Shaolin Zhu

7.0k total citations · 1 hit paper
88 papers, 5.9k citations indexed

About

Shaolin Zhu is a scholar working on Organic Chemistry, Inorganic Chemistry and Pharmaceutical Science. According to data from OpenAlex, Shaolin Zhu has authored 88 papers receiving a total of 5.9k indexed citations (citations by other indexed papers that have themselves been cited), including 88 papers in Organic Chemistry, 49 papers in Inorganic Chemistry and 8 papers in Pharmaceutical Science. Recurrent topics in Shaolin Zhu's work include Catalytic C–H Functionalization Methods (72 papers), Asymmetric Hydrogenation and Catalysis (49 papers) and Catalytic Cross-Coupling Reactions (32 papers). Shaolin Zhu is often cited by papers focused on Catalytic C–H Functionalization Methods (72 papers), Asymmetric Hydrogenation and Catalysis (49 papers) and Catalytic Cross-Coupling Reactions (32 papers). Shaolin Zhu collaborates with scholars based in China, United States and Canada. Shaolin Zhu's co-authors include Yuli He, Stephen L. Buchwald, You Wang, Nootaree Niljianskul, Yao Zhang, Dawei Ma, David W. C. MacMillan, Shouyun Yu, Fang Zhou and Jian Chen 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

Shaolin Zhu

84 papers receiving 5.8k citations

Hit Papers

NiH-Catalyzed Functionalization of Remote and Proximal Ol... 2022 2026 2023 2024 2022 50 100 150

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shaolin Zhu China 43 5.6k 2.6k 630 467 181 88 5.9k
Yi‐Xia Jia China 42 5.5k 1.0× 1.4k 0.5× 466 0.7× 406 0.9× 55 0.3× 102 5.6k
Dong‐Hui Wang China 23 9.7k 1.8× 2.1k 0.8× 333 0.5× 267 0.6× 171 0.9× 38 10.0k
Wangqing Kong China 43 5.9k 1.1× 1.3k 0.5× 339 0.5× 1.3k 2.7× 174 1.0× 89 6.2k
Jaesook Yun South Korea 39 4.8k 0.9× 2.1k 0.8× 956 1.5× 128 0.3× 160 0.9× 98 5.1k
Kami L. Hull United States 23 4.6k 0.8× 1.1k 0.4× 279 0.4× 488 1.0× 129 0.7× 51 4.8k
Boshun Wan China 40 4.6k 0.8× 908 0.3× 318 0.5× 242 0.5× 118 0.7× 124 4.8k
Kandikere Ramaiah Prabhu India 44 5.3k 0.9× 985 0.4× 537 0.9× 180 0.4× 118 0.7× 129 5.5k
Ming‐Yu Ngai United States 34 3.5k 0.6× 1.3k 0.5× 434 0.7× 1.1k 2.3× 131 0.7× 57 3.9k
Guangrong Meng United States 33 4.6k 0.8× 1.1k 0.4× 1.3k 2.0× 183 0.4× 97 0.5× 59 4.8k
Kyle W. Quasdorf United States 12 3.5k 0.6× 749 0.3× 238 0.4× 249 0.5× 110 0.6× 16 3.7k

Countries citing papers authored by Shaolin Zhu

Since Specialization
Citations

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

Fields of papers citing papers by Shaolin Zhu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Shaolin Zhu. 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 Shaolin Zhu. The network helps show where Shaolin Zhu may publish in the future.

Co-authorship network of co-authors of Shaolin Zhu

This figure shows the co-authorship network connecting the top 25 collaborators of Shaolin Zhu. A scholar is included among the top collaborators of Shaolin Zhu 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 Shaolin Zhu. Shaolin Zhu 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.
Yang, Jingjie, Xinyu Li, Xinyun Wang, et al.. (2025). Migratory C(sp 2 )–H/C(sp 3 )–H Cross‐Coupling Enabled by Metallaphotoredox Catalysis. Angewandte Chemie International Edition. 65(5). e18972–e18972.
2.
Yang, Jingjie, et al.. (2025). Through‐Space 1,4‐Ni/H Shift: Unlocking Migration along Coupling Partners in Olefin Borylcarbofunctionalization. Angewandte Chemie International Edition. 64(25). e202503671–e202503671. 1 indexed citations
5.
He, Yuli, et al.. (2024). Ligand Relay Catalysis Enables Asymmetric Migratory Hydroarylation for the Concise Synthesis of Chiral α‐(Hetero)Aryl‐Substituted Amines. Advanced Science. 11(16). e2306447–e2306447. 7 indexed citations
6.
Yang, Jingjie, et al.. (2023). Functionalization of Olefinic C−H Bonds by an Aryl‐to‐Vinyl 1,4‐Nickel Migration/Reductive Coupling Sequence. Angewandte Chemie. 135(28). 1 indexed citations
7.
Chen, Changpeng & Shaolin Zhu. (2023). Rhodium-Catalyzed Migratory 1,n-Diborylation of Alkynes and Migratory Hydroboration of Vinylboronates. Chinese Journal of Organic Chemistry. 43(1). 368–368. 1 indexed citations
8.
Yang, Jingjie, et al.. (2023). Functionalization of Olefinic C−H Bonds by an Aryl‐to‐Vinyl 1,4‐Nickel Migration/Reductive Coupling Sequence. Angewandte Chemie International Edition. 62(28). e202304713–e202304713. 24 indexed citations
9.
Chen, Changpeng, et al.. (2023). Synthesis of Enantioenriched 1,2‐ cis Disubstituted Cycloalkanes by Convergent NiH Catalysis. Angewandte Chemie International Edition. 62(36). e202308320–e202308320. 15 indexed citations
10.
Wang, You, et al.. (2022). NiH-catalyzed asymmetric hydroalkynylation of α,β-unsaturated amides. Green Synthesis and Catalysis. 3(4). 377–379. 25 indexed citations
11.
12.
He, Yuli, et al.. (2022). Regio- and enantioselective remote hydroarylation using a ligand-relay strategy. Nature Communications. 13(1). 2471–2471. 45 indexed citations
13.
Liu, Jiandong, Hegui Gong, & Shaolin Zhu. (2021). BH3 ⋅ Me2S: An Alternative Hydride Source for NiH‐Catalyzed Reductive Migratory Hydroarylation and Hydroalkenylation of Alkenes. European Journal of Organic Chemistry. 2021(10). 1543–1546. 9 indexed citations
14.
Jiang, Xiaoli, et al.. (2021). Nickel-catalysed migratory hydroalkynylation and enantioselective hydroalkynylation of olefins with bromoalkynes. Nature Communications. 12(1). 3792–3792. 67 indexed citations
15.
He, Yuli, Jian Chen, Xiaoli Jiang, & Shaolin Zhu. (2021). Enantioselective NiH‐Catalyzed Reductive Hydrofunctionalization of Alkenes. Chinese Journal of Chemistry. 40(5). 651–661. 103 indexed citations
16.
He, Yuli & Shaolin Zhu. (2020). Quinim Ligand-Enabled Ni-Catalyzed Asymmetric 1,2-Carbamoyl-Alkylation of Unactivated Alkenes. Chinese Journal of Organic Chemistry. 40(12). 4377–4377. 6 indexed citations
17.
He, Yuli, et al.. (2020). Enantio‐ and Regioselective NiH‐Catalyzed Reductive Hydroarylation of Vinylarenes with Aryl Iodides. Angewandte Chemie International Edition. 59(48). 21530–21534. 115 indexed citations
18.
He, Yuli, et al.. (2018). Remote sp3 C–H Amination of Alkenes with Nitroarenes. Chem. 4(7). 1645–1657. 187 indexed citations
19.
Niljianskul, Nootaree, Shaolin Zhu, & Stephen L. Buchwald. (2014). Enantioselective Synthesis of α‐Aminosilanes by Copper‐Catalyzed Hydroamination of Vinylsilanes. Angewandte Chemie International Edition. 54(5). 1638–1641. 127 indexed citations
20.
Zhu, Shaolin, Shouyun Yu, You Wang, & Dawei Ma. (2010). Organocatalytic Michael Addition of Aldehydes to Protected 2‐Amino‐1‐Nitroethenes: The Practical Syntheses of Oseltamivir (Tamiflu) and Substituted 3‐Aminopyrrolidines. Angewandte Chemie International Edition. 49(27). 4656–4660. 133 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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