Yoshitaka Numajiri

534 total citations
15 papers, 447 citations indexed

About

Yoshitaka Numajiri is a scholar working on Organic Chemistry, Pharmacology and Molecular Biology. According to data from OpenAlex, Yoshitaka Numajiri has authored 15 papers receiving a total of 447 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Organic Chemistry, 5 papers in Pharmacology and 3 papers in Molecular Biology. Recurrent topics in Yoshitaka Numajiri's work include Catalytic C–H Functionalization Methods (5 papers), Alkaloids: synthesis and pharmacology (5 papers) and Chemical synthesis and alkaloids (5 papers). Yoshitaka Numajiri is often cited by papers focused on Catalytic C–H Functionalization Methods (5 papers), Alkaloids: synthesis and pharmacology (5 papers) and Chemical synthesis and alkaloids (5 papers). Yoshitaka Numajiri collaborates with scholars based in United States, Japan and Germany. Yoshitaka Numajiri's co-authors include Brian M. Stoltz, Beau P. Pritchett, Takayuki Doi, Jun Kikuchi, Takashi Takahashi, Takashi Takahashi, Motoki Takagi, Gonzalo Jiménez‐Osés, Bo Wang and K. N. Houk and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Tetrahedron.

In The Last Decade

Yoshitaka Numajiri

15 papers receiving 443 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yoshitaka Numajiri United States 12 357 128 113 83 79 15 447
Shupeng Zhou China 10 324 0.9× 162 1.3× 81 0.7× 104 1.3× 61 0.8× 12 459
Narendra B. Ambhaikar United States 8 466 1.3× 155 1.2× 115 1.0× 88 1.1× 40 0.5× 12 543
Benjamin D. Hafensteiner United States 8 431 1.2× 134 1.0× 118 1.0× 93 1.1× 40 0.5× 8 505
Zachary G. Brill United States 7 418 1.2× 174 1.4× 115 1.0× 47 0.6× 120 1.5× 9 551
Yosuke Kaburagi Japan 9 450 1.3× 110 0.9× 73 0.6× 76 0.9× 47 0.6× 10 518
Gerald D. Artman United States 10 374 1.0× 116 0.9× 133 1.2× 77 0.9× 67 0.8× 16 481
Yian Guo China 12 307 0.9× 90 0.7× 88 0.8× 33 0.4× 64 0.8× 29 390
François‐Hugues Porée France 14 458 1.3× 140 1.1× 89 0.8× 62 0.7× 93 1.2× 30 558
Fuzhuo Li China 12 271 0.8× 212 1.7× 129 1.1× 77 0.9× 74 0.9× 18 482
Stéphane Dorich Canada 9 546 1.5× 127 1.0× 88 0.8× 43 0.5× 55 0.7× 15 622

Countries citing papers authored by Yoshitaka Numajiri

Since Specialization
Citations

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

Fields of papers citing papers by Yoshitaka Numajiri

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yoshitaka Numajiri

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

All Works

15 of 15 papers shown
1.
Stoltz, Brian M., Beau P. Pritchett, Jun Kikuchi, & Yoshitaka Numajiri. (2017). A Fischer Indolization Strategy toward the Total Synthesis of (–)-Goniomitine. Heterocycles. 95(2). 1245–1245. 13 indexed citations
2.
Pritchett, Beau P., Jun Kikuchi, Yoshitaka Numajiri, & Brian M. Stoltz. (2016). Enantioselective Pd‐Catalyzed Allylic Alkylation Reactions of Dihydropyrido[1,2‐a]indolone Substrates: Efficient Syntheses of (−)‐Goniomitine, (+)‐Aspidospermidine, and (−)‐Quebrachamine. Angewandte Chemie International Edition. 55(43). 13529–13532. 69 indexed citations
3.
Pritchett, Beau P., Jun Kikuchi, Yoshitaka Numajiri, & Brian M. Stoltz. (2016). Enantioselective Pd‐Catalyzed Allylic Alkylation Reactions of Dihydropyrido[1,2‐a]indolone Substrates: Efficient Syntheses of (−)‐Goniomitine, (+)‐Aspidospermidine, and (−)‐Quebrachamine. Angewandte Chemie. 128(43). 13727–13730. 23 indexed citations
4.
Marziale, Alexander N., Robert A. Craig, Kelly E. Kim, et al.. (2015). An Efficient Protocol for the Palladium‐Catalyzed Asymmetric Decarboxylative Allylic Alkylation Using Low Palladium Concentrations and a Palladium(II) Precatalyst. Advanced Synthesis & Catalysis. 357(10). 2238–2245. 19 indexed citations
5.
Li, Zining, Qian Geng, Beau P. Pritchett, et al.. (2015). Selective syntheses of leuconolam, leuconoxine, and mersicarpine alkaloids from a common intermediate through regiocontrolled cyclizations by Staudinger reactions. Organic Chemistry Frontiers. 2(3). 236–240. 34 indexed citations
6.
Takahashi, Eiki, et al.. (2015). Identification of alpha-substituted acylamines as novel, potent, and orally active mGluR5 negative allosteric modulators. Bioorganic & Medicinal Chemistry Letters. 25(16). 3135–3141. 1 indexed citations
7.
Numajiri, Yoshitaka, Gonzalo Jiménez‐Osés, Bo Wang, K. N. Houk, & Brian M. Stoltz. (2015). Enantioselective Synthesis of DialkylatedN-Heterocycles by Palladium-Catalyzed Allylic Alkylation. Organic Letters. 17(5). 1082–1085. 49 indexed citations
8.
Kita, Yusuke, Yoshitaka Numajiri, Noriko Okamoto, & Brian M. Stoltz. (2015). Construction of tertiary chiral centers by Pd-catalyzed asymmetric allylic alkylation of prochiral enolate equivalents. Tetrahedron. 71(37). 6349–6353. 15 indexed citations
9.
Numajiri, Yoshitaka, et al.. (2015). Enantioselective Synthesis of α-Quaternary Mannich Adducts by Palladium-Catalyzed Allylic Alkylation: Total Synthesis of (+)-Sibirinine. Journal of the American Chemical Society. 137(3). 1040–1043. 61 indexed citations
10.
Doi, Takayuki, Yoshitaka Numajiri, Takashi Takahashi, Motoki Takagi, & Kazuo Shin‐ya. (2010). Solid‐phase Total Synthesis of (−)‐Apratoxin A and Its Analogues and Their Biological Evaluation. Chemistry - An Asian Journal. 6(1). 180–188. 31 indexed citations
11.
Numajiri, Yoshitaka, Takashi Takahashi, Motoki Takagi, Kazuo Shin‐ya, & Takayuki Doi. (2009). Total Synthesis of Largazole and Its Biological Evaluation. 2008. 41–44. 2 indexed citations
12.
Miyamoto, Shigeru, et al.. (2009). Stereoselective one-pot three-component coupling approach towards the synthesis of the AC ring system of taxanes. Tetrahedron Letters. 50(26). 3408–3410. 7 indexed citations
13.
Numajiri, Yoshitaka, Takashi Takahashi, & Takayuki Doi. (2008). Total Synthesis of (−)‐Apratoxin A, 34‐Epimer, and Its Oxazoline Analogue. Chemistry - An Asian Journal. 4(1). 111–125. 40 indexed citations
14.
Doi, Takayuki, Yoshitaka Numajiri, Takashi Takahashi, Motoki Takagi, & Kazuo Shin‐ya. (2008). Total Synthesis of Largazoleand Its Biological Evaluation. Synlett. 2008(16). 2483–2486. 15 indexed citations
15.
Doi, Takayuki, et al.. (2006). Total Synthesis of Apratoxin A. Organic Letters. 8(3). 531–534. 68 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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