Taichi Nakano

749 total citations
47 papers, 534 citations indexed

About

Taichi Nakano is a scholar working on Organic Chemistry, Inorganic Chemistry and Pharmaceutical Science. According to data from OpenAlex, Taichi Nakano has authored 47 papers receiving a total of 534 indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Organic Chemistry, 9 papers in Inorganic Chemistry and 7 papers in Pharmaceutical Science. Recurrent topics in Taichi Nakano's work include Synthetic Organic Chemistry Methods (13 papers), Organoboron and organosilicon chemistry (12 papers) and Chemical Synthesis and Reactions (12 papers). Taichi Nakano is often cited by papers focused on Synthetic Organic Chemistry Methods (13 papers), Organoboron and organosilicon chemistry (12 papers) and Chemical Synthesis and Reactions (12 papers). Taichi Nakano collaborates with scholars based in Japan. Taichi Nakano's co-authors include Yasuyoshi Nagai, Hideyuki Matsumoto, Hamao Watanabe, Takeshi Arai, Masatoshi Takahashi, Toshihiko Migita, Takashi Miyamoto, Miyuki Kasahara, Hiromichi Kono and Minoru Hasegawa and has published in prestigious journals such as Biochemical and Biophysical Research Communications, The Journal of Organic Chemistry and Tetrahedron Letters.

In The Last Decade

Taichi Nakano

47 papers receiving 511 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Taichi Nakano Japan 13 480 179 56 41 32 47 534
Saburo Nakanishi Japan 12 405 0.8× 192 1.1× 39 0.7× 47 1.1× 36 1.1× 63 479
Christophe Rousset United States 13 809 1.7× 267 1.5× 84 1.5× 34 0.8× 35 1.1× 18 869
Masato Oshima Japan 12 427 0.9× 237 1.3× 48 0.9× 31 0.8× 17 0.5× 27 511
Attila Aranyos Sweden 8 735 1.5× 308 1.7× 78 1.4× 32 0.8× 43 1.3× 9 808
Nicholas A. Cortese United States 11 458 1.0× 126 0.7× 116 2.1× 45 1.1× 42 1.3× 12 532
Go Hata United States 12 483 1.0× 226 1.3× 73 1.3× 35 0.9× 22 0.7× 21 553
Daniel A. Lev United States 9 487 1.0× 238 1.3× 58 1.0× 34 0.8× 20 0.6× 10 548
Michael G. Fickes United States 10 524 1.1× 323 1.8× 72 1.3× 49 1.2× 25 0.8× 13 614
John C. Tebby United Kingdom 15 656 1.4× 187 1.0× 76 1.4× 39 1.0× 39 1.2× 91 756
A Meisters Australia 14 336 0.7× 107 0.6× 62 1.1× 29 0.7× 24 0.8× 27 444

Countries citing papers authored by Taichi Nakano

Since Specialization
Citations

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

Fields of papers citing papers by Taichi Nakano

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Taichi Nakano

This figure shows the co-authorship network connecting the top 25 collaborators of Taichi Nakano. A scholar is included among the top collaborators of Taichi Nakano 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 Taichi Nakano. Taichi Nakano 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.
Ito, Ryo, Masanobu Morita, Taichi Nakano, et al.. (2020). The establishment of a novel high-throughput screening system using RNA-guided genome editing to identify chemicals that suppress aldosterone synthase expression. Biochemical and Biophysical Research Communications. 534. 672–679. 6 indexed citations
2.
3.
Nakano, Taichi, et al.. (2005). Acid‐dependent selective formation of trans‐aryl(germyl)ethenes or 1‐aryl‐1‐germylethenes by the protodestannylation of (Z)‐germyl(stannyl)ethenes. Applied Organometallic Chemistry. 19(4). 563–569. 6 indexed citations
4.
Nakano, Taichi, et al.. (2001). HIGH-YIELD FORMATION OF ALLYLIC GERMANES BY Pd2(dba)3-CATALYZED REACTION OF ALLYLIC HALIDES WITH DIGERMANES. Main Group Metal Chemistry. 24(2). 67–76. 2 indexed citations
5.
6.
Nakano, Taichi, et al.. (1989). A convenient synthesis of .GAMMA.-alkyl-.ALPHA.-hydroxy-.GAMMA.-lactones as a food intake-control substance.. Chemistry Letters. 567–568. 1 indexed citations
7.
Nakano, Taichi, et al.. (1987). Free Radical Addition of 2-Bromoalkanoic Acids to Alkenes. Bulletin of the Chemical Society of Japan. 60(3). 1049–1052. 12 indexed citations
8.
Matsumoto, Hideyuki, Miyuki Kasahara, Masatoshi Takahashi, et al.. (1983). Conversion of disilanes to functional monosilanes. Journal of Organometallic Chemistry. 250(1). 99–107. 26 indexed citations
9.
Nakano, Taichi, et al.. (1982). THE PALLADIUM(0)-CATALYZED REDUCTIVE COUPLING OF HALIDES USING sym-DICHLOROTETRAMETHYLDISILANE AS A REDUCING AGENT. Chemistry Letters. 11(5). 613–616. 14 indexed citations
10.
Matsumoto, Hideyuki, et al.. (1982). A NEW REDUCTIVE SILYLATION OF p-QUINONES WITH HEXAMETHYLDISILANE CATALYZED BY IODINE. Chemistry Letters. 11(4). 533–534. 9 indexed citations
11.
Nakano, Taichi, et al.. (1981). FREE RADICAL ADDITION OF α-BROMOCARBOXYLIC ACIDS TO OLEFINS LEADING TO γ-BUTYROLACTONES. Chemistry Letters. 10(3). 415–418. 5 indexed citations
12.
Matsumoto, Hideyuki, et al.. (1980). A FACILE SILYLATION OF CARBOXYLIC ACIDS WITH HEXAMETHYLDISILOXANE. Chemistry Letters. 9(12). 1475–1478. 8 indexed citations
13.
Matsumoto, Hideyuki, et al.. (1979). A one-step and convenient synthesis of .ALPHA.-chloro-.GAMMA.-butyrolactones, precursors of .DELTA..ALPHA.,.BETA.-butenolides and .ALPHA.-methylene .GAMMA.-butyrolactones.. Chemistry Letters. 1011–1014. 1 indexed citations
14.
15.
Matsumoto, Hideyuki, et al.. (1978). SIDE-CHAIN MONOCHLORINATION OF TOLUENES WITH SULFURYL CHLORIDE CATALYZED BY TETRAKIS(TRIPHENYLPHOSPHINE)PALLADIUM(0). Chemistry Letters. 7(2). 223–226. 9 indexed citations
16.
Matsumoto, Hideyuki, et al.. (1978). Radical reactions in the coordination sphere. 4. Addition of carbon tetrachloride to cis-cyclooctene catalyzed by dichlorotris(triphenylphosphine)ruthenium(II). The Journal of Organic Chemistry. 43(9). 1734–1736. 35 indexed citations
17.
Matsumoto, Hideyuki, et al.. (1978). ADDITION OF CARBON TETRACHLORIDE TO CONJUGATED 1,3-DIENES CATALYZED BY DICHLOROTRIS(TRIPHENYLPHOSPHINE)RUTHENIUM(II). Chemistry Letters. 7(1). 115–116. 18 indexed citations
18.
Watanabe, Hamao, et al.. (1974). The reaction of organosilicon hydrides with carbomethoxycarbene generated from methyl diazoacetate. Journal of Organometallic Chemistry. 69(3). 389–396. 19 indexed citations
19.
Nagai, Yasuyoshi, Hideyuki Matsumoto, Taichi Nakano, & Hamao Watanabe. (1972). Polar Substituent Constants for Substituted Phenyl Groups. The Extended Taft Equation.. Bulletin of the Chemical Society of Japan. 45(8). 2560–2565. 20 indexed citations
20.
Nakano, Taichi, et al.. (1972). Correlaiton of Hammett σ constants withNMR parameters for substituted phenylsilanes, phenylmethylsilanes and phenyldimethylsilanes. Journal of Organometallic Chemistry. 35(1). 81–90. 28 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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