Takuya Washio

495 total citations
11 papers, 413 citations indexed

About

Takuya Washio is a scholar working on Organic Chemistry, Biochemistry and Pharmacology. According to data from OpenAlex, Takuya Washio has authored 11 papers receiving a total of 413 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Organic Chemistry, 3 papers in Biochemistry and 2 papers in Pharmacology. Recurrent topics in Takuya Washio's work include Asymmetric Synthesis and Catalysis (9 papers), Synthetic Organic Chemistry Methods (8 papers) and Cyclopropane Reaction Mechanisms (4 papers). Takuya Washio is often cited by papers focused on Asymmetric Synthesis and Catalysis (9 papers), Synthetic Organic Chemistry Methods (8 papers) and Cyclopropane Reaction Mechanisms (4 papers). Takuya Washio collaborates with scholars based in Japan. Takuya Washio's co-authors include Masahiro Anada, Shunichi Hashimoto, Masahiko Tanaka, Naoyuki Shimada, Takumi Abe, Shinji Kitagaki, Motoo Shiro, Makoto Nakajima, Minoru Yamawaki and Hisanori Nambu and has published in prestigious journals such as Angewandte Chemie International Edition, Chemical Communications and Tetrahedron.

In The Last Decade

Takuya Washio

11 papers receiving 409 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Takuya Washio Japan 11 389 96 39 35 26 11 413
Clarisse Olier France 5 391 1.0× 68 0.7× 55 1.4× 43 1.2× 21 0.8× 6 403
Prashant Borkar India 13 434 1.1× 59 0.6× 53 1.4× 37 1.1× 15 0.6× 18 454
Kai E. O. Ylijoki Canada 9 518 1.3× 62 0.6× 60 1.5× 21 0.6× 24 0.9× 21 552
Pamela J. Lombardi United States 5 332 0.9× 64 0.7× 68 1.7× 23 0.7× 11 0.4× 7 346
Anyu He United States 12 412 1.1× 106 1.1× 84 2.2× 29 0.8× 9 0.3× 17 446
Yoshimitsu Hashimoto Japan 13 371 1.0× 44 0.5× 36 0.9× 23 0.7× 17 0.7× 42 389
Michelle Riener United States 4 513 1.3× 46 0.5× 48 1.2× 23 0.7× 18 0.7× 5 562
Jérôme Thibonnet France 9 328 0.8× 37 0.4× 54 1.4× 21 0.6× 17 0.7× 21 355
Jean Marc Campagne France 3 386 1.0× 82 0.9× 57 1.5× 18 0.5× 18 0.7× 3 398
Helge Menz Germany 13 805 2.1× 121 1.3× 57 1.5× 22 0.6× 28 1.1× 18 825

Countries citing papers authored by Takuya Washio

Since Specialization
Citations

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

Fields of papers citing papers by Takuya Washio

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Takuya Washio

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

All Works

11 of 11 papers shown
2.
Hashimoto, Shunichi, et al.. (2010). The Mukaiyama Aldol and Mukaiyama–Michael Reactions Promoted by Commercially Available Molecular Sieves. Heterocycles. 80(2). 1489–1489. 10 indexed citations
3.
Anada, Masahiro, et al.. (2010). A Short, Catalytic, Asymmetric Synthesis of Diospongins A and B by a One‐Pot, Sequential Hetero‐Diels–Alder/Mukaiyama–Michael Reaction Process. European Journal of Organic Chemistry. 2010(35). 6850–6854. 19 indexed citations
4.
5.
Washio, Takuya, Hisanori Nambu, Masahiro Anada, & Shunichi Hashimoto. (2007). Catalytic asymmetric hetero-Diels–Alder route to a key intermediate for the synthesis of calyxin L. Tetrahedron Asymmetry. 18(21). 2606–2612. 21 indexed citations
7.
Anada, Masahiro, Masahiko Tanaka, Takuya Washio, et al.. (2007). Catalytic Enantioselective Amination of Silyl Enol Ethers Using Chiral Dirhodium(II) Carboxylates:  Asymmetric Formal Synthesis of (−)-Metazocine. Organic Letters. 9(22). 4559–4562. 86 indexed citations
9.
Hashimoto, Shunichi, Takuya Washio, Seiichi Nakamura, & Masahiro Anada. (2005). Dirhodium(II) Tetrakis[N-benzene-fused Phthaloyl-(S)-piperidinonate] as a Chiral Lewis Acid: Catalytic Enantioselective Aldol Reactions of Acetate-derived Silylketene Acetals and Aldehydes. Heterocycles. 66(1). 567–567. 12 indexed citations
10.
Anada, Masahiro, Takuya Washio, Naoyuki Shimada, et al.. (2004). A New Dirhodium(II) Carboxamidate Complex as a Chiral Lewis Acid Catalyst for Enantioselective Hetero‐Diels–Alder Reactions. Angewandte Chemie International Edition. 43(20). 2665–2668. 102 indexed citations
11.
Anada, Masahiro, Takuya Washio, Naoyuki Shimada, et al.. (2004). A New Dirhodium(II) Carboxamidate Complex as a Chiral Lewis Acid Catalyst for Enantioselective Hetero‐Diels–Alder Reactions. Angewandte Chemie. 116(20). 2719–2722. 27 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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