Mamoru Kaname

518 total citations
29 papers, 418 citations indexed

About

Mamoru Kaname is a scholar working on Organic Chemistry, Molecular Biology and Toxicology. According to data from OpenAlex, Mamoru Kaname has authored 29 papers receiving a total of 418 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Organic Chemistry, 9 papers in Molecular Biology and 9 papers in Toxicology. Recurrent topics in Mamoru Kaname's work include Sulfur-Based Synthesis Techniques (10 papers), Organoselenium and organotellurium chemistry (9 papers) and Synthesis and Reactivity of Sulfur-Containing Compounds (5 papers). Mamoru Kaname is often cited by papers focused on Sulfur-Based Synthesis Techniques (10 papers), Organoselenium and organotellurium chemistry (9 papers) and Synthesis and Reactivity of Sulfur-Containing Compounds (5 papers). Mamoru Kaname collaborates with scholars based in Japan. Mamoru Kaname's co-authors include Haruki Sashida, Shigeyuki Yoshifuji, Mao Minoura, Hirokazu Suzuki, Takashi Tsuchiya and Chao Pan and has published in prestigious journals such as Tetrahedron, Molecules and Tetrahedron Letters.

In The Last Decade

Mamoru Kaname

28 papers receiving 406 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mamoru Kaname Japan 14 367 119 108 69 20 29 418
Xinyue Fang China 12 350 1.0× 70 0.6× 93 0.9× 57 0.8× 19 0.9× 16 415
Basi Reddy India 12 428 1.2× 67 0.6× 27 0.3× 29 0.4× 33 1.6× 29 458
Lorenzo Caruana Italy 12 1.1k 2.9× 82 0.7× 77 0.7× 98 1.4× 33 1.6× 13 1.1k
Senthil Narayanaperumal Brazil 13 352 1.0× 44 0.4× 169 1.6× 54 0.8× 4 0.2× 16 390
Divya K. Nair India 10 476 1.3× 93 0.8× 108 1.0× 16 0.2× 31 1.6× 15 539
Carlos Jarava‐Barrera Spain 9 476 1.3× 48 0.4× 25 0.2× 64 0.9× 12 0.6× 12 525
Thomas Buyck Switzerland 8 546 1.5× 89 0.7× 27 0.3× 108 1.6× 12 0.6× 10 594
Manisha Swain India 12 411 1.1× 64 0.5× 16 0.1× 51 0.7× 44 2.2× 17 437
Mi Lian China 9 572 1.6× 57 0.5× 19 0.2× 38 0.6× 11 0.6× 11 594
Fang‐Xin Wang China 10 815 2.2× 69 0.6× 49 0.5× 32 0.5× 58 2.9× 17 850

Countries citing papers authored by Mamoru Kaname

Since Specialization
Citations

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

Fields of papers citing papers by Mamoru Kaname

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mamoru Kaname

This figure shows the co-authorship network connecting the top 25 collaborators of Mamoru Kaname. A scholar is included among the top collaborators of Mamoru Kaname 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 Mamoru Kaname. Mamoru Kaname 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.
2.
Kaname, Mamoru, Shigeyuki Yoshifuji, & Haruki Sashida. (2011). Ruthenium Tetroxide Oxidation of <i>N</i>-Acyl Amines and Related Compounds. Journal of Synthetic Organic Chemistry Japan. 69(10). 1109–1121.
3.
Kaname, Mamoru & Haruki Sashida. (2011). Tandem addition–cyclization of o-ethynylphenyl isothiocyanates with N nucleophiles; difference of cyclization mode between primary and secondary amines. Tetrahedron Letters. 53(7). 748–751. 16 indexed citations
4.
5.
Kaname, Mamoru & Haruki Sashida. (2011). Tandem addition–cyclization of o-ethynylphenyllithiums and isoselenocyanates: a convenient preparation of functionalized benzo[c]selenophenes. Tetrahedron Letters. 52(26). 3279–3282. 13 indexed citations
6.
Sashida, Haruki, et al.. (2010). Novel Oxidative Ring Opening Reaction of 1H-Isotelluro-chromenes to Bis(o-formylstyryl) Ditellurides. Molecules. 15(3). 1466–1472. 11 indexed citations
7.
Kaname, Mamoru, Mao Minoura, & Haruki Sashida. (2010). One-pot copper-catalyzed tandem addition–cyclization of 2-iodoanilines with isoselenocyanates for the practical preparation of 2-aminobenzoselenazoles. Tetrahedron Letters. 52(4). 505–508. 36 indexed citations
8.
Sashida, Haruki, et al.. (2010). A straightforward double intramolecular cyclization of dibenzyl dichalcogenols into a triple bond. Tetrahedron. 66(27-28). 5149–5157. 18 indexed citations
9.
Sashida, Haruki, et al.. (2010). 2-Substituted Isotellurochromenium Salt Derivatives: Preparations, Structures, Spectroscopic Properties. Heterocycles. 80(2). 1339–1339. 11 indexed citations
10.
Sashida, Haruki, Chao Pan, Mamoru Kaname, & Mao Minoura. (2010). A Facile and Practical Solvent-Free One-Pot Synthesis of (Z)-4-Methylene-3-selenaquinoline Derivatives from o-Ethynylanilines and Isoselenocyanates¹. Synthesis. 2010(18). 3091–3096. 14 indexed citations
11.
Kaname, Mamoru, Shigeyuki Yoshifuji, & Haruki Sashida. (2008). Ruthenium tetroxide oxidation of cyclic N-acylamines by a single layer method: formation of ω-amino acids. Tetrahedron Letters. 49(17). 2786–2788. 24 indexed citations
12.
Sashida, Haruki, et al.. (2008). Ruthenium Tetroxide Oxidation of N-Acyl Cyclic Amine-2-phosphonic Acid Diesters. Heterocycles. 76(1). 429–429. 3 indexed citations
13.
Sashida, Haruki, et al.. (2008). A New One-Pot Synthetic Methodfor Selenium-Containing Medium-Sized α,β-UnsaturatedCyclic Ketones. Synthesis. 2008(20). 3229–3236. 30 indexed citations
14.
Kaname, Mamoru, et al.. (2004). Synthesis of Hexahydropyridazine-3-phosphonic Acid. Chemical and Pharmaceutical Bulletin. 52(1). 160–162. 3 indexed citations
15.
Kaname, Mamoru, et al.. (2001). Chemical Conversion of Cyclic .ALPHA.-Amino Acids to Cyclic .ALPHA.-Aminophosphonic Acids.. Chemical and Pharmaceutical Bulletin. 49(5). 531–536. 20 indexed citations
16.
Yoshifuji, Shigeyuki & Mamoru Kaname. (1995). Stereospecific Synthesis of (R)- and (S)-Baclofen and (R)- and (S)-PCPGABA (4-Amino-2-(4-chlorophenyl)butyric Acid) via (R)- and (S)-3-(4-Chlorophenyl)pyrrolidines.. Chemical and Pharmaceutical Bulletin. 43(8). 1302–1306. 29 indexed citations
17.
Yoshifuji, Shigeyuki & Mamoru Kaname. (1995). Asymmetric Synthesis of Lycoperdic Acid.. Chemical and Pharmaceutical Bulletin. 43(10). 1617–1620. 29 indexed citations
18.
Kaname, Mamoru & Shigeyuki Yoshifuji. (1992). First synthesis of lycoperdic acid. Tetrahedron Letters. 33(52). 8103–8104. 32 indexed citations
19.
Sashida, Haruki, Mamoru Kaname, & Takashi Tsuchiya. (1990). Studies of seven-membered heterocycles. XXXII. Synthesis of N-unsubstituted 1H-1,4-benzodiazepines stabilized by intramolecular hydrogen bonding.. Chemical and Pharmaceutical Bulletin. 38(11). 2919–2925. 6 indexed citations
20.
Sashida, Haruki, Mamoru Kaname, & Takashi Tsuchiya. (1987). The first examples of isolated N-unsubstituted 1H-1,4-benzodiazepines.. Chemical and Pharmaceutical Bulletin. 35(11). 4676–4679. 1 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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