Yoichi Hoshimoto

1.8k total citations
55 papers, 1.5k citations indexed

About

Yoichi Hoshimoto is a scholar working on Organic Chemistry, Inorganic Chemistry and Process Chemistry and Technology. According to data from OpenAlex, Yoichi Hoshimoto has authored 55 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Organic Chemistry, 18 papers in Inorganic Chemistry and 12 papers in Process Chemistry and Technology. Recurrent topics in Yoichi Hoshimoto's work include N-Heterocyclic Carbenes in Organic and Inorganic Chemistry (20 papers), Catalytic Cross-Coupling Reactions (16 papers) and Catalytic C–H Functionalization Methods (16 papers). Yoichi Hoshimoto is often cited by papers focused on N-Heterocyclic Carbenes in Organic and Inorganic Chemistry (20 papers), Catalytic Cross-Coupling Reactions (16 papers) and Catalytic C–H Functionalization Methods (16 papers). Yoichi Hoshimoto collaborates with scholars based in Japan, United Kingdom and Spain. Yoichi Hoshimoto's co-authors include Sensuke Ogoshi, Masato Ohashi, Ravindra Kumar, Takuya Kinoshita, Haruka Suzuki, Wenjie Tao, Jean‐François Carpentier, Kyoko Nozaki, Kazushi Mashima and Yasuhito Nakahara and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Nature Communications.

In The Last Decade

Yoichi Hoshimoto

54 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yoichi Hoshimoto Japan 23 1.4k 558 166 146 100 55 1.5k
Antoine Simonneau France 23 1.8k 1.3× 648 1.2× 107 0.6× 124 0.8× 73 0.7× 48 1.9k
Carl Deutsch Germany 13 994 0.7× 431 0.8× 96 0.6× 163 1.1× 62 0.6× 25 1.1k
Marc Magre Germany 20 910 0.7× 595 1.1× 144 0.9× 138 0.9× 150 1.5× 31 1.1k
Rositha Kuniyil Germany 24 1.6k 1.2× 382 0.7× 91 0.5× 166 1.1× 102 1.0× 51 1.8k
Jennifer V. Obligacion United States 13 2.2k 1.6× 993 1.8× 168 1.0× 197 1.3× 132 1.3× 17 2.4k
Supriya Rej Japan 18 1.9k 1.4× 497 0.9× 60 0.4× 93 0.6× 93 0.9× 32 2.0k
Zhenhua Zhang China 21 2.0k 1.5× 335 0.6× 71 0.4× 157 1.1× 170 1.7× 45 2.2k
Thomas M. Gøgsig Denmark 18 1.1k 0.8× 276 0.5× 85 0.5× 131 0.9× 162 1.6× 22 1.2k
Manuel R. Fructos Spain 22 2.3k 1.7× 425 0.8× 47 0.3× 98 0.7× 72 0.7× 35 2.3k
Erik A. Romero United States 13 790 0.6× 316 0.6× 116 0.7× 87 0.6× 35 0.3× 20 892

Countries citing papers authored by Yoichi Hoshimoto

Since Specialization
Citations

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

Fields of papers citing papers by Yoichi Hoshimoto

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yoichi Hoshimoto

This figure shows the co-authorship network connecting the top 25 collaborators of Yoichi Hoshimoto. A scholar is included among the top collaborators of Yoichi Hoshimoto 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 Yoichi Hoshimoto. Yoichi Hoshimoto 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.
Hoshimoto, Yoichi, et al.. (2025). An Isolated Lithium ortho-Carboranyl Cuprate Complex for the Synthesis of Multiple-Carborane-Substituted Arenes from (Hetero)Aryl Bromides and Chlorides. Journal of the American Chemical Society. 147(41). 37677–37687. 3 indexed citations
2.
Manna, Sourav, et al.. (2024). Palladium‐Catalyzed γ‐Arylation of Acylketene Synthons with Aryl Chlorides Enabled by Ylide‐Functionalized Phosphines (YPhos). Advanced Synthesis & Catalysis. 366(5). 1107–1112. 3 indexed citations
3.
Hoshimoto, Yoichi, et al.. (2024). Recent Trends in Triarylborane Chemistry: Diversification of Structures and Reactivity via meta-Substitution of the Aryl Groups. Synthesis. 56(22). 3421–3430. 5 indexed citations
4.
Yamauchi, Yasuhiro, Sensuke Ogoshi, Yuta Uetake, & Yoichi Hoshimoto. (2024). Reversible modulation of the local environment around metal centers bearing multifunctional carbenes. Chemistry Letters. 53(3). 2 indexed citations
5.
6.
Ogoshi, Sensuke, et al.. (2024). Triarylborane Catalysis: From Hydrogenation of Unsaturated Molecules to H<sub>2</sub> Purification. Journal of Synthetic Organic Chemistry Japan. 82(11). 1097–1106. 1 indexed citations
7.
Ogoshi, Sensuke, et al.. (2023). N -Borane-Substituted Cyclic Phosphine Imides (BCPIs). Bulletin of the Chemical Society of Japan. 96(12). 1346–1353.
8.
Ogoshi, Sensuke, et al.. (2023). Strategic use of crude H2 for the catalytic reduction of carbonyl compounds. SHILAP Revista de lepidopterología. 9. 100059–100059. 5 indexed citations
9.
Yamauchi, Yasuhiro, Yuta Uetake, Yasuo Takeichi, et al.. (2023). Reversible Modulation of the Electronic and Spatial Environment around Ni(0) Centers Bearing Multifunctional Carbene Ligands with Triarylaluminum. Journal of the American Chemical Society. 145(30). 16938–16947. 6 indexed citations
10.
Hoshimoto, Yoichi, et al.. (2022). Complexation-induced N‒P axial chirality in Sm(II) N -phosphine oxide-substituted imidazolylidene and imidazolinylidene complexes. Canadian Journal of Chemistry. 101(7). 429–433. 2 indexed citations
11.
Ogoshi, Sensuke, et al.. (2022). Main group catalysis for H 2 purification based on liquid organic hydrogen carriers. Science Advances. 8(43). eade0189–eade0189. 33 indexed citations
12.
Hoshimoto, Yoichi, et al.. (2021). A boron-transfer mechanism mediating the thermally induced revival of frustrated carbene–borane pairs from their shelf-stable adducts. Communications Chemistry. 4(1). 137–137. 4 indexed citations
13.
Kumar, Ravindra, et al.. (2017). Two-step synthesis of chiral fused tricyclic scaffolds from phenols via desymmetrization on nickel. Nature Communications. 8(1). 32–32. 72 indexed citations
14.
Hoshimoto, Yoichi, Ravindra Kumar, Ken Kamikawa, et al.. (2017). Efficient Synthesis of Polycyclic γ‐Lactams by Catalytic Carbonylation of Ene‐Imines via Nickelacycle Intermediates. Angewandte Chemie. 129(28). 8318–8322. 18 indexed citations
15.
Hoshimoto, Yoichi, Takuya Kinoshita, Masato Ohashi, & Sensuke Ogoshi. (2015). A Strategy to Control the Reactivation of Frustrated Lewis Pairs from Shelf‐Stable Carbene Borane Complexes. Angewandte Chemie International Edition. 54(40). 11666–11671. 41 indexed citations
16.
Hoshimoto, Yoichi, Takuya Kinoshita, Masato Ohashi, & Sensuke Ogoshi. (2015). A Strategy to Control the Reactivation of Frustrated Lewis Pairs from Shelf‐Stable Carbene Borane Complexes. Angewandte Chemie. 127(40). 11832–11837. 8 indexed citations
17.
Kita, Yusuke, Hironobu Sakaguchi, Yoichi Hoshimoto, et al.. (2015). Pentacoordinated Carboxylate π‐Allyl Nickel Complexes as Key Intermediates for the Ni‐Catalyzed Direct Amination of Allylic Alcohols. Chemistry - A European Journal. 21(41). 14571–14578. 68 indexed citations
18.
Hoshimoto, Yoichi, et al.. (2014). Highly Efficient Activation of Organosilanes with η2-Aldehyde Nickel Complexes: Key for Catalytic Syntheses of Aryl-, Vinyl-, and Alkynyl-Benzoxasiloles. Journal of the American Chemical Society. 136(48). 16752–16755. 29 indexed citations
19.
Hoshimoto, Yoichi, et al.. (2012). Synthesis of Five‐ and Six‐Membered Benzocyclic Ketones through Intramolecular Alkene Hydroacylation Catalyzed by Nickel(0)/N‐Heterocyclic Carbenes. Angewandte Chemie International Edition. 51(43). 10812–10815. 67 indexed citations
20.
Ogoshi, Sensuke, Yoichi Hoshimoto, & Masato Ohashi. (2010). Nickel-catalyzed Tishchenko reaction via hetero-nickelacycles by oxidative cyclization of aldehydes with nickel(0) complex. Chemical Communications. 46(19). 3354–3354. 59 indexed citations

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