Etsuko Tokunaga

8.3k total citations · 1 hit paper
158 papers, 6.9k citations indexed

About

Etsuko Tokunaga is a scholar working on Pharmaceutical Science, Organic Chemistry and Inorganic Chemistry. According to data from OpenAlex, Etsuko Tokunaga has authored 158 papers receiving a total of 6.9k indexed citations (citations by other indexed papers that have themselves been cited), including 122 papers in Pharmaceutical Science, 116 papers in Organic Chemistry and 40 papers in Inorganic Chemistry. Recurrent topics in Etsuko Tokunaga's work include Fluorine in Organic Chemistry (122 papers), Cyclopropane Reaction Mechanisms (36 papers) and Inorganic Fluorides and Related Compounds (35 papers). Etsuko Tokunaga is often cited by papers focused on Fluorine in Organic Chemistry (122 papers), Cyclopropane Reaction Mechanisms (36 papers) and Inorganic Fluorides and Related Compounds (35 papers). Etsuko Tokunaga collaborates with scholars based in Japan, China and Spain. Etsuko Tokunaga's co-authors include Norio Shibata, Motoo Shiro, Hiroyuki Kawai, Kenji Hirai, Osamu Kobayashi, Yuta Ogawa, Yudong Yang, Satoshi Okusu, Tatsuya Furukawa and Yoshinori Nomura 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

Etsuko Tokunaga

158 papers receiving 6.8k citations

Hit Papers

Current Contributions of ... 2020 2026 2022 2024 2020 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Etsuko Tokunaga Japan 45 5.1k 4.5k 2.0k 886 340 158 6.9k
Shuichi Nakamura Japan 57 8.1k 1.6× 2.9k 0.7× 2.7k 1.3× 1.6k 1.8× 469 1.4× 233 9.4k
Alexander E. Sorochinsky Ukraine 34 5.7k 1.1× 5.0k 1.1× 1.7k 0.8× 2.0k 2.3× 215 0.6× 76 7.6k
Günter Haufe Germany 35 3.8k 0.7× 2.6k 0.6× 948 0.5× 1.6k 1.8× 388 1.1× 291 5.5k
José Luis Aceña Spain 35 8.1k 1.6× 6.7k 1.5× 2.4k 1.2× 2.4k 2.8× 280 0.8× 100 10.4k
Takeshi Toru Japan 45 5.7k 1.1× 2.3k 0.5× 1.6k 0.8× 1.2k 1.3× 429 1.3× 211 6.7k
Peter R. Moore United Kingdom 17 5.8k 1.1× 5.5k 1.2× 1.9k 0.9× 953 1.1× 195 0.6× 39 7.5k
Kunisuke Izawa Japan 27 4.0k 0.8× 3.1k 0.7× 1.4k 0.7× 1.3k 1.5× 177 0.5× 110 5.4k
María Sánchez‐Roselló Spain 29 6.0k 1.2× 3.9k 0.9× 1.4k 0.7× 1.1k 1.3× 161 0.5× 68 7.1k
Steve Swallow United Kingdom 7 5.2k 1.0× 5.2k 1.2× 1.7k 0.8× 843 1.0× 151 0.4× 10 6.9k
Carlos del Pozo Spain 31 5.8k 1.1× 3.9k 0.9× 1.5k 0.7× 1.2k 1.3× 167 0.5× 111 7.0k

Countries citing papers authored by Etsuko Tokunaga

Since Specialization
Citations

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

Fields of papers citing papers by Etsuko Tokunaga

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Etsuko Tokunaga

This figure shows the co-authorship network connecting the top 25 collaborators of Etsuko Tokunaga. A scholar is included among the top collaborators of Etsuko Tokunaga 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 Etsuko Tokunaga. Etsuko Tokunaga 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
2.
Yamanaka, Satoshi, Daisuke Saito, Gembu Abe, et al.. (2021). Thalidomide and its metabolite 5‐hydroxythalidomide induce teratogenicity via the cereblon neosubstrate PLZF. The EMBO Journal. 40(4). e105375–e105375. 59 indexed citations
5.
Tokunaga, Etsuko, Takeshi Yamamoto, Emi Ito, & Norio Shibata. (2018). Understanding the Thalidomide Chirality in Biological Processes by the Self-disproportionation of Enantiomers. Scientific Reports. 8(1). 17131–17131. 114 indexed citations
7.
Tokunaga, Etsuko, et al.. (2018). Defluorosilylation of fluoroarenes and fluoroalkanes. Nature Communications. 9(1). 4393–4393. 108 indexed citations
8.
Mori, Tomoyuki, Takumi Ito, Shujie Liu, et al.. (2018). Structural basis of thalidomide enantiomer binding to cereblon. Scientific Reports. 8(1). 1294–1294. 86 indexed citations
9.
Tokunaga, Etsuko, et al.. (2018). Synthesis of fluoro-functionalized diaryl-λ3-iodonium salts and their cytotoxicity against human lymphoma U937 cells. Beilstein Journal of Organic Chemistry. 14. 364–372. 6 indexed citations
10.
Tokunaga, Etsuko, et al.. (2017). Biological evaluation of both enantiomers of fluoro-thalidomide using human myeloma cell line H929 and others. PLoS ONE. 12(8). e0182152–e0182152. 23 indexed citations
11.
Wang, Jiandong, et al.. (2017). Synthesis of Sulfur Perfluorophenyl Compounds Using a Pentafluorobenzenesulfonyl Hypervalent Iodonium Ylide. The Journal of Organic Chemistry. 82(22). 11939–11945. 6 indexed citations
12.
Okusu, Satoshi, Etsuko Tokunaga, & Norio Shibata. (2015). Difluoromethylation of Terminal Alkynes by Fluoroform. Organic Letters. 17(15). 3802–3805. 59 indexed citations
14.
Wang, Xin, Guo‐Kai Liu, Xiu‐Hua Xu, et al.. (2014). S‐((Phenylsulfonyl)difluoromethyl)thiophenium Salts: Carbon‐Selective Electrophilic Difluoromethylation of β‐Ketoesters, β‐Diketones, and Dicyanoalkylidenes. Angewandte Chemie. 126(7). 1858–1862. 52 indexed citations
15.
Liu, Guo‐Kai, Xiu‐Hua Xu, Norio Shibata, et al.. (2014). S‐((Phenylsulfonyl)difluoromethyl)thiophenium Salts: Carbon‐Selective Electrophilic Difluoromethylation of β‐Ketoesters, β‐Diketones, and Dicyanoalkylidenes. Angewandte Chemie International Edition. 53(7). 1827–1831. 62 indexed citations
16.
Nishimine, Takayuki, Kazunobu Fukushi, Etsuko Tokunaga, et al.. (2013). Kinetic Resolution of Allyl Fluorides by Enantioselective Allylic Trifluoromethylation Based on Silicon‐Assisted CF Bond Cleavage. Angewandte Chemie. 126(2). 527–530. 26 indexed citations
17.
Kawai, Hiroyuki, Zhe Yuan, Etsuko Tokunaga, & Norio Shibata. (2013). A sterically demanding organo-superbase avoids decomposition of a naked trifluoromethyl carbanion directly generated from fluoroform. Organic & Biomolecular Chemistry. 11(9). 1446–1446. 94 indexed citations
18.
Shibata, Norio, Norio Shibata, Takayuki Nishimine, et al.. (2013). Asymmetric Mannich reaction between (S)-N-(tert-butanesulfinyl)-3,3,3-trifluoroacetaldimine and malonic acid derivatives. Stereodivergent synthesis of (R)- and (S)-3-amino-4,4,4-trifluorobutanoic acids. Organic & Biomolecular Chemistry. 12(9). 1454–1454. 39 indexed citations
19.
Nishimine, Takayuki, et al.. (2013). Kinetic Resolution of Allyl Fluorides by Enantioselective Allylic Trifluoromethylation Based on Silicon‐Assisted CF Bond Cleavage. Angewandte Chemie International Edition. 53(2). 517–520. 89 indexed citations
20.
Kawai, Hiroyuki, Tatsuya Furukawa, Akihiro Kusuda, et al.. (2010). Enantioselective Synthesis of Trifluoromethyl‐Substituted 2‐Isoxazolines: Asymmetric Hydroxylamine/Enone Cascade Reaction. Angewandte Chemie International Edition. 49(33). 5762–5766. 113 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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