Toshikatsu Maki

1.2k total citations
17 papers, 995 citations indexed

About

Toshikatsu Maki is a scholar working on Organic Chemistry, Inorganic Chemistry and Molecular Biology. According to data from OpenAlex, Toshikatsu Maki has authored 17 papers receiving a total of 995 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Organic Chemistry, 8 papers in Inorganic Chemistry and 7 papers in Molecular Biology. Recurrent topics in Toshikatsu Maki's work include Asymmetric Hydrogenation and Catalysis (8 papers), Chemical Synthesis and Analysis (7 papers) and Chemical Synthesis and Reactions (6 papers). Toshikatsu Maki is often cited by papers focused on Asymmetric Hydrogenation and Catalysis (8 papers), Chemical Synthesis and Analysis (7 papers) and Chemical Synthesis and Reactions (6 papers). Toshikatsu Maki collaborates with scholars based in Japan and United States. Toshikatsu Maki's co-authors include Kazuaki Ishihara, Hisashi Yamamoto, Manabu Hatano, Katsuhiko Moriyama, Yoshiro Furuya, Yuka Nakamura, Tatsuro Yasukata, Takayuki Tsuritani, Atsushi Satô and Xiaowei Wang and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Tetrahedron.

In The Last Decade

Toshikatsu Maki

17 papers receiving 975 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Toshikatsu Maki Japan 12 925 387 368 59 50 17 995
Stefan Klaus Germany 17 860 0.9× 269 0.7× 162 0.4× 48 0.8× 31 0.6× 32 973
Joanna Paradowska Poland 9 650 0.7× 196 0.5× 250 0.7× 52 0.9× 33 0.7× 9 729
Jean‐Simon Suppo France 8 824 0.9× 640 1.7× 262 0.7× 47 0.8× 22 0.4× 11 935
Valmik S. Shinde India 13 1.1k 1.2× 186 0.5× 363 1.0× 79 1.3× 56 1.1× 17 1.2k
David Madec France 20 1.2k 1.2× 163 0.4× 325 0.9× 58 1.0× 27 0.5× 70 1.2k
Dirk Strübing Germany 17 803 0.9× 280 0.7× 159 0.4× 46 0.8× 21 0.4× 25 919
Laurent Giordano France 22 1.4k 1.5× 170 0.4× 732 2.0× 65 1.1× 47 0.9× 54 1.5k
James M. Longmire United States 10 871 0.9× 179 0.5× 443 1.2× 50 0.8× 51 1.0× 11 983
Timothy A. Ayers United States 12 796 0.9× 238 0.6× 566 1.5× 38 0.6× 49 1.0× 19 928
Ulrike Nettekoven Austria 17 945 1.0× 184 0.5× 553 1.5× 50 0.8× 26 0.5× 29 1.1k

Countries citing papers authored by Toshikatsu Maki

Since Specialization
Citations

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

Fields of papers citing papers by Toshikatsu Maki

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Toshikatsu Maki

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

All Works

17 of 17 papers shown
1.
Maki, Toshikatsu, et al.. (2024). Practical Manufacturing Process for Baloxavir Marboxil: Efficient Route to a Tricyclic Triazinanone Scaffold. Organic Process Research & Development. 28(6). 2128–2138. 4 indexed citations
2.
3.
Maki, Toshikatsu, Takayuki Tsuritani, & Tatsuro Yasukata. (2014). A Mild Method for the Synthesis of Carbamate-Protected Guanidines Using the Burgess Reagent. Organic Letters. 16(7). 1868–1871. 23 indexed citations
4.
Hatano, Manabu, Katsuhiko Moriyama, Toshikatsu Maki, & Kazuaki Ishihara. (2010). Which Is the Actual Catalyst: Chiral Phosphoric Acid or Chiral Calcium Phosphate?. Angewandte Chemie International Edition. 49(22). 3823–3826. 208 indexed citations
5.
Hatano, Manabu, Katsuhiko Moriyama, Toshikatsu Maki, & Kazuaki Ishihara. (2010). Titelbild: Which Is the Actual Catalyst: Chiral Phosphoric Acid or Chiral Calcium Phosphate? (Angew. Chem. 22/2010). Angewandte Chemie. 122(22). 3783–3783. 1 indexed citations
6.
Hatano, Manabu, et al.. (2010). Ligand-Assisted Rate Acceleration in Lanthanum(III) Isopropoxide Catalyzed Transesterification of Carboxylic Esters. Organic Letters. 13(3). 426–429. 71 indexed citations
7.
Hatano, Manabu, Katsuhiko Moriyama, Toshikatsu Maki, & Kazuaki Ishihara. (2010). Which Is the Actual Catalyst: Chiral Phosphoric Acid or Chiral Calcium Phosphate?. Angewandte Chemie. 122(22). 3911–3914. 78 indexed citations
8.
Hatano, Manabu, et al.. (2009). Pyridinium 1,1′-Binaphthyl-2,2′-disulfonates as Highly Effective Chiral Brønsted Acid−Base Combined Salt Catalysts for Enantioselective Mannich-Type Reaction. Journal of the American Chemical Society. 131(33). 12015–12015. 1 indexed citations
9.
Hatano, Manabu, et al.. (2008). Pyridinium 1,1′-Binaphthyl-2,2′-disulfonates as Highly Effective Chiral Brønsted Acid−Base Combined Salt Catalysts for Enantioselective Mannich-Type Reaction. Journal of the American Chemical Society. 130(50). 16858–16860. 146 indexed citations
10.
Maki, Toshikatsu, Kazuaki Ishihara, & Hisashi Yamamoto. (2007). New boron(III)-catalyzed amide and ester condensation reactions. Tetrahedron. 63(35). 8645–8657. 148 indexed citations
11.
Nakamura, Yuka, Toshikatsu Maki, Xiaowei Wang, Kazuaki Ishihara, & Hisashi Yamamoto. (2006). Iron(III)–Zirconium(IV) Combined Salt Immobilized on N‐(Polystyrylbutyl)pyridinium Triflylimide as a Reusable Catalyst for a Dehydrative Esterification Reaction. Advanced Synthesis & Catalysis. 348(12-13). 1505–1510. 21 indexed citations
12.
Maki, Toshikatsu, Kazuaki Ishihara, & Hisashi Yamamoto. (2006). 4,5,6,7-Tetrachlorobenzo[d][1,3,2]dioxaborol- 2-ol as an Effective Catalyst for the Amide Condensation of Sterically Demanding Carboxylic Acids. Organic Letters. 8(7). 1431–1434. 98 indexed citations
13.
Maki, Toshikatsu, Kazuaki Ishihara, & Hisashi Yamamoto. (2005). N-Alkyl-4-boronopyridinium Halides versus Boric Acid as Catalysts for the Esterification of α-Hydroxycarboxylic Acids. Organic Letters. 7(22). 5047–5050. 63 indexed citations
14.
Satô, Atsushi, Yuka Nakamura, Toshikatsu Maki, Kazuaki Ishihara, & Hisashi Yamamoto. (2005). Zr(IV)Fe(III), Ga(III), and Sn(IV) Binary Metal Complexes as Synergistic and Reusable Esterification Catalysts. Advanced Synthesis & Catalysis. 347(10). 1337–1340. 27 indexed citations
15.
Maki, Toshikatsu, Kazuaki Ishihara, & Hisashi Yamamoto. (2005). N-Alkyl-4-boronopyridinium Salts as Thermally Stable and Reusable Amide Condensation Catalysts. Organic Letters. 7(22). 5043–5046. 89 indexed citations
16.
Maki, Toshikatsu, Kazuaki Ishihara, & Hisashi Yamamoto. (2004). Arylboronic Acid Catalyzed Direct Condensation of Carboxylic Acids with Ureas.. ChemInform. 35(45). 1 indexed citations
17.
Ishihara, Kazuaki, Hisashi Yamamoto, & Toshikatsu Maki. (2004). Arylboronic Acid-Catalyzed Direct Condensation of Carboxylic Acids with Ureas. Synlett. 1355–1358. 12 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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