Daisuke Uraguchi

7.6k total citations · 1 hit paper
107 papers, 6.5k citations indexed

About

Daisuke Uraguchi is a scholar working on Organic Chemistry, Inorganic Chemistry and Molecular Biology. According to data from OpenAlex, Daisuke Uraguchi has authored 107 papers receiving a total of 6.5k indexed citations (citations by other indexed papers that have themselves been cited), including 101 papers in Organic Chemistry, 30 papers in Inorganic Chemistry and 20 papers in Molecular Biology. Recurrent topics in Daisuke Uraguchi's work include Asymmetric Synthesis and Catalysis (59 papers), Asymmetric Hydrogenation and Catalysis (24 papers) and Synthesis and Catalytic Reactions (22 papers). Daisuke Uraguchi is often cited by papers focused on Asymmetric Synthesis and Catalysis (59 papers), Asymmetric Hydrogenation and Catalysis (24 papers) and Synthesis and Catalytic Reactions (22 papers). Daisuke Uraguchi collaborates with scholars based in Japan, United States and Ukraine. Daisuke Uraguchi's co-authors include Takashi Ooi, Masahiro Terada, Yusuke Ueki, Keiichi Sorimachi, Natsuko Kinoshita, Kyohei Koshimoto, Tomohito Kizu, Tetsu Yamakawa, Ken Yoshioka and Shinji Nakamura and has published in prestigious journals such as Science, Journal of the American Chemical Society and Angewandte Chemie International Edition.

In The Last Decade

Daisuke Uraguchi

106 papers receiving 6.5k citations

Hit Papers

Chiral Brønsted Acid-Catalyzed Direct Mannich Reactions v... 2004 2026 2011 2018 2004 400 800 1.2k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Daisuke Uraguchi Japan 43 6.1k 2.0k 1.2k 667 396 107 6.5k
Luca Bernardi Italy 44 5.5k 0.9× 1.3k 0.7× 1.1k 0.9× 348 0.5× 354 0.9× 121 5.9k
Koichi Narasaka Japan 46 7.7k 1.3× 1.1k 0.6× 1.4k 1.1× 457 0.7× 490 1.2× 254 8.3k
Gonzalo Blay Spain 38 3.8k 0.6× 1.2k 0.6× 792 0.6× 450 0.7× 254 0.6× 191 4.4k
Marino Petrini Italy 38 5.3k 0.9× 896 0.5× 1.2k 1.0× 230 0.3× 242 0.6× 171 5.7k
Kiitirô Utimoto Japan 48 6.7k 1.1× 1.4k 0.7× 1.0k 0.8× 602 0.9× 194 0.5× 236 7.3k
Francisco Foubelo Spain 33 5.9k 1.0× 2.1k 1.1× 998 0.8× 214 0.3× 147 0.4× 167 6.3k
Peter O’Brien United Kingdom 41 5.2k 0.9× 1.3k 0.7× 1.0k 0.8× 129 0.2× 226 0.6× 171 5.7k
Alexandre Alexakis Switzerland 67 14.7k 2.4× 5.6k 2.9× 2.4k 2.0× 555 0.8× 632 1.6× 296 15.3k
Dieter Hoppe Germany 42 6.6k 1.1× 1.2k 0.6× 1.0k 0.9× 316 0.5× 378 1.0× 289 6.9k
Petri M. Pihko Finland 36 5.0k 0.8× 1.4k 0.7× 1.1k 0.9× 286 0.4× 249 0.6× 108 5.5k

Countries citing papers authored by Daisuke Uraguchi

Since Specialization
Citations

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

Fields of papers citing papers by Daisuke Uraguchi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Daisuke Uraguchi

This figure shows the co-authorship network connecting the top 25 collaborators of Daisuke Uraguchi. A scholar is included among the top collaborators of Daisuke Uraguchi 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 Daisuke Uraguchi. Daisuke Uraguchi 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.
Shimazu, Toru, et al.. (2025). Olefin‐Catalyzed Aromatic Bromination toward Biocompatible Tyrosine Modification. Chemistry - A European Journal. 31(39). e202501554–e202501554.
3.
Uraguchi, Daisuke, et al.. (2024). Synthesis of Substituted Cyclooctenes through Cross-Coupling Reactions. Synlett. 36(1). 69–74. 2 indexed citations
4.
Hori, Yuichiro, et al.. (2024). BODNs as biocompatible brominating reagents: visible-light photocatalytic tyrosine modification under physiologically favorable conditions. Chemical Communications. 60(85). 12381–12384. 3 indexed citations
5.
Matsubara, Seijiro, et al.. (2023). trans‐Cyclooctenes as Scavengers of Bromine Involved in Catalytic Bromination. Chemistry - A European Journal. 30(8). e202303399–e202303399. 1 indexed citations
6.
Uraguchi, Daisuke, et al.. (2021). Catalytic asymmetric synthesis of 5-membered alicyclic α-quaternary β-amino acids via [3 + 2]-photocycloaddition of α-substituted acrylates. Organic & Biomolecular Chemistry. 19(8). 1744–1747. 27 indexed citations
7.
Uraguchi, Daisuke, et al.. (2021). o-Quinone methide with overcrowded olefin component as a dehydridation catalyst under aerobic photoirradiation conditions. Chemical Science. 12(8). 2778–2783. 1 indexed citations
8.
Uraguchi, Daisuke, et al.. (2020). A Structurally Robust Chiral Borate Ion: Molecular Design, Synthesis, and Asymmetric Catalysis. Angewandte Chemie. 132(28). 11553–11558. 2 indexed citations
9.
Uraguchi, Daisuke, et al.. (2020). Redox-regulated divergence in photocatalytic addition of α-nitro alkyl radicals to styrenes. Chemical Communications. 56(75). 11014–11017. 19 indexed citations
10.
Hong, Yongseok, Daisuke Uraguchi, Takashi Ooi, et al.. (2019). Inserting Nitrogen: An Effective Concept To Create Nonplanar and Stimuli-Responsive Perylene Bisimide Analogues. Journal of the American Chemical Society. 141(50). 19807–19816. 49 indexed citations
11.
Uraguchi, Daisuke, et al.. (2019). Photocatalytic borylcyclopropanation of α-boryl styrenes. Organic Chemistry Frontiers. 6(11). 1734–1737. 25 indexed citations
12.
Uraguchi, Daisuke, et al.. (2019). Unveiling Latent Photoreactivity of Imines. Angewandte Chemie International Edition. 59(9). 3665–3670. 34 indexed citations
13.
Uraguchi, Daisuke, et al.. (2019). Unveiling Latent Photoreactivity of Imines. Angewandte Chemie. 132(9). 3694–3699. 5 indexed citations
14.
Uraguchi, Daisuke, Kohei Yamada, Makoto Sato, & Takashi Ooi. (2018). Catalyst-Directed Guidance of Sulfur-Substituted Enediolates to Stereoselective Carbon–Carbon Bond Formation with Aldehydes. Journal of the American Chemical Society. 140(15). 5110–5117. 24 indexed citations
15.
Uraguchi, Daisuke, et al.. (2018). Catalyst‐Enabled Site‐Divergent Stereoselective Michael Reactions: Overriding Intrinsic Reactivity of Enynyl Carbonyl Acceptors. Angewandte Chemie. 130(17). 4822–4826. 16 indexed citations
16.
Uraguchi, Daisuke, Keiko Kuwata, Yuh Hijikata, et al.. (2018). A femtomolar-range suicide germination stimulant for the parasitic plant Striga hermonthica. Science. 362(6420). 1301–1305. 96 indexed citations
17.
Uraguchi, Daisuke, et al.. (2018). Molecular Design, Synthesis, and Asymmetric Catalysis of a Hexacoordinated Chiral Phosphate Ion. Journal of the American Chemical Society. 140(8). 2765–2768. 17 indexed citations
18.
Uraguchi, Daisuke, Ken Yoshioka, & Takashi Ooi. (2017). Complete diastereodivergence in asymmetric 1,6-addition reactions enabled by minimal modification of a chiral catalyst. Nature Communications. 8(1). 14793–14793. 82 indexed citations
19.
Yoshioka, Ken, Kohei Yamada, Daisuke Uraguchi, & Takashi Ooi. (2017). Unique site-selectivity control in asymmetric Michael addition of azlactone to alkenyl dienyl ketones enabled by P-spiro chiral iminophosphorane catalysis. Chemical Communications. 53(40). 5495–5498. 29 indexed citations
20.
Yamanaka, Masahiro, Ken Sakata, Ken Yoshioka, Daisuke Uraguchi, & Takashi Ooi. (2016). Origin of High Regio-, Diastereo-, and Enantioselectivities in 1,6-Addition of Azlactones to Dienyl N-Acylpyrroles: A Computational Study. The Journal of Organic Chemistry. 82(1). 541–548. 15 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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