Fumito Ishibashi

2.3k total citations
72 papers, 2.0k citations indexed

About

Fumito Ishibashi is a scholar working on Organic Chemistry, Molecular Biology and Biotechnology. According to data from OpenAlex, Fumito Ishibashi has authored 72 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Organic Chemistry, 23 papers in Molecular Biology and 9 papers in Biotechnology. Recurrent topics in Fumito Ishibashi's work include Synthesis and Characterization of Pyrroles (18 papers), Plant-derived Lignans Synthesis and Bioactivity (12 papers) and Marine Sponges and Natural Products (9 papers). Fumito Ishibashi is often cited by papers focused on Synthesis and Characterization of Pyrroles (18 papers), Plant-derived Lignans Synthesis and Bioactivity (12 papers) and Marine Sponges and Natural Products (9 papers). Fumito Ishibashi collaborates with scholars based in Japan, France and United Kingdom. Fumito Ishibashi's co-authors include Masatomo Iwao, Tsutomu Fukuda, Shotaro Hirao, Eiji Taniguchi, Yuji Fujita, Mochammad Amin Alamsjah, Takeshi Ohta, Tomohiro Yamaguchi, Naotaka Fujikawa and Chutamas Satasook and has published in prestigious journals such as Journal of Medicinal Chemistry, The Journal of Organic Chemistry and Tetrahedron.

In The Last Decade

Fumito Ishibashi

68 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fumito Ishibashi Japan 24 1.3k 482 235 227 162 72 2.0k
Dušan Sladić Serbia 25 900 0.7× 397 0.8× 150 0.6× 225 1.0× 59 0.4× 96 1.7k
Philip Proteau United States 24 543 0.4× 1.2k 2.5× 114 0.5× 385 1.7× 168 1.0× 45 2.4k
Takashi Tokoroyama Japan 20 873 0.7× 684 1.4× 57 0.2× 234 1.0× 241 1.5× 119 1.7k
Yu Tang China 23 1.1k 0.9× 299 0.6× 64 0.3× 126 0.6× 92 0.6× 74 1.5k
Takenori Kusumi Japan 21 533 0.4× 409 0.8× 33 0.1× 278 1.2× 79 0.5× 68 1.3k
Eduardo G. Gros Argentina 23 690 0.5× 889 1.8× 53 0.2× 125 0.6× 321 2.0× 182 2.0k
Hidetoshi Yamada Japan 27 1.4k 1.1× 1.3k 2.8× 68 0.3× 227 1.0× 241 1.5× 153 2.4k
Hou‐Ming Wu China 25 659 0.5× 651 1.4× 202 0.9× 528 2.3× 267 1.6× 75 1.7k
Lorenzo De Napoli Italy 23 561 0.4× 1.1k 2.2× 65 0.3× 199 0.9× 107 0.7× 117 1.6k
Christos Roussakis France 27 852 0.7× 748 1.6× 42 0.2× 705 3.1× 187 1.2× 91 2.3k

Countries citing papers authored by Fumito Ishibashi

Since Specialization
Citations

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

Fields of papers citing papers by Fumito Ishibashi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fumito Ishibashi

This figure shows the co-authorship network connecting the top 25 collaborators of Fumito Ishibashi. A scholar is included among the top collaborators of Fumito Ishibashi 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 Fumito Ishibashi. Fumito Ishibashi 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.
Ishibashi, Fumito, et al.. (2024). Design, synthesis, and biological evaluation of novel benzo[6,7]indolo[3,4-c]isoquinolines as anticancer agents with topoisomerase I inhibition. Bioorganic & Medicinal Chemistry Letters. 104. 129710–129710. 3 indexed citations
2.
Ishibashi, Fumito, et al.. (2024). Numerical Simulation Study on Enhanced Efficiency of Geological CO2 Storage with Nanoparticle. International Petroleum Technology Conference. 1 indexed citations
3.
Fukuda, Tsutomu, Kentaro Yamashita, Fumito Ishibashi, et al.. (2021). Synthesis and evaluation of azalamellarin N and its A-ring-modified analogues as non-covalent inhibitors of the EGFR T790M/L858R mutant. Bioorganic & Medicinal Chemistry. 34. 116039–116039. 9 indexed citations
4.
Fukuda, Tsutomu, Fumito Ishibashi, & Masatomo Iwao. (2020). Lamellarin alkaloids: Isolation, synthesis, and biological activity. PubMed. 83. 1–112. 59 indexed citations
5.
6.
Fukuda, Tsutomu, Xiang Gao, Yuki Yoshida, et al.. (2017). Design, synthesis, and evaluation of A-ring-modified lamellarin N analogues as noncovalent inhibitors of the EGFR T790M/L858R mutant. Bioorganic & Medicinal Chemistry. 25(24). 6563–6580. 22 indexed citations
7.
Ishibashi, Fumito, et al.. (2013). Algicidal Sesquiterpene Hydroquinones from the Brown AlgaDictyopteris undulata. Bioscience Biotechnology and Biochemistry. 77(5). 1120–1122. 17 indexed citations
8.
Tanaka, Junji, Nadège Loaëc, Olivier Lozach, et al.. (2013). Synthesis, Resolution, and Biological Evaluation of Atropisomeric (aR)- and (aS)-16-Methyllamellarins N: Unique Effects of the Axial Chirality on the Selectivity of Protein Kinases Inhibition. Journal of Medicinal Chemistry. 56(18). 7289–7301. 57 indexed citations
9.
Kubo, Yoshinao, Hironori Sato, Naoki Yamamoto, et al.. (2011). Synthesis, structure–activity relationships, and mechanism of action of anti-HIV-1 lamellarin α 20-sulfate analogues. Bioorganic & Medicinal Chemistry. 19(24). 7541–7550. 44 indexed citations
10.
Fukuda, Tsutomu, Fumito Ishibashi, & Masatomo Iwao. (2011). ChemInform Abstract: Synthesis and Biological Activity of Lamellarin Alkaloids: An Overview. ChemInform. 42(32). 1 indexed citations
11.
Hirao, Shotaro, et al.. (2009). Synthetic Approach to Telomerase Inhibitor Dictyodendrin B: Synthesis of the Pyrrolo[2,3-c]carbazole Core. Bioscience Biotechnology and Biochemistry. 73(8). 1764–1772. 25 indexed citations
12.
Alamsjah, Mochammad Amin, Fumito Ishibashi, Hitoshi Kitamura, & Yuji Fujita. (2006). The Effectiveness of Ulva fasciata and U. pertusa (Ulvales, Chlorophyta) as Algicidal Substances on Harmful Algal Bloom Species. 54(3). 325–334. 1 indexed citations
13.
Kim, Ji Yeon, et al.. (2006). Algicidal Diterpenes from the Brown AlgaDictyota dichotoma. Bioscience Biotechnology and Biochemistry. 70(10). 2571–2574. 29 indexed citations
14.
Alamsjah, Mochammad Amin, Shotaro Hirao, Fumito Ishibashi, & Yuji Fujita. (2005). Isolation and Structure Determination of Algicidal Compounds fromUlva fasciata. Bioscience Biotechnology and Biochemistry. 69(11). 2186–2192. 78 indexed citations
15.
Iwao, Masatomo, et al.. (1998). New synthetic approach to pyrroloiminoquinone marine alkaloids. Total synthesis of makaluvamines A, D, I, and K. Tetrahedron. 54(31). 8999–9010. 43 indexed citations
16.
Ishibashi, Fumito, et al.. (1997). Total Synthesis of (+)-Paulownin. Bioscience Biotechnology and Biochemistry. 61(4). 743–745. 7 indexed citations
17.
Ishibashi, Fumito, Yoshitsugu Miyazaki, & Masatomo Iwao. (1997). ChemInform Abstract: Total Syntheses of Lamellarin D and H. The First Synthesis of Lamellarin‐Class Marine Alkaloids.. ChemInform. 28(37). 2 indexed citations
18.
Satasook, Chutamas, et al.. (1994). Insecticidal bioactivity of crude extracts of Aglaia species (meliaceae). Biochemical Systematics and Ecology. 22(2). 121–127. 21 indexed citations
19.
Taniguchi, Eiji & Fumito Ishibashi. (1989). NOESY Spectra of 1-Acetoxy-6-aryl-2-aryloxy-3,7-dioxabicyclo[3.3.0]octanes. Revision of the Absolute Configuration of (+)-Phrymarolin I. Chemistry Letters. 18(2). 313–316. 1 indexed citations
20.
Ishibashi, Fumito & Eiji Taniguchi. (1986). Synthesis and Absolute Configuration of (+)-Phrymarolin I, a Lignan. Chemistry Letters. 15(10). 1771–1774. 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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