Jun Shi

1.5k total citations
76 papers, 1.2k citations indexed

About

Jun Shi is a scholar working on Organic Chemistry, Molecular Biology and Spectroscopy. According to data from OpenAlex, Jun Shi has authored 76 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Organic Chemistry, 14 papers in Molecular Biology and 10 papers in Spectroscopy. Recurrent topics in Jun Shi's work include Catalytic C–H Functionalization Methods (18 papers), Oxidative Organic Chemistry Reactions (14 papers) and Synthesis and biological activity (9 papers). Jun Shi is often cited by papers focused on Catalytic C–H Functionalization Methods (18 papers), Oxidative Organic Chemistry Reactions (14 papers) and Synthesis and biological activity (9 papers). Jun Shi collaborates with scholars based in China, United States and Canada. Jun Shi's co-authors include Phil S. Baran, Xiaoping Bao, Carlos A. Guerrero, Ryan A. Shenvi, Na Luo, Chuang‐Chuang Li, Thomas J. Maimone, Shinji Ashida, Hiroki Shigehisa and Hai Ren and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Journal of Hazardous Materials.

In The Last Decade

Jun Shi

70 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jun Shi China	16	675	252	147	145	123	76	1.2k
Perry T. Kaye South Africa	24	1.5k 2.2×	556 2.2×	67 0.5×	134 0.9×	88 0.7×	165	2.1k
Ana G. Petrovic United States	26	675 1.0×	576 2.3×	76 0.5×	107 0.7×	325 2.6×	75	1.8k
G. Paul Savage Australia	23	1.3k 1.9×	670 2.7×	59 0.4×	30 0.2×	161 1.3×	114	1.9k
George I. Birnbaum Canada	20	473 0.7×	649 2.6×	56 0.4×	42 0.3×	121 1.0×	80	1.2k
Brian L. Bray United States	13	596 0.9×	591 2.3×	53 0.4×	63 0.4×	100 0.8×	22	1.1k
Sung Keon Namgoong South Korea	15	674 1.0×	530 2.1×	50 0.3×	61 0.4×	125 1.0×	41	1.2k
Hamilton B. Napolitano Brazil	22	951 1.4×	493 2.0×	14 0.1×	117 0.8×	284 2.3×	150	1.9k
Lester A. Dolak United States	18	572 0.8×	334 1.3×	147 1.0×	24 0.2×	28 0.2×	36	1.0k
Najim A. Al‐Masoudi Germany	25	2.3k 3.4×	668 2.7×	46 0.3×	33 0.2×	78 0.6×	175	2.7k
T. R. Bailey United States	20	953 1.4×	322 1.3×	61 0.4×	16 0.1×	32 0.3×	41	1.3k

Countries citing papers authored by Jun Shi

Since Specialization

Citations

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

Fields of papers citing papers by Jun Shi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jun Shi

This figure shows the co-authorship network connecting the top 25 collaborators of Jun Shi. A scholar is included among the top collaborators of Jun Shi 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 Jun Shi. Jun Shi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Pan, Renjie, Zongchen Li, Tian‐Yang Zhang, et al.. (2025). Amino-functionalized MIL-101(Fe)-NH2 as efficient peracetic acid activator for selective contaminant degradation: Unraveling the role of electron-donating ligands in Fe(IV) generation. Journal of Hazardous Materials. 491. 138028–138028. 4 indexed citations

Shi, Jun, et al.. (2025). Single-electron transfer enables enantioselective synthesis of spirooxindoles via dual copper and phosphoric acid catalysis. Chinese Chemical Letters. 37(4). 111250–111250.

Ren, Hai, et al.. (2024). Copper‐Catalyzed Tunable Oxygenative Rearrangement of Tetrahydrocarbazoles. Chemistry - A European Journal. 30(44). e202401293–e202401293. 1 indexed citations

Shi, Jun, et al.. (2024). Design, Synthesis, and Insecticidal Activity of Isoxazoline Derivatives Incorporating an Acylhydrazine Moiety. Journal of Agricultural and Food Chemistry. 72(38). 20974–20980. 9 indexed citations

Shi, Jun, et al.. (2023). Catalyst‐Free [3+2] Cycloaddition of Isoquinolinium/Pyridinium Ylides and Electron‐Deficient Alkenes. European Journal of Organic Chemistry. 26(37). 3 indexed citations

Wang, Wei, Jun Shi, Wei Wu, et al.. (2023). Copper‐Catalyzed Oxygenative Skeletal Rearrangement of Tetrahydro‐β‐carbolines Using H₂O and O₂ as Oxygen Sources. Angewandte Chemie International Edition. 62(51). e202313687–e202313687. 6 indexed citations

Ren, Hai, et al.. (2023). Electrochemical bromocyclization enables 3,5-diversification of heterocyclic indolines. Organic & Biomolecular Chemistry. 21(36). 7290–7294. 3 indexed citations

Yao, Tong, et al.. (2022). Designing a toroidal crystal for monochromatic X-ray imaging of a laser-produced He-like plasma. High Power Laser Science and Engineering. 10. 5 indexed citations

Song, Jun‐Rong, et al.. (2022). Water enables the tunable electrochemical synthesis of heterocyclic 3a- or 5a-bromoindolines. Green Chemistry. 24(17). 6720–6726. 17 indexed citations

10.

Du, Huan, et al.. (2020). Design, synthesis, crystal structure and in vitro antimicrobial activity of novel 1,2,4-triazolo[1,5-a]pyrimidine-containing quinazolinone derivatives. Molecular Diversity. 25(2). 711–722. 19 indexed citations

11.

Liu, Daying, Tingting Zhang, Mingyang Zhang, et al.. (2020). Water-soluble fluorescent sensor for Zn2+ with high selectivity and sensitivity imaging in living cells. Bioorganic & Medicinal Chemistry Letters. 30(8). 127073–127073. 12 indexed citations

12.

Liu, Daying, Jun Shi, Xinxin Deng, et al.. (2019). A 1,8-naphthalimide-based fluorescent sensor with high selectivity and sensitivity for Hg²⁺ in aqueous solution and living cells. Analytical Methods. 11(25). 3150–3154. 15 indexed citations

13.

Shi, Jun, et al.. (2018). Synthesis and antimicrobial evaluation of novel 1,2,4-triazole thioether derivatives bearing a quinazoline moiety. Molecular Diversity. 22(3). 657–667. 30 indexed citations

14.

Wang, Yanyan, Jun Shi, Jiahong Xu, et al.. (2018). Synthesis and larvicidal activity of 1,3,4-oxadiazole derivatives containing a 3-chloropyridin-2-yl-1H-pyrazole scaffold. Monatshefte für Chemie - Chemical Monthly. 149(3). 611–623. 8 indexed citations

15.

Shi, Jun, et al.. (2010). 1,5-Dimethyl-4-{[1-(3-methyl-5-oxo-1-phenyl-4,5-dihydro-1H-pyrazol-4-ylidene)ethyl]amino}-2-phenyl-1H-pyrazol-3(2H)-one. Acta Crystallographica Section E Structure Reports Online. 66(7). o1583–o1583. 4 indexed citations

16.

Wei, Zhen, et al.. (2010). Bis(4-acetyl-3-methyl-1-phenyl-1H-pyrazol-5-olato-κ²O,O′)bis(N,N-dimethylformamide-κO)nickel(II). Acta Crystallographica Section E Structure Reports Online. 66(8). m904–m904. 4 indexed citations

17.

Liu, Yu, et al.. (2007). Thermodynamics of Molecular Recognition of Bile Salts by 3,6- (Oligoethylenediamino-Bridged) β-Cyclodextrin Dimers. Combinatorial Chemistry & High Throughput Screening. 10(5). 350–357. 5 indexed citations

18.

Shi, Jun. (2005). (E)-4-[4-(Benzyloxy)-3-methoxybenzylideneamino]-1,5-dimethyl-2-phenyl-1H-pyrazol-3(2H)-one. Acta Crystallographica Section E Structure Reports Online. 61(11). o3893–o3894. 1 indexed citations

19.

Shi, Jun. (2003). Micromation and applications of spectrometers. 4 indexed citations

20.

Shi, Jun. (2001). EXPERIMENTAL RESEARCH ON TREATMENT OF Cr(VI)-BEARING WASTEWATER BY PYRITE. 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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