Masatoshi Asami

2.7k total citations
92 papers, 2.0k citations indexed

About

Masatoshi Asami is a scholar working on Organic Chemistry, Spectroscopy and Inorganic Chemistry. According to data from OpenAlex, Masatoshi Asami has authored 92 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 78 papers in Organic Chemistry, 23 papers in Spectroscopy and 20 papers in Inorganic Chemistry. Recurrent topics in Masatoshi Asami's work include Asymmetric Synthesis and Catalysis (48 papers), Synthetic Organic Chemistry Methods (22 papers) and Asymmetric Hydrogenation and Catalysis (17 papers). Masatoshi Asami is often cited by papers focused on Asymmetric Synthesis and Catalysis (48 papers), Synthetic Organic Chemistry Methods (22 papers) and Asymmetric Hydrogenation and Catalysis (17 papers). Masatoshi Asami collaborates with scholars based in Japan, United States and Germany. Masatoshi Asami's co-authors include Seiichi Inoue, Suguru Ito, Teruaki Mukaiyama, Kiyoshi Honda, Yoshitaka Yamaguchi, Takashi Ubukata, Susumu Kobayashi, Hiroyasu Watanabe, Takeshi Yamada and Tomohiro Taguchi and has published in prestigious journals such as Chemical Communications, Biochemical and Biophysical Research Communications and The Journal of Organic Chemistry.

In The Last Decade

Masatoshi Asami

91 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Masatoshi Asami Japan 26 1.6k 495 453 434 378 92 2.0k
Mary F. Mahon United Kingdom 25 1.2k 0.7× 395 0.8× 263 0.6× 475 1.1× 290 0.8× 75 1.7k
Saumitra Sengupta India 26 1.7k 1.0× 325 0.7× 142 0.3× 207 0.5× 365 1.0× 89 2.1k
Richard P. Bonar‐Law United Kingdom 23 851 0.5× 366 0.7× 339 0.7× 255 0.6× 537 1.4× 30 1.3k
Ottorino De Lucchi Italy 29 2.9k 1.8× 335 0.7× 461 1.0× 391 0.9× 439 1.2× 212 3.2k
J.A.J.M. Vekemans Netherlands 21 932 0.6× 378 0.8× 179 0.4× 192 0.4× 350 0.9× 47 1.6k
Hongwen Hu China 29 2.4k 1.5× 275 0.6× 157 0.3× 442 1.0× 403 1.1× 148 2.8k
Ei‐ichi Negishi United States 23 4.5k 2.7× 417 0.8× 119 0.3× 666 1.5× 492 1.3× 59 4.9k
Luis Simón Spain 21 1.4k 0.9× 270 0.5× 524 1.2× 483 1.1× 476 1.3× 63 2.1k
Haruo Matsuyama Japan 21 1.3k 0.8× 279 0.6× 172 0.4× 112 0.3× 240 0.6× 110 1.6k
Xin‐Yan Wu China 35 2.6k 1.6× 339 0.7× 153 0.3× 699 1.6× 769 2.0× 163 3.4k

Countries citing papers authored by Masatoshi Asami

Since Specialization
Citations

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

Fields of papers citing papers by Masatoshi Asami

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Masatoshi Asami

This figure shows the co-authorship network connecting the top 25 collaborators of Masatoshi Asami. A scholar is included among the top collaborators of Masatoshi Asami 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 Masatoshi Asami. Masatoshi Asami 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.
Asami, Masatoshi, et al.. (2022). Dual-channel recognition of Al3+ and Cu2+ ions using a chiral pyrene-based fluorescent sensor. New Journal of Chemistry. 46(17). 7864–7871. 7 indexed citations
2.
Ito, Suguru, et al.. (2021). Mechanochromic Luminescence and Solid‐State Circularly Polarized Luminescence of a Chiral Diamine‐Linked Bispyrene. ChemPhotoChem. 5(10). 920–925. 19 indexed citations
3.
Asami, Masatoshi, et al.. (2020). Two types of two-step mechanochromic luminescence of phenanthroimidazolylbenzothiadiazoles. Materials Advances. 1(4). 708–719. 42 indexed citations
4.
Tachikawa, Takashi, et al.. (2019). Efficient and versatile mechanochromic luminescence of phenanthroimidazolylbenzothiadiazoles: tricolor switching and directional control over the chromism. Journal of Materials Chemistry C. 7(17). 4988–4998. 64 indexed citations
5.
Ito, Suguru, et al.. (2019). Switching the Direction of Mechano-responsive Emission Color Change of Triphenylimidazolylbenzothiadiazole. Chemistry Letters. 48(12). 1492–1495. 16 indexed citations
6.
7.
Ito, Suguru, Tomohiro Taguchi, Takeshi Yamada, et al.. (2017). Indolylbenzothiadiazoles with varying substituents on the indole ring: a systematic study on the self-recovering mechanochromic luminescence. RSC Advances. 7(28). 16953–16962. 62 indexed citations
8.
Ito, Suguru, et al.. (2017). Differentiation of enantiomeric anions by NMR spectroscopy with chiral bisurea receptors. Organic & Biomolecular Chemistry. 16(2). 213–222. 21 indexed citations
9.
10.
Asami, Masatoshi, et al.. (2016). Enantioselective addition of diethylzinc to aldehydes catalyzed by o-xylylene-type chiral 1,4-amino alcohols with an aminal structure. Tetrahedron Asymmetry. 27(7-8). 322–329. 12 indexed citations
11.
Ito, Suguru, Takeshi Yamada, & Masatoshi Asami. (2016). Two‐Step Mechanochromic Luminescence of N,N′‐Bis‐Boc‐3,3′‐di(pyren‐1‐yl)‐2,2′‐biindole. ChemPlusChem. 81(12). 1272–1275. 18 indexed citations
12.
13.
Yoshida, Takashi, Kazuhisa Sakakibara, & Masatoshi Asami. (2003). Theoretical Evaluation of the Reaction Intermediate Complex for an Asymmetric Reaction Using a Chiral Lithium Amide by the Molecular Mechanics (MM3) Calculations. Chemistry Letters. 32(2). 150–151. 6 indexed citations
14.
Asami, Masatoshi. (1996). Asymmetric Transformation of meso-Epoxides by Chiral Lithium Amides.. Journal of Synthetic Organic Chemistry Japan. 54(3). 188–199. 33 indexed citations
15.
Asami, Masatoshi, Toshiki Kuno, Hideyuki Mukai, & Chikako Tanaka. (1993). Detection of the FK506-FKBP-Calcineurin Complex by a Simple Binding Assay. Biochemical and Biophysical Research Communications. 192(3). 1388–1394. 25 indexed citations
16.
Asami, Masatoshi, Makoto Owhashi, Toru Abe, & Yukifumi Nawa. (1991). Susceptibility of multipotent haemopoietic stem cell deficient W/Wv mice to Plasmodiumberghei‐infection. Immunology and Cell Biology. 69(5). 355–360. 9 indexed citations
17.
Asami, Masatoshi & Seiichi Inoue. (1991). Enantioselective Addition of Diethylzinc to Aldehydes Catalyzed by Chiral Hydroxy Aminal. Chemistry Letters. 20(4). 685–688. 13 indexed citations
18.
Asami, Masatoshi. (1990). A Novel Asymmetric Synthesis of Chiral Cyclopentanoid Building Blocks by the Use of Chiral Lithium Amide. Bulletin of the Chemical Society of Japan. 63(5). 1402–1408. 43 indexed citations
19.
Sakito, Yoji, Masatoshi Asami, & Teruaki Mukaiyama. (1980). An asymmetric synthesis of .BETA.-formyl .BETA.-hydroxy esters.. Chemistry Letters. 455–458. 1 indexed citations
20.
Mukaiyama, Teruaki, et al.. (1979). A convenient method for the preparation of .ALPHA.-chloronitriles.. Chemistry Letters. 1117–1118. 1 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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