Yu‐Lin Tsai

582 total citations
29 papers, 488 citations indexed

About

Yu‐Lin Tsai is a scholar working on Organic Chemistry, Pharmacology and Molecular Biology. According to data from OpenAlex, Yu‐Lin Tsai has authored 29 papers receiving a total of 488 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Organic Chemistry, 4 papers in Pharmacology and 2 papers in Molecular Biology. Recurrent topics in Yu‐Lin Tsai's work include Catalytic C–H Functionalization Methods (12 papers), Sulfur-Based Synthesis Techniques (9 papers) and Asymmetric Synthesis and Catalysis (7 papers). Yu‐Lin Tsai is often cited by papers focused on Catalytic C–H Functionalization Methods (12 papers), Sulfur-Based Synthesis Techniques (9 papers) and Asymmetric Synthesis and Catalysis (7 papers). Yu‐Lin Tsai collaborates with scholars based in Taiwan, Mexico and Germany. Yu‐Lin Tsai's co-authors include Meng‐Yang Chang, Chieh‐Kai Chan, Hanyu Chen, Wen Ju, Alexander Bagger, Huan Wang, Jan Rossmeisl, Tim Möller, Xingli Wang and Fang Luo and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Science of The Total Environment and The Journal of Organic Chemistry.

In The Last Decade

Yu‐Lin Tsai

29 papers receiving 482 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yu‐Lin Tsai Taiwan 13 277 161 82 58 48 29 488
Maximilian Selt Germany 10 925 3.3× 224 1.4× 48 0.6× 46 0.8× 33 0.7× 10 1.1k
Hirofumi Maekawa Japan 15 571 2.1× 73 0.5× 31 0.4× 43 0.7× 88 1.8× 85 688
Barbara Riehl Germany 6 794 2.9× 178 1.1× 33 0.4× 27 0.5× 38 0.8× 7 936
Miguel Paradas Spain 8 307 1.1× 61 0.4× 23 0.3× 45 0.8× 40 0.8× 9 407
Sarah E. Braley United States 9 362 1.3× 136 0.8× 142 1.7× 62 1.1× 27 0.6× 11 511
Yajie Fu China 15 235 0.8× 38 0.2× 171 2.1× 146 2.5× 71 1.5× 27 501
Xinhua Xu China 12 348 1.3× 53 0.3× 22 0.3× 68 1.2× 36 0.8× 33 447
Renier Crous South Africa 10 135 0.5× 36 0.2× 169 2.1× 152 2.6× 33 0.7× 15 369
Mu Lin China 13 646 2.3× 60 0.4× 17 0.2× 101 1.7× 32 0.7× 23 793
Sebastian Wertz Germany 8 607 2.2× 33 0.2× 31 0.4× 72 1.2× 27 0.6× 9 663

Countries citing papers authored by Yu‐Lin Tsai

Since Specialization
Citations

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

Fields of papers citing papers by Yu‐Lin Tsai

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yu‐Lin Tsai

This figure shows the co-authorship network connecting the top 25 collaborators of Yu‐Lin Tsai. A scholar is included among the top collaborators of Yu‐Lin Tsai 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 Yu‐Lin Tsai. Yu‐Lin Tsai 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.
2.
Tsai, Yu‐Lin, et al.. (2022). Nickel-Catalyzed Denitrogenative Cyclization of 1,2,3,4-Benzothiatriazin-1,1(2H)-dioxides with Arynes To Synthesize Biaryl Sultams. Organic Letters. 24(15). 2915–2920. 8 indexed citations
3.
Tsai, Yu‐Lin, et al.. (2020). Bayesian inference of nonylphenol exposure for assessing human dietary risk. The Science of The Total Environment. 713. 136710–136710. 10 indexed citations
4.
Chang, Meng‐Yang & Yu‐Lin Tsai. (2020). One-Pot Amberlyst 15-Controlled Cyclocondensation of Piperidines and Arylaldehydes: Synthesis of 3,5-Diarylmethylpyridines. The Journal of Organic Chemistry. 85(8). 5651–5659. 2 indexed citations
5.
Chang, Meng‐Yang, Yu‐Lin Tsai, & Hsing‐Yin Chen. (2020). CuBr2-Mediated One-Pot Synthesis of Sulfonyl 9-Fluorenylidenes. The Journal of Organic Chemistry. 85(11). 6897–6909. 2 indexed citations
6.
Ju, Wen, Alexander Bagger, Xingli Wang, et al.. (2019). Unraveling Mechanistic Reaction Pathways of the Electrochemical CO2 Reduction on Fe–N–C Single-Site Catalysts. ACS Energy Letters. 4(7). 1663–1671. 167 indexed citations
7.
Chang, Meng‐Yang, Kuan‐Ting Chen, Yu‐Lin Tsai, & Hanyu Chen. (2019). One-Pot Access to 2-Aryl-3-(arylmethyl)chromones. Synthesis. 52(6). 861–872. 2 indexed citations
8.
Chang, Meng‐Yang & Yu‐Lin Tsai. (2019). Samarium triflate-catalyzed dimerization of vinylarenes. SHILAP Revista de lepidopterología. 2019(6). 200–211. 1 indexed citations
9.
Chang, Meng‐Yang, et al.. (2019). Synthesis of 2-Sulfonyl Indenes and Indanes. The Journal of Organic Chemistry. 84(18). 11699–11723. 13 indexed citations
10.
Chang, Meng‐Yang, Hanyu Chen, & Yu‐Lin Tsai. (2019). NH2OH–HCl-Mediated Umpolung α-Methylsulfonylation of α-Sulfonyl Ketones with Methylsulfoxides: Synthesis of α,β-Bis-sulfonyl Arylketones. Organic Letters. 21(6). 1832–1836. 27 indexed citations
11.
12.
Chang, Meng‐Yang, Hanyu Chen, & Yu‐Lin Tsai. (2018). Intramolecular Benzannulation of 3-Sulfonyl-2-benzylchromen-4-ones: Synthesis of Sulfonyl Dibenzooxabicyclo[3.3.1]nonanes. The Journal of Organic Chemistry. 84(1). 443–449. 7 indexed citations
13.
Chang, Meng‐Yang, Hanyu Chen, & Yu‐Lin Tsai. (2018). Temperature-Controlled Desulfonylative Condensation of α-Sulfonyl o-Hydroxyacetophenones and 2-Formyl Azaarenes: Synthesis of Azaaryl Aurones and Flavones. The Journal of Organic Chemistry. 84(1). 326–337. 33 indexed citations
14.
Chang, Meng‐Yang & Yu‐Lin Tsai. (2018). Stereocontrolled Synthesis of 3-Sulfonyl Chroman-4-ols. The Journal of Organic Chemistry. 83(12). 6798–6804. 8 indexed citations
15.
Chan, Chieh‐Kai, et al.. (2017). Synthesis of polyoxygenated dibenzo[ a , e ]cycloheptatrienes. Tetrahedron. 73(15). 2074–2088. 3 indexed citations
16.
Chan, Chieh‐Kai, Yu‐Lin Tsai, & Meng‐Yang Chang. (2017). CuI Mediated One-Pot Cycloacetalization/Ketalization of o-Carbonyl Allylbenzenes: Synthesis of Benzobicyclo[3.2.1]octane Core. Organic Letters. 19(7). 1870–1873. 23 indexed citations
17.
Chan, Chieh‐Kai, et al.. (2017). Bi(OTf)3-Mediated Intramolecular Olefinic Cyclization: Synthesis of Substituted Aryl-Dihydronaphthalenes and Indenes. The Journal of Organic Chemistry. 82(13). 7077–7084. 16 indexed citations
18.
Chan, Chieh‐Kai, Yu‐Hsin Chen, Yu‐Lin Tsai, & Meng‐Yang Chang. (2017). Synthesis of Substituted 1,6-Diarylnaphthalenes via a Tandem Claisen Rearrangement and Ene Reaction Protocol. The Journal of Organic Chemistry. 82(6). 3317–3326. 21 indexed citations
19.
Chan, Chieh‐Kai, et al.. (2016). One-Pot Synthesis of 2-Cyano-1,4-diketones: Applications to Synthesis of Cyanosubstituted Furans, Pyrroles, and Dihydropyridazines. The Journal of Organic Chemistry. 81(17). 8112–8120. 28 indexed citations
20.
Chen, Hsuan‐Ying, et al.. (2016). Stepwise and Self-Assembly Synthesis of Tetranuclear Iron-Thiolate-Diisocyanide Metallocyclophane Complexes. Journal of the Chinese Chemical Society. 64(1). 94–102. 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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