Masahiro Ikejiri

646 total citations
24 papers, 521 citations indexed

About

Masahiro Ikejiri is a scholar working on Molecular Biology, Organic Chemistry and Infectious Diseases. According to data from OpenAlex, Masahiro Ikejiri has authored 24 papers receiving a total of 521 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 10 papers in Organic Chemistry and 4 papers in Infectious Diseases. Recurrent topics in Masahiro Ikejiri's work include Synthetic Organic Chemistry Methods (5 papers), Click Chemistry and Applications (4 papers) and Microbial Natural Products and Biosynthesis (4 papers). Masahiro Ikejiri is often cited by papers focused on Synthetic Organic Chemistry Methods (5 papers), Click Chemistry and Applications (4 papers) and Microbial Natural Products and Biosynthesis (4 papers). Masahiro Ikejiri collaborates with scholars based in Japan and United States. Masahiro Ikejiri's co-authors include Takeshi Imanishi, Mayland Chang, Shahriar Mobashery, Rafael Fridman, M. Margarida Bernardo, Kazuyuki Miyashita, Kazuyuki Miyashita, Márta Tóth, R. Daniel Bonfil and Takafumi Hosokawa and has published in prestigious journals such as Journal of the American Chemical Society, Journal of Biological Chemistry and SHILAP Revista de lepidopterología.

In The Last Decade

Masahiro Ikejiri

24 papers receiving 513 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Masahiro Ikejiri Japan 11 246 182 146 111 58 24 521
Thomas E. Barta United States 15 253 1.0× 319 1.8× 81 0.6× 89 0.8× 55 0.9× 25 649
Marie Suggitt United Kingdom 8 116 0.5× 201 1.1× 65 0.4× 147 1.3× 26 0.4× 9 435
C. Yu United States 6 153 0.6× 484 2.7× 54 0.4× 148 1.3× 62 1.1× 7 654
Jacob A. Kaizerman United States 11 296 1.2× 230 1.3× 126 0.9× 65 0.6× 27 0.5× 12 560
Noriaki Tatsuta United States 12 123 0.5× 426 2.3× 67 0.5× 125 1.1× 15 0.3× 21 731
Mihiret T. Sisay Germany 9 83 0.3× 214 1.2× 57 0.4× 53 0.5× 44 0.8× 12 365
Jean‐Claude Jardillier France 16 100 0.4× 373 2.0× 81 0.6× 213 1.9× 50 0.9× 29 670
Qizhuang Ye United States 11 118 0.5× 212 1.2× 54 0.4× 199 1.8× 20 0.3× 21 470
Sarah Bregant France 15 323 1.3× 408 2.2× 85 0.6× 113 1.0× 34 0.6× 27 601
Mary K. Wolpert-DeFilippes United States 10 126 0.5× 268 1.5× 60 0.4× 215 1.9× 47 0.8× 13 507

Countries citing papers authored by Masahiro Ikejiri

Since Specialization
Citations

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

Fields of papers citing papers by Masahiro Ikejiri

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Masahiro Ikejiri

This figure shows the co-authorship network connecting the top 25 collaborators of Masahiro Ikejiri. A scholar is included among the top collaborators of Masahiro Ikejiri 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 Masahiro Ikejiri. Masahiro Ikejiri 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.
Ikejiri, Masahiro, Takuya Ito, Katsuhito Nagai, et al.. (2023). Impact of Different Attitudes toward Face-to-Face and Online Classes on Learning Outcomes in Japan. SHILAP Revista de lepidopterología. 11(1). 16–16. 1 indexed citations
2.
Ikejiri, Masahiro, et al.. (2019). Synthesis and environment-dependent fluorescence behavior of a biaryl-conjugated (diphenylmethylene)imidazolinone. Organic & Biomolecular Chemistry. 17(36). 8443–8449. 1 indexed citations
3.
Ikejiri, Masahiro, et al.. (2018). Synthesis and properties of geometrical 4-diarylmethylene analogs of the green fluorescent protein chromophore. Organic & Biomolecular Chemistry. 16(14). 2397–2401. 8 indexed citations
4.
Ikejiri, Masahiro, et al.. (2017). A hybrid molecule of a GFP chromophore analogue and cholestene as a viscosity-dependent and cholesterol-responsive fluorescent sensor. Organic & Biomolecular Chemistry. 15(33). 6948–6958. 6 indexed citations
5.
Ikejiri, Masahiro, Kousuke Matsumoto, Daisuke Yamaguchi, et al.. (2015). Synthesis and fluorescence properties of 4-diarylmethylene analogues of the green fluorescent protein chromophore. Tetrahedron. 71(30). 4987–4998. 10 indexed citations
6.
Lee, Mijoon, Masahiro Ikejiri, Márta Tóth, et al.. (2012). Structure–Activity Relationship for Thiirane-Based Gelatinase Inhibitors. ACS Medicinal Chemistry Letters. 3(6). 490–495. 31 indexed citations
7.
Ikejiri, Masahiro, et al.. (2012). Design and Concise Synthesis of a Novel Type of Green Fluorescent Protein Chromophore Analogue. Organic Letters. 14(17). 4406–4409. 19 indexed citations
8.
Sakakibara, Norikazu, Paula Ordonez, Takayuki Hamasaki, et al.. (2011). Synthesis of 1-benzyl-3-(3,5-dimethylbenzyl)Uracil Derivatives with Potential Anti-HIV Activity. Antiviral chemistry & chemotherapy. 22(2). 57–65. 14 indexed citations
9.
Gooyit, Major, Mijoon Lee, Valerie A. Schroeder, et al.. (2011). Selective Water-Soluble Gelatinase Inhibitor Prodrugs. Journal of Medicinal Chemistry. 54(19). 6676–6690. 42 indexed citations
10.
Ikejiri, Masahiro, et al.. (2008). Synthesis and evaluation of 5′-modified 2′-deoxyadenosine analogues as anti-hepatitis C virus agents. Bioorganic & Medicinal Chemistry Letters. 18(16). 4638–4641. 6 indexed citations
11.
Miyashita, Kazuyuki, et al.. (2008). Total Synthesis of Leustroducsin B. The Journal of Organic Chemistry. 73(14). 5360–5370. 32 indexed citations
12.
Ikejiri, Masahiro, Masayuki Saijo, Shigeru Morikawa, et al.. (2007). Synthesis and biological evaluation of nucleoside analogues having 6-chloropurine as anti-SARS-CoV agents. Bioorganic & Medicinal Chemistry Letters. 17(9). 2470–2473. 28 indexed citations
13.
Miyashita, Kazuyuki, et al.. (2007). Synthetic Studies on Fostriecin and Related Natural Products. Journal of Synthetic Organic Chemistry Japan. 65(9). 874–887. 8 indexed citations
14.
Ikejiri, Masahiro, Takayuki Ohshima, Keizo Kato, et al.. (2007). 5′-O-Masked 2′-deoxyadenosine analogues as lead compounds for hepatitis C virus (HCV) therapeutic agents. Bioorganic & Medicinal Chemistry. 15(22). 6882–6892. 9 indexed citations
15.
Miyashita, Kazuyuki, et al.. (2007). Total synthesis of leustroducsin B via a convergent route. Tetrahedron Letters. 48(22). 3829–3833. 24 indexed citations
16.
Ikejiri, Masahiro, Masayuki Saijo, Shigeru Morikawa, et al.. (2006). Anti-SARS-CoV activity of nucleoside analogs having 6-chloropurine as a nucleobase. Nucleic Acids Symposium Series. 50(1). 113–114. 3 indexed citations
17.
Ikejiri, Masahiro, M. Margarida Bernardo, R. Daniel Bonfil, et al.. (2005). Potent Mechanism-based Inhibitors for Matrix Metalloproteinases. Journal of Biological Chemistry. 280(40). 33992–34002. 114 indexed citations
18.
Hari, Yoshiyuki, et al.. (2005). Synthesis and Triplex-Forming Ability of 2',4'-BNAs Bearing Imidazoles as a Nucleobase. Chemical and Pharmaceutical Bulletin. 53(7). 843–846. 9 indexed citations
19.
Ikejiri, Masahiro, M. Margarida Bernardo, Samy O. Meroueh, et al.. (2005). Design, Synthesis, and Evaluation of a Mechanism-Based Inhibitor for Gelatinase A. The Journal of Organic Chemistry. 70(14). 5709–5712. 36 indexed citations
20.
Miyashita, Kazuyuki, et al.. (2002). Total synthesis of fostriecin (CI-920) via a convergent route. Chemical Communications. 742–743. 39 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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