Nobuhiro Kanomata

1.0k total citations
44 papers, 819 citations indexed

About

Nobuhiro Kanomata is a scholar working on Organic Chemistry, Molecular Biology and Biomedical Engineering. According to data from OpenAlex, Nobuhiro Kanomata has authored 44 papers receiving a total of 819 indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Organic Chemistry, 11 papers in Molecular Biology and 4 papers in Biomedical Engineering. Recurrent topics in Nobuhiro Kanomata's work include Asymmetric Synthesis and Catalysis (9 papers), Synthetic Organic Chemistry Methods (9 papers) and Synthesis and Properties of Aromatic Compounds (6 papers). Nobuhiro Kanomata is often cited by papers focused on Asymmetric Synthesis and Catalysis (9 papers), Synthetic Organic Chemistry Methods (9 papers) and Synthesis and Properties of Aromatic Compounds (6 papers). Nobuhiro Kanomata collaborates with scholars based in Japan, United States and Belarus. Nobuhiro Kanomata's co-authors include Tadashi Nakata, Makoto Nitta, Tsuyoshi Ueda, Masaru Tada, Tatsuya Hattori, Naokazu Inoue, Reiko Kobayakawa, Ko Kobayakawa, Akari Asaba and Takefumi Kikusui and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Angewandte Chemie International Edition.

In The Last Decade

Nobuhiro Kanomata

41 papers receiving 774 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nobuhiro Kanomata Japan 16 630 178 94 92 91 44 819
Akio Minato Japan 15 1.1k 1.7× 179 1.0× 195 2.1× 62 0.7× 49 0.5× 27 1.6k
María Eugenia Castro Mexico 16 170 0.3× 90 0.5× 176 1.9× 104 1.1× 45 0.5× 81 719
Frank Lehmann Germany 17 220 0.3× 242 1.4× 8 0.1× 90 1.0× 92 1.0× 29 775
Qing‐Qing Yang China 25 1.7k 2.8× 155 0.9× 239 2.5× 39 0.4× 26 0.3× 73 2.0k
James P. Wepsiec United States 11 691 1.1× 339 1.9× 88 0.9× 182 2.0× 35 0.4× 18 972
Yasushi Sugiura Japan 9 536 0.9× 165 0.9× 106 1.1× 34 0.4× 47 0.5× 16 728
Eric Brenner France 21 1.1k 1.7× 279 1.6× 188 2.0× 44 0.5× 16 0.2× 44 1.3k
R. W. TURNER United Kingdom 16 407 0.6× 122 0.7× 169 1.8× 78 0.8× 14 0.2× 47 677
Graham J. Durant United States 18 443 0.7× 478 2.7× 50 0.5× 83 0.9× 9 0.1× 32 960

Countries citing papers authored by Nobuhiro Kanomata

Since Specialization
Citations

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

Fields of papers citing papers by Nobuhiro Kanomata

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nobuhiro Kanomata

This figure shows the co-authorship network connecting the top 25 collaborators of Nobuhiro Kanomata. A scholar is included among the top collaborators of Nobuhiro Kanomata 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 Nobuhiro Kanomata. Nobuhiro Kanomata 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.
Ogawa, Narihito, et al.. (2020). Biomimetic systems involving sequential redox reactions in glycolysis – the sulfur effect. Chemical Communications. 56(85). 12917–12920. 1 indexed citations
2.
Matsuo, Tomohiko, Tatsuya Hattori, Akari Asaba, et al.. (2015). Genetic dissection of pheromone processing reveals main olfactory system-mediated social behaviors in mice. Proceedings of the National Academy of Sciences. 112(3). E311–20. 68 indexed citations
3.
Kanomata, Nobuhiro, et al.. (2015). Remote steric effects of C2-symmetric planar-chiral terpyridine ligands on copper-catalyzed asymmetric cyclopropanation reactions. Tetrahedron Letters. 56(14). 1898–1903. 6 indexed citations
4.
Maeda, Ryo, et al.. (2011). Planar-to-Planar Chirality Transfer in the Excited State. Enantiodifferentiating Photoisomerization of Cyclooctenes Sensitized by Planar-Chiral Paracyclophane. Journal of the American Chemical Society. 133(27). 10379–10381. 47 indexed citations
5.
Kanomata, Nobuhiro, et al.. (2011). Formal total synthesis of aspergillide A. Tetrahedron Asymmetry. 22(2). 246–251. 18 indexed citations
6.
Kanomata, Nobuhiro, et al.. (2009). Synthesis of planar-chiral bridged bipyridines and terpyridines by metal-mediated coupling reactions of pyridinophanes. Tetrahedron Letters. 50(23). 2740–2743. 10 indexed citations
7.
Emoto, Makoto, et al.. (2009). Novel chemoembolization using calcium‐phosphate ceramic microsphere incorporating TNP‐470, an anti‐angiogenic agent. Cancer Science. 101(4). 984–990. 8 indexed citations
8.
Kanomata, Nobuhiro, et al.. (2008). Synchronized stereocontrol of planar chirality by crystallization-induced asymmetric transformation. Tetrahedron Letters. 50(4). 409–412. 21 indexed citations
9.
Kanomata, Nobuhiro, et al.. (2006). Synthesis of bridged nicotinates having [n](2,5)pyridinophane skeletons (n=8–14). Tetrahedron. 62(17). 4128–4138. 11 indexed citations
10.
Kanomata, Nobuhiro. (2003). Studies on Syntheses and Functional Properties of Structurally Unique Nitrogen Aromatics. Journal of Synthetic Organic Chemistry Japan. 61(4). 352–359. 2 indexed citations
11.
Kanomata, Nobuhiro & Tadashi Nakata. (2000). A Compact Chemical Miniature of a Holoenzyme, Coenzyme NADH Linked Dehydrogenase. Design and Synthesis of Bridged NADH Models and Their Highly Enantioselective Reduction1. Journal of the American Chemical Society. 122(19). 4563–4568. 89 indexed citations
12.
Kanomata, Nobuhiro. (1999). Biomimetic Oxidation and Asymmetric Reduction with Coenzyme NAD Analogs.. Journal of Synthetic Organic Chemistry Japan. 57(6). 512–522. 5 indexed citations
13.
14.
Kanomata, Nobuhiro, et al.. (1998). Biomimetic Oxidation of Aldehyde with NAD+ Models: Glycolysis-Type Hydrogen Transfer in an NAD+/NADH Model System. Angewandte Chemie International Edition. 37(10). 1410–1412. 23 indexed citations
15.
LUKIN, K. A., Jianchang Li, Philip E. Eaton, et al.. (1997). Synthesis and Chemistry of 1,3,5,7-Tetranitrocubane Including Measurement of Its Acidity, Formation of o-Nitro Anions, and the First Preparations of Pentanitrocubane and Hexanitrocubane1. Journal of the American Chemical Society. 119(41). 9591–9602. 54 indexed citations
16.
Kanomata, Nobuhiro & Tadashi Nakata. (1997). Hochenantioselektive Reduktion mit neuartigen verbrückten NADH‐Modellverbindungen. Angewandte Chemie. 109(11). 1263–1266. 12 indexed citations
17.
Balaban, Alexandrù T., et al.. (1992). Bridge Flipping Data from Dynamic 1H‐NMR Spectra of 2,6‐Dimethyl‐[9](3,5)‐Pyridophane and its Pyrylium and N‐Methylpyridinium Analogs. Bulletin des Sociétés Chimiques Belges. 101(12). 1047–1051. 1 indexed citations
18.
Kanomata, Nobuhiro, et al.. (1992). On the reaction of (vinylimino)phosphorane and related compounds. 22. Syntheses and structural studies of methanocycloundeca[b]pyrrole ring systems. The Journal of Organic Chemistry. 57(20). 5313–5318. 7 indexed citations
19.
20.
Nitta, Makoto, et al.. (1987). Synthesis and Properties of Norcaradiene-Cycloheptatriene System Fused with Isoxazole Ring. Heterocycles. 26(12). 3105–3105.

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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