Nobuhito Tabuchi

407 total citations
18 papers, 315 citations indexed

About

Nobuhito Tabuchi is a scholar working on Organic Chemistry, Inorganic Chemistry and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Nobuhito Tabuchi has authored 18 papers receiving a total of 315 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Organic Chemistry, 6 papers in Inorganic Chemistry and 5 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Nobuhito Tabuchi's work include Asymmetric Synthesis and Catalysis (6 papers), Asymmetric Hydrogenation and Catalysis (6 papers) and Synthetic Organic Chemistry Methods (6 papers). Nobuhito Tabuchi is often cited by papers focused on Asymmetric Synthesis and Catalysis (6 papers), Asymmetric Hydrogenation and Catalysis (6 papers) and Synthetic Organic Chemistry Methods (6 papers). Nobuhito Tabuchi collaborates with scholars based in Japan. Nobuhito Tabuchi's co-authors include Yuji Hanzawa, Takeo Taguchi, Susumu Harada, Satoshi Noguchi, Kosuke Saito, Akira Murakami, Hiroshi Toshida, Yasuo Dobashi, Akira Dobashi and Daisuke Koike and has published in prestigious journals such as Angewandte Chemie International Edition, Langmuir and Tetrahedron.

In The Last Decade

Nobuhito Tabuchi

18 papers receiving 311 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nobuhito Tabuchi Japan 12 226 63 51 45 26 18 315
Shiao Y. Chow Sweden 11 204 0.9× 39 0.6× 22 0.4× 103 2.3× 25 1.0× 18 322
Hagen Hauptmann Germany 13 208 0.9× 94 1.5× 7 0.1× 88 2.0× 10 0.4× 28 370
Carlos Lázaro‐Milla Spain 14 405 1.8× 35 0.6× 8 0.2× 34 0.8× 87 3.3× 30 562
Min Li Leow Singapore 13 407 1.8× 40 0.6× 7 0.1× 118 2.6× 15 0.6× 15 491
Inna Perepichka Canada 8 265 1.2× 56 0.9× 7 0.1× 30 0.7× 5 0.2× 19 318
Alejandra Salerno Argentina 11 298 1.3× 18 0.3× 31 0.6× 67 1.5× 8 0.3× 39 343
Qingxuan Tang China 8 165 0.7× 35 0.6× 35 0.7× 46 1.0× 23 0.9× 15 309
Nisha Devi India 13 537 2.4× 24 0.4× 4 0.1× 241 5.4× 9 0.3× 21 588
Dafydd A. Thomas United Kingdom 8 197 0.9× 50 0.8× 5 0.1× 67 1.5× 7 0.3× 14 271
E Winkelmann Germany 5 130 0.6× 41 0.7× 8 0.2× 32 0.7× 6 0.2× 13 187

Countries citing papers authored by Nobuhito Tabuchi

Since Specialization
Citations

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

Fields of papers citing papers by Nobuhito Tabuchi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nobuhito Tabuchi

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

All Works

18 of 18 papers shown
1.
Yoshida, Masataka, et al.. (2020). Effect of Mineral-Oil Addition on Film Stability of Polar Lipid Constituents Derived from Meibum. Journal of Oleo Science. 69(5). 429–436. 1 indexed citations
2.
Yoshida, Masataka, et al.. (2019). Role of Endogenous Ingredients in Meibum and Film Structures on Stability of the Tear Film Lipid Layer against Lateral Compression. Langmuir. 35(25). 8445–8451. 14 indexed citations
3.
Tabuchi, Nobuhito, et al.. (2018). Membrane permeation of giant unilamellar vesicles and corneal epithelial cells with lipophilic vitamin nanoemulsions. Colloids and Surfaces B Biointerfaces. 169. 444–452. 18 indexed citations
4.
Toshida, Hiroshi, Toshinari Funaki, Koichi Ono, et al.. (2017). Efficacy and safety of retinol palmitate ophthalmic solution in the treatment of dry eye: a Japanese Phase II clinical trial. Drug Design Development and Therapy. Volume 11. 1871–1879. 18 indexed citations
5.
Tabuchi, Nobuhito, Hiroshi Toshida, Daisuke Koike, et al.. (2016). Effect of Retinol Palmitate on Corneal and Conjunctival Mucin Gene Expression in a Rat Dry Eye Model After Injury. Journal of Ocular Pharmacology and Therapeutics. 33(1). 24–33. 11 indexed citations
6.
Toshida, Hiroshi, Nobuhito Tabuchi, Daisuke Koike, et al.. (2012). The Effects of Vitamin A Compounds on Hyaluronic Acid Released from Cultured Rabbit Corneal Epithelial Cells and Keratocytes. Journal of Nutritional Science and Vitaminology. 58(4). 223–229. 14 indexed citations
7.
Tabuchi, Nobuhito, et al.. (2009). Adsorption of Actives in Ophthalmological Drugs for Over-The-Counter on Soft Contact Lens Surfaces. Journal of Oleo Science. 58(1). 43–52. 6 indexed citations
8.
Tabuchi, Nobuhito, et al.. (2003). Fractional determination of sodium chondroitin sulfate/hydroxypropylmethylcellulose mixture using Alucian Blue 8GX.. BUNSEKI KAGAKU. 52(4). 259–263. 2 indexed citations
9.
Hanzawa, Yuji, et al.. (2002). Pd-catalyzed regioselective acylation of α,β-unsaturated ketone derivatives by acylzirconocene chloride as an acyl group donor. Tetrahedron. 58(38). 7559–7571. 20 indexed citations
10.
Hanzawa, Yuji, et al.. (2001). Pd-catalyzed acylation of α,β-ynone with acylzirconocene chloride and one-pot formation of cyclopentenone derivatives. Tetrahedron Letters. 42(9). 1737–1739. 12 indexed citations
11.
Hanzawa, Yuji, Nobuhito Tabuchi, Kosuke Saito, Satoshi Noguchi, & Takeo Taguchi. (1999). Acylzirconocenchlorid als „unmaskiertes” Acylanion: enantioselektive 1,2-Addition anα,β-ungesättigte Ketone. Angewandte Chemie. 111(16). 2552–2555. 3 indexed citations
12.
Hanzawa, Yuji, Nobuhito Tabuchi, Kosuke Saito, Satoshi Noguchi, & Takeo Taguchi. (1999). Acylzirconocene Chloride as an “Unmasked” Acyl Anion: Enantioselective 1,2-Addition toα,β-Unsaturated Ketone Derivatives. Angewandte Chemie International Edition. 38(16). 2395–2398. 36 indexed citations
13.
Hanzawa, Yuji, Nobuhito Tabuchi, Kosuke Saito, Satoshi Noguchi, & Takeo Taguchi. (1999). Acylzirconocene Chloride as an “Unmasked” Acyl Anion: Enantioselective 1,2-Addition to ,-Unsaturated Ketone Derivatives. Angewandte Chemie International Edition. 38(16). 2395–2398. 1 indexed citations
14.
Harada, Susumu, et al.. (1998). Acylzirconocene Chloride as an “Unmasked” Acyl Anion. Angewandte Chemie International Edition. 37(12). 1696–1698. 57 indexed citations
15.
Harada, Susumu, Nobuhito Tabuchi, Takeo Taguchi, et al.. (1998). Hydrozirconation of alkenyloxirane derivatives: Preparation of cycloalkylmethanols. Tetrahedron. 54(5-6). 753–766. 18 indexed citations
16.
Hanzawa, Yuji, Nobuhito Tabuchi, & Takeo Taguchi. (1998). Palladium-catalyzed acylation reactions of α,β-unsaturated ketones with acylzirconocene chloride: Remarkable control of 1,2- and 1,4-selectivity by the catalyst. Tetrahedron Letters. 39(44). 8141–8144. 25 indexed citations
17.
Harada, Susumu, et al.. (1998). Acylzirconocenchlorid als „nichtmaskiertes” Acylanionenäquivalent. Angewandte Chemie. 110(12). 1796–1798. 6 indexed citations
18.
Hanzawa, Yuji, Nobuhito Tabuchi, & Takeo Taguchi. (1998). Palladium-catalyzed reactions of acylzirconocene chloride with organic halides. Tetrahedron Letters. 39(34). 6249–6252. 53 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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