Li‐Jie Cheng

1.3k total citations
28 papers, 1.0k citations indexed

About

Li‐Jie Cheng is a scholar working on Organic Chemistry, Inorganic Chemistry and Pharmaceutical Science. According to data from OpenAlex, Li‐Jie Cheng has authored 28 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Organic Chemistry, 10 papers in Inorganic Chemistry and 5 papers in Pharmaceutical Science. Recurrent topics in Li‐Jie Cheng's work include Catalytic C–H Functionalization Methods (19 papers), Catalytic Cross-Coupling Reactions (13 papers) and Asymmetric Hydrogenation and Catalysis (8 papers). Li‐Jie Cheng is often cited by papers focused on Catalytic C–H Functionalization Methods (19 papers), Catalytic Cross-Coupling Reactions (13 papers) and Asymmetric Hydrogenation and Catalysis (8 papers). Li‐Jie Cheng collaborates with scholars based in China, United States and United Kingdom. Li‐Jie Cheng's co-authors include Neal P. Mankad, C. Cordier, Shahidul M. Islam, Dominic R. Pye, Qi‐Lin Zhou, Jian‐Hua Xie, Yong Chen, Lixin Wang, Donghao Jiang and Cheng Wang 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

Li‐Jie Cheng

27 papers receiving 1.0k 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‐Jie Cheng China 16 962 273 112 95 78 28 1.0k
Yuan‐Zhao Hua China 22 976 1.0× 327 1.2× 59 0.5× 104 1.1× 100 1.3× 53 1.0k
Xi‐Jie Dai Canada 19 1.0k 1.0× 440 1.6× 72 0.6× 94 1.0× 110 1.4× 24 1.1k
Xiaoming Jie China 19 1.7k 1.8× 418 1.5× 54 0.5× 59 0.6× 78 1.0× 34 1.8k
Soumik Biswas United States 11 954 1.0× 307 1.1× 41 0.4× 84 0.9× 63 0.8× 14 1.0k
Amparo Sanz‐Marco Spain 19 836 0.9× 296 1.1× 47 0.4× 180 1.9× 136 1.7× 47 957
Faben A. Cruz United States 8 916 1.0× 392 1.4× 55 0.5× 47 0.5× 85 1.1× 8 965
David Schönbauer Austria 5 1.4k 1.4× 296 1.1× 38 0.3× 74 0.8× 63 0.8× 8 1.4k
Daniel S. Müller France 20 1.3k 1.3× 302 1.1× 60 0.5× 43 0.5× 126 1.6× 39 1.4k
Togati Naveen India 20 1.5k 1.6× 238 0.9× 32 0.3× 67 0.7× 85 1.1× 41 1.6k
Arghya Banerjee India 24 1.7k 1.8× 184 0.7× 38 0.3× 75 0.8× 82 1.1× 33 1.8k

Countries citing papers authored by Li‐Jie Cheng

Since Specialization
Citations

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

Fields of papers citing papers by Li‐Jie Cheng

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Li‐Jie Cheng

This figure shows the co-authorship network connecting the top 25 collaborators of Li‐Jie Cheng. A scholar is included among the top collaborators of Li‐Jie Cheng 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‐Jie Cheng. Li‐Jie Cheng 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.
Li, Wei, et al.. (2025). Cobalt-Catalyzed Markovnikov Hydroarylcarbonylation of Unactivated Alkenes via Distal Aryl Migration. CCS Chemistry. 1–11. 4 indexed citations
2.
Jiang, Donghao, et al.. (2025). Cobalt-Catalyzed Intramolecular Fluoroalkylative Carbonylation of Unactivated Alkenes. Organic Letters. 27(40). 11351–11355.
3.
Cheng, Li‐Jie, et al.. (2024). BF3 ⋅ OEt2 and Visible Light‐Controlled [3,3]‐ or [1,3]‐Rearrangement of Quinazolinone N−O Aryl Moieties. Advanced Synthesis & Catalysis. 366(9). 2056–2062. 3 indexed citations
4.
Jiang, Donghao, et al.. (2024). Cobalt‐Catalyzed Intramolecular Markovnikov Hydrocarbonylation of Unactivated Alkenes via Hydrogen Atom Transfer. Angewandte Chemie International Edition. 63(46). e202412828–e202412828. 9 indexed citations
5.
6.
Jiang, Donghao, et al.. (2024). Cobalt‐Catalyzed Intramolecular Markovnikov Hydrocarbonylation of Unactivated Alkenes via Hydrogen Atom Transfer. Angewandte Chemie. 136(46). 1 indexed citations
7.
Wang, Cheng, et al.. (2024). Copper-Catalyzed Protoarylation of gem-Difluoroallenes. Organic Letters. 26(2). 525–529. 4 indexed citations
8.
Li, Wei, Donghao Jiang, Cheng Wang, & Li‐Jie Cheng. (2023). Recent Advances in Base‐Metal‐Catalyzed Carbonylation of Unactivated Alkyl Electrophiles†. Chinese Journal of Chemistry. 41(23). 3419–3432. 19 indexed citations
9.
Cheng, Li‐Jie, et al.. (2020). One‐Step Synthesis of Acylboron Compounds via Copper‐Catalyzed Carbonylative Borylation of Alkyl Halides**. Angewandte Chemie International Edition. 60(4). 2094–2098. 38 indexed citations
10.
Cheng, Li‐Jie, et al.. (2020). One‐Step Synthesis of Acylboron Compounds via Copper‐Catalyzed Carbonylative Borylation of Alkyl Halides**. Angewandte Chemie. 133(4). 2122–2126. 9 indexed citations
11.
Cheng, Li‐Jie & Neal P. Mankad. (2019). Heterobimetallic Control of Regioselectivity in Alkyne Hydrostannylation: Divergent Syntheses of α- and (E)-β-Vinylstannanes via Cooperative Sn–H Bond Activation. Journal of the American Chemical Society. 141(8). 3710–3716. 36 indexed citations
12.
Cordier, C., et al.. (2018). From Propargylic Fluorinations to [1,3]-Rearrangements: Anion and Ligand Effects in Cu-Acetylide Chemistry. Synlett. 29(13). 1675–1682. 3 indexed citations
13.
Cheng, Li‐Jie & Neal P. Mankad. (2018). Copper‐Catalyzed Borocarbonylative Coupling of Internal Alkynes with Unactivated Alkyl Halides: Modular Synthesis of Tetrasubstituted β‐Borylenones. Angewandte Chemie. 130(32). 10485–10489. 14 indexed citations
14.
Pye, Dominic R., Li‐Jie Cheng, & Neal P. Mankad. (2017). Cu/Mn bimetallic catalysis enables carbonylative Suzuki–Miyaura coupling with unactivated alkyl electrophiles. Chemical Science. 8(7). 4750–4755. 64 indexed citations
15.
Cordier, C., et al.. (2017). Recent Advances in Catalytic Transformations Involving Copper Acetylides. Synthesis. 49(4). 790–801. 31 indexed citations
16.
Cheng, Li‐Jie, et al.. (2017). Enantioselective propargylic [1,3]-rearrangements: copper-catalyzed O-to-N migrations toward C–N bond formation. Chemical Science. 8(6). 4299–4305. 56 indexed citations
17.
Cheng, Li‐Jie & Neal P. Mankad. (2017). Cu-Catalyzed Hydrocarbonylative C–C Coupling of Terminal Alkynes with Alkyl Iodides. Journal of the American Chemical Society. 139(30). 10200–10203. 94 indexed citations
18.
19.
Cheng, Li‐Jie & C. Cordier. (2015). Catalytic Nucleophilic Fluorination of Secondary and Tertiary Propargylic Electrophiles with a Copper–N‐Heterocyclic Carbene Complex. Angewandte Chemie. 127(46). 13938–13942. 11 indexed citations
20.
Cheng, Li‐Jie & C. Cordier. (2015). Catalytic Nucleophilic Fluorination of Secondary and Tertiary Propargylic Electrophiles with a Copper–N‐Heterocyclic Carbene Complex. Angewandte Chemie International Edition. 54(46). 13734–13738. 27 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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