Kei Muto

4.7k total citations · 2 hit papers
63 papers, 3.9k citations indexed

About

Kei Muto is a scholar working on Organic Chemistry, Inorganic Chemistry and Molecular Biology. According to data from OpenAlex, Kei Muto has authored 63 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 60 papers in Organic Chemistry, 6 papers in Inorganic Chemistry and 3 papers in Molecular Biology. Recurrent topics in Kei Muto's work include Catalytic C–H Functionalization Methods (50 papers), Catalytic Cross-Coupling Reactions (42 papers) and Sulfur-Based Synthesis Techniques (17 papers). Kei Muto is often cited by papers focused on Catalytic C–H Functionalization Methods (50 papers), Catalytic Cross-Coupling Reactions (42 papers) and Sulfur-Based Synthesis Techniques (17 papers). Kei Muto collaborates with scholars based in Japan, United States and China. Kei Muto's co-authors include Junichiro Yamaguchi, Kenichiro Itami, Ryosuke Takise, Ryota Isshiki, Djamaladdin G. Musaev, Kazuma Amaike, Toshimasa Okita, Aiwen Lei, Lingkui Meng and Takuya Yamamoto and has published in prestigious journals such as Journal of the American Chemical Society, Chemical Society Reviews and Angewandte Chemie International Edition.

In The Last Decade

Kei Muto

62 papers receiving 3.9k citations

Hit Papers

Recent Progress in Nickel‐Catalyzed Biaryl Coupling 2012 2026 2016 2021 2012 2017 100 200 300 400

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kei Muto Japan 30 3.8k 770 316 222 97 63 3.9k
Baomin Fan China 34 2.6k 0.7× 1.5k 1.9× 404 1.3× 292 1.3× 143 1.5× 168 3.3k
Huailong Teng China 25 1.7k 0.5× 529 0.7× 222 0.7× 109 0.5× 50 0.5× 51 2.0k
Alison J. Frontier United States 33 3.4k 0.9× 413 0.5× 648 2.1× 80 0.4× 42 0.4× 90 3.8k
Ming‐Yu Ngai United States 34 3.5k 0.9× 1.3k 1.7× 434 1.4× 1.1k 4.8× 131 1.4× 57 3.9k
Rolf H. Taaning Denmark 21 1.5k 0.4× 506 0.7× 314 1.0× 259 1.2× 328 3.4× 26 1.8k
Ryan R. Walvoord United States 10 1.5k 0.4× 372 0.5× 231 0.7× 51 0.2× 48 0.5× 14 1.9k
Rita Skoda‐Földes Hungary 21 1.5k 0.4× 319 0.4× 415 1.3× 47 0.2× 123 1.3× 112 1.9k
Xiang‐Ying Tang China 36 3.3k 0.9× 279 0.4× 262 0.8× 224 1.0× 19 0.2× 116 3.5k
Keiichi Sorimachi Japan 17 2.3k 0.6× 899 1.2× 576 1.8× 131 0.6× 9 0.1× 20 2.4k
Fang Ke China 18 983 0.3× 122 0.2× 189 0.6× 85 0.4× 16 0.2× 70 1.3k

Countries citing papers authored by Kei Muto

Since Specialization
Citations

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

Fields of papers citing papers by Kei Muto

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kei Muto

This figure shows the co-authorship network connecting the top 25 collaborators of Kei Muto. A scholar is included among the top collaborators of Kei Muto 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 Kei Muto. Kei Muto 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.
Yokogawa, Daisuke, et al.. (2025). Facile generation of ortho-quinodimethanes toward polycyclic compounds. Chem. 11(11). 102615–102615. 2 indexed citations
2.
Muto, Kei, et al.. (2024). Cine- Substitution of Enolates: Enolate Dance/Coupling of Cycloalkenyl Pivalates by Nickel Catalysis. ACS Catalysis. 14(13). 10412–10417. 3 indexed citations
3.
Muto, Kei, et al.. (2023). Chloroacetyl boronate N -tosylhydrazone as a versatile synthetic building block. Chemical Communications. 59(48). 7419–7422. 2 indexed citations
4.
Muto, Kei, et al.. (2023). Concise Synthesis of (±)‐Fortuneicyclidins and (±)‐Cephalotine B Enabled by Pd‐Catalyzed Dearomative Spirocyclization**. Chemistry - A European Journal. 29(68). 4 indexed citations
5.
Isshiki, Ryota, et al.. (2022). Decarbonylative Reductive Coupling of Aromatic Esters by Nickel and Palladium Catalyst. Chemistry Letters. 51(7). 749–753. 5 indexed citations
6.
Muto, Kei, et al.. (2022). Aryl sulfide synthesis via aryl exchange reaction. Trends in Chemistry. 5(1). 102–103. 1 indexed citations
7.
Kashihara, Myuto, et al.. (2021). Development of Pd-Catalyzed Denitrative Couplings. Journal of Synthetic Organic Chemistry Japan. 79(1). 11–21. 2 indexed citations
8.
Muto, Kei, et al.. (2021). Convergent Azaspirocyclization of Bromoarenes with N -Tosylhydrazones by a Palladium Catalyst. ACS Catalysis. 11(16). 10429–10435. 23 indexed citations
9.
Muto, Kei, et al.. (2020). Dearomative Allylation of Naphthyl Cyanohydrins by Palladium Catalysis: Catalyst-Enhanced Site Selectivity. Organic Letters. 22(9). 3423–3427. 21 indexed citations
10.
Isshiki, Ryota, et al.. (2020). Catalytic Deoxygenative Coupling of Aromatic Esters with Organophosphorus Compounds. Journal of the American Chemical Society. 142(16). 7386–7392. 33 indexed citations
11.
Muto, Kei, et al.. (2019). Pd-Catalyzed Dearomative Three-Component Reaction of Bromoarenes with Diazo Compounds and Allylborates. ACS Catalysis. 9(10). 8991–8995. 39 indexed citations
12.
Isshiki, Ryota, Toshimasa Okita, Kei Muto, & Junichiro Yamaguchi. (2018). Decarbonylative Coupling Reaction of Aromatic Esters. Journal of Synthetic Organic Chemistry Japan. 76(4). 300–314. 2 indexed citations
13.
Muto, Kei, et al.. (2018). Synthesis of Fully Arylated (Hetero) arenes by Coupling Reaction. Journal of Synthetic Organic Chemistry Japan. 76(2). 98–110. 2 indexed citations
14.
Yamaguchi, Junichiro, Kei Muto, & Kenichiro Itami. (2016). Nickel-Catalyzed Aromatic C–H Functionalization. Topics in Current Chemistry. 374(4). 55–55. 73 indexed citations
15.
Yamanaka, Iori, Anupriya Kumar, Junichiro Yamaguchi, et al.. (2015). CH Activation Generates Period‐Shortening Molecules That Target Cryptochrome in the Mammalian Circadian Clock. Angewandte Chemie International Edition. 54(24). 7193–7197. 61 indexed citations
16.
Takise, Ryosuke, Kei Muto, Junichiro Yamaguchi, & Kenichiro Itami. (2014). Nickel‐Catalyzed α‐Arylation of Ketones with Phenol Derivatives. Angewandte Chemie International Edition. 53(26). 6791–6794. 151 indexed citations
17.
Yamaguchi, Junichiro, Kei Muto, Kazuma Amaike, Takuya Yamamoto, & Kenichiro Itami. (2013). Nickel-Catalyzed Direct Coupling of Heteroarenes. Journal of Synthetic Organic Chemistry Japan. 71(6). 576–587. 3 indexed citations
18.
Muto, Kei, Junichiro Yamaguchi, Aiwen Lei, & Kenichiro Itami. (2013). Isolation, Structure, and Reactivity of an Arylnickel(II) Pivalate Complex in Catalytic C–H/C–O Biaryl Coupling. Journal of the American Chemical Society. 135(44). 16384–16387. 144 indexed citations
19.
Meng, Lingkui, et al.. (2013). CH Alkenylation of Azoles with Enols and Esters by Nickel Catalysis. Angewandte Chemie International Edition. 52(38). 10048–10051. 138 indexed citations
20.
Yamamoto, Takuya, et al.. (2011). Nickel‐Catalyzed CH Arylation of Azoles with Haloarenes: Scope, Mechanism, and Applications to the Synthesis of Bioactive Molecules. Chemistry - A European Journal. 17(36). 10113–10122. 177 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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