Masaki Nishiuchi

535 total citations
29 papers, 429 citations indexed

About

Masaki Nishiuchi is a scholar working on Organic Chemistry, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Masaki Nishiuchi has authored 29 papers receiving a total of 429 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Organic Chemistry, 9 papers in Molecular Biology and 4 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Masaki Nishiuchi's work include Organic Chemistry Cycloaddition Reactions (6 papers), Asymmetric Synthesis and Catalysis (5 papers) and Chemical Synthesis and Analysis (4 papers). Masaki Nishiuchi is often cited by papers focused on Organic Chemistry Cycloaddition Reactions (6 papers), Asymmetric Synthesis and Catalysis (5 papers) and Chemical Synthesis and Analysis (4 papers). Masaki Nishiuchi collaborates with scholars based in Japan, United States and China. Masaki Nishiuchi's co-authors include Shuji Kanemasa, Kenzi Hori, Akio Kamimura, Shigeru Kobayashi, Yasuhiko Kawamura, Eiji Wada, Masao Tsukayama, Hitoshi Nishizawa, Hiyoshizo Kotsuki and Tetsuo Iwasawa and has published in prestigious journals such as Journal of the American Chemical Society, Chemical Communications and The Journal of Organic Chemistry.

In The Last Decade

Masaki Nishiuchi

28 papers receiving 415 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Masaki Nishiuchi Japan 11 376 113 41 27 23 29 429
Sergey E. Pipko Ukraine 13 307 0.8× 125 1.1× 46 1.1× 28 1.0× 28 1.2× 25 371
Adam T. Gillmore United Kingdom 9 399 1.1× 92 0.8× 23 0.6× 28 1.0× 21 0.9× 13 483
Hildegard Nimmesgern Germany 9 346 0.9× 66 0.6× 24 0.6× 18 0.7× 15 0.7× 18 410
Р. С. Сагитуллин Russia 11 319 0.8× 70 0.6× 19 0.5× 17 0.6× 14 0.6× 68 361
Niklas Wahlström Sweden 9 294 0.8× 82 0.7× 14 0.3× 51 1.9× 13 0.6× 9 391
Francesco Montalbano Portugal 6 495 1.3× 162 1.4× 18 0.4× 39 1.4× 20 0.9× 7 546
Shin Chung South Korea 9 275 0.7× 95 0.8× 49 1.2× 30 1.1× 94 4.1× 17 364
Ulrich Schwartz Germany 11 224 0.6× 84 0.7× 14 0.3× 89 3.3× 30 1.3× 12 320
Shaojing Hu Canada 11 393 1.0× 77 0.7× 27 0.7× 24 0.9× 43 1.9× 15 458
Takayuki Tsuritani Japan 15 505 1.3× 109 1.0× 18 0.4× 16 0.6× 11 0.5× 22 531

Countries citing papers authored by Masaki Nishiuchi

Since Specialization
Citations

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

Fields of papers citing papers by Masaki Nishiuchi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Masaki Nishiuchi

This figure shows the co-authorship network connecting the top 25 collaborators of Masaki Nishiuchi. A scholar is included among the top collaborators of Masaki Nishiuchi 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 Masaki Nishiuchi. Masaki Nishiuchi 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.
Isaka, Tamami, et al.. (2023). Comparison of different approaches in complete thoracoscopic segmentectomy of lung lower lobe. Journal of Thoracic Disease. 15(6). 2958–2970. 1 indexed citations
2.
Nishiuchi, Masaki, et al.. (2014). Regioisomeric allene dimer formation by the reaction of tetraarylbutatrienes with tetracyanoethene. Organic & Biomolecular Chemistry. 12(17). 2784–2784. 8 indexed citations
3.
Yagishita, Fumitoshi, et al.. (2014). One-pot synthesis of novel polysubstituted 1,1′-phenylene-bipyrrole via the double [3+2] cycloaddition reaction. Tetrahedron. 71(22). 3614–3618. 3 indexed citations
4.
Ooi, Takashi, et al.. (2008). Thermal cyclotrimerization of tetraphenyl[5]cumulene(tetraphenylhexapentaene) to a tricyclodecadiene derivative. Chemical Communications. 574–576. 19 indexed citations
5.
Iwasawa, Tetsuo, et al.. (2008). Straightforward access to functionalized pentaarylbenzene derivatives through a quick lithiation. Tetrahedron Letters. 49(36). 5244–5246. 7 indexed citations
6.
Iwasawa, Tetsuo, et al.. (2008). A functionalized phosphine ligand with a pentaarylbenzene moiety in palladium-catalyzed Suzuki–Miyaura coupling of aryl chlorides. Tetrahedron Letters. 49(52). 7430–7433. 12 indexed citations
7.
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Shimizu, Mayumi, et al.. (2003). Long-term survival in adult mediastinal neuroblastoma. The Japanese Journal of Thoracic and Cardiovascular Surgery. 51(7). 326–329. 6 indexed citations
10.
Kawamura, Yasuhiko, et al.. (2002). Photoreactions of 1,3-Dipolar Cycloadducts of Mesoionic Compounds with Buckminsterfullerene. Molecular Crystals and Liquid Crystals. 376(1). 219–224. 1 indexed citations
11.
Kanzaki, Masato, et al.. (2002). Bronchoplasty with Plication of the Proximal Bronchial Membranous Portion. Asian Cardiovascular and Thoracic Annals. 10(4). 372–373. 2 indexed citations
12.
13.
Tsukayama, Masao, et al.. (2000). Regioselective Synthesis of Prenylisoflavones: Syntheses of Luteone and Luteone Hydrate. Chemistry Letters. 29(12). 1362–1363. 3 indexed citations
14.
Tsukayama, Masao, et al.. (1998). Regioselective Synthesis of Prenylisoflavones. Syntheses of Lupiwighteone, Lupiwighteone Hydrate and Related Compounds. Journal of Chemical Research Synopses. 238–239. 3 indexed citations
15.
Nishiuchi, Masaki, et al.. (1996). Stereocontrol by Lewis Acids in the Hetero-Diels-Alder Reaction Leading to a Key 1β-Methylcarbapenem Intermediate. Chemistry Letters. 25(4). 321–322. 5 indexed citations
16.
Kanemasa, Shuji, Masaki Nishiuchi, Akio Kamimura, & Kenzi Hori. (1994). First Successful Metal Coordination Control in 1,3-Dipolar Cycloadditions. High-Rate Acceleration and Regio- and Stereocontrol of Nitrile Oxide Cycloadditions to the Magnesium Alkoxides of Allylic and Homoallylic Alcohols. Journal of the American Chemical Society. 116(6). 2324–2339. 149 indexed citations
17.
Kanemasa, Shuji & Masaki Nishiuchi. (1993). A highly effective quenching method of 1,3-dipolar cycloadditions of nitrile oxides or nitrile oxide/Lewis acid complexes by use of 2-propenyloxymagnesium bromide. Tetrahedron Letters. 34(25). 4011–4014. 13 indexed citations
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19.
Kanemasa, Shuji, Masaki Nishiuchi, & Eiji Wada. (1992). Regiocontrol of nitrile oxide cycloadditions to allyl alcohols. Synthesis of 4-substituted and 4,4-disubstituted 5-hydroxymethyl-2-isoxazolines. Tetrahedron Letters. 33(10). 1357–1360. 45 indexed citations
20.
Kotsuki, Hiyoshizo, Masaki Nishiuchi, Shigeru Kobayashi, & Hitoshi Nishizawa. (1990). High-pressure organic chemistry. 10. Novel neutral alkylations of indoles and pyrroles with vinyl epoxides at high pressure. The Journal of Organic Chemistry. 55(9). 2969–2972. 38 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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