Mitsuhiro Yoshimatsu

1.1k total citations
68 papers, 788 citations indexed

About

Mitsuhiro Yoshimatsu is a scholar working on Organic Chemistry, Toxicology and Pharmaceutical Science. According to data from OpenAlex, Mitsuhiro Yoshimatsu has authored 68 papers receiving a total of 788 indexed citations (citations by other indexed papers that have themselves been cited), including 61 papers in Organic Chemistry, 14 papers in Toxicology and 13 papers in Pharmaceutical Science. Recurrent topics in Mitsuhiro Yoshimatsu's work include Sulfur-Based Synthesis Techniques (25 papers), Catalytic Alkyne Reactions (17 papers) and Organoselenium and organotellurium chemistry (13 papers). Mitsuhiro Yoshimatsu is often cited by papers focused on Sulfur-Based Synthesis Techniques (25 papers), Catalytic Alkyne Reactions (17 papers) and Organoselenium and organotellurium chemistry (13 papers). Mitsuhiro Yoshimatsu collaborates with scholars based in Japan. Mitsuhiro Yoshimatsu's co-authors include Tadashi Kataoka, Hiroshi Shimizu, Genzoh Tanabe, Osamu Muraoka, Igor Minia, Naoko Matsunaga, Tsuneyasu Kaisho, Osamu Hazeki, Yuji Iizawa and Katsunori Takashima and has published in prestigious journals such as Chemical Communications, Electrochimica Acta and The Journal of Organic Chemistry.

In The Last Decade

Mitsuhiro Yoshimatsu

63 papers receiving 757 citations

Peers

Mitsuhiro Yoshimatsu

IMMUN

TOXIC

Michal Uher Slovakia

Donn G. Wishka United States

Jianqing Li United States

Tryfon Zarganes‐Tzitzikas Netherlands

Sandra Leitza United States

Jeffrey Cohen United States

Hachemi Kadri United Kingdom

Yanpeng Xing China

Eirik Sundby Norway

John W. Dankwardt United States

Michal Uher Slovakia

Mitsuhiro Yoshimatsu

281 ×0.5

87 ×0.7

IMMUN

181 ×1.6

62 ×0.6

TOXIC

23 ×0.3

Citations per year, relative to Mitsuhiro Yoshimatsu Mitsuhiro Yoshimatsu (= 1×) peers Michal Uher

Countries citing papers authored by Mitsuhiro Yoshimatsu

Since Specialization

Citations

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

Fields of papers citing papers by Mitsuhiro Yoshimatsu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mitsuhiro Yoshimatsu

This figure shows the co-authorship network connecting the top 25 collaborators of Mitsuhiro Yoshimatsu. A scholar is included among the top collaborators of Mitsuhiro Yoshimatsu 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 Mitsuhiro Yoshimatsu. Mitsuhiro Yoshimatsu 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

Kato, Y., et al.. (2024). Radical Nitrososulfonation of Propargyl Alcohols: Thiazolidine-2,4-dione-Assisted Synthesis of 5-Alykyl-4-sulfonylisoxazoles. Organic Letters. 26(9). 1753–1757. 2 indexed citations

Sakai, Yoko, et al.. (2021). Synthesis of Azepino[1,2‐a]indole‐10‐amines via [6+1] Annulation of Ynenitriles with Reformatsky Reagent. European Journal of Organic Chemistry. 2021(10). 1553–1558. 12 indexed citations

Ogawa, Takahiro, Genzoh Tanabe, Osamu Muraoka, et al.. (2019). Synthesis of Thiazinoimidazoles by Lewis Acid–Catalyzed [3+3] Cycloaddition Reactions of Propargyl Alcohols with 2‐Mercaptoimidazoles. European Journal of Organic Chemistry. 2019(20). 3117–3121. 4 indexed citations

Wasada, Hiroaki, et al.. (2018). Unprecedented nucleophile-promoted 1,7-S or Se shift reactions under Pummerer reaction conditions of 4-alkenyl-3-sulfinylmethylpyrroles. Beilstein Journal of Organic Chemistry. 14. 2722–2729. 4 indexed citations

Yoshimatsu, Mitsuhiro, Genzoh Tanabe, & Osamu Muraoka. (2013). Chemistry of Propargyl Compounds Activated by Sulfur Functional Groups^|^mdash;Development of Methodology for the Synthesis of Heterocyles Triggered by Functionalizations. Journal of Synthetic Organic Chemistry Japan. 71(12). 1282–1293. 3 indexed citations

Yoshimatsu, Mitsuhiro, et al.. (2012). Propargyl Hydrazides: Synthesis and Conversion Into Pyrazoles Through Hydroamination. Chemistry - A European Journal. 18(49). 15602–15606. 35 indexed citations

Yoshimatsu, Mitsuhiro, et al.. (2010). Convenient preparation of 4-arylmethyl- and 4-hetarylmethyl thiazoles by regioselective cycloaddition reactions of 3-sulfanyl- and selanylpropargyl alcohols. Tetrahedron. 66(40). 7975–7987. 14 indexed citations

Takashima, Katsunori, Naoko Matsunaga, Mitsuhiro Yoshimatsu, et al.. (2009). Analysis of binding site for the novel small‐molecule TLR4 signal transduction inhibitor TAK‐242 and its therapeutic effect on mouse sepsis model. British Journal of Pharmacology. 157(7). 1250–1262. 198 indexed citations

Yoshimatsu, Mitsuhiro, et al.. (2005). First Lewis Acid Catalyzed Generation and Reaction of α‐Organylsulfanyl and α‐Organylselanyl Carbenium Ions Using Ethyl α‐Fluoroacetate Derivatives. European Journal of Organic Chemistry. 2005(14). 2884–2887. 4 indexed citations

10.

Yoshimatsu, Mitsuhiro, et al.. (2005). Z-Selective or Stereospecific Alkenylation Reaction: A Novel Synthetic Method for α-Fluoro-α,β-unsaturated Esters. Chemistry Letters. 34(7). 998–999. 16 indexed citations

11.

Yoshimatsu, Mitsuhiro, et al.. (2004). A Study on the Electronic Effect of Reactions of π-Allylpalladiums Using 2-Arylsulfonyloxy-3-chloropropenes with Ethyl Malonate and Their Synthetic Utilization. Chemistry Letters. 33(10). 1322–1323. 2 indexed citations

12.

Yoshimatsu, Mitsuhiro. (2002). Organic Synthesis Using .BETA.-Alhoxyalkenyllithiums.. Journal of Synthetic Organic Chemistry Japan. 60(9). 847–858. 3 indexed citations

13.

Yoshimatsu, Mitsuhiro, et al.. (2000). Direct Lithiation and Alkylation of Trifluoromethyl Enol Ethers Having a .BETA.-Sulfur Substituent.. Chemical and Pharmaceutical Bulletin. 48(1). 145–147. 1 indexed citations

14.

Yoshimatsu, Mitsuhiro & M. Hibino. (2000). First Synthesis of a .ALPHA.-Trifluoromethyl Allenol Ether via the Julia-Lythgoe Process.. Chemical and Pharmaceutical Bulletin. 48(9). 1395–1398. 7 indexed citations

15.

Yoshimatsu, Mitsuhiro, et al.. (2000). Organic chemistry of enyne sulfones: convenient one-pot synthesis of 2-ethoxy-3-ethynyl-4-methylene-2-perfluoroalkyl-3-(phenylsulfonyl)tetrahydrofurans. Journal of the Chemical Society Perkin Transactions 1. 4427–4431. 1 indexed citations

16.

Yoshimatsu, Mitsuhiro, et al.. (1997). Regio- and stereo-selective additions of sodium selenides to conjugate enyne sulfones: a convenient synthesis of 4-seleno-1-sulfonylbuta-1,3-dienes. Journal of the Chemical Society Perkin Transactions 1. 211–216. 21 indexed citations

17.

Yoshimatsu, Mitsuhiro, et al.. (1996). Regio- and stereoselective vinylic substitution reactions of α-haloenyne sulfones. Tetrahedron Letters. 37(41). 7381–7382. 8 indexed citations

18.

Yoshimatsu, Mitsuhiro, et al.. (1995). A useful synthesis of α,β‐bis(methylseleno)alkanes and α,δ‐bis(methylseleno)alk‐2‐enes by the reactions of alkenes and 1,3‐dienes with B(SeMe)₃‐Lewis acid. Heteroatom Chemistry. 6(3). 259–264.

19.

Hori, Mikio, et al.. (1990). Novel Reaction of a Stable Selenanaphthalene, 1-Cyano-2-methyl-2-selenanaphthalene with Electrophiles. Heterocycles. 30(1). 295–295. 5 indexed citations

20.

Kataoka, Tadashi, et al.. (1990). The C-O Bond Cleavage of Cyclic Ethers with Tris(phenylseleno)borane-Lewis Acid. Heterocycles. 31(5). 889–889. 3 indexed citations

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