Li Hai

1.6k total citations
97 papers, 1.4k citations indexed

About

Li Hai is a scholar working on Organic Chemistry, Molecular Biology and Biomaterials. According to data from OpenAlex, Li Hai has authored 97 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 66 papers in Organic Chemistry, 27 papers in Molecular Biology and 12 papers in Biomaterials. Recurrent topics in Li Hai's work include Catalytic C–H Functionalization Methods (34 papers), Synthesis and Catalytic Reactions (17 papers) and Cyclopropane Reaction Mechanisms (13 papers). Li Hai is often cited by papers focused on Catalytic C–H Functionalization Methods (34 papers), Synthesis and Catalytic Reactions (17 papers) and Cyclopropane Reaction Mechanisms (13 papers). Li Hai collaborates with scholars based in China, South Korea and United States. Li Hai's co-authors include Yong Wu, Li Guo, Qiantao Wang, Songyang Lv, Chen Zhang, Yi Zhao, Yuesen Shi, Ruizhi Lai, Xiaocen Li and Zhen Zhan and has published in prestigious journals such as Chemical Communications, ACS Applied Materials & Interfaces and Nanoscale.

In The Last Decade

Li Hai

94 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Li Hai China 23 824 330 229 175 111 97 1.4k
Alessandro Sacchetti Italy 26 1.2k 1.4× 793 2.4× 342 1.5× 328 1.9× 141 1.3× 125 2.3k
Subrata Shaw United States 13 549 0.7× 372 1.1× 122 0.5× 167 1.0× 141 1.3× 22 1.1k
Marco Blangetti Italy 19 572 0.7× 210 0.6× 62 0.3× 185 1.1× 178 1.6× 50 1.1k
Hyuk Lee South Korea 23 797 1.0× 748 2.3× 418 1.8× 368 2.1× 83 0.7× 45 1.9k
Valentina Oliveri Italy 22 428 0.5× 561 1.7× 234 1.0× 161 0.9× 211 1.9× 57 1.7k
Jiayan Shi China 22 336 0.4× 263 0.8× 149 0.7× 348 2.0× 287 2.6× 55 1.8k
Huoji Chen China 29 1.8k 2.2× 347 1.1× 91 0.4× 127 0.7× 116 1.0× 56 2.4k
Xing Zheng China 23 404 0.5× 683 2.1× 312 1.4× 267 1.5× 206 1.9× 86 2.0k
Lantao Liu China 27 1.2k 1.4× 375 1.1× 54 0.2× 217 1.2× 220 2.0× 119 2.3k
Beena G. Singh India 17 240 0.3× 220 0.7× 169 0.7× 113 0.6× 88 0.8× 62 867

Countries citing papers authored by Li Hai

Since Specialization
Citations

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

Fields of papers citing papers by Li Hai

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Li Hai

This figure shows the co-authorship network connecting the top 25 collaborators of Li Hai. A scholar is included among the top collaborators of Li Hai 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 Li Hai. Li Hai 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
2.
Lai, Ruizhi, Li Hai, Ruifang Nie, et al.. (2024). Discovery, synthesis and biological evaluation of novel isoquinoline derivatives as potent indoleamine 2, 3-dioxygenase 1 and tryptophan 2, 3-dioxygenase dual inhibitors. European Journal of Medicinal Chemistry. 279. 116852–116852. 3 indexed citations
3.
Lai, Ruizhi, Li Hai, Zhongzhen Yang, et al.. (2024). Novel berberine derivatives as p300 histone acetyltransferase inhibitors in combination treatment for breast cancer. European Journal of Medicinal Chemistry. 266. 116116–116116. 5 indexed citations
4.
Liu, Xingyu, Guanghui Lv, Xue Zhang, et al.. (2024). Visible-Light-Driven Coupling of 1,3,4-Oxadiazoles and Hydroxamic Acid Derivatives. The Journal of Organic Chemistry. 89(14). 10012–10020. 6 indexed citations
5.
Zhang, Xue, Xingyu Liu, Jian Chen, et al.. (2024). Organic Photoredox-Catalyzed Site-Selective Alkylation of Glycine Derivatives and Peptides via Infrequent 1,2-Hydrogen Atom Transfer of Amidyl Radicals. Organic Letters. 26(36). 7638–7643. 13 indexed citations
6.
Chen, Jian, et al.. (2020). Synthesis of 4-ethenyl quinazolines via rhodium(iii)-catalyzed [5 + 1] annulation reaction of N-arylamidines with cyclopropenones. Organic Chemistry Frontiers. 7(4). 672–677. 30 indexed citations
7.
Liu, Qi‐Jun, et al.. (2020). Biotin and glucose co-modified multi-targeting liposomes for efficient delivery of chemotherapeutics for the treatment of glioma. Bioorganic & Medicinal Chemistry. 29. 115852–115852. 23 indexed citations
8.
Zhao, Yi, et al.. (2019). Ascorbic acid-modified brain-specific liposomes drug delivery system with “lock-in” function. Chemistry and Physics of Lipids. 224. 104727–104727. 24 indexed citations
9.
Zhang, Chen, Xiaomei Chen, Yi Luo, et al.. (2018). Imidazolium-Based Ionic Liquid: An Efficient, Normalized, and Recyclable Platform for Rh(III)-Catalyzed Directed C–H Carbenoid Coupling Reactions. ACS Sustainable Chemistry & Engineering. 6(10). 13473–13479. 22 indexed citations
10.
Zhang, Li, Yi Zhao, Li Hai, et al.. (2018). Preparation and Characterization of GLUT1-mediated Novel Brain Targeting Magnetic Nanoparticles. Letters in Drug Design & Discovery. 15(12). 1308–1313. 3 indexed citations
11.
Lv, Songyang, Yaling Li, Tian Yao, et al.. (2018). Rhodium-Catalyzed Direct C-H Bond Cyanation in Ionic Liquids. Organic Letters. 20(16). 4994–4997. 45 indexed citations
12.
Jiang, Chong, et al.. (2017). Potassium tert-Butanolate promoted reaction of benzaldehydes and indoles: a new strategy for synthesis of bis(indolyl)arylmethanes. Chemical Research in Chinese Universities. 33(2). 200–205. 2 indexed citations
13.
Li, Renjun, Yan Zhou, Yang Zheng, Li Hai, & Yong Wu. (2016). The synthesis and biological evaluation of unsymmetrical 2,2-di(1H-indol-3-yl)-N-phenylacetamide derivatives. Tetrahedron Letters. 57(26). 2829–2832. 10 indexed citations
14.
He, Yun, Yang Zheng, Li Hai, & Yong Wu. (2014). A Versatile Total Synthesis of 8‐Oxyberberine and Oxohomoberberines. Chinese Journal of Chemistry. 32(11). 1121–1127. 4 indexed citations
15.
16.
Li, Xiaocen, et al.. (2013). Design, synthesis and biological evaluation for docetaxel-loaded brain targeting liposome with “lock-in” function. Journal of drug targeting. 22(3). 251–261. 20 indexed citations
17.
Li, Xiaocen, et al.. (2013). Design, synthesis and biological evaluation of multivalent glucosides with high affinity as ligands for brain targeting liposomes. European Journal of Medicinal Chemistry. 72. 110–118. 50 indexed citations
18.
Fan, Lei, et al.. (2011). Design, synthesis and preliminary bio-evaluation of glucose–cholesterol derivatives as ligands for brain targeting liposomes. Chinese Chemical Letters. 22(7). 831–834. 20 indexed citations
19.
Li, Xiaocen, et al.. (2010). Design, Synthesis and Biological Evaluation of Lipophilic Analogs of Anethol Trithione. Letters in Drug Design & Discovery. 7(10). 747–753. 1 indexed citations
20.
Li, Jie, et al.. (2008). Study on synthesis and distribution in vivo of 5-Fu-cholic acid conjugate. Chinese Chemical Letters. 20(2). 136–138. 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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