Makoto Ebine

801 total citations
28 papers, 649 citations indexed

About

Makoto Ebine is a scholar working on Organic Chemistry, Environmental Chemistry and Biotechnology. According to data from OpenAlex, Makoto Ebine has authored 28 papers receiving a total of 649 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Organic Chemistry, 19 papers in Environmental Chemistry and 9 papers in Biotechnology. Recurrent topics in Makoto Ebine's work include Marine Toxins and Detection Methods (19 papers), Synthetic Organic Chemistry Methods (12 papers) and Marine Sponges and Natural Products (9 papers). Makoto Ebine is often cited by papers focused on Marine Toxins and Detection Methods (19 papers), Synthetic Organic Chemistry Methods (12 papers) and Marine Sponges and Natural Products (9 papers). Makoto Ebine collaborates with scholars based in Japan and United States. Makoto Ebine's co-authors include Makoto Sasaki, Haruhiko Fuwa, Tohru Oishi, Chihiro Tsukano, Daniel G. Baden, Andrea J. Bourdelais, Nobuaki Matsumori, Michio Murata, Yoshiyuki Manabe and Kohei Torikai and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and The Journal of Organic Chemistry.

In The Last Decade

Makoto Ebine

28 papers receiving 625 citations

Peers

Makoto Ebine
Noriaki Uesaka United States
Robert J. Aversa United States
F. PERRON United States
J. Tiebes United States
F. P. J. T. Rutjes United States
Édouard Untersteller United States
Noriaki Uesaka United States
Makoto Ebine
Citations per year, relative to Makoto Ebine Makoto Ebine (= 1×) peers Noriaki Uesaka

Countries citing papers authored by Makoto Ebine

Since Specialization
Citations

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

Fields of papers citing papers by Makoto Ebine

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Makoto Ebine

This figure shows the co-authorship network connecting the top 25 collaborators of Makoto Ebine. A scholar is included among the top collaborators of Makoto Ebine 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 Makoto Ebine. Makoto Ebine 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.
Ebine, Makoto, et al.. (2020). Total Synthesis of Amphidinol 3: A General Strategy for Synthesizing Amphidinol Analogues and Structure–Activity Relationship Study. Journal of the American Chemical Society. 142(7). 3472–3478. 31 indexed citations
2.
Ebine, Makoto, et al.. (2018). Synthesis and Stereochemical Revision of the C31–C67 Fragment of Amphidinol 3. Angewandte Chemie International Edition. 57(21). 6060–6064. 25 indexed citations
3.
Ebine, Makoto, et al.. (2018). Synthesis and Stereochemical Revision of the C31–C67 Fragment of Amphidinol 3. Angewandte Chemie. 130(21). 6168–6172. 4 indexed citations
4.
Watanabe, Tomohiro, Hajime Shibata, Makoto Ebine, et al.. (2018). Synthesis and Complete Structure Determination of a Sperm-Activating and -Attracting Factor Isolated from the Ascidian Ascidia sydneiensis. Journal of Natural Products. 81(4). 985–997. 9 indexed citations
5.
Oishi, Tohru, Hiroki Yamamoto, Kohei Torikai, & Makoto Ebine. (2018). Synthesis of 6/6/6-Tricyclic Ether System via Achmatowicz and Intramolecular Oxa-Michael Reactions. Heterocycles. 97(1). 158–158. 6 indexed citations
6.
Konoki, Keiichi, et al.. (2017). Syntheses and Biological Activities of the LMNO, ent-LMNO, and NOPQR(S) Ring Systems of Maitotoxin. The Journal of Organic Chemistry. 82(18). 9595–9618. 12 indexed citations
7.
Ebine, Makoto, et al.. (2017). Synthesis of a Truncated Analog of Amphidinol 3 Corresponding to the C21–C39/C52–C67 Section. Chemistry Letters. 46(5). 662–664. 11 indexed citations
8.
Torikai, Kohei, et al.. (2017). Convergent Syntheses of the WXYZ Ring of Maitotoxin and the HIJK Ring of Brevisulcenal-F. Chemistry Letters. 47(3). 265–268. 9 indexed citations
9.
Ebine, Makoto, et al.. (2014). Stereoselective Synthesis of the C1–C29 Part of Amphidinol 3. The Journal of Organic Chemistry. 80(2). 859–871. 22 indexed citations
10.
Konoki, Keiichi, et al.. (2014). Synthesis and Biological Activity of the QRS Ring System of Maitotoxin. Chemistry Letters. 43(12). 1904–1906. 13 indexed citations
11.
Ebine, Makoto, Yoshiyuki Manabe, Ken Sakai, et al.. (2013). Synthesis and Structure Revision of the C43–C67 Part of Amphidinol 3. Organic Letters. 15(11). 2846–2849. 27 indexed citations
12.
Koshiyama, Tomomi, Akihiro Hori, Ryo Ohtani, et al.. (2013). Guest responsivity of a two-dimensional coordination polymer incorporating a cholesterol-based co-ligand. Dalton Transactions. 42(45). 15893–15893. 4 indexed citations
13.
Tamura, Satoru, Makoto Ebine, Izumi Iwakura, et al.. (2012). Triazoyl–phenyl linker system enhancing the aqueous solubility of a molecular probe and its efficiency in affinity labeling of a target protein for jasmonate glucoside. Bioorganic & Medicinal Chemistry Letters. 23(1). 188–193. 9 indexed citations
14.
Manabe, Yoshiyuki, Makoto Ebine, Nobuaki Matsumori, Michio Murata, & Tohru Oishi. (2012). Confirmation of the Absolute Configuration at C45 of Amphidinol 3. Journal of Natural Products. 75(11). 2003–2006. 21 indexed citations
15.
Fuwa, Haruhiko, Makoto Ebine, & Makoto Sasaki. (2011). Recent Applications of the Suzuki-Miyaura Cross-coupling to Complex Polycyclic Ether Synthesis. Journal of Synthetic Organic Chemistry Japan. 69(11). 1251–1262. 1 indexed citations
16.
Nakamura, Yoko, et al.. (2010). “Click-made” biaryl-linker improving efficiency in proteinlabelling for the membrane target protein of a bioactive compound. Organic & Biomolecular Chemistry. 9(1). 83–85. 18 indexed citations
17.
Ebine, Makoto, et al.. (2009). Highly efficient synthesis of medium-sized lactones via oxidative lactonization: concise total synthesis of isolaurepan. Organic & Biomolecular Chemistry. 8(1). 39–42. 43 indexed citations
18.
Fuwa, Haruhiko, Makoto Ebine, Andrea J. Bourdelais, Daniel G. Baden, & Makoto Sasaki. (2006). Total Synthesis, Structure Revision, and Absolute Configuration of (−)-Brevenal. Journal of the American Chemical Society. 128(51). 16989–16999. 104 indexed citations
19.
Fuwa, Haruhiko, Makoto Ebine, & Makoto Sasaki. (2006). Total Synthesis of the Proposed Structure of Brevenal. Journal of the American Chemical Society. 128(30). 9648–9650. 51 indexed citations
20.
Sasaki, Makoto, Makoto Ebine, Hiroyuki Takagi, et al.. (2004). Synthesis of the CDE/FG Ring Models of Prymnesins:  Reassignment of the Relative Configuration of the E/F Ring Juncture. Organic Letters. 6(9). 1501–1504. 27 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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