Fu‐She Han

3.6k total citations · 1 hit paper
82 papers, 3.1k citations indexed

About

Fu‐She Han is a scholar working on Organic Chemistry, Molecular Biology and Inorganic Chemistry. According to data from OpenAlex, Fu‐She Han has authored 82 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 74 papers in Organic Chemistry, 15 papers in Molecular Biology and 14 papers in Inorganic Chemistry. Recurrent topics in Fu‐She Han's work include Catalytic C–H Functionalization Methods (27 papers), Catalytic Cross-Coupling Reactions (19 papers) and Asymmetric Hydrogenation and Catalysis (14 papers). Fu‐She Han is often cited by papers focused on Catalytic C–H Functionalization Methods (27 papers), Catalytic Cross-Coupling Reactions (19 papers) and Asymmetric Hydrogenation and Catalysis (14 papers). Fu‐She Han collaborates with scholars based in China, Japan and Russia. Fu‐She Han's co-authors include Lianxun Gao, Guo‐Jie Wu, Yu‐Long Zhao, Jing Guan, You Li, Zhijun Du, Dongxing Tan, Jinying Ding, Xue Zhong and Qi Shuai and has published in prestigious journals such as Journal of the American Chemical Society, Chemical Society Reviews and Angewandte Chemie International Edition.

In The Last Decade

Fu‐She Han

80 papers receiving 3.1k citations

Hit Papers

Transition-metal-catalyzed Suzuki–Miyaura cross-coupling ... 2013 2026 2017 2021 2013 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fu‐She Han China 29 2.9k 691 279 232 125 82 3.1k
Lei Jiao China 37 4.2k 1.5× 851 1.2× 318 1.1× 268 1.2× 130 1.0× 84 4.9k
José C. González‐Gómez Spain 24 3.0k 1.0× 676 1.0× 457 1.6× 158 0.7× 61 0.5× 67 3.2k
Brian L. Pagenkopf United States 33 3.0k 1.0× 353 0.5× 373 1.3× 317 1.4× 78 0.6× 78 3.4k
Steven W. M. Crossley United States 11 1.8k 0.6× 528 0.8× 443 1.6× 154 0.7× 132 1.1× 12 2.4k
Ryo Takita Japan 25 1.9k 0.7× 496 0.7× 288 1.0× 181 0.8× 76 0.6× 73 2.3k
Boris J. Nachtsheim Germany 34 4.0k 1.4× 945 1.4× 481 1.7× 279 1.2× 108 0.9× 84 4.3k
Jerry A. Murry United States 28 2.4k 0.8× 571 0.8× 526 1.9× 171 0.7× 105 0.8× 53 2.7k
Kyle W. Quasdorf United States 12 3.5k 1.2× 749 1.1× 238 0.9× 102 0.4× 107 0.9× 16 3.7k
Ilija Čorić Germany 19 1.8k 0.6× 713 1.0× 237 0.8× 253 1.1× 49 0.4× 27 2.2k
Yuki Yabe Japan 17 1.7k 0.6× 664 1.0× 241 0.9× 161 0.7× 71 0.6× 21 2.1k

Countries citing papers authored by Fu‐She Han

Since Specialization
Citations

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

Fields of papers citing papers by Fu‐She Han

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Fu‐She Han. 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 Fu‐She Han. The network helps show where Fu‐She Han may publish in the future.

Co-authorship network of co-authors of Fu‐She Han

This figure shows the co-authorship network connecting the top 25 collaborators of Fu‐She Han. A scholar is included among the top collaborators of Fu‐She Han 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 Fu‐She Han. Fu‐She Han 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.
Tan, Dongxing, Jie Zhou, Chengyu Gu, et al.. (2025). Enantioselective total syntheses of melotenine-, voacafrine-, and tabersonine-type Aspidosperma indole alkaloids. Chem. 11(6). 102440–102440. 3 indexed citations
2.
Shahzad, Sohail Anjum, et al.. (2024). Drug molecules beyond chemical biology: fluorescence- and DFT-based investigations for fluoride ion sensing and the trace detection of chloroform. RSC Advances. 14(51). 37993–38001. 4 indexed citations
3.
Zhao, Yan, Guo‐Jie Wu, Dongxing Tan, & Fu‐She Han. (2024). Pd-catalyzed room temperature hydrodeoxygenation of aryl sulfonates by tuning the stereoelectronic nature of ligands. Tetrahedron. 162. 134120–134120.
4.
Li, Zongjun, et al.. (2024). N,N-Dimethylformamide-Promoted Synthesis of Fullerene-Fused Oxazoline Derivatives. Chinese Journal of Organic Chemistry. 44(1). 242–242. 1 indexed citations
6.
Wu, Guo‐Jie, et al.. (2018). Total synthesis of cyrneines A–B and glaucopine C. Nature Communications. 9(1). 2148–2148. 25 indexed citations
8.
Wu, Guo‐Jie, Fu‐She Han, & Yu‐Long Zhao. (2015). Palladacycles derived from arylphosphinamides for mild Suzuki–Miyaura cross-couplings. RSC Advances. 5(85). 69776–69781. 18 indexed citations
9.
Li, Yu, et al.. (2014). The Development of Copper‐Catalyzed Aerobic Oxidative Coupling of H‐Tetrazoles with Boronic Acids and an Insight into the Reaction Mechanism. Chemistry - A European Journal. 20(8). 2373–2381. 53 indexed citations
10.
Zhao, Yu‐Long, Guo‐Jie Wu, You Li, Lianxun Gao, & Fu‐She Han. (2012). [NiCl2(dppp)]‐Catalyzed Cross‐Coupling of Aryl Halides with Dialkyl Phosphite, Diphenylphosphine Oxide, and Diphenylphosphine. Chemistry - A European Journal. 18(31). 9622–9627. 152 indexed citations
11.
Li, Yu, Lianxun Gao, & Fu‐She Han. (2012). Efficient synthesis of 2,5-disubstituted tetrazoles via the Cu2O-catalyzed aerobic oxidative direct cross-coupling of N–H free tetrazoles with boronic acids. Chemical Communications. 48(21). 2719–2719. 50 indexed citations
12.
Zhong, Xue, You Li, & Fu‐She Han. (2012). Al‐Catalyzed Facile Construction of Quaternary CC Bonds by the Allylic Substitution of Tertiary Alcohols: A Concise and Formal Synthesis of (±)‐Mersicarpine. Chemistry - A European Journal. 18(32). 9784–9788. 59 indexed citations
13.
Zhao, Yu‐Long, Guo‐Jie Wu, & Fu‐She Han. (2012). Ni-catalyzed construction of C–P bonds from electron-deficient phenols via the in situ aryl C–O activation by PyBroP. Chemical Communications. 48(47). 5868–5868. 98 indexed citations
14.
Gao, Lianxun, et al.. (2011). PdCl2-catalyzed efficient allylation and benzylation of heteroarenes under ligand, base/acid, and additive-free conditions. Chemical Communications. 47(18). 5289–5289. 51 indexed citations
15.
Kang, Chuanqing, Zheng Bian, Yabing He, et al.. (2011). An organogel formed from a cyclic β-aminoalcohol. Chemical Communications. 47(38). 10746–10746. 12 indexed citations
16.
Zhao, Yu‐Long, You Li, Li Yu, Lianxun Gao, & Fu‐She Han. (2010). Aryl Phosphoramides: Useful Electrophiles for Suzuki–Miyaura Coupling Catalyzed by a NiCl2/dppp System (dppp=1,3‐Bis(diphenylphosphino)propane). Chemistry - A European Journal. 16(17). 4991–4994. 49 indexed citations
17.
Yu, Haijun, Lianxun Gao, & Fu‐She Han. (2010). Reliable and Diverse Synthesis of Aryl Azides through Copper‐Catalyzed Coupling of Boronic Acids or Esters with TMSN3. Chemistry - A European Journal. 16(27). 7969–7972. 75 indexed citations
18.
Han, Fu‐She, Masayoshi Higuchi, & Dirk G. Kurth. (2008). Synthesis of π-conjugated, pyridine ring functionalized bis-terpyridines with efficient green, blue, and purple emission. Tetrahedron. 64(38). 9108–9116. 29 indexed citations
19.
Sureshan, Kana M., et al.. (2004). Resolution of synthetically useful myo-inositol derivatives using the chiral auxiliary O-acetylmandelic acid. Tetrahedron Asymmetry. 16(1). 231–241. 7 indexed citations
20.
Han, Fu‐She, Minoru Hayashi, & Yutaka Watanabe. (2003). Regioselective phosphorylation of vicinal 3,4-hydroxy myo-inositol derivative promoted practical synthesis of d-PtdIns(4,5)P2 and d-Ins(1,4,5)P3. Tetrahedron. 59(39). 7703–7711. 10 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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