Mao‐Lin Li

2.1k total citations
34 papers, 1.7k citations indexed

About

Mao‐Lin Li is a scholar working on Organic Chemistry, Inorganic Chemistry and Molecular Biology. According to data from OpenAlex, Mao‐Lin Li has authored 34 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Organic Chemistry, 10 papers in Inorganic Chemistry and 4 papers in Molecular Biology. Recurrent topics in Mao‐Lin Li's work include Catalytic C–H Functionalization Methods (14 papers), Cyclopropane Reaction Mechanisms (14 papers) and Asymmetric Hydrogenation and Catalysis (10 papers). Mao‐Lin Li is often cited by papers focused on Catalytic C–H Functionalization Methods (14 papers), Cyclopropane Reaction Mechanisms (14 papers) and Asymmetric Hydrogenation and Catalysis (10 papers). Mao‐Lin Li collaborates with scholars based in China, United States and France. Mao‐Lin Li's co-authors include Qi‐Lin Zhou, Shou‐Fei Zhu, Guofang Chen, Jian‐Hua Xie, Jinhan Yu, Bin Xu, Li‐Jun Xiao, Lei Cheng, Weimin Feng and Zi‐Qi Li and has published in prestigious journals such as Science, Journal of the American Chemical Society and Angewandte Chemie International Edition.

In The Last Decade

Mao‐Lin Li

34 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mao‐Lin Li China 20 1.5k 519 230 189 150 34 1.7k
Ke‐Fang Yang China 25 1.4k 0.9× 378 0.7× 289 1.3× 169 0.9× 98 0.7× 70 1.7k
Balaram S. Takale United States 22 1.1k 0.7× 322 0.6× 365 1.6× 171 0.9× 163 1.1× 46 1.4k
Francesco Ferretti Italy 19 1.4k 0.9× 677 1.3× 421 1.8× 108 0.6× 134 0.9× 48 1.6k
Thomas Schareina Germany 20 2.2k 1.5× 559 1.1× 244 1.1× 238 1.3× 64 0.4× 40 2.5k
Kai Xu China 25 1.3k 0.8× 333 0.6× 526 2.3× 143 0.8× 90 0.6× 66 1.9k
Hui Zhou China 24 781 0.5× 429 0.8× 345 1.5× 168 0.9× 133 0.9× 73 1.4k
Jinho Kim South Korea 20 1.9k 1.3× 459 0.9× 223 1.0× 220 1.2× 47 0.3× 61 2.2k
Tomohiro Yasukawa Japan 21 1.2k 0.8× 648 1.2× 432 1.9× 207 1.1× 337 2.2× 49 1.6k
Clara I. Herrerı́as Spain 25 1.5k 1.0× 631 1.2× 320 1.4× 255 1.3× 351 2.3× 48 2.0k
Koichi Mitsudo Japan 29 2.1k 1.4× 334 0.6× 239 1.0× 273 1.4× 117 0.8× 115 2.4k

Countries citing papers authored by Mao‐Lin Li

Since Specialization
Citations

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

Fields of papers citing papers by Mao‐Lin Li

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mao‐Lin Li

This figure shows the co-authorship network connecting the top 25 collaborators of Mao‐Lin Li. A scholar is included among the top collaborators of Mao‐Lin Li 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 Mao‐Lin Li. Mao‐Lin Li 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.
Zhang, Zhengyi, Mao‐Lin Li, & Huimin Zhao. (2025). Mechanistic investigation of repurposed photoenzymes with new-to-nature reactivity. Current Opinion in Green and Sustainable Chemistry. 52. 101009–101009. 1 indexed citations
2.
Li, Mao‐Lin, et al.. (2024). Breaking the activity-selectivity trade-off in photocatalytic semihydrogenation of alkynes over palladium nanoparticles with phosphate modification. Applied Catalysis B: Environmental. 365. 124948–124948. 6 indexed citations
3.
Harrison, Wesley, et al.. (2024). Photoenzymatic Asymmetric Hydroamination for Chiral Alkyl Amine Synthesis. Journal of the American Chemical Society. 146(15). 10716–10722. 26 indexed citations
4.
Li, Mao‐Lin, et al.. (2024). Asymmetric photoenzymatic incorporation of fluorinated motifs into olefins. Science. 385(6707). 416–421. 49 indexed citations
5.
Ren, Hengqian, Chunshuai Huang, Haiyang Cui, et al.. (2024). Non-modular fatty acid synthases yield distinct N-terminal acylation in ribosomal peptides. Nature Chemistry. 16(8). 1320–1329. 12 indexed citations
6.
Yang, Zhi‐Chun, et al.. (2023). Enantioselective Synthesis of Chiral Amides by a Phosphoric Acid Catalyzed Asymmetric Wolff Rearrangement**. Angewandte Chemie International Edition. 62(39). e202308122–e202308122. 19 indexed citations
7.
Shi, Yifan, et al.. (2023). A Spiro Phosphamide Catalyzed Enantioselective Proton Transfer of Ylides in a Free Carbene Insertion into N−H Bonds. Angewandte Chemie. 135(15). 5 indexed citations
8.
Li, Mao‐Lin, Wesley Harrison, Zhengyi Zhang, Yujie Yuan, & Huimin Zhao. (2023). Remote stereocontrol with azaarenes via enzymatic hydrogen atom transfer. Nature Chemistry. 16(2). 277–284. 54 indexed citations
9.
Yang, Zhi‐Chun, et al.. (2023). Enantioselective Synthesis of Chiral Amides by a Phosphoric Acid Catalyzed Asymmetric Wolff Rearrangement**. Angewandte Chemie. 135(39). 3 indexed citations
10.
Shi, Yifan, et al.. (2023). A Spiro Phosphamide Catalyzed Enantioselective Proton Transfer of Ylides in a Free Carbene Insertion into N−H Bonds. Angewandte Chemie International Edition. 62(15). e202300691–e202300691. 30 indexed citations
11.
Li, You, et al.. (2022). Enantioselective Synthesis of Unnatural Carbamate-Protected α-Alkyl Amino Esters via N–H Bond Insertion Reactions. ACS Catalysis. 12(21). 13143–13148. 15 indexed citations
12.
Li, Mao‐Lin, et al.. (2019). Highly enantioselective carbene insertion into N–H bonds of aliphatic amines. Science. 366(6468). 990–994. 227 indexed citations
13.
Li, Yi‐Pan, Zi‐Qi Li, Biying Zhou, et al.. (2019). Chiral Spiro Phosphoric Acid-Catalyzed Friedel–Crafts Conjugate Addition/Enantioselective Protonation Reactions. ACS Catalysis. 9(7). 6522–6529. 64 indexed citations
14.
15.
Xiao, Li‐Jun, Lei Cheng, Weimin Feng, et al.. (2017). Nickel(0)‐Catalyzed Hydroarylation of Styrenes and 1,3‐Dienes with Organoboron Compounds. Angewandte Chemie. 130(2). 470–473. 38 indexed citations
16.
Xiao, Li‐Jun, Lei Cheng, Weimin Feng, et al.. (2017). Nickel(0)‐Catalyzed Hydroarylation of Styrenes and 1,3‐Dienes with Organoboron Compounds. Angewandte Chemie International Edition. 57(2). 461–464. 168 indexed citations
17.
Li, Mao‐Lin, Shuang Yang, Xun‐Cheng Su, et al.. (2016). Mechanism Studies of Ir-Catalyzed Asymmetric Hydrogenation of Unsaturated Carboxylic Acids. Journal of the American Chemical Society. 139(1). 541–547. 54 indexed citations
18.
Xu, Bin, Mao‐Lin Li, Xiao‐Dong Zuo, Shou‐Fei Zhu, & Qi‐Lin Zhou. (2015). Catalytic Asymmetric Arylation of α-Aryl-α-diazoacetates with Aniline Derivatives. Journal of the American Chemical Society. 137(27). 8700–8703. 148 indexed citations
19.
20.
Li, Mao‐Lin & Guofang Chen. (2013). Revisiting catalytic model reaction p-nitrophenol/NaBH4 using metallic nanoparticles coated on polymeric spheres. Nanoscale. 5(23). 11919–11919. 175 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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