Suguru Yoshida

5.8k total citations · 1 hit paper
182 papers, 4.7k citations indexed

About

Suguru Yoshida is a scholar working on Organic Chemistry, Molecular Biology and Pharmaceutical Science. According to data from OpenAlex, Suguru Yoshida has authored 182 papers receiving a total of 4.7k indexed citations (citations by other indexed papers that have themselves been cited), including 131 papers in Organic Chemistry, 49 papers in Molecular Biology and 17 papers in Pharmaceutical Science. Recurrent topics in Suguru Yoshida's work include Cyclization and Aryne Chemistry (49 papers), Click Chemistry and Applications (36 papers) and Chemical Synthesis and Analysis (33 papers). Suguru Yoshida is often cited by papers focused on Cyclization and Aryne Chemistry (49 papers), Click Chemistry and Applications (36 papers) and Chemical Synthesis and Analysis (33 papers). Suguru Yoshida collaborates with scholars based in Japan, United States and United Kingdom. Suguru Yoshida's co-authors include Takamitsu Hosoya, Keisuke Uchida, Koichiro Oshima, Hideki Yorimitsu, Kazutaka Nishikawa, Kiyoshi YAMAGATA, Sunao Hasegawa, T. Fujii, Kazuya Kanemoto and Young‐Chan Kim and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Nucleic Acids Research.

In The Last Decade

Suguru Yoshida

174 papers receiving 4.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Forced convective heat transfer to supercritical water flowing in tubes

1972 524 citations Suguru Yoshida et al. profile →

Peers

Suguru Yoshida

OC

MB

CM

BE

PS

Chi‐Wan Lee South Korea

Cheng‐Chung Chang Taiwan

Hai‐Yu Hu China

Michael Caplow United States

Carsten Baldauf Germany

Jun Takagi Japan

Da Ma China

Stefan Abele Switzerland

Alessandro Contini Italy

Chi‐Wan Lee South Korea

Suguru Yoshida

734 ×0.2

OC

628 ×0.6

MB

29 ×0.0

CM

215 ×0.3

BE

27 ×0.1

PS

Citations per year, relative to Suguru Yoshida Suguru Yoshida (= 1×) peers Chi‐Wan Lee

Countries citing papers authored by Suguru Yoshida

Since Specialization

Citations

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

Fields of papers citing papers by Suguru Yoshida

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Suguru Yoshida

This figure shows the co-authorship network connecting the top 25 collaborators of Suguru Yoshida. A scholar is included among the top collaborators of Suguru Yoshida 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 Suguru Yoshida. Suguru Yoshida is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

1.

Kobayashi, Akihiro, et al.. (2024). Facile synthesis of dibenzothiophene S-oxides from sulfinate esters. Chemical Communications. 60(12). 1611–1614. 2 indexed citations

2.

Yoshida, Suguru, et al.. (2022). Synthesis of Multisubstituted Benzenes from Phenols via Multisubstituted Benzynes. Synthesis. 54(22). 5017–5025. 2 indexed citations

3.

Kobayashi, Akihiro, et al.. (2022). Modular synthesis of triazoles from 2-azidoacrylamides having a nucleophilic amino group. Organic & Biomolecular Chemistry. 20(30). 6007–6011. 5 indexed citations

4.

Hosoya, Takamitsu, et al.. (2021). Transition-Metal-Free Synthesis of N-Arylphenothiazines through an N- and S-Arylation Sequence. Organic Letters. 23(6). 2347–2352. 18 indexed citations

5.

Kanemoto, Kazuya, et al.. (2021). Palladium-Catalyzed Sulfinylation of Aryl- and Alkenylborons with Sulfinate Esters. Organic Letters. 23(9). 3793–3797. 10 indexed citations

6.

Uchida, Keisuke, et al.. (2021). Acylalkylation of Arynes Generated from o-Iodoaryl Triflates with Hydrosilanes and Cesium Fluoride. Organic Letters. 23(5). 1868–1873. 10 indexed citations

7.

Hosoya, Takamitsu, et al.. (2020). 2-Azidoacrylamides as compact platforms for efficient modular synthesis. Chemical Communications. 56(99). 15541–15544. 10 indexed citations

8.

Kim, Young‐Chan, et al.. (2020). Single C–F Transformations of o-Hydrosilyl Benzotrifluorides with Trityl Compounds as All-in-One Reagents. Organic Letters. 22(23). 9292–9297. 45 indexed citations

9.

Igawa, Kazunobu, et al.. (2020). Selective strain-promoted azide–alkyne cycloadditions through transient protection of bicyclo[6.1.0]nonynes with silver or gold. Chemical Communications. 56(68). 9823–9826. 11 indexed citations

10.

Inouye, S, et al.. (2020). A novel yellow fluorescent protein of recombinant apoPholasin with dehydrocoelenterazine. Biochemical and Biophysical Research Communications. 526(2). 404–409. 4 indexed citations

11.

Igawa, Kazunobu, et al.. (2020). (Hexafluoroacetylacetonato)copper(i)–cycloalkyne complexes as protected cycloalkynes. Chemical Communications. 56(77). 11449–11452. 7 indexed citations

12.

Nakamura, Yu, et al.. (2020). Synthesis of Functionalized Benzopyran/Coumarin-Derived Aryne Precursors and Their Applications. Organic Letters. 22(21). 8505–8510. 18 indexed citations

13.

Yoshida, Suguru, et al.. (2020). Assembly of four modules onto a tetraazide platform by consecutive 1,2,3-triazole formations. Chemical Communications. 57(7). 899–902. 14 indexed citations

14.

Hosoya, Takamitsu, et al.. (2020). Synthesis of Diverse Aromatic Ketones through C−F Cleavage of Trifluoromethyl Group. Chemistry - A European Journal. 26(54). 12333–12337. 25 indexed citations

15.

Minami, Yasunori, et al.. (2020). Synthesis of multisubstituted cycloalkenes through carbomagnesiation of strained cycloalkynes. Chemical Communications. 56(52). 7147–7150. 4 indexed citations

16.

Uchida, Keisuke, Yasunori Minami, Suguru Yoshida, & Takamitsu Hosoya. (2019). Synthesis of Diverse γ-Aryl-β-ketoesters via Aryne Intermediates Generated by C–C Bond Cleavage. Organic Letters. 21(22). 9019–9023. 20 indexed citations

17.

Yoshida, Suguru, et al.. (2018). Transient Protection of Organic Azides from Click Reactions with Alkynes by Phosphazide Formation. Organic Letters. 20(13). 4126–4130. 34 indexed citations

18.

Yoshida, Suguru, et al.. (2018). Convergent synthesis of trifunctional molecules by three sequential azido-type-selective cycloadditions. Chemical Communications. 54(30). 3705–3708. 29 indexed citations

19.

Nishiyama, Yoshitake, Yuki Hazama, Suguru Yoshida, & Takamitsu Hosoya. (2017). Synthesis of Unsymmetrical Tertiary Phosphine Oxides via Sequential Substitution Reaction of Phosphonic Acid Dithioesters with Grignard Reagents. Organic Letters. 19(14). 3899–3902. 28 indexed citations

20.

Uchida, Keisuke, Suguru Yoshida, & Takamitsu Hosoya. (2017). Three-Component Coupling of Triflyloxy-Substituted Benzocyclobutenones, Organolithium Reagents, and Arynophiles Promoted by Generation of Aryne via Carbon–Carbon Bond Cleavage. Organic Letters. 19(5). 1184–1187. 41 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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