Naoki Kakusawa

1.1k total citations
64 papers, 839 citations indexed

About

Naoki Kakusawa is a scholar working on Organic Chemistry, Toxicology and Inorganic Chemistry. According to data from OpenAlex, Naoki Kakusawa has authored 64 papers receiving a total of 839 indexed citations (citations by other indexed papers that have themselves been cited), including 62 papers in Organic Chemistry, 9 papers in Toxicology and 8 papers in Inorganic Chemistry. Recurrent topics in Naoki Kakusawa's work include Catalytic Cross-Coupling Reactions (23 papers), Sulfur-Based Synthesis Techniques (19 papers) and Catalytic C–H Functionalization Methods (17 papers). Naoki Kakusawa is often cited by papers focused on Catalytic Cross-Coupling Reactions (23 papers), Sulfur-Based Synthesis Techniques (19 papers) and Catalytic C–H Functionalization Methods (17 papers). Naoki Kakusawa collaborates with scholars based in Japan. Naoki Kakusawa's co-authors include Jyoji Kurita, Shuji Yasuike, Mio Matsumura, Kentaro Yamaguchi, Yuki Murata, Takashi Tsuchiya, Hiroko Seki, Masatoshi Kawahata, Yuki Kitamura and Atsuya Muranaka and has published in prestigious journals such as Tetrahedron, The Journal of Physical Chemistry A and Tetrahedron Letters.

In The Last Decade

Naoki Kakusawa

62 papers receiving 822 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Naoki Kakusawa Japan 17 789 187 94 93 49 64 839
Osamu Niyomura Japan 14 490 0.6× 193 1.0× 41 0.4× 147 1.6× 24 0.5× 29 554
Morgan Donnard France 14 924 1.2× 148 0.8× 110 1.2× 24 0.3× 25 0.5× 44 1.0k
George Y. Li United States 8 1.0k 1.3× 235 1.3× 80 0.9× 35 0.4× 18 0.4× 8 1.1k
M. N. V. Sastry Taiwan 12 1.1k 1.4× 110 0.6× 111 1.2× 45 0.5× 10 0.2× 18 1.1k
Shiro Matsukawa Japan 17 622 0.8× 281 1.5× 82 0.9× 20 0.2× 32 0.7× 40 742
Jörg Rust Germany 15 516 0.7× 213 1.1× 42 0.4× 21 0.2× 140 2.9× 32 614
Rahul Kadu India 12 387 0.5× 130 0.7× 32 0.3× 67 0.7× 126 2.6× 19 452
Stéphane Perrio France 19 864 1.1× 107 0.6× 88 0.9× 30 0.3× 15 0.3× 44 936
Thiruvellore Thatai Jayanth Taiwan 11 975 1.2× 86 0.5× 36 0.4× 46 0.5× 17 0.3× 11 1.0k
L. Yu. Ukhin Russia 10 293 0.4× 62 0.3× 67 0.7× 27 0.3× 40 0.8× 97 408

Countries citing papers authored by Naoki Kakusawa

Since Specialization
Citations

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

Fields of papers citing papers by Naoki Kakusawa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Naoki Kakusawa

This figure shows the co-authorship network connecting the top 25 collaborators of Naoki Kakusawa. A scholar is included among the top collaborators of Naoki Kakusawa 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 Naoki Kakusawa. Naoki Kakusawa 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.
Matsumura, Mio, Masatoshi Kawahata, Yuki Murata, et al.. (2017). Antimony–lithium exchange reaction: Synthesis of 1,4,5-trisubstituted-1,2,3-triazoles by triazolyllithium with electrophiles. Journal of Organometallic Chemistry. 834. 83–87. 12 indexed citations
2.
Takahashi, Tsutomu, M. Hasegawa, Mio Matsumura, et al.. (2017). Synthesis, antitumor activity, and cytotoxicity of 4-substituted 1-benzyl-5-diphenylstibano-1H-1,2,3-triazoles. Bioorganic & Medicinal Chemistry Letters. 28(2). 152–154. 25 indexed citations
3.
Kitamura, Yuki, Mio Matsumura, Yuki Murata, et al.. (2017). A versatile synthesis of triarylantimony difluorides by fluorination of triarylstibanes with nitrosyl tetrafluoroborate and their antitumor activity. Journal of Fluorine Chemistry. 199. 1–6. 11 indexed citations
4.
Matsumura, Mio, Atsuya Muranaka, Naoki Kakusawa, et al.. (2017). Synthesis and photophysical properties of novel benzophospholo[3,2-b]indole derivatives. Beilstein Journal of Organic Chemistry. 13. 2304–2309. 13 indexed citations
5.
Murata, Yuki, et al.. (2017). Microwave-Assisted Debromination of α-Bromoketones with Triarylstibanes in Water. Chemical and Pharmaceutical Bulletin. 65(11). 1081–1084. 1 indexed citations
6.
Matsumura, Mio, Yuki Uchida, Masatoshi Kawahata, et al.. (2016). Copper-catalyzed [3 + 2] cycloaddition of (phenylethynyl)di-p-tolylstibane with organic azides. Beilstein Journal of Organic Chemistry. 12. 1309–1313. 14 indexed citations
7.
Yasuike, Shuji, et al.. (2015). Synthesis of Unsymmetrical Diaryl Selenides: Copper-Catalyzed Se-Arylation of Diaryl Diselenides with Triarylbismuthanes. Synthesis. 48(5). 730–736. 14 indexed citations
8.
Kakusawa, Naoki, Shuji Yasuike, Jyoji Kurita, et al.. (2012). A novel organobismuth compound, 1-[(2-di-p-tolylbismuthanophenyl)diazenyl]pyrrolidine, induces apoptosis in the human acute promyelocytic leukemia cell line NB4 via reactive oxygen species. Journal of Inorganic Biochemistry. 117. 77–84. 28 indexed citations
9.
Kurita, Jyoji, Shuji Yasuike, Satoshi Tsukada, Naoki Kakusawa, & Takashi Tsuchiya. (2012). Syntheses of Novel Dibenzo[d,f]heteronins Incorporating Group 15 and 16 Heavier Elements. Heterocycles. 86(2). 941–941.
10.
Kakusawa, Naoki, Shuji Yasuike, & Jyoji Kurita. (2010). ChemInform Abstract: Rhodium‐Catalyzed 1,2‐Addition of Sb‐Phenyl‐1,5‐azastibocines to Functionalized Aldehydes.. ChemInform. 41(21). 1 indexed citations
11.
Kurita, Jyoji, Naoki Kakusawa, & Shuji Yasuike. (2009). Rhodium-Catalyzed Conjugate Addition of Sb-Aryl-1,5-azastibocines to α,β-Unsaturated Carbonyl Compounds. Heterocycles. 77(2). 1269–1269. 8 indexed citations
12.
Kakusawa, Naoki & Jyoji Kurita. (2006). Carbonylative Cross-Coupling Reaction of Ethynylstibane with Aryl Iodides. Chemical and Pharmaceutical Bulletin. 54(5). 699–702. 13 indexed citations
13.
Kakusawa, Naoki & Jyoji Kurita. (2005). Microwave-Assisted Cross-Coupling Reaction of Alkynylstibanes with Aryl Iodides in the Presence of Ammonium Salt. Chemical and Pharmaceutical Bulletin. 53(10). 1369–1371. 11 indexed citations
14.
15.
Okajima, Satoru, Shuji Yasuike, Naoki Kakusawa, et al.. (2002). Synthesis of Sb-chiral organoantimony compounds having intramolecular Sb⋯N interaction and their separation into optically pure compounds via ortho-palladated benzylamine complexes. Journal of Organometallic Chemistry. 656(1-2). 234–242. 36 indexed citations
16.
Kakusawa, Naoki, et al.. (2000). Palladium-catalyzed cross-coupling reactions between 1-alkynylstibines and acyl chlorides. Tetrahedron Letters. 41(21). 4143–4146. 54 indexed citations
17.
Kurita, Jyoji, Naoki Kakusawa, Shuji Yasuike, & Takashi Tsuchiya. (1991). ChemInform Abstract: Reaction of Pyridazine N‐Oxides with Pyridynes: Formation of the First Examples of Pyridooxepins.. ChemInform. 22(14). 2 indexed citations
18.
Tanaka, Tomoko, K. HORITA, N. Nakajima, et al.. (1987). 12員環マクロライド抗生物質メチマイシンのアグリコンであるメチノリドの高立体選択的全合成 I D-グルコースからのPrelog-Djerassi型キラル合成中間体の合成. Chemical and Pharmaceutical Bulletin. 35(6). 2184–2195. 1 indexed citations
19.
Kurita, Jyoji, Naoki Kakusawa, & Takashi Tsuchiya. (1987). Reactions of 1H-1,2- and 1H-1,3-diazepines with dimethyl acetylenedicarboxylate. Journal of the Chemical Society Chemical Communications. 1880–1880. 1 indexed citations
20.
Oikawa, Yuji, Tatsuyoshi Tanaka, Kiyoshi Horita, et al.. (1987). Highly stereoselective total synthesis of methynolide, the aglycon of the 12-membered macrolide antibiotic methymycin. I. Synthesis of a prelog-djerassi lactone-type chiral intermediate from D-glucose.. Chemical and Pharmaceutical Bulletin. 35(6). 2184–2195. 11 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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