Fa‐Jie Chen

1.5k total citations
22 papers, 1.3k citations indexed

About

Fa‐Jie Chen is a scholar working on Organic Chemistry, Molecular Biology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Fa‐Jie Chen has authored 22 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Organic Chemistry, 11 papers in Molecular Biology and 7 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Fa‐Jie Chen's work include Chemical Synthesis and Analysis (10 papers), Click Chemistry and Applications (10 papers) and Catalytic C–H Functionalization Methods (9 papers). Fa‐Jie Chen is often cited by papers focused on Chemical Synthesis and Analysis (10 papers), Click Chemistry and Applications (10 papers) and Catalytic C–H Functionalization Methods (9 papers). Fa‐Jie Chen collaborates with scholars based in China and United States. Fa‐Jie Chen's co-authors include Bing‐Feng Shi, Kai Chen, Qi Zhang, Yuejun Zhang, Wei‐Hao Rao, Sheng Zhao, Jianmin Gao, Fang Hu, Shuo‐Qing Zhang and Xin Li and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Nature Communications.

In The Last Decade

Fa‐Jie Chen

19 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fa‐Jie Chen China 14 1.2k 213 193 65 43 22 1.3k
Heather Burks United States 8 983 0.8× 318 1.5× 273 1.4× 43 0.7× 22 0.5× 10 1.1k
Schubert Pereira United States 7 589 0.5× 173 0.8× 125 0.6× 53 0.8× 11 0.3× 11 611
Saegun Kim South Korea 19 939 0.8× 161 0.8× 64 0.3× 7 0.1× 57 1.3× 31 1.0k
Scott N. Mlynarski United States 6 859 0.7× 205 1.0× 175 0.9× 37 0.6× 22 0.5× 11 892
Dipankar Koley India 19 755 0.6× 115 0.5× 160 0.8× 5 0.1× 46 1.1× 38 816
Subramani Rajkumar China 13 395 0.3× 142 0.7× 68 0.4× 27 0.4× 9 0.2× 22 447
Jongwoo Son United States 11 543 0.5× 65 0.3× 178 0.9× 16 0.2× 79 1.8× 19 584
Guangjun Bao China 15 504 0.4× 72 0.3× 188 1.0× 7 0.1× 32 0.7× 32 569
Gennadij V. Latyshev Russia 17 640 0.5× 50 0.2× 133 0.7× 9 0.1× 33 0.8× 48 687
Trinadh Kaicharla India 16 744 0.6× 114 0.5× 55 0.3× 10 0.2× 24 0.6× 20 799

Countries citing papers authored by Fa‐Jie Chen

Since Specialization
Citations

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

Fields of papers citing papers by Fa‐Jie Chen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fa‐Jie Chen

This figure shows the co-authorship network connecting the top 25 collaborators of Fa‐Jie Chen. A scholar is included among the top collaborators of Fa‐Jie Chen 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 Fa‐Jie Chen. Fa‐Jie Chen 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.
Ding, Xin, et al.. (2025). Polyfluorinated reagents for peptide stapling. Organic Chemistry Frontiers. 12(8). 2777–2789.
2.
Chen, Fa‐Jie. (2024). Another side of side chains. Nature Reviews Chemistry. 8(6). 406–407. 1 indexed citations
3.
Chen, Fa‐Jie, et al.. (2024). Strategies for the Construction of Multicyclic Phage Display Libraries. ChemBioChem. 25(9). e202400072–e202400072. 16 indexed citations
4.
Chen, Fa‐Jie, et al.. (2024). Non-symmetric stapling of native peptides. Nature Reviews Chemistry. 8(5). 304–318. 17 indexed citations
5.
Huang, Jingrong, et al.. (2024). Synthesis of Glycoconjugates through Chlorooxime–Thiol Conjugation. The Journal of Organic Chemistry. 89(9). 6364–6370. 1 indexed citations
6.
Chen, Fa‐Jie, et al.. (2023). A Cysteine‐Directed Proximity‐Driven Crosslinking Method for Native Peptide Bicyclization. Angewandte Chemie International Edition. 62(31). e202306813–e202306813. 32 indexed citations
7.
Chen, Fa‐Jie, et al.. (2023). A Cysteine‐Directed Proximity‐Driven Crosslinking Method for Native Peptide Bicyclization. Angewandte Chemie. 135(31).
8.
Huang, Jingrong, et al.. (2023). Cu-catalyzed arylation of S-tosyl peptides with arylboronic acids. Organic Chemistry Frontiers. 11(1). 53–59. 6 indexed citations
9.
Chen, Fa‐Jie & Jianmin Gao. (2022). Fast Cysteine Bioconjugation Chemistry. Chemistry - A European Journal. 28(66). e202201843–e202201843. 37 indexed citations
10.
Zheng, Mengmeng, et al.. (2022). Lysine-Targeted Reversible Covalent Ligand Discovery for Proteins via Phage Display. Journal of the American Chemical Society. 144(34). 15885–15893. 44 indexed citations
11.
Chen, Fa‐Jie, Phani Mamidipalli, Venkata R. Sabbasani, et al.. (2021). Three-component coupling reaction for the synthesis of fully substituted triazoles: reactivity control of Cu-acetylide toward alkyl azides and diazo compounds. Organic Chemistry Frontiers. 8(21). 6095–6107. 3 indexed citations
12.
13.
Hu, Rong, Fa‐Jie Chen, Xiaofeng Zhang, Min Zhang, & Weiping Su. (2019). Copper-catalyzed dehydrogenative γ-C(sp3)-H amination of saturated ketones for synthesis of polysubstituted anilines. Nature Communications. 10(1). 3681–3681. 22 indexed citations
14.
Zhao, Sheng, Fa‐Jie Chen, Bin Liu, & Bing‐Feng Shi. (2015). Copper-catalyzed direct acyloxylation of C(sp2)-H bonds with Benzoic acids. Science China Chemistry. 58(8). 1302–1309. 23 indexed citations
15.
Zhao, Sheng, Yue‐Jin Liu, Sheng‐Yi Yan, et al.. (2015). Copper-/Silver-Mediated Arylation of C(sp2)–H Bonds with 2-Thiophenecarboxylic Acids. Organic Letters. 17(13). 3338–3341. 67 indexed citations
16.
Chen, Fa‐Jie, Gang Liao, Xin Li, Jun Wu, & Bing‐Feng Shi. (2014). Cu(II)-Mediated C–S/N–S Bond Formation via C–H Activation: Access to Benzoisothiazolones Using Elemental Sulfur. Organic Letters. 16(21). 5644–5647. 172 indexed citations
17.
Li, Xin, Yanhua Liu, Wenjia Gu, et al.. (2014). Copper-Mediated Hydroxylation of Arenes and Heteroarenes Directed by a Removable Bidentate Auxiliary. Organic Letters. 16(15). 3904–3907. 120 indexed citations
18.
Zhang, Qi, Kai Chen, Wei‐Hao Rao, et al.. (2013). Stereoselective Synthesis of Chiral α‐Amino‐β‐Lactams through Palladium(II)‐Catalyzed Sequential Monoarylation/Amidation of C(sp3)H Bonds. Angewandte Chemie International Edition. 52(51). 13588–13592. 307 indexed citations
19.
Zhang, Qi, Kai Chen, Wei‐Hao Rao, et al.. (2013). Stereoselective Synthesis of Chiral α‐Amino‐β‐Lactams through Palladium(II)‐Catalyzed Sequential Monoarylation/Amidation of C(sp3)H Bonds. Angewandte Chemie. 125(51). 13833–13837. 98 indexed citations
20.
Chen, Fa‐Jie, Sheng Zhao, Fang Hu, et al.. (2013). Pd(ii)-catalyzed alkoxylation of unactivated C(sp3)–H and C(sp2)–H bonds using a removable directing group: efficient synthesis of alkyl ethers. Chemical Science. 4(11). 4187–4187. 283 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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