Jiaji Zhao

927 total citations
19 papers, 819 citations indexed

About

Jiaji Zhao is a scholar working on Organic Chemistry, Molecular Biology and Pharmaceutical Science. According to data from OpenAlex, Jiaji Zhao has authored 19 papers receiving a total of 819 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Organic Chemistry, 2 papers in Molecular Biology and 1 paper in Pharmaceutical Science. Recurrent topics in Jiaji Zhao's work include Catalytic C–H Functionalization Methods (15 papers), Asymmetric Synthesis and Catalysis (4 papers) and Synthesis and Catalytic Reactions (3 papers). Jiaji Zhao is often cited by papers focused on Catalytic C–H Functionalization Methods (15 papers), Asymmetric Synthesis and Catalysis (4 papers) and Synthesis and Catalytic Reactions (3 papers). Jiaji Zhao collaborates with scholars based in China, Japan and Hong Kong. Jiaji Zhao's co-authors include Qiang Zhu, Jinbo Huang, Lanying Liu, Yimiao He, Ziwei Hu, Dong‐Dong Liang, Changlan Peng, Jiangling Peng, Yong Wang and Zhonghua Xia and has published in prestigious journals such as Chemical Communications, The Journal of Organic Chemistry and Organic Letters.

In The Last Decade

Jiaji Zhao

19 papers receiving 810 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jiaji Zhao China 14 805 74 53 33 16 19 819
Yuanxun Zhu China 17 936 1.2× 85 1.1× 63 1.2× 29 0.9× 34 2.1× 20 955
Marcos Escolano Spain 11 371 0.5× 51 0.7× 56 1.1× 40 1.2× 13 0.8× 20 402
Sourav Kumar Santra India 19 751 0.9× 61 0.8× 88 1.7× 35 1.1× 11 0.7× 25 761
Mi Lian China 9 572 0.7× 57 0.8× 38 0.7× 17 0.5× 11 0.7× 11 594
Swathi Mohan United States 4 510 0.6× 60 0.8× 73 1.4× 25 0.8× 10 0.6× 4 532
Suchithra Madhavan India 9 425 0.5× 104 1.4× 49 0.9× 19 0.6× 17 1.1× 24 448
Ho‐Yan Sun Canada 5 629 0.8× 34 0.5× 73 1.4× 23 0.7× 16 1.0× 5 651
Tian‐Yu Liu China 8 681 0.8× 113 1.5× 126 2.4× 23 0.7× 21 1.3× 12 703
Tsung‐Hsun Chuang Taiwan 12 353 0.4× 88 1.2× 70 1.3× 33 1.0× 13 0.8× 24 374
Ming‐Kui Zhu China 9 700 0.9× 83 1.1× 117 2.2× 32 1.0× 12 0.8× 9 715

Countries citing papers authored by Jiaji Zhao

Since Specialization
Citations

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

Fields of papers citing papers by Jiaji Zhao

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jiaji Zhao

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

All Works

19 of 19 papers shown
1.
Wang, Xilong, et al.. (2023). CPA-catalyzed asymmetric domino thia-Michael/aldol reactions for simultaneous chiral center and axial chirality formation. Organic & Biomolecular Chemistry. 21(33). 6697–6701. 8 indexed citations
2.
He, Jiaming, et al.. (2023). Base-Catalyzed One-Pot Synthesis of 2,3,6-Substituted Pyridines. The Journal of Organic Chemistry. 88(16). 11450–11459. 2 indexed citations
3.
Hu, Weiming, Xilong Wang, Yan Peng, et al.. (2022). Synthesis of 7-Arylthiomethyl Dibenzo[b,d]azepines through Imidoylative Heck Cyclization and CPA-Catalyzed Thio-Michael Addition/Enantioselective Protonation. Organic Letters. 24(20). 3642–3646. 21 indexed citations
4.
Zhao, Jiaji, et al.. (2022). Photocatalytic C–H Disulfuration for the Preparation of Indolizine-3-disulfides. The Journal of Organic Chemistry. 87(24). 16297–16306. 18 indexed citations
5.
6.
Ma, Yan‐Long, et al.. (2021). Recent advances in the synthesis of indolizine and its derivatives by radical cyclization/cross-coupling. Organic & Biomolecular Chemistry. 19(47). 10245–10258. 50 indexed citations
7.
Xia, Zhonghua, Jinbo Huang, Yimiao He, et al.. (2014). Arylative Cyclization of 2-Isocyanobiphenyls with Anilines: One-Pot Synthesis of 6-Arylphenanthridines via Competitive Reaction Pathways. Organic Letters. 16(9). 2546–2549. 117 indexed citations
8.
Zhao, Jiaji, et al.. (2014). Palladium-Catalyzed C(sp2)–H Arylation Using Formamide as a Transformable Directing Group. The Journal of Organic Chemistry. 79(10). 4751–4756. 13 indexed citations
9.
Li, Jing, Yasuhiro Okuda, Jiaji Zhao, Seiji Mori, & Yasushi Nishihara. (2014). Skeletal Rearrangement of Cyano-Substituted Iminoisobenzofurans into Alkyl 2-Cyanobenzoates Catalyzed by B(C6F5)3. Organic Letters. 16(19). 5220–5223. 10 indexed citations
10.
Zhao, Jiaji, Yong Wang, Yimiao He, Lanying Liu, & Qiang Zhu. (2012). Cu-Catalyzed Oxidative C(sp2)–H Cycloetherification ofo-Arylphenols for the Preparation of Dibenzofurans. Organic Letters. 14(4). 1078–1081. 114 indexed citations
11.
Hu, Ziwei, Dong‐Dong Liang, Jiaji Zhao, Jinbo Huang, & Qiang Zhu. (2012). Palladium-catalyzed cyclization of o-alkynyltrifluoroacetanilides followed by isocyanide insertion: synthesis of 2-substituted 1H-indole-3-carboxamides. Chemical Communications. 48(59). 7371–7371. 82 indexed citations
12.
Zhao, Jiaji, Qi Zhang, Lanying Liu, et al.. (2012). CuI-Mediated Sequential Iodination/Cycloetherification ofo-Arylphenols: Synthesis of 2- or 4-Iododibenzofurans and Mechanistic Studies. Organic Letters. 14(20). 5362–5365. 50 indexed citations
13.
Peng, Jiangling, Jiaji Zhao, Ziwei Hu, et al.. (2012). Palladium-Catalyzed C(sp2)–H Cyanation Using Tertiary Amine Derived Isocyanide as a Cyano Source. Organic Letters. 14(18). 4966–4969. 142 indexed citations
14.
15.
Wang, Honggen, Jiaji Zhao, Jiancun Zhang, & Qiang Zhu. (2011). Brønsted Acid‐Promoted Sequential Hydroarylation– Hydroamidation of Arene‐Tethered 1‐(2‐Alkynylphenyl)ureas: Direct Access to 4,4‐Spiro‐3,4‐dihydro‐2‐(1H)‐quinazolinones. Advanced Synthesis & Catalysis. 353(14-15). 2653–2658. 15 indexed citations
16.
Peng, Changlan, Yong Wang, Lanying Liu, et al.. (2010). p‐Toluenesulfonic Acid Promoted Annulation of 2‐Alkynylanilines with Activated Ketones: Efficient Synthesis of 4‐Alkyl‐2,3‐Disubstituted Quinolines. European Journal of Organic Chemistry. 2010(5). 818–822. 35 indexed citations
17.
Zhao, Jiaji, Changlan Peng, Lanying Liu, Yong Wang, & Qiang Zhu. (2010). Synthesis of 2-Alkoxy(aroxy)-3-substituted Quinolines by DABCO-Promoted Cyclization of o-Alkynylaryl Isocyanides. The Journal of Organic Chemistry. 75(21). 7502–7504. 53 indexed citations
18.
Liu, Lanying, Yong Wang, Honggen Wang, et al.. (2009). Tetrabutylammonium chloride-triggered 6-endo cyclization of o-alkynylisocyanobenzenes: an efficient synthesis of 2-chloro-3-substituted quinolines. Tetrahedron Letters. 50(48). 6715–6719. 32 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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