Masaru Hashimoto

5.8k total citations
223 papers, 4.6k citations indexed

About

Masaru Hashimoto is a scholar working on Organic Chemistry, Molecular Biology and Pharmacology. According to data from OpenAlex, Masaru Hashimoto has authored 223 papers receiving a total of 4.6k indexed citations (citations by other indexed papers that have themselves been cited), including 60 papers in Organic Chemistry, 55 papers in Molecular Biology and 43 papers in Pharmacology. Recurrent topics in Masaru Hashimoto's work include Microbial Natural Products and Biosynthesis (32 papers), Marine Sponges and Natural Products (22 papers) and Molecular spectroscopy and chirality (21 papers). Masaru Hashimoto is often cited by papers focused on Microbial Natural Products and Biosynthesis (32 papers), Marine Sponges and Natural Products (22 papers) and Molecular spectroscopy and chirality (21 papers). Masaru Hashimoto collaborates with scholars based in Japan, United States and Canada. Masaru Hashimoto's co-authors include Koji Nakanishi, Janet R. Sparrow, Craig A. Parish, Masami Yamada, Shiro Terashima, James Dillon, Kazuaki Tanaka, H. Seki, Y. Ishida and Takanori Murakami and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Angewandte Chemie International Edition.

In The Last Decade

Masaru Hashimoto

215 papers receiving 4.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Masaru Hashimoto Japan 33 1.4k 1.1k 612 605 603 223 4.6k
Andrew R. Harvey United Kingdom 33 930 0.7× 227 0.2× 229 0.4× 64 0.1× 472 0.8× 232 4.7k
Louise C. Serpell United Kingdom 66 11.0k 8.1× 2.0k 1.8× 105 0.2× 43 0.1× 632 1.0× 174 17.2k
P. C. W. Fung Hong Kong 25 308 0.2× 112 0.1× 29 0.0× 201 0.3× 173 0.3× 207 2.7k
Valerie Daggett United States 69 12.9k 9.5× 510 0.5× 37 0.1× 82 0.1× 159 0.3× 234 15.9k
Donald C. Chang Hong Kong 41 3.3k 2.4× 152 0.1× 83 0.1× 22 0.0× 378 0.6× 134 6.5k
Shin‐ichi Sasaki Japan 38 1.2k 0.9× 584 0.5× 109 0.2× 11 0.0× 69 0.1× 335 5.4k
Annette Tardieu France 40 5.0k 3.7× 1.0k 0.9× 122 0.2× 23 0.0× 32 0.1× 82 6.9k
Scott E. Feller United States 41 8.7k 6.4× 1.0k 0.9× 25 0.0× 19 0.0× 180 0.3× 84 11.6k
Masaaki Yoshida Japan 33 1.2k 0.9× 92 0.1× 159 0.3× 29 0.0× 73 0.1× 247 4.0k
Svend Erik Nielsen Denmark 27 1.9k 1.4× 389 0.4× 22 0.0× 66 0.1× 254 0.4× 106 5.8k

Countries citing papers authored by Masaru Hashimoto

Since Specialization
Citations

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

Fields of papers citing papers by Masaru Hashimoto

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Masaru Hashimoto

This figure shows the co-authorship network connecting the top 25 collaborators of Masaru Hashimoto. A scholar is included among the top collaborators of Masaru Hashimoto 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 Masaru Hashimoto. Masaru Hashimoto 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.
Maeda, H., et al.. (2024). Highly Functionalized Spirobisnaphthalenes from Roussoella sp. KT4147. Journal of Natural Products. 87(7). 1798–1807. 7 indexed citations
3.
Wu, Jing, Masaru Hashimoto, Mitsuru Kondo, et al.. (2023). “Fruiting Liquid” of Mushroom-Forming Fungi, A Novel Source of Bioactive Compounds – Fruiting-Body Inducer and HIF and Axl Inhibitors. Journal of Agricultural and Food Chemistry. 71(36). 13338–13345. 3 indexed citations
4.
Ishibashi, Osamu, et al.. (2021). Semipinacol rearrangement of a bicyclo[7.2.0]undecane framework into a bicyclo[6.3.0]undecane skeleton: a model study on the biosynthesis of seiridiasteriscane A. Bioscience Biotechnology and Biochemistry. 85(7). 1621–1627. 1 indexed citations
5.
Uesugi, Shota, et al.. (2019). Identification of neomacrophorins isolated from Trichoderma sp. 1212-03 as proteasome inhibitors. Bioorganic & Medicinal Chemistry. 27(24). 115161–115161. 14 indexed citations
6.
Hashimoto, Masaru, et al.. (2017). Development of novel textile and yarn actuators using plasticized PVC gel. Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE. 10163. 1016327–1016327. 11 indexed citations
7.
Kudo, Shinji, et al.. (2014). Lambertellin system, the mechanism for fungal replacement of Monilinia fructigena with Lambertella corni-maris without competitive inhibition on agar media. Bioorganic & Medicinal Chemistry. 22(8). 2489–2495. 6 indexed citations
8.
Hashimoto, Masaru, et al.. (2013). Isolation and Structure Elucidation of Potential Anti-Dengue Metabolites from Tawa-tawa (Euphorbia hirta Linn.). SHILAP Revista de lepidopterología. 11 indexed citations
9.
Tanaka, Kazuaki, et al.. (2011). Absolute Stereochemistry of Novel Isochromanone Derivatives fromLeptosphaeriasp. KTC 727. Bioscience Biotechnology and Biochemistry. 75(12). 2390–2393. 18 indexed citations
10.
Hashimoto, Masaru, et al.. (2010). Brans-Dicke model constrained from the Big Bang nucleosynthesis and magnitude redshift relations of supernovae. Springer Link (Chiba Institute of Technology). 5 indexed citations
11.
Yamamoto, Kazunori, et al.. (2009). Synthesis of a trigalacturonic acid analogue mimicking the expected transition state in the glycosidases. Carbohydrate Research. 345(5). 572–585. 5 indexed citations
12.
Hashimoto, Masaru, Takanori Murakami, Takashi Tokunaga, et al.. (2006). An RNA polymerase inhibitor, cyclothiazomycin B1, and its isomer. Bioorganic & Medicinal Chemistry. 14(24). 8259–8270. 38 indexed citations
13.
Murakami, Takanori, Akane Sasaki, Eri Fukushi, et al.. (2005). Optimization of isotope-labeling conditions for lambertellin based on isotope patterns observed by mass spectrometry. Bioorganic & Medicinal Chemistry Letters. 15(10). 2591–2594. 6 indexed citations
14.
Murakami, Takanori, Akane Sasaki, Eri Fukushi, et al.. (2005). Lambertellol C, a labile and novel biosynthetic congener of lambertellols A and B. Bioorganic & Medicinal Chemistry Letters. 15(10). 2587–2590. 17 indexed citations
15.
Matsuda, Hiroko, et al.. (2005). Synthetic studies on oligosaccharides composed of 5-thioglucopyranose units. Bioorganic & Medicinal Chemistry. 13(17). 5113–5144. 9 indexed citations
16.
Matsuda, Hiroko, et al.. (2003). α-Selective glycosylation with 5-thioglucopyranosyl donors; synthesis of an IsoMaltotetraoside mimic composed of 5-thioglucopyranose units. Bioorganic & Medicinal Chemistry Letters. 13(6). 1063–1066. 7 indexed citations
17.
Takahashi, Mihoko, et al.. (2002). Total Synthesis of Both Enantiomers of Dictyochromenol and their (Z)-Isomers. Bioscience Biotechnology and Biochemistry. 66(9). 1915–1924. 4 indexed citations
18.
Thielemann, F.‐K., C. Freiburghaus, Stephan Rosswog, et al.. (2000). Type II supernova nucleosynthesis and early galactic evolution.. MmSAI. 71. 483–498. 1 indexed citations
19.
Hashimoto, Masaru, et al.. (1972). Change of the Orientation with Cold-drawing, Heat-treatment and Swelling for 6-Nylon Fiber. NIPPON KAGAKU KAISHI. 454–458. 2 indexed citations
20.
Hashimoto, Masaru. (1960). The distribution of active marrow in the bones of normal adult.. 11(3). 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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