Fu‐Yu Tsai

1.8k total citations
58 papers, 1.5k citations indexed

About

Fu‐Yu Tsai is a scholar working on Organic Chemistry, Materials Chemistry and Inorganic Chemistry. According to data from OpenAlex, Fu‐Yu Tsai has authored 58 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Organic Chemistry, 10 papers in Materials Chemistry and 9 papers in Inorganic Chemistry. Recurrent topics in Fu‐Yu Tsai's work include Catalytic Cross-Coupling Reactions (30 papers), Catalytic C–H Functionalization Methods (18 papers) and Catalytic Alkyne Reactions (9 papers). Fu‐Yu Tsai is often cited by papers focused on Catalytic Cross-Coupling Reactions (30 papers), Catalytic C–H Functionalization Methods (18 papers) and Catalytic Alkyne Reactions (9 papers). Fu‐Yu Tsai collaborates with scholars based in Taiwan, Japan and Ireland. Fu‐Yu Tsai's co-authors include Wei‐Yi Wu, Martin Kotora, Tamotsu Takahashi, Yanzhong Li, Kiyohiko Nakajima, Chung‐Yuan Mou, Tamotsu Takahashi, Masamichi Yamanaka, Hui Wang and Yoshihiko Kondo and has published in prestigious journals such as Journal of the American Chemical Society, Langmuir and ACS Applied Materials & Interfaces.

In The Last Decade

Fu‐Yu Tsai

58 papers receiving 1.5k citations

Peers

Fu‐Yu Tsai

EEE

Prasenjit Saha India

Danilo Zim Brazil

Zoltán Hell Hungary

Thorsten Lauterbach Germany

Jean‐Francis Spindler France

Chandra Sekhar Vasam India

Dilip Konwar India

Xin‐Fang Duan China

Katrin M. Dyballa Germany

K. Surendra India

Prasenjit Saha India

Fu‐Yu Tsai

1.3k ×1.0

192 ×0.9

157 ×1.0

140 ×1.4

25 ×0.7

EEE

Citations per year, relative to Fu‐Yu Tsai Fu‐Yu Tsai (= 1×) peers Prasenjit Saha

Countries citing papers authored by Fu‐Yu Tsai

Since Specialization

Citations

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

Fields of papers citing papers by Fu‐Yu Tsai

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

This figure shows the co-authorship network connecting the top 25 collaborators of Fu‐Yu Tsai. A scholar is included among the top collaborators of Fu‐Yu 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 Fu‐Yu Tsai. Fu‐Yu Tsai 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

Suzuki, Noriyuki, et al.. (2024). Palladium-catalysed reactions in water using catalysts covalently tethered on a thermo-responsive polymer. Catalysis Science & Technology. 15(3). 696–707. 1 indexed citations

Chang, Ya‐Ting, et al.. (2021). Stille coupling for the synthesis of isoflavones by a reusable palladium catalyst in water. Journal of the Chinese Chemical Society. 68(3). 469–475. 3 indexed citations

Lin, Che-Yi, Mei‐Yeh Jade Lu, Jia‐Xing Yue, et al.. (2020). Molecular asymmetry in the cephalochordate embryo revealed by single-blastomere transcriptome profiling. PLoS Genetics. 16(12). e1009294–e1009294. 5 indexed citations

Wu, Wei‐Yi, et al.. (2016). A Highly Efficient and Reusable Palladium(II)/Cationic 2,2’-Bipyridyl-Catalyzed Stille Coupling in Water. Molecules. 21(9). 1205–1205. 7 indexed citations

Hsu, I‐Jui, et al.. (2013). A Fluorescent Organic Nanotube Assembled from Novel p-Phenylene Ethynylene-Based Dicationic Amphiphiles. Langmuir. 29(8). 2580–2587. 5 indexed citations

Tsai, Fu‐Yu, et al.. (2012). Sonogashira–Hagihara Coupling towards Diaryl Alkynes Catalyzed by FeCl₃⋅6 H₂O/Cationic 2,2'‐Bipyridyl. ChemCatChem. 4(4). 540–545. 25 indexed citations

Tsai, Fu‐Yu, et al.. (2012). Deformation twinning in LiAlO2 at elevated temperatures. Materials Science and Engineering A. 551. 218–221. 2 indexed citations

Chen, Junrong, et al.. (2010). Palladium(II)/Cationic 2,2’-Bipyridyl System as a Highly Efficient and Reusable Catalyst for the Mizoroki-Heck Reaction in Water. Molecules. 15(1). 315–330. 45 indexed citations

Tsai, Fu‐Yu, et al.. (2010). pH‐Dependent conjugate addition of arylboronic acids to α,β‐unsaturated enones catalyzed by a reusable palladium(II)/cationic 2,2′‐bipyridyl system in water under air. Applied Organometallic Chemistry. 24(9). 619–624. 15 indexed citations

10.

Mou, Chung‐Yuan, et al.. (2009). Highly-efficient and recyclable nanosized MCM-41 anchored palladium bipyridyl complex-catalyzed coupling of acyl chlorides and terminal alkynes for the formation of ynones. Tetrahedron. 65(49). 10134–10141. 35 indexed citations

11.

Tsai, Fu‐Yu, et al.. (2009). Reusable and Efficient Cul/TBAB‐Catalyzed Iodination of Terminal Alkynes in Water under Air. Journal of the Chinese Chemical Society. 56(5). 1078–1081. 11 indexed citations

12.

Wu, Wei‐Yi, et al.. (2008). Homocoupling reaction of terminal alkynes catalyzed by a reusable cationic 2,2′-bipyridyl palladium(II)/CuI system in water. Green Chemistry. 11(2). 269–274. 107 indexed citations

13.

Wang, Yunhua & Fu‐Yu Tsai. (2007). Reusable Rhodium(I)/Cationic Bipyridyl-catalyzed Polymerization of Phenylacetylenes in Water under Aerobic Conditions. Chemistry Letters. 36(12). 1492–1493. 14 indexed citations

14.

Takahashi, Tamotsu, Fu‐Yu Tsai, Yanzhong Li, et al.. (2002). Selective Preparation of Pyridines, Pyridones, and Iminopyridines from Two Different Alkynes via Azazirconacycles. Journal of the American Chemical Society. 124(18). 5059–5067. 159 indexed citations

15.

Takahashi, Tamotsu, Yanzhong Li, Fu‐Yu Tsai, & Kiyohiko Nakajima. (2001). Cyclopentenone Formation by Regioselective Intermolecular Coupling of Trisubstituted Alkenes, Alkynes, and Isocyanates. Organometallics. 20(4). 595–597. 18 indexed citations

16.

Takahashi, Tamotsu, Yanzhong Li, Yasuyuki Ura, Fu‐Yu Tsai, & Feng Xu. (2001). Preparation of Benzoheterocycles Containing Group 14 Elements Using Zirconacyclopentadienes. Heterocycles. 54(2). 943–943. 6 indexed citations

17.

Takahashi, Tamotsu, Yasuyuki Ura, Yanzhong Li, et al.. (2000). Preparation of Sn-, Ge-, and Si-Heterocycles from Zirconacycles. Heterocycles. 52(3). 1171–1171. 21 indexed citations

18.

Takahashi, Tamotsu, Fu‐Yu Tsai, & Martin Kotora. (2000). ChemInform Abstract: Selective Formation of Substituted Pyridines from Two Different Alkynes and a Nitrile: Novel Coupling Reaction of Azazirconacyclopentadienes with Alkynes.. ChemInform. 31(39). 1 indexed citations

19.

Tsai, Fu‐Yu, et al.. (1998). A new stable intermediary mode between η3-2-aminoallyl complexes and metallacyclobutanimines. Synthesis and structural characteristic of η3-azatrimethylenemethane and N-protonated, N-alkylated, N-arylated η3-azatrimethylenemethane complexes of Pt and Pd. Journal of Organometallic Chemistry. 569(1-2). 39–54. 15 indexed citations

20.

Froment, G.F., et al.. (1985). Aromatics from Light Hydrocarbons. 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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