Kan Wakamatsu

1.1k total citations
67 papers, 945 citations indexed

About

Kan Wakamatsu is a scholar working on Organic Chemistry, Materials Chemistry and Spectroscopy. According to data from OpenAlex, Kan Wakamatsu has authored 67 papers receiving a total of 945 indexed citations (citations by other indexed papers that have themselves been cited), including 58 papers in Organic Chemistry, 15 papers in Materials Chemistry and 8 papers in Spectroscopy. Recurrent topics in Kan Wakamatsu's work include Synthesis and Properties of Aromatic Compounds (25 papers), Radical Photochemical Reactions (18 papers) and Sulfur-Based Synthesis Techniques (11 papers). Kan Wakamatsu is often cited by papers focused on Synthesis and Properties of Aromatic Compounds (25 papers), Radical Photochemical Reactions (18 papers) and Sulfur-Based Synthesis Techniques (11 papers). Kan Wakamatsu collaborates with scholars based in Japan, China and Chile. Kan Wakamatsu's co-authors include Shinji Toyota, Akihiro Orita, Tetsuo Iwanaga, Eiji Tsurumaki, Junzo Otera, Yuta Yamamoto, Tsutomu Miyashi, Kôichi Kikuchi, Yasutake Takahashi and De Lie An and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Chemical Communications.

In The Last Decade

Kan Wakamatsu

66 papers receiving 931 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kan Wakamatsu Japan 20 743 336 133 111 111 67 945
Manabu Yanase Japan 12 823 1.1× 482 1.4× 108 0.8× 138 1.2× 136 1.2× 14 1.0k
Katsuya Sako Japan 17 539 0.7× 318 0.9× 98 0.7× 175 1.6× 115 1.0× 46 813
B. Içli Switzerland 8 446 0.6× 599 1.8× 100 0.8× 188 1.7× 127 1.1× 10 943
Ephrath Solel Israel 15 373 0.5× 219 0.7× 139 1.0× 141 1.3× 72 0.6× 25 626
Myriam Linke France 9 463 0.6× 526 1.6× 141 1.1× 163 1.5× 71 0.6× 11 696
N.N.P. Moonen Switzerland 14 623 0.8× 493 1.5× 141 1.1× 91 0.8× 306 2.8× 17 1.0k
Joakim Kärnbratt Sweden 10 411 0.6× 693 2.1× 136 1.0× 97 0.9× 189 1.7× 10 879
Damien Jouvenot France 16 467 0.6× 389 1.2× 54 0.4× 104 0.9× 123 1.1× 31 787
Lioudmila Fomina Mexico 16 401 0.5× 288 0.9× 102 0.8× 87 0.8× 160 1.4× 85 754
José Osío Barcina Spain 18 466 0.6× 205 0.6× 134 1.0× 91 0.8× 109 1.0× 60 765

Countries citing papers authored by Kan Wakamatsu

Since Specialization
Citations

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

Fields of papers citing papers by Kan Wakamatsu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kan Wakamatsu

This figure shows the co-authorship network connecting the top 25 collaborators of Kan Wakamatsu. A scholar is included among the top collaborators of Kan Wakamatsu 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 Kan Wakamatsu. Kan Wakamatsu 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.
Yamamoto, Kōji, et al.. (2024). Phenothiazine cyclic hexamers: synthesis, properties, and complexation behavior with C60. Chemical Communications. 60(16). 2220–2223. 2 indexed citations
2.
Tsurumaki, Eiji, et al.. (2024). Structures, Chiroptical Properties, and Unexpectedly Facile Helical Inversion of Highly Elongated Anthracene‐Fused Expanded Helicenes. Chemistry - A European Journal. 31(10). e202404348–e202404348. 5 indexed citations
3.
Watanabe, Hikaru, Shunsuke Yamada, Yasuhiro Okuda, et al.. (2024). Synthesis of (Z)-Enediynes via Stereoinvertive Nucleophilic Substitution of (E)-Sulfonylethenes with Arylethynide, and Their Aggregation-Induced Optical Properties. The Journal of Organic Chemistry. 89(23). 17122–17132. 1 indexed citations
4.
Watanabe, Hikaru, Takuma Sato, T. Tokuyama, et al.. (2023). Effective synthesis of 1,4-diarylbutadienes via reductive desulfonylation of 1,3-butadienyl sulfones by proper choice of regioisomeric π-expanded pyrene photocatalysts. Bulletin of the Chemical Society of Japan. 97(2). 1 indexed citations
5.
Hasegawa, Eietsu, et al.. (2023). Desulfonylative Radical Truce–Smiles Rearrangement Utilizing the Benzimidazoline and Benzimidazolium Redox Couple. Synlett. 35(3). 352–356. 2 indexed citations
6.
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Tsurumaki, Eiji, et al.. (2021). Structure and Photophysical Properties of 1,1,2,2‐Tetra(1‐anthryl)ethane: A C(sp3)−C(sp3) Bond Substituted with Four Anthracene Units. ChemPlusChem. 87(1). e202100447–e202100447. 3 indexed citations
8.
Tsurumaki, Eiji, et al.. (2021). Construction of Helical Structures with Multiple Fused Anthracenes: Structures and Properties of Long Expanded Helicenes. Chemistry - A European Journal. 27(14). 4477–4477. 2 indexed citations
9.
Orita, Akihiro, et al.. (2021). Custom-Made Pyrene Photocatalyst-Promoted Desulfonylation of Arylethenyl Sulfones Using Green-Light-Emitting Diodes. Synthesis. 53(17). 2984–2994. 6 indexed citations
10.
Hasegawa, Eietsu, et al.. (2020). Sterically Regulated α-Oxygenation of α-Bromocarbonyl Compounds Promoted Using 2-Aryl-1,3-dimethylbenzimidazolines and Air. ACS Omega. 5(13). 7651–7665. 16 indexed citations
11.
Watanabe, Hikaru, Kazumasa Adachi, Yasuhiro Okuda, et al.. (2020). Syntheses of Diarylethenes by Perylene-catalyzed Photodesulfonylation from Ethenyl Sulfones. Chemistry Letters. 49(4). 409–412. 13 indexed citations
12.
Toyota, Shinji, Yuta Yamamoto, Kan Wakamatsu, Eiji Tsurumaki, & Alvaro Muñoz‐Castro. (2019). Nano-Saturn with an Ellipsoidal Body: Anthracene Macrocyclic Ring–C70 Complex. Bulletin of the Chemical Society of Japan. 92(10). 1721–1728. 21 indexed citations
13.
Hasegawa, Eietsu, Keisuke Matsumoto, Tomoaki Miura, et al.. (2018). Visible Light and Hydroxynaphthylbenzimidazoline Promoted Transition-Metal-Catalyst-Free Desulfonylation of N-Sulfonylamides and N-Sulfonylamines. The Journal of Organic Chemistry. 83(18). 10813–10825. 38 indexed citations
14.
Yamamoto, Yuta, Eiji Tsurumaki, Kan Wakamatsu, & Shinji Toyota. (2018). Nano‐Saturn: Experimental Evidence of Complex Formation of an Anthracene Cyclic Ring with C60. Angewandte Chemie. 130(27). 8331–8334. 20 indexed citations
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Wakamatsu, Kan, et al.. (2013). Strained and Fluxional Macrocyclic Framework of Anthracene–Diacetylene Cyclic Pentamers. Chemistry Letters. 42(5). 559–561. 19 indexed citations
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Wakamatsu, Kan. (2004). Quinone imine dye formation via photocycloaddition between isocyanates and chloranil. Tetrahedron Letters. 45(24). 4627–4630. 1 indexed citations
20.
Kikuchi, Kôichi, Yasutake Takahashi, Kazuhide Koike, et al.. (1990). The Free Enthalpy Dependence of Rate Constants of Return Electron Transfer within Photoproduced Geminate Radical Ion Pairs. Zeitschrift für Physikalische Chemie. 167(1). 27–39. 26 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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