Tatsuro Yasukata

573 total citations
20 papers, 342 citations indexed

About

Tatsuro Yasukata is a scholar working on Molecular Biology, Organic Chemistry and Infectious Diseases. According to data from OpenAlex, Tatsuro Yasukata has authored 20 papers receiving a total of 342 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 10 papers in Organic Chemistry and 5 papers in Infectious Diseases. Recurrent topics in Tatsuro Yasukata's work include Chemical Synthesis and Analysis (6 papers), Cancer therapeutics and mechanisms (3 papers) and Asymmetric Hydrogenation and Catalysis (3 papers). Tatsuro Yasukata is often cited by papers focused on Chemical Synthesis and Analysis (6 papers), Cancer therapeutics and mechanisms (3 papers) and Asymmetric Hydrogenation and Catalysis (3 papers). Tatsuro Yasukata collaborates with scholars based in Japan and United States. Tatsuro Yasukata's co-authors include Kenji Koga, Kenji Koga, Masatoshi Murakata, Takashi Nomura, Takayuki Tsuritani, Toshikatsu Maki, Janet L. Gunzner, Yukitoshi Narukawa, Barry M. Trost and Yasuhiro Nishitani and has published in prestigious journals such as Tetrahedron, Organic Letters and Tetrahedron Letters.

In The Last Decade

Tatsuro Yasukata

18 papers receiving 327 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Tatsuro Yasukata Japan	12	268	113	63	33	28	20	342
Sigmond G. Johnson United States	8	342 1.3×	164 1.5×	59 0.9×	37 1.1×	40 1.4×	10	471
C. L. Viswanathan India	10	265 1.0×	125 1.1×	25 0.4×	26 0.8×	19 0.7×	19	380
Eric J. Stoner United States	10	323 1.2×	115 1.0×	59 0.9×	53 1.6×	17 0.6×	13	420
Sandeep R. Ghorpade India	10	235 0.9×	161 1.4×	43 0.7×	31 0.9×	21 0.8×	14	330
R. M. PURICK United States	8	252 0.9×	114 1.0×	48 0.8×	45 1.4×	22 0.8×	9	333
George Burton United States	11	450 1.7×	126 1.1×	39 0.6×	40 1.2×	59 2.1×	33	560
A. W. FRITZ United States	9	227 0.8×	113 1.0×	19 0.3×	40 1.2×	34 1.2×	11	294
Pau Ruiz‐Sanchis Denmark	7	451 1.7×	113 1.0×	55 0.9×	37 1.1×	38 1.4×	7	572
D. Sriram India	5	391 1.5×	119 1.1×	44 0.7×	43 1.3×	30 1.1×	8	470
Ann E. DeCamp United States	9	382 1.4×	126 1.1×	58 0.9×	17 0.5×	36 1.3×	11	435

Countries citing papers authored by Tatsuro Yasukata

Since Specialization

Citations

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

Fields of papers citing papers by Tatsuro Yasukata

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tatsuro Yasukata

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

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

Maki, Toshikatsu, et al.. (2024). Practical Manufacturing Process for Baloxavir Marboxil: Effective Selection and Replacement of Protective Group toward Enhancement of Crystallization-Induced Diastereomer Transformation. Organic Process Research & Development. 28(6). 2139–2149. 4 indexed citations

Yasukata, Tatsuro & Yasunori Aoyama. (2020). Development of Practical Synthetic Method for the Preparation of Dolutegravir Sodium, a Potent HIV-1 Integrase Inhibitor for the Treatment of HIV Infectious Disease. Journal of Synthetic Organic Chemistry Japan. 78(1). 2–10. 1 indexed citations

Yasukata, Tatsuro, Moriyasu Masui, Kazuya Okamoto, et al.. (2019). Practical Synthetic Method for the Preparation of Pyrone Diesters: An Efficient Synthetic Route for the Synthesis of Dolutegravir Sodium. Organic Process Research & Development. 23(4). 565–570. 22 indexed citations

Aoyama, Yasunori, Toshikazu Hakogi, Yuki Fukui, et al.. (2019). Practical and Scalable Synthetic Method for Preparation of Dolutegravir Sodium: Improvement of a Synthetic Route for Large-Scale Synthesis. Organic Process Research & Development. 23(4). 558–564. 16 indexed citations

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

Suzuki, Hideyuki, et al.. (2013). Antibacterial oxazolidinone analogues having a N-hydroxyacetyl-substituted seven-membered [1,2,5]triazepane or [1,2,5]oxadiazepane C-ring unit. European Journal of Medicinal Chemistry. 63. 811–825. 11 indexed citations

Suzuki, Hideyuki, et al.. (2013). Synthesis and in vitro/in vivo antibacterial activity of oxazolidinones having thiocarbamate at C-5 on the A-ring and an amide- or urea-substituted [1,2,5]triazepane or [1,2,5]oxadiazepane as the C-ring. European Journal of Medicinal Chemistry. 69. 262–277. 19 indexed citations

Iida, Akira, et al.. (2012). Practical Synthesis of Ethyl 1-(tert-Butoxycarbonyl)-4-(1-pyrrolidinyl)-4-piperidineacetate, an Intermediate of a Novel Antiarteriosclerotic, Utilizing Aza-Michael Addition Promoted by LiBr. Chemistry Letters. 41(12). 1703–1705.

10.

Yamawaki, Kenji, Takashi Nomura, Tatsuro Yasukata, et al.. (2007). A novel series of parenteral cephalosporins exhibiting potent activities against Pseudomonas aeruginosa and other Gram-negative pathogens: Synthesis and structure–activity relationships. Bioorganic & Medicinal Chemistry. 15(21). 6716–6732. 22 indexed citations

11.

Yamawaki, Kenji, Takashi Nomura, Tatsuro Yasukata, et al.. (2007). A novel series of parenteral cephalosporins exhibiting potent activities against both Pseudomonas aeruginosa and other Gram-negative pathogens. Part 2: Synthesis and structure–activity relationships. Bioorganic & Medicinal Chemistry. 16(4). 1632–1647. 7 indexed citations

12.

Nomura, Takashi, Tsutomu Iwaki, Tatsuro Yasukata, et al.. (2005). A new type of ketolides bearing an N-aryl-alkyl acetamide moiety at the C-9 iminoether synthesis and structure–activity relationships. Bioorganic & Medicinal Chemistry. 13(24). 6615–6628. 15 indexed citations

13.

Nomura, Takashi, et al.. (2005). 9-Oxime-3-ketolides: Modification at the C-11,12-diol moiety and antibacterial activities against key respiratory pathogens. Bioorganic & Medicinal Chemistry. 13(21). 6054–6063. 15 indexed citations

14.

Yoshida, Osamu, et al.. (2002). Novel semi-synthetic glycopeptide antibiotics active against methicillin-resistant staphylococcus aureus (MRSA) and vancomycin-resistant Enterococci (VRE): doubly-modified water-soluble derivatives of chloroorienticin B. Bioorganic & Medicinal Chemistry Letters. 12(21). 3027–3031. 15 indexed citations

15.

Yasukata, Tatsuro, et al.. (2002). An efficient and practical method for solid-phase synthesis of tripeptide-bearing glycopeptide antibiotics: combinatorial parallel synthesis of carboxamide derivatives of chloroorienticin B. Bioorganic & Medicinal Chemistry Letters. 12(21). 3033–3036. 8 indexed citations

16.

Trost, Barry M., Janet L. Gunzner, & Tatsuro Yasukata. (2001). An unusual regioselectivity in the Pd-catalyzed cross coupling of alkynes. A correction. Tetrahedron Letters. 42(23). 3775–3778. 26 indexed citations

17.

Murakata, Masatoshi, et al.. (1998). Stereoselective reactions. 30. Enantioselective alkylation of the lithium enolates of six-membered cyclic ketones using tetradentate chiral amines in the presence of lithium bromide. Tetrahedron. 54(11). 2449–2458. 24 indexed citations

18.

Shirai, Ryuichi, Kazumasa Aoki, Daisaku Sato, et al.. (1994). Stereoselective Reactions. XXII. Design and Synthesis of Chiral Chelated Lithium Amides for Enantioselective Reactions.. Chemical and Pharmaceutical Bulletin. 42(3). 690–693. 48 indexed citations

19.

Yasukata, Tatsuro & Kenji Koga. (1993). Enantioselective protonation of achiral lithium enolates using a chiral amine in the presence of lithium bromide. Tetrahedron Asymmetry. 4(1). 35–38. 62 indexed citations

20.

Yasukata, Tatsuro, Shigeki Sasaki, & Kenji Koga. (1991). Novel bicyclic chiral crown ethers having a p-xylenedioxy unit with improved complex stability and rate-enhancement in the intra-complex thiolysis of .ALPHA.-amino acid ester salts.. Chemical and Pharmaceutical Bulletin. 39(2). 530–532.

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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