Haruro Ishitani

7.7k total citations · 1 hit paper
97 papers, 6.4k citations indexed

About

Haruro Ishitani is a scholar working on Organic Chemistry, Inorganic Chemistry and Biomedical Engineering. According to data from OpenAlex, Haruro Ishitani has authored 97 papers receiving a total of 6.4k indexed citations (citations by other indexed papers that have themselves been cited), including 82 papers in Organic Chemistry, 45 papers in Inorganic Chemistry and 30 papers in Biomedical Engineering. Recurrent topics in Haruro Ishitani's work include Asymmetric Synthesis and Catalysis (49 papers), Asymmetric Hydrogenation and Catalysis (44 papers) and Innovative Microfluidic and Catalytic Techniques Innovation (27 papers). Haruro Ishitani is often cited by papers focused on Asymmetric Synthesis and Catalysis (49 papers), Asymmetric Hydrogenation and Catalysis (44 papers) and Innovative Microfluidic and Catalytic Techniques Innovation (27 papers). Haruro Ishitani collaborates with scholars based in Japan and United States. Haruro Ishitani's co-authors include Shu̅ Kobayashi, Masaharu Ueno, Susumu Komiyama, Yasuhiro Yamashita, Iwao Hachiya, Mitsuharu Araki, Satoshi Nagayama, Haruka Shimizu, Yuki Saito and Masakazu Iwamoto and has published in prestigious journals such as Chemical Reviews, Proceedings of the National Academy of Sciences and Journal of the American Chemical Society.

In The Last Decade

Haruro Ishitani

94 papers receiving 6.2k citations

Hit Papers

Catalytic Enantioselective Addition to Imines 1999 2026 2008 2017 1999 400 800 1.2k

Peers

Haruro Ishitani
Jung Woon Yang South Korea
Haruro Ishitani
Citations per year, relative to Haruro Ishitani Haruro Ishitani (= 1×) peers Jung Woon Yang

Countries citing papers authored by Haruro Ishitani

Since Specialization
Citations

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

Fields of papers citing papers by Haruro Ishitani

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Haruro Ishitani

This figure shows the co-authorship network connecting the top 25 collaborators of Haruro Ishitani. A scholar is included among the top collaborators of Haruro Ishitani 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 Haruro Ishitani. Haruro Ishitani 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.
Ishitani, Haruro, et al.. (2025). Efficient low-temperature depolymerization of polycarbonate catalyzed by lanthanum β-diketonate complexes. Green Chemistry. 27(25). 7544–7550.
3.
Ishitani, Haruro, et al.. (2024). Sequential‐Flow Synthesis of Donepezil: A Green and Sustainable Strategy Featuring Heterogeneous Catalysis and Hydrogenation. Chemistry - A European Journal. 30(59). e202402128–e202402128. 3 indexed citations
4.
Ishitani, Haruro, et al.. (2024). Structure-Directed Quaternary Ammonium Hydroxide Resins: High-Performance Heterogeneous Base Catalysts for Continuous-Flow Carbon–Carbon Bond-Forming Reactions. The Journal of Organic Chemistry. 89(19). 14081–14089. 2 indexed citations
5.
Ishitani, Haruro, Tomoya Kawase, Amrita Das, & Shu̅ Kobayashi. (2023). Catalytic hydrogenative dechlorination reaction for efficient synthesis of a key intermediate of SDHI fungicides under continuous-flow conditions. Catalysis Science & Technology. 13(11). 3282–3291. 4 indexed citations
7.
Ishitani, Haruro, et al.. (2017). Synthesis of (±)‐Pregabalin by Utilizing a Three‐Step Sequential‐Flow System with Heterogeneous Catalysts. European Journal of Organic Chemistry. 2017(44). 6491–6494. 28 indexed citations
8.
Ishitani, Haruro, et al.. (2015). Friedel-crafts alkylation on mesoporous W-Zr composite oxide catalysts prepared by a wall ionexchange method. 8(3). 3–4. 1 indexed citations
9.
Ishitani, Haruro, Hirotsugu Suzuki, Yuki Saito, Yasuhiro Yamashita, & Shu̅ Kobayashi. (2015). Hafnium Trifluoromethanesulfonate [Hf(OTf)4] as a Unique Lewis Acid in Organic Synthesis. European Journal of Organic Chemistry. 2015(25). 5485–5499. 30 indexed citations
10.
Yasuda, Satoshi, H. Kitagawa, Masaharu Ueno, et al.. (2013). A novel inhibitor of ceramide trafficking from endoplasmic reticulum to the site of sphingomyelin synthesis.. Journal of Biological Chemistry. 288(33). 24162–24162. 6 indexed citations
11.
Ishitani, Haruro, et al.. (2010). Highly ordered aluminium-planted mesoporous silica as active catalyst for Biginelli reaction and formyl C–H insertion reaction with diazoester. Physical Chemistry Chemical Physics. 12(43). 14452–14452. 8 indexed citations
12.
Ishitani, Haruro, et al.. (2010). Synthesis of Biginelli dihydropyrimidinone derivatives with various substituents on aluminium-planted mesoporous silica catalyst. Organic & Biomolecular Chemistry. 8(5). 1202–1202. 60 indexed citations
13.
Kobayashi, Shu̅, et al.. (2004). A Novel Dinuclear Chiral Niobium Complex for Lewis Acid Catalyzed Enantioselective Reactions: Design of a Tridentate Ligand and Elucidation of the Catalyst Structure. Angewandte Chemie International Edition. 44(5). 761–764. 47 indexed citations
14.
Yamashita, Yasuhiro, Haruro Ishitani, Haruka Shimizu, & Shu̅ Kobayashi. (2002). Highly anti-Selective Asymmetric Aldol Reactions Using Chiral Zirconium Catalysts. Improvement of Activities, Structure of the Novel Zirconium Complexes, and Effect of a Small Amount of Water for the Preparation of the Catalysts. Journal of the American Chemical Society. 124(13). 3292–3302. 103 indexed citations
15.
Yasuda, Satoshi, H. Kitagawa, Masaharu Ueno, et al.. (2001). A Novel Inhibitor of Ceramide Trafficking from the Endoplasmic Reticulum to the Site of Sphingomyelin Synthesis. Journal of Biological Chemistry. 276(47). 43994–44002. 116 indexed citations
16.
Kobayashi, Sh & Haruro Ishitani. (2000). Novel binuclear chiral zirconium catalysts used in enantioselective strecker reactions. Chirality. 12(5-6). 540–543. 40 indexed citations
17.
Kobayashi, Shu̅, et al.. (1999). Catalytic Asymmetric Synthesis of Antimalarial Alkaloids Febrifugine and Isofebrifugine and Their Biological Activity. The Journal of Organic Chemistry. 64(18). 6833–6841. 107 indexed citations
18.
Kobayashi, Shu̅, Susumu Komiyama, & Haruro Ishitani. (1998). The First Enantioselective Aza-Diels-Alder Reactions of Imino Dienophiles on Use of a Chiral Zirconium Catalyst. Angewandte Chemie International Edition. 37(7). 979–981. 125 indexed citations
19.
Ishitani, Haruro, Susumu Komiyama, & Shu̅ Kobayashi. (1998). Catalytic, Enantioselective Synthesis ofα-Aminonitriles with a Novel Zirconium Catalyst. Angewandte Chemie International Edition. 37(22). 3186–3188. 135 indexed citations
20.
Kobayashi, Shu̅ & Haruro Ishitani. (1998). Catalytic Activation of Imine Derivatives Using Novel Lewis Acids.. Journal of Synthetic Organic Chemistry Japan. 56(5). 357–367. 4 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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