Hai‐Lei Cui

3.5k total citations
93 papers, 3.1k citations indexed

About

Hai‐Lei Cui is a scholar working on Organic Chemistry, Inorganic Chemistry and Molecular Biology. According to data from OpenAlex, Hai‐Lei Cui has authored 93 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 90 papers in Organic Chemistry, 12 papers in Inorganic Chemistry and 8 papers in Molecular Biology. Recurrent topics in Hai‐Lei Cui's work include Catalytic C–H Functionalization Methods (45 papers), Asymmetric Synthesis and Catalysis (34 papers) and Synthesis and Characterization of Pyrroles (31 papers). Hai‐Lei Cui is often cited by papers focused on Catalytic C–H Functionalization Methods (45 papers), Asymmetric Synthesis and Catalysis (34 papers) and Synthesis and Characterization of Pyrroles (31 papers). Hai‐Lei Cui collaborates with scholars based in China, Japan and United States. Hai‐Lei Cui's co-authors include Ying‐Chun Chen, Jing Peng, Kun Jiang, Jie Lei, Xinliang Feng, Fujie Tanaka, Xin Huang, Tianyu Liu, Lin Jiang and Wei Du and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Chemical Communications.

In The Last Decade

Hai‐Lei Cui

90 papers receiving 3.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hai‐Lei Cui China 27 3.0k 562 497 186 108 93 3.1k
Matthias R. M. Hüttl Germany 8 3.4k 1.2× 649 1.2× 749 1.5× 182 1.0× 44 0.4× 11 3.5k
Pankaj Chauhan India 27 3.7k 1.2× 511 0.9× 397 0.8× 217 1.2× 46 0.4× 70 3.8k
Zhaobin Wang China 32 3.4k 1.2× 630 1.1× 336 0.7× 174 0.9× 56 0.5× 68 3.6k
Dolores Badı́a Spain 27 2.4k 0.8× 513 0.9× 652 1.3× 87 0.5× 157 1.5× 86 2.5k
Mariafrancesca Fochi Italy 28 2.8k 0.9× 508 0.9× 451 0.9× 126 0.7× 45 0.4× 100 2.9k
So Won Youn South Korea 32 3.2k 1.1× 511 0.9× 291 0.6× 72 0.4× 91 0.8× 69 3.3k
Søren Bertelsen Denmark 15 2.6k 0.9× 659 1.2× 580 1.2× 102 0.5× 34 0.3× 21 2.7k
Doris Fielenbach Denmark 11 2.6k 0.9× 620 1.1× 519 1.0× 390 2.1× 21 0.2× 12 2.7k
Wenjun Li China 33 2.9k 1.0× 250 0.4× 486 1.0× 107 0.6× 46 0.4× 90 2.9k
Jesús M. Garcı́a Spain 26 2.1k 0.7× 517 0.9× 550 1.1× 129 0.7× 29 0.3× 63 2.2k

Countries citing papers authored by Hai‐Lei Cui

Since Specialization
Citations

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

Fields of papers citing papers by Hai‐Lei Cui

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hai‐Lei Cui

This figure shows the co-authorship network connecting the top 25 collaborators of Hai‐Lei Cui. A scholar is included among the top collaborators of Hai‐Lei Cui 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 Hai‐Lei Cui. Hai‐Lei Cui 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.
Liu, Yang, et al.. (2025). CuI-Catalyzed Dearomatization/Peroxidation/Cyclization Cascade of Pyrrole-Tethered Indoles. The Journal of Organic Chemistry. 90(10). 3639–3652. 1 indexed citations
2.
Jiang, Man, et al.. (2025). Sulfoxide-Controlled Chlorination of Pyrrolo[2,1-a]isoquinoline with Acetyl Chloride. The Journal of Organic Chemistry. 90(30). 10994–11003.
3.
Zhou, Jing, et al.. (2024). HCl/DMSO/HFIP-Mediated Chlorination of Pyrrolo[2,1-a]isoquinolines and Other Electron-Rich Heteroarenes. The Journal of Organic Chemistry. 89(14). 9789–9799. 8 indexed citations
4.
Cui, Hai‐Lei. (2024). Recent advances in oxidative chlorination. Organic & Biomolecular Chemistry. 22(8). 1580–1601. 12 indexed citations
5.
Huang, Xiang, Wanzhen Li, Shuchen Pei, & Hai‐Lei Cui. (2023). Iron-catalyzed dimerization of pyrrolo[2,1-a]isoquinolines and pyrrolo[1,2-a]quinolines. Tetrahedron Letters. 126. 154657–154657. 2 indexed citations
6.
Cui, Hai‐Lei, et al.. (2021). Synthesis of Imidazo[2,3‐a]isoquinoline and Imidazo[3,2‐a]quinoline Derivatives with Ynones, Isoquinolines and Quinolines. Asian Journal of Organic Chemistry. 10(8). 2170–2173. 4 indexed citations
7.
8.
Cui, Hai‐Lei, et al.. (2020). Palladium Catalyzed Direct Alkenylation of Dihydropyrrolo[2,1‐a]isoquinolines through the Oxidative Heck Reaction. European Journal of Organic Chemistry. 2020(35). 5729–5734. 5 indexed citations
9.
Ma, Dandan, et al.. (2020). Iron Catalyzed [3+2] Cycloaddition of Tetrahydroisoquinoline: Synthesis of Dihydropyrrolo[2,1‐ a ]isoquinolines. Asian Journal of Organic Chemistry. 9(10). 1617–1622. 12 indexed citations
10.
Yang, Ming-Cheng, et al.. (2017). K 3 PO 4 promoted dipolar [3+3] cyclization: Direct synthesis of pyrazino[2,1- a ]isoquinoline derivatives. Tetrahedron Letters. 59(2). 138–142. 6 indexed citations
11.
Zhang, Dongxin, et al.. (2014). Synthesis of Furanose Spirooxindoles via 1,8‐Diazabicyclo[5.4.0]undec‐7‐ene (DBU)‐Catalyzed Aldol Reactions of a Pyruvic Aldehyde Derivative. Asian Journal of Organic Chemistry. 3(4). 391–394. 15 indexed citations
12.
Cui, Hai‐Lei & Fujie Tanaka. (2013). Catalytic Enantioselective Formal Hetero‐Diels–Alder Reactions of Enones with Isatins to Give Spirooxindole Tetrahydropyranones. Chemistry - A European Journal. 19(20). 6213–6216. 82 indexed citations
13.
Chouthaiwale, Pandurang V., et al.. (2013). Fluorogenic probes for aldol reactions: tuning of fluorescence using π-conjugation systems. Tetrahedron Letters. 55(1). 74–78. 7 indexed citations
14.
Huang, Ji‐Rong, et al.. (2011). Organocatalytic chemoselective asymmetric N-allylic alkylation of enamides. Chemical Communications. 47(16). 4784–4784. 44 indexed citations
15.
Lei, Jie, et al.. (2010). Tributyltin hydride-mediated radical cyclisation reactions: efficient construction of multiply substituted cyclopentanes. Organic & Biomolecular Chemistry. 8(12). 2840–2840. 4 indexed citations
16.
Cui, Hai‐Lei, Jing Peng, Xinliang Feng, et al.. (2009). Dual Organocatalysis: Asymmetric Allylic–Allylic Alkylation of α,α‐Dicyanoalkenes and Morita–Baylis–Hillman Carbonates. Chemistry - A European Journal. 15(7). 1574–1577. 122 indexed citations
17.
Cui, Hai‐Lei & Ying‐Chun Chen. (2009). α,α-Dicyanoalkenes: versatile vinylogous nucleophiles for organic synthesis. Chemical Communications. 4479–4479. 120 indexed citations
18.
Cui, Hai‐Lei, et al.. (2009). Chemoselective Asymmetric N‐Allylic Alkylation of Indoles with Morita–Baylis–Hillman Carbonates. Angewandte Chemie International Edition. 48(31). 5737–5740. 229 indexed citations
19.
Feng, Xinliang, et al.. (2009). Organocatalytic peroxy-asymmetric allylic alkylation. Organic & Biomolecular Chemistry. 7(18). 3660–3660. 61 indexed citations
20.
Liu, Tian‐Yu, Hai‐Lei Cui, Yan Zhang, et al.. (2008). ChemInform Abstract: Organocatalytic and Highly Enantioselective Direct α‐Amination of Aromatic Ketones.. ChemInform. 39(4). 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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