Kosuke Yasui

507 total citations
26 papers, 405 citations indexed

About

Kosuke Yasui is a scholar working on Organic Chemistry, Inorganic Chemistry and Pharmaceutical Science. According to data from OpenAlex, Kosuke Yasui has authored 26 papers receiving a total of 405 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Organic Chemistry, 4 papers in Inorganic Chemistry and 2 papers in Pharmaceutical Science. Recurrent topics in Kosuke Yasui's work include Catalytic C–H Functionalization Methods (14 papers), Catalytic Cross-Coupling Reactions (14 papers) and N-Heterocyclic Carbenes in Organic and Inorganic Chemistry (7 papers). Kosuke Yasui is often cited by papers focused on Catalytic C–H Functionalization Methods (14 papers), Catalytic Cross-Coupling Reactions (14 papers) and N-Heterocyclic Carbenes in Organic and Inorganic Chemistry (7 papers). Kosuke Yasui collaborates with scholars based in Japan, United States and France. Kosuke Yasui's co-authors include Mamoru Tobisu, Naoto Chatani, Hayato Fujimoto, Hugh Nakamura, Yuzuru Kanda, Phil S. Baran, Yoshinori Aihara, Takuya Kodama, Keisuke Nakamura and Masaya Sawamura and has published in prestigious journals such as Science, Journal of the American Chemical Society and Angewandte Chemie International Edition.

In The Last Decade

Kosuke Yasui

25 papers receiving 399 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kosuke Yasui Japan 12 374 69 36 24 22 26 405
Hiromichi Fujioka Japan 13 521 1.4× 88 1.3× 30 0.8× 49 2.0× 24 1.1× 24 558
Brendan C. Lainhart United States 8 497 1.3× 112 1.6× 31 0.9× 46 1.9× 38 1.7× 9 548
I. F. Dempsey Hyatt United States 10 321 0.9× 65 0.9× 28 0.8× 14 0.6× 20 0.9× 18 351
Chang‐Jiang Yang China 13 602 1.6× 124 1.8× 44 1.2× 42 1.8× 16 0.7× 30 654
Benjamin D. A. Shennan United Kingdom 7 238 0.6× 72 1.0× 33 0.9× 58 2.4× 10 0.5× 8 295
Matthew A. Horwitz United States 11 483 1.3× 96 1.4× 38 1.1× 78 3.3× 24 1.1× 14 528
Ze‐Xin Zhang United Kingdom 9 442 1.2× 90 1.3× 35 1.0× 50 2.1× 13 0.6× 11 478
Rei Matsuura United States 7 410 1.1× 77 1.1× 15 0.4× 20 0.8× 14 0.6× 7 436
Toshihiko Sone Japan 8 334 0.9× 88 1.3× 28 0.8× 54 2.3× 14 0.6× 11 370
Chi Yang China 10 523 1.4× 54 0.8× 29 0.8× 27 1.1× 15 0.7× 14 540

Countries citing papers authored by Kosuke Yasui

Since Specialization
Citations

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

Fields of papers citing papers by Kosuke Yasui

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kosuke Yasui

This figure shows the co-authorship network connecting the top 25 collaborators of Kosuke Yasui. A scholar is included among the top collaborators of Kosuke Yasui 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 Kosuke Yasui. Kosuke Yasui 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.
Yasui, Kosuke, et al.. (2025). Stereoselective Preparation and Palladium‐Catalyzed Suzuki–Miyaura Cross‐Coupling of Alkenyl Sulfoximines. Angewandte Chemie International Edition. 64(11). e202420949–e202420949. 4 indexed citations
3.
Nakamura, Shōgo, et al.. (2025). CuH-Catalyzed Regio- and Stereoselective Hydroalkoxylation of Styrenes with Acetal-Based Peroxides. ACS Catalysis. 15(10). 8353–8360. 2 indexed citations
4.
Tokura, Yu, et al.. (2024). Pd-catalysed C–H alkynylation of benzophospholes. Chemical Communications. 60(20). 2792–2795. 7 indexed citations
5.
Yasui, Kosuke, et al.. (2024). Nickel-Catalyzed Electrophilic Amination of the Biphenylene C–C σ-Bond. Organic Letters. 26(20). 4268–4273. 2 indexed citations
6.
Yasui, Kosuke, Itsunari Minami, Motonari Uesugi, et al.. (2024). Molecular Design for Cardiac Cell Differentiation Using a Small Data Set and Decorated Shape Features. Journal of Chemical Information and Modeling. 64(23). 8824–8837. 1 indexed citations
7.
Kojima, Yuki, et al.. (2024). Synthesis of highly condensed phospholes by the Lewis acid-assisted dehydrogenative Mallory reaction under visible light irradiation. Chemical Science. 15(48). 20413–20420. 4 indexed citations
8.
9.
Fujimoto, Hayato, et al.. (2023). Single–carbon atom transfer to α,β-unsaturated amides from N-heterocyclic carbenes. Science. 379(6631). 484–488. 52 indexed citations
10.
Fujimoto, Hayato, Kosuke Yasui, & Mamoru Tobisu. (2023). Non-Classical Molecular Activation by Phosphines and N-Heterocyclic Carbenes and Its Application to Catalytic Reactions. Bulletin of the Chemical Society of Japan. 96(9). 872–886. 7 indexed citations
11.
Hayakawa, Masahiro, Satoshi Horike, Yuh Hijikata, et al.. (2022). Late-stage modification of π-electron systems based on asymmetric oxidation of a medium-sized sulfur-containing ring. Chemical Communications. 58(15). 2548–2551. 2 indexed citations
12.
Yasui, Kosuke, et al.. (2021). Construction of Tricyclic Nitrogen Heterocycles by a Gold(I)‐Catalyzed Cascade Cyclization of Allenynes and Application to Polycyclic π‐Electron Systems. Angewandte Chemie International Edition. 60(52). 27019–27025. 16 indexed citations
13.
14.
Tobisu, Mamoru, et al.. (2021). Late-Stage Derivatization of Buflavine by Nickel-Catalyzed Direct Substitution of a Methoxy Group via C–O Bond Activation. Synthesis. 53(17). 3037–3044. 1 indexed citations
15.
Nakamura, Hugh, Kosuke Yasui, Yuzuru Kanda, & Phil S. Baran. (2019). 11-Step Total Synthesis of Teleocidins B-1–B-4. Journal of the American Chemical Society. 141(4). 1494–1497. 64 indexed citations
16.
Yasui, Kosuke, et al.. (2019). N‐Heterocyclic Carbene Catalyzed Concerted Nucleophilic Aromatic Substitution of Aryl Fluorides Bearing α,β‐Unsaturated Amides. Angewandte Chemie International Edition. 58(40). 14157–14161. 42 indexed citations
17.
Yasui, Kosuke, Naoto Chatani, & Mamoru Tobisu. (2018). Rhodium-Catalyzed C–O Bond Alkynylation of Aryl Carbamates with Propargyl Alcohols. Organic Letters. 20(7). 2108–2111. 20 indexed citations
18.
Tobisu, Mamoru, Kosuke Yasui, Yoshinori Aihara, & Naoto Chatani. (2017). C−O Activation by a Rhodium Bis(N‐Heterocyclic Carbene) Catalyst: Aryl Carbamates as Arylating Reagents in Directed C−H Arylation. Angewandte Chemie International Edition. 56(7). 1877–1880. 29 indexed citations
19.
Nakamura, Keisuke, Kosuke Yasui, Mamoru Tobisu, & Naoto Chatani. (2015). Rhodium-catalyzed cross-coupling of aryl carbamates with arylboron reagents. Tetrahedron. 71(26-27). 4484–4489. 26 indexed citations
20.
Yasui, Kosuke & J. Kanasaki. (2011). Scanning tunneling microscopic studies of laser-induced modifications of Si(001)-(2 × 1) surface. Journal of Applied Physics. 110(10). 3 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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