Li‐Biao Han

8.5k total citations
193 papers, 7.2k citations indexed

About

Li‐Biao Han is a scholar working on Organic Chemistry, Inorganic Chemistry and Molecular Biology. According to data from OpenAlex, Li‐Biao Han has authored 193 papers receiving a total of 7.2k indexed citations (citations by other indexed papers that have themselves been cited), including 187 papers in Organic Chemistry, 99 papers in Inorganic Chemistry and 24 papers in Molecular Biology. Recurrent topics in Li‐Biao Han's work include Asymmetric Hydrogenation and Catalysis (89 papers), Organophosphorus compounds synthesis (86 papers) and Catalytic C–H Functionalization Methods (64 papers). Li‐Biao Han is often cited by papers focused on Asymmetric Hydrogenation and Catalysis (89 papers), Organophosphorus compounds synthesis (86 papers) and Catalytic C–H Functionalization Methods (64 papers). Li‐Biao Han collaborates with scholars based in Japan, China and United States. Li‐Biao Han's co-authors include Tieqiao Chen, Masato Tanaka, Chang‐Qiu Zhao, Qing Xu, Yongbo Zhou, Midori Goto, Shuang‐Feng Yin, Jia Yang, Ruwei Shen and Shigeru Shimada and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Nature Communications.

In The Last Decade

Li‐Biao Han

187 papers receiving 7.0k 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‐Biao Han Japan 48 6.8k 2.8k 768 362 322 193 7.2k
Marc Taillefer France 40 7.7k 1.1× 1.6k 0.6× 852 1.1× 546 1.5× 540 1.7× 133 8.3k
Kálmán J. Szabó Sweden 54 7.6k 1.1× 2.5k 0.9× 766 1.0× 1.5k 4.2× 248 0.8× 179 8.3k
Teruyuki Kondo Japan 43 6.1k 0.9× 2.4k 0.8× 760 1.0× 137 0.4× 586 1.8× 169 6.8k
Mamoru Tobisu Japan 57 10.6k 1.6× 2.2k 0.8× 614 0.8× 777 2.1× 313 1.0× 191 11.1k
Yasushi Nishihara Japan 47 5.4k 0.8× 995 0.4× 379 0.5× 572 1.6× 1.1k 3.5× 203 6.9k
Anant R. Kapdi India 34 6.5k 1.0× 1.3k 0.5× 496 0.6× 241 0.7× 354 1.1× 112 6.9k
Seung Hwan Cho South Korea 40 8.1k 1.2× 1.4k 0.5× 912 1.2× 243 0.7× 257 0.8× 78 8.4k
Xihe Bi China 50 7.7k 1.1× 867 0.3× 651 0.8× 1.1k 3.0× 251 0.8× 185 8.2k
Xiu‐Li Sun China 48 6.0k 0.9× 1.0k 0.4× 475 0.6× 162 0.4× 325 1.0× 124 6.4k
Rebecca L. Melen United Kingdom 35 3.3k 0.5× 1.6k 0.6× 348 0.5× 213 0.6× 410 1.3× 129 3.7k

Countries citing papers authored by Li‐Biao Han

Since Specialization
Citations

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

Fields of papers citing papers by Li‐Biao Han

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Li‐Biao Han

This figure shows the co-authorship network connecting the top 25 collaborators of Li‐Biao Han. A scholar is included among the top collaborators of Li‐Biao 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 Li‐Biao Han. Li‐Biao 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
2.
Su, Lebin, Jianyu Dong, Yangyang Shen, et al.. (2025). General (hetero)polyaryl amine synthesis via multicomponent cycloaromatization of amines. Nature Communications. 16(1). 169–169. 8 indexed citations
3.
5.
Han, Li‐Biao, et al.. (2024). Chiral α-Aminophosphonates as Ligands in Copper-Catalyzed Asymmetric Oxidative Coupling of 2-Naphthols. Organic Letters. 26(25). 5274–5279. 5 indexed citations
6.
Xiao, Jing, Yichun Xie, & Li‐Biao Han. (2024). Advances in Organic Reactions Using Phosphorus Acid as Reducing Agent. Chinese Journal of Organic Chemistry. 44(12). 3702–3702. 3 indexed citations
7.
Xu, Tianhao, Lingling Wang, Jingwei Zhao, et al.. (2023). Metal-free highly chemo-selective bisphosphorylation and deoxyphosphorylation of carboxylic acids. Chemical Science. 14(20). 5519–5526. 10 indexed citations
8.
Zhang, Jianqiu, Shun‐ya Onozawa, Shu̅ Kobayashi, et al.. (2020). Ready Approach to Organophosphines from ArCl via Selective Cleavage of C–P Bonds by Sodium. Organometallics. 39(14). 2682–2694. 44 indexed citations
9.
Onozawa, Shun‐ya, et al.. (2020). Wet and Dry Processes for the Selective Transformation of Phosphonates to Phosphonic Acids Catalyzed by Brønsted Acids. The Journal of Organic Chemistry. 85(22). 14411–14419. 11 indexed citations
10.
Han, Li‐Biao, Shang‐Dong Yang, Rory Waterman, & Jan J. Weigand. (2020). Love in the Time of COVID. The Journal of Organic Chemistry. 85(22). 14273–14275. 1 indexed citations
11.
Zhang, Jianqiu, et al.. (2020). Conversion of triphenylphosphine oxide to organophosphorus via selective cleavage of C-P, O-P, and C-H bonds with sodium. Communications Chemistry. 3(1). 1–1. 116 indexed citations
12.
Zhang, Jianqiu, Shang‐Dong Yang, & Li‐Biao Han. (2019). Facial conversion of secondary phosphine oxides R1R2P(O)H to chlorophosphines R1R2PCl by acetyl chloride. Tetrahedron Letters. 61(10). 151556–151556. 5 indexed citations
13.
Yoshimura, Aya, et al.. (2015). Organosulfide‐Catalyzed Diboration of Terminal Alkynes under Light. Chemistry - A European Journal. 21(40). 13930–13933. 71 indexed citations
14.
15.
Xiong, Biquan, Ruwei Shen, Midori Goto, Shuang‐Feng Yin, & Li‐Biao Han. (2012). Highly Selective 1,4‐ and 1,6‐Addition of P(O)H Compounds to p‐Quinones: A Divergent Method for the Synthesis of C‐ and O‐Phosphoryl Hydroquinone Derivatives. Chemistry - A European Journal. 18(52). 16902–16910. 30 indexed citations
16.
Zhou, Yongbo, Shuang‐Feng Yin, Yuxing Gao, et al.. (2010). Selective PP and POP Bond Formations through Copper‐Catalyzed Aerobic Oxidative Dehydrogenative Couplings of H‐Phosphonates. Angewandte Chemie International Edition. 49(38). 6852–6855. 73 indexed citations
17.
Xu, Qing, Ruwei Shen, Yutaka Ono, et al.. (2010). A new oxapalladacycle generated via ortho C–H activation of phenylphosphinic acid: an efficient catalyst for Markovnikov-type additions of E–H bonds to alkynes. Chemical Communications. 47(8). 2333–2335. 27 indexed citations
18.
Zhao, Chang‐Qiu, Li‐Biao Han, Midori Goto, & Masato Tanaka. (2001). Rhodium-Catalyzed Hydrophosphorylation of Terminal Alkynes Leading to Highly Selective Formation of (E)-Alkenylphosphonates: Complete Reversal of Regioselectivity to the Palladium-Catalyzed Counterpart We are grateful to the Japan Science and Technology Corporation (JST) for financial support through the CREST (Core Research for Evolutional Science and Technology) program and for a postdoctoral fellowship to C.-Q.Z.. PubMed. 40(10). 1929–1932. 78 indexed citations
19.
Zhao, Chang‐Qiu, Li‐Biao Han, & Masato Tanaka. (2001). ChemInform Abstract: Palladium‐Catalyzed Hydrophosphorylation of Allenes Leading to Regio‐ and Stereoselective Formation of Allylphosphonates.. ChemInform. 32(2). 1 indexed citations
20.

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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