Baohua Chen

3.4k total citations
154 papers, 2.9k citations indexed

About

Baohua Chen is a scholar working on Organic Chemistry, Molecular Biology and Inorganic Chemistry. According to data from OpenAlex, Baohua Chen has authored 154 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 137 papers in Organic Chemistry, 21 papers in Molecular Biology and 14 papers in Inorganic Chemistry. Recurrent topics in Baohua Chen's work include Catalytic C–H Functionalization Methods (57 papers), Synthesis and Biological Evaluation (32 papers) and Catalytic Cross-Coupling Reactions (28 papers). Baohua Chen is often cited by papers focused on Catalytic C–H Functionalization Methods (57 papers), Synthesis and Biological Evaluation (32 papers) and Catalytic Cross-Coupling Reactions (28 papers). Baohua Chen collaborates with scholars based in China, France and Indonesia. Baohua Chen's co-authors include Xu Meng, Dong Wang, Yongxin Chen, Xin Guo, Jihui Li, Mingming Zhao, Ping Wu, Na Li, Dong Tang and Ma Yongxiang and has published in prestigious journals such as Chemical Communications, Green Chemistry and The Journal of Organic Chemistry.

In The Last Decade

Baohua Chen

152 papers receiving 2.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Baohua Chen China 29 2.6k 461 295 294 191 154 2.9k
Fan Xu China 29 1.9k 0.7× 468 1.0× 522 1.8× 184 0.6× 72 0.4× 85 2.2k
Gabriel Radivoy Argentina 26 2.0k 0.8× 588 1.3× 376 1.3× 325 1.1× 70 0.4× 74 2.3k
Heng Zhang China 37 3.9k 1.5× 288 0.6× 613 2.1× 317 1.1× 319 1.7× 114 4.5k
Charlotte E. Willans United Kingdom 29 1.7k 0.6× 191 0.4× 690 2.3× 325 1.1× 205 1.1× 65 2.3k
Eietsu Hasegawa Japan 27 2.2k 0.8× 233 0.5× 191 0.6× 207 0.7× 204 1.1× 111 2.4k
Rosa López Spain 25 2.0k 0.8× 563 1.2× 528 1.8× 309 1.1× 49 0.3× 65 2.6k
Yanhui Shi China 28 1.9k 0.7× 181 0.4× 760 2.6× 504 1.7× 115 0.6× 126 2.5k
K. Rajender Reddy India 33 2.5k 1.0× 447 1.0× 882 3.0× 408 1.4× 121 0.6× 84 3.1k
Cong‐Ying Zhou China 31 2.9k 1.1× 166 0.4× 878 3.0× 468 1.6× 148 0.8× 78 3.3k
Takanori Iwasaki Japan 29 2.3k 0.9× 322 0.7× 608 2.1× 201 0.7× 69 0.4× 100 2.7k

Countries citing papers authored by Baohua Chen

Since Specialization
Citations

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

Fields of papers citing papers by Baohua Chen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Baohua Chen

This figure shows the co-authorship network connecting the top 25 collaborators of Baohua Chen. A scholar is included among the top collaborators of Baohua Chen 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 Baohua Chen. Baohua Chen 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.
Yu, Bin, Jian Wu, Baohua Chen, et al.. (2025). Biomechanical analysis of axial-radial integrated functional gradient material implants in healthy and osteoporotic bones. Dental Materials Journal. 44(2). 179–189.
2.
Zhai, Rui, Baohua Chen, Xiaoxiao Jiang, et al.. (2023). One-pot synthesis of rod-like lignin@zeolitic imidazolate framework-8 with enhanced immobilization of β-glucosidase. Industrial Crops and Products. 196. 116473–116473. 7 indexed citations
3.
4.
Liu, Yafeng, et al.. (2020). Rhodium-catalyzed ortho-acrylation of aryl ketone O-methyl oximes with cyclopropenones. Organic & Biomolecular Chemistry. 18(20). 3823–3826. 6 indexed citations
5.
Liu, Xiang, Xu Meng, Jihui Li, et al.. (2019). Recent Developments in the Synthesis of Nitrogen-Containing Heterocycles through C–H/N–H Bond Functionalizations and Oxidative Cyclization. Synlett. 30(9). 1026–1036. 25 indexed citations
6.
7.
Han, Jianwei, et al.. (2018). CuBr‐Catalyzed Synthesis of Indolizines from Pyridine, Acetophenone and Chalcone under Solvent‐Free Conditions. ChemistrySelect. 3(11). 3014–3017. 9 indexed citations
8.
9.
Chen, Baohua, Lei Deng, Yueqi Duan, Zhixiang Chen, & Jie Zhou. (2016). Multiple model fusion in 3-D reconstruction: Illumination and scale invariance. Journal of Tsinghua University(Science and Technology). 56(9). 969–973. 2 indexed citations
10.
Fu, Yajie, Panpan Wang, Xin Guo, et al.. (2016). Synthesis of Polyfunctional Pyridines via Copper-Catalyzed Oxidative Coupling Reactions. The Journal of Organic Chemistry. 81(23). 11671–11677. 48 indexed citations
11.
Yang, Xiaodong, et al.. (2016). Iodothiocyanation/Nitration of Allenes with Potassium Thiocyanate/Silver Nitrite and Iodine. Advanced Synthesis & Catalysis. 358(19). 3130–3134. 28 indexed citations
12.
Chen, Baohua, Ji‐Tai Li, & Guofeng Chen. (2014). Efficient synthesis of 2,3-disubstituted-2,3-dihydroquinazolin-4(1H)-ones catalyzed by dodecylbenzenesulfonic acid in aqueous media under ultrasound irradiation. Ultrasonics Sonochemistry. 23. 59–65. 53 indexed citations
13.
Chen, Guofeng, Haidong Shen, Liyan Zhang, et al.. (2013). Eco-Friendly Synthesis of 2-Substituted Benzimidazoles Using Air as the Oxidant. Australian Journal of Chemistry. 66(2). 262–266. 14 indexed citations
14.
Chen, Wenlin, et al.. (2012). Iodine-induced regioselective direct alkylation of azoles via in situ formed alkyliodide. Tetrahedron. 68(38). 7956–7959. 9 indexed citations
15.
Wang, Dong, Mingming Zhao, Xiang Liu, et al.. (2011). Quick and highly efficient copper-catalyzed cycloaddition of organic azides with terminal alkynes. Organic & Biomolecular Chemistry. 10(2). 229–231. 44 indexed citations
16.
Liu, Jia‐Cheng, Jing Cao, Wen‐Ting Deng, & Baohua Chen. (2011). Synthesis, Crystal Structure, Photoluminescent, and Electrochemical Properties of a Novel 2-D silver(I) Coordination Polymer with 1H-1,2,4-Triazole-1-Methylene-1H-Benzimidazole-1-Acetic Acid. Journal of Chemical Crystallography. 41(6). 806–810. 12 indexed citations
17.
Zhang, Cunli, et al.. (2008). Convenient and rapid palladium-catalyzed coupling reaction between ferrocenylethyne and aryl iodides. Catalysis Communications. 10(6). 1006–1009. 4 indexed citations
18.
Ma, Fangfang, et al.. (2005). Highly Efficient Solid‐State Synthesis of α,β‐Epoxy Ketones.. ChemInform. 36(52). 1 indexed citations
19.
Li, Bang‐Jing, et al.. (2003). Preparation, spectroscopy and electrochemistry of some ferrocenyl Schiff base derivatives with NLO responses. Lanzhou University Institutional Repository. 42(10). 2643–2648. 2 indexed citations
20.
Xu, Qihai, Baohua Chen, Yongxiang Ma, Wanyi Liu, & Yong‐Min Liang. (2002). MICROWAVE-ASSISTED SYNTHESIS OF SUBSTITUTED CYCLOPROPYL, FERROCENYL KETONES BY A SULFUR YLIDE REACTION UNDER SOLID-STATE CONDITIONS. Organic Preparations and Procedures International. 34(2). 194–198. 1 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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