Takanao Matsui

1.1k total citations
53 papers, 850 citations indexed

About

Takanao Matsui is a scholar working on Organic Chemistry, Molecular Biology and Materials Chemistry. According to data from OpenAlex, Takanao Matsui has authored 53 papers receiving a total of 850 indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Organic Chemistry, 17 papers in Molecular Biology and 10 papers in Materials Chemistry. Recurrent topics in Takanao Matsui's work include Oxidative Organic Chemistry Reactions (13 papers), Synthetic Organic Chemistry Methods (11 papers) and Porphyrin and Phthalocyanine Chemistry (7 papers). Takanao Matsui is often cited by papers focused on Oxidative Organic Chemistry Reactions (13 papers), Synthetic Organic Chemistry Methods (11 papers) and Porphyrin and Phthalocyanine Chemistry (7 papers). Takanao Matsui collaborates with scholars based in Japan and United States. Takanao Matsui's co-authors include Yoh‐ichi Matsushita, Kazuhiro Sugamoto, Mitsuru Nakayama, James D. White, Hirotaka Mori, Tadashi Sakai, Satoru Yoshida, Yasushi Nishikawa, Jim A. Thomas and D.M.S. Munasinghe and has published in prestigious journals such as The Journal of Organic Chemistry, Cellular and Molecular Life Sciences and Tetrahedron.

In The Last Decade

Takanao Matsui

49 papers receiving 817 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Takanao Matsui Japan 18 475 273 96 96 94 53 850
Paulo Marcos Donate Brazil 19 339 0.7× 355 1.3× 80 0.8× 118 1.2× 98 1.0× 70 954
René Miranda Mexico 20 729 1.5× 243 0.9× 88 0.9× 136 1.4× 152 1.6× 115 1.4k
Julio A. Seijas Spain 23 917 1.9× 368 1.3× 133 1.4× 93 1.0× 82 0.9× 98 1.8k
Manas Chakrabarty India 21 1.0k 2.1× 269 1.0× 50 0.5× 107 1.1× 78 0.8× 105 1.4k
Archimede Rotondo Italy 23 709 1.5× 423 1.5× 118 1.2× 148 1.5× 59 0.6× 81 1.5k
Giancarlo Verardo Italy 22 693 1.5× 433 1.6× 102 1.1× 242 2.5× 71 0.8× 106 1.5k
Kourosch Abbaspour Tehrani Belgium 24 1.3k 2.8× 361 1.3× 80 0.8× 137 1.4× 84 0.9× 82 1.9k
Maurizio Barontini Italy 18 415 0.9× 248 0.9× 36 0.4× 73 0.8× 52 0.6× 27 769
Héctor Luna Mexico 16 558 1.2× 491 1.8× 79 0.8× 75 0.8× 26 0.3× 62 946
Manuel González Sierra Argentina 18 290 0.6× 437 1.6× 67 0.7× 217 2.3× 65 0.7× 52 958

Countries citing papers authored by Takanao Matsui

Since Specialization
Citations

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

Fields of papers citing papers by Takanao Matsui

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Takanao Matsui

This figure shows the co-authorship network connecting the top 25 collaborators of Takanao Matsui. A scholar is included among the top collaborators of Takanao Matsui 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 Takanao Matsui. Takanao Matsui 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.
Sugamoto, Kazuhiro, Yoh‐ichi Matsushita, & Takanao Matsui. (2012). Solvent-Free Oxidative Coupling of 2-Naphthols Catalyzed by Hydrotalcite-Like Compounds in Aerobic Conditions. Letters in Organic Chemistry. 9(4). 263–266. 1 indexed citations
3.
4.
Sugamoto, Kazuhiro, et al.. (2008). Synthesis of 4-hydroxyderricin and related derivatives. Tetrahedron Letters. 49(47). 6639–6641. 21 indexed citations
5.
Matsushita, Yoh‐ichi, et al.. (2008). Chemical changes in terpenes of sugi (Cryptomeria japonica) wood during steam drying in kiln at high temperature. Journal of Wood Science. 54(6). 476–482. 8 indexed citations
6.
Matsushita, Yoh‐ichi, et al.. (2005). Preparation and Properties of Gelatin-Immobilized β-Glucosidase fromPyrococcus furiosus. Bioscience Biotechnology and Biochemistry. 69(1). 128–136. 20 indexed citations
7.
Sugamoto, Kazuhiro, et al.. (2005). Antimicrobial Effect of the Wood Vinegar from Cryptomeria japonica Sapwood on Plant Pathogenic Microorganisms. Journal of Microbiology and Biotechnology. 15(5). 1106–1109. 47 indexed citations
8.
Sugamoto, Kazuhiro, et al.. (2004). Carbonization of wood biomass. TANSO. 2004(212). 69–74. 7 indexed citations
9.
Matsushita, Yoh‐ichi, Kazuhiro Sugamoto, & Takanao Matsui. (2004). The Friedel–Crafts acylation of aromatic compounds with carboxylic acids by the combined use of perfluoroalkanoic anhydride and bismuth or scandium triflate. Tetrahedron Letters. 45(24). 4723–4727. 49 indexed citations
10.
Matsushita, Yoh‐ichi, et al.. (2003). Enantioselective reduction of γ-hydroperoxy-α,β-unsaturated carbonyl compounds catalyzed by lipid-coated peroxidase in organic solvents. Tetrahedron Asymmetry. 14(16). 2339–2350. 3 indexed citations
11.
Munasinghe, D.M.S., et al.. (2003). Lipid peroxidation-derived cytotoxic aldehyde, 4-hydroxy-2-nonenal in smoked pork. Meat Science. 63(3). 377–380. 23 indexed citations
12.
Hayashi, Yoshiki, Yasushi Nishikawa, Hirotaka Mori, et al.. (1998). Evaluation of the Cytotoxic Activity of Chiral (E)-13-Hydroxy-10-oxo-11-octadecenoic Acid and Its Lactone. Bioscience Biotechnology and Biochemistry. 62(9). 1771–1773. 6 indexed citations
13.
Matsushita, Yoh‐ichi, et al.. (1995). γ-selective hydroxylation of α,β,γ,δ-unsaturated carbonyl compounds and its application to syntheses of (±)-6-hydroxyshogaol and related furanoids. Tetrahedron Letters. 36(11). 1879–1882. 10 indexed citations
14.
Matsushita, Yoh‐ichi, et al.. (1994). Total Synthesis of (−)-Pyrenophorin via Cobalt(II) Porphyrin-Catalyzed Oxygenation of Ethyl (2E,4E,7R)-7-Acetoxy-2,4-octadienoate. Chemistry Letters. 23(6). 1083–1084. 11 indexed citations
15.
Matsushita, Yoh‐ichi, Kei Sakamoto, Taro Murakami, & Takanao Matsui. (1994). A Convenient Synthesis of Methyl 4-Substituted Benzoates via Diels-Alder Reaction in the Presence of Palladium on Activated Carbon. Synthetic Communications. 24(22). 3307–3313. 17 indexed citations
16.
Matsushita, Yoh‐ichi & Takanao Matsui. (1993). Synthesis of aminomethylated calix[4]resorcinarenes. Tetrahedron Letters. 34(46). 7433–7436. 111 indexed citations
17.
18.
Matsui, Takanao & Mitsuru Nakayama. (1983). Photochemical Synthesis of the Acetylene Adducts and Dimers of 2H- and 4H-1-Benzopyranones. Bulletin of the Chemical Society of Japan. 56(11). 3531–3532. 5 indexed citations
19.
Nakayama, Mitsuru, Shinji Nishimura, Takanao Matsui, S. Hayashi, & Kenji Fukui. (1970). The Syntheses of Isoevodionol and Its Derivatives. Nippon kagaku zassi. 91(11). 1092–1094. 4 indexed citations
20.
Fukui, Kenji, Mitsuru Nakayama, Takanao Matsui, Mitsuo Masumura, & Tokunaru Hòrie. (1969). The Syntheses of Pedalitin and Related Compounds. Nippon kagaku zassi. 90(12). 1270–1274. 7 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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