Nobuaki Kambe

11.8k total citations
328 papers, 9.3k citations indexed

About

Nobuaki Kambe is a scholar working on Organic Chemistry, Toxicology and Inorganic Chemistry. According to data from OpenAlex, Nobuaki Kambe has authored 328 papers receiving a total of 9.3k indexed citations (citations by other indexed papers that have themselves been cited), including 304 papers in Organic Chemistry, 72 papers in Toxicology and 48 papers in Inorganic Chemistry. Recurrent topics in Nobuaki Kambe's work include Sulfur-Based Synthesis Techniques (107 papers), Catalytic C–H Functionalization Methods (102 papers) and Catalytic Cross-Coupling Reactions (82 papers). Nobuaki Kambe is often cited by papers focused on Sulfur-Based Synthesis Techniques (107 papers), Catalytic C–H Functionalization Methods (102 papers) and Catalytic Cross-Coupling Reactions (82 papers). Nobuaki Kambe collaborates with scholars based in Japan, China and United States. Nobuaki Kambe's co-authors include Jun Terao, Hitoshi Kuniyasu, Noboru Sonoda, Takanori Iwasaki, Akiya Ogawa, Ilhyong Ryu, Aki Ikumi, Renhua Qiu, Shin‐ichi Fujiwara and Hirohisa Todo and has published in prestigious journals such as Journal of the American Chemical Society, Chemical Society Reviews and Angewandte Chemie International Edition.

In The Last Decade

Nobuaki Kambe

321 papers receiving 9.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nobuaki Kambe Japan 48 8.5k 1.5k 1.1k 1.0k 584 328 9.3k
Shinji Murai Japan 62 11.8k 1.4× 4.0k 2.8× 405 0.4× 475 0.5× 602 1.0× 292 12.8k
David J. Procter United Kingdom 63 10.8k 1.3× 1.6k 1.1× 227 0.2× 971 0.9× 440 0.8× 230 12.1k
L. Brandsma Netherlands 35 5.6k 0.7× 1.1k 0.7× 230 0.2× 433 0.4× 454 0.8× 359 6.5k
Kouichi Ohe Japan 48 6.0k 0.7× 1.4k 1.0× 269 0.3× 171 0.2× 789 1.4× 202 6.8k
Valentine G. Nenajdenko Russia 42 6.3k 0.7× 1.2k 0.8× 169 0.2× 2.3k 2.2× 921 1.6× 435 7.8k
Yoshiaki Nishibayashi Japan 74 13.4k 1.6× 6.5k 4.5× 503 0.5× 579 0.6× 2.6k 4.5× 328 18.1k
Toshikazu Hirao Japan 45 6.0k 0.7× 1.8k 1.2× 176 0.2× 258 0.2× 1.7k 2.9× 284 7.6k
Alexander Villinger Germany 40 6.8k 0.8× 3.7k 2.6× 142 0.1× 436 0.4× 637 1.1× 533 8.0k
Chao‐Guo Yan China 42 6.6k 0.8× 1.3k 0.9× 322 0.3× 292 0.3× 1.7k 2.9× 440 8.3k
Paolo Melchiorre Spain 80 19.4k 2.3× 3.3k 2.3× 162 0.2× 1.7k 1.7× 927 1.6× 209 20.6k

Countries citing papers authored by Nobuaki Kambe

Since Specialization
Citations

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

Fields of papers citing papers by Nobuaki Kambe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nobuaki Kambe

This figure shows the co-authorship network connecting the top 25 collaborators of Nobuaki Kambe. A scholar is included among the top collaborators of Nobuaki Kambe 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 Nobuaki Kambe. Nobuaki Kambe 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.
Zhou, Wenjun, Youwen Chen, Youwen Chen, et al.. (2025). Synthesis and application of organostibines. Coordination Chemistry Reviews. 548. 217200–217200.
2.
Yang, Tianbao, Chunyi Tong, Shuang‐Feng Yin, et al.. (2024). Rapid copper-catalyzed friedel-crafts alkylation of indoles in 25 Minutes. Journal of Organometallic Chemistry. 1011. 123119–123119. 2 indexed citations
3.
Iwasaki, Takanori & Nobuaki Kambe. (2023). Cross‐ and Multi‐Coupling Reactions Using Monofluoroalkanes. The Chemical Record. 23(9). e202300033–e202300033. 2 indexed citations
4.
Peng, Lifen, Lifen Peng, Zhi Xu, et al.. (2022). One-pot synthesis of phosphorylnaphth[2,1-d]oxazoles and products as P,N-ligands in C–N and C–C formation. Organic & Biomolecular Chemistry. 20(20). 4110–4114. 2 indexed citations
5.
Lu, Dingheng, Tianbao Yang, Chenghan Li, et al.. (2022). A pH-Dependent rhodamine fluorophore with antiproliferative activity of bladder cancer in Vitro/Vivo and apoptosis mechanism. European Journal of Medicinal Chemistry. 236. 114293–114293. 6 indexed citations
6.
Deng, Wei, Renhua Qiu, Tianbao Yang, et al.. (2022). UV-Light-Induced Dehydrogenative N-Acylation of Amines with 2-Nitrobenzaldehydes To Give 2-Aminobenzamides. Synthesis. 54(10). 2361–2372. 6 indexed citations
7.
Iwasaki, Takanori, et al.. (2013). Co-Catalyzed Cross-Coupling of Alkyl Halides with Tertiary Alkyl Grignard Reagents Using a 1,3-Butadiene Additive. Journal of the American Chemical Society. 135(26). 9604–9607. 102 indexed citations
8.
Iwasaki, Takanori, V. Prakash Reddy, Yukari Fujimoto, et al.. (2013). NickelButadiene Catalytic System for the Cross‐Coupling of Bromoalkanoic Acids with Alkyl Grignard Reagents: A Practical and Versatile Method for Preparing Fatty Acids. Chemistry - A European Journal. 19(9). 2956–2960. 18 indexed citations
9.
Fujiwara, Shin‐ichi, et al.. (2012). Palladium-catalyzed vinylselenation of allenes. Tetrahedron. 68(51). 10523–10529. 6 indexed citations
10.
Terao, Jun, Hirohisa Todo, Shameem Ara Begum, Hitoshi Kuniyasu, & Nobuaki Kambe. (2007). Copper‐Catalyzed Cross‐Coupling Reaction of Grignard Reagents with Primary‐Alkyl Halides: Remarkable Effect of 1‐Phenylpropyne. Angewandte Chemie. 119(12). 2132–2135. 173 indexed citations
11.
Kuniyasu, Hitoshi, et al.. (2007). Definitive Evidence for the Insertion of Terminal Alkynes into ArylSPt Bonds: “o‐Halogen Effect” in Stoichiometric and Catalytic Reactions. Angewandte Chemie International Edition. 46(31). 5929–5933. 40 indexed citations
12.
Terao, Jun, et al.. (2004). Palladium-Catalyzed Dimerization Disilylation of 1,3-Butadiene with Chlorosilanes. Organic Letters. 6(19). 3341–3344. 14 indexed citations
13.
Ryu, Ilhyong, et al.. (1997). Synthesis of macrocyclic ketoesters by an n + 1 strategy based on free-radical carbonylation. Tetrahedron. 53(43). 14615–14626. 16 indexed citations
14.
Maeda, Hajime, Nobuaki Kambe, Noboru Sonoda, Shin‐ichi Fujiwara, & Tsutomu Shin‐ike. (1997). Synthesis of 1,3-selenazoles and 2-imidazolin-5-selones from isoselenocyanates and isocyanides. Tetrahedron. 53(40). 13667–13680. 24 indexed citations
15.
Ryu, Ilhyong, et al.. (1997). Intramolecular Homolytic Substitution Behavior of Acyl Radicals at Sulfur:  New Carbonylative Access to γ-Thiolactones. The Journal of Organic Chemistry. 62(22). 7550–7551. 40 indexed citations
16.
Kambe, Nobuaki, et al.. (1995). Synthesis and Structures of Tricyclic Diureas. The Journal of Organic Chemistry. 60(21). 7058–7062. 13 indexed citations
17.
Kuniyasu, Hitoshi, et al.. (1992). The first example of transition-metal-catalyzed addition of aromatic thiols to acetylenes. Journal of the American Chemical Society. 114(14). 5902–5903. 208 indexed citations
18.
Nakahira, Hiroyuki, et al.. (1991). β‐Lithioketoenolate: Erzeugung und Reaktionen mit Elektrophilen. Angewandte Chemie. 103(2). 178–179. 1 indexed citations
19.
Kambe, Nobuaki, et al.. (1987). A new reduction with hydrogen telluride.. NIPPON KAGAKU KAISHI. 1152–1162. 2 indexed citations
20.
Miyoshi, Noritaka, Tetsuya Yamamoto, Nobuaki Kambe, Shinji Murai, & Noboru Sonoda. (1982). A convenient method for the synthesis of α-phenylselenenyl carbonyl compounds. Tetrahedron Letters. 23(46). 4813–4816. 24 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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