authorship network connecting the top 25 collaborators of Hongbo Dong. A scholar is included among the top collaborators of Hongbo Dong 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 Hongbo Dong. Hongbo Dong 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

Song, Weijie, Wenqiang Ma, Qi Sun, et al.. (2025). A biotin-conjugated highly stable cationic viologen derivative for live-cell imaging. Journal of Materials Chemistry B. 13(42). 13715–13724.

Wang, Na, Zhanjun Hou, Yinghui Wang, et al.. (2025). Design, synthesis, and biological evaluation of membrane-active cannabichromene derivatives as potent antibacterial agents. European Journal of Medicinal Chemistry. 296. 117888–117888. 1 indexed citations

Tan, Fei, Zaili Luo, Ting Peng, et al.. (2025). Total synthesis and reconfirmation of the absolute configuration of melanochromone. Tetrahedron. 185. 134808–134808.

Liao, Li, et al.. (2024). Total synthesis and antibacterial evaluation of lupalbigenin and isolupalbigenin. Journal of Asian Natural Products Research. 27(4). 556–567. 2 indexed citations

Dong, Hongbo, Pei Yu, Ting Peng, et al.. (2023). Total Synthesis of Kuwanons A and B and Discovery of Their Antibacterial Mechanism. Journal of Natural Products. 86(8). 2022–2030. 13 indexed citations

Yu, Pei, et al.. (2023). Total syntheses of pongaflavone and its natural analogues. Journal of Asian Natural Products Research. 25(11). 1085–1096. 3 indexed citations

Dong, Hongbo, et al.. (2023). Total syntheses and antibacterial evaluations of cudraflavones A-C and related Flavones. Bioorganic Chemistry. 140. 106764–106764. 15 indexed citations

Snyder, Larry, Taavi K. Neklesa, Xin Chen, et al.. (2023). Abstract ND03: Discovery of ARV-766, an androgen receptor degrading PROTAC® for the treatment of men with metastatic castration resistant prostate cancer. Cancer Research. 83(7_Supplement). ND03–ND03. 12 indexed citations

Li, Ying, et al.. (2022). Total Synthesis and Anti-Inflammatory Activity of Velutone F. Natural Product Communications. 17(2). 2 indexed citations

10.

Wu, Min, et al.. (2021). First total syntheses of four natural bioactive glucosides. Synthetic Communications. 1–6. 1 indexed citations

11.

Dong, Hongbo, et al.. (2020). First total syntheses of two natural glycosides. Carbohydrate Research. 499. 108200–108200. 4 indexed citations

12.

Dong, Hongbo, et al.. (2017). First total synthesis of a new phenylpropanoid glycoside: natural cytotoxic compound from Cirsium japonicum. Journal of Asian Natural Products Research. 20(12). 1154–1161. 6 indexed citations

13.

Winkler, Julia, Kanak Raina, Martha Altieri, et al.. (2016). PROTAC BET degraders are more broadly effective than BET inhibitors. European Journal of Cancer. 69. S10–S10. 3 indexed citations

14.

Xu, Zhi-Hong, et al.. (2015). Synthesis and Biological Activity of Novel 4-Methyl-3-substituted-phenyl-2-benzoylimine Thiazolines with Hydantion. Chinese Journal of Organic Chemistry. 35(2). 411–411. 2 indexed citations

15.

Zhao, Jin, et al.. (2014). Synthesis and antifungal activity of 7-methyl-7-hydroxy-2,3-benzo[c]octa-1,6-olide. Journal of Asian Natural Products Research. 16(3). 312–317. 9 indexed citations

16.

Dong, Hongbo, et al.. (2014). Asymmetric total synthesis of all four isomers of 6-acetoxy-5-hexadecanolide: the major component of mosquito oviposition attractant pheromones. Tetrahedron Asymmetry. 25(8). 610–616. 9 indexed citations

17.

Dong, Hongbo, Mingyan Yang, Bin Liu, & Mingan Wang. (2014). Concise stereoselective total synthesis of (+)-muricatacin and (+)-epi-muricatacin. Journal of Asian Natural Products Research. 16(8). 847–853. 5 indexed citations

18.

Dong, Hongbo, et al.. (2013). Total synthesis of 3,7-dimethyl-7-hydroxy-2-octen-1,6-olide and 3,7-dimethyl-2,6-octadien-1,6-olide. Journal of Asian Natural Products Research. 15(8). 880–884. 9 indexed citations

19.

Wang, Jinmin, et al.. (2013). Synthesis and Biological Activity of Novel Phosphoramidate with Hydantoin. Chinese Journal of Organic Chemistry. 33(3). 596–596. 2 indexed citations

20.

Dong, Hongbo. (1997). The formal stereoselective synthesis of (+)-preussin. Chinese Chemical Letters. 8. 693–694. 7 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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