Yuuya Nagata

4.3k total citations
121 papers, 3.7k citations indexed

About

Yuuya Nagata is a scholar working on Organic Chemistry, Materials Chemistry and Spectroscopy. According to data from OpenAlex, Yuuya Nagata has authored 121 papers receiving a total of 3.7k indexed citations (citations by other indexed papers that have themselves been cited), including 93 papers in Organic Chemistry, 49 papers in Materials Chemistry and 22 papers in Spectroscopy. Recurrent topics in Yuuya Nagata's work include Synthesis and Properties of Aromatic Compounds (53 papers), Luminescence and Fluorescent Materials (32 papers) and Organoboron and organosilicon chemistry (17 papers). Yuuya Nagata is often cited by papers focused on Synthesis and Properties of Aromatic Compounds (53 papers), Luminescence and Fluorescent Materials (32 papers) and Organoboron and organosilicon chemistry (17 papers). Yuuya Nagata collaborates with scholars based in Japan, France and China. Yuuya Nagata's co-authors include Michinori Suginome, Takeshi Yamamoto, Yoshiki Chujo, Tsuyoshi Nishikawa, Tetsuya Yamada, Yuto Akai, Kenta Kokado, Atsushi Nagai, Tadashi Mori and Ryohei Takeda and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Nature Communications.

In The Last Decade

Yuuya Nagata

114 papers receiving 3.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yuuya Nagata Japan 32 2.9k 1.5k 759 704 434 121 3.7k
Max von Delius Germany 29 2.3k 0.8× 1.3k 0.8× 579 0.8× 493 0.7× 514 1.2× 81 3.3k
Massimo Baroncini Italy 29 1.9k 0.6× 2.1k 1.4× 986 1.3× 620 0.9× 525 1.2× 75 3.5k
Chuyang Cheng United States 24 1.8k 0.6× 1.1k 0.7× 736 1.0× 562 0.8× 395 0.9× 36 2.6k
Bo Song China 33 1.6k 0.6× 1.4k 0.9× 781 1.0× 731 1.0× 309 0.7× 79 2.9k
Michael Pittelkow Denmark 34 2.2k 0.8× 1.3k 0.8× 761 1.0× 253 0.4× 648 1.5× 110 3.3k
Paul R. McGonigal United Kingdom 30 2.3k 0.8× 2.4k 1.6× 1.1k 1.4× 551 0.8× 596 1.4× 59 4.2k
Simin Liu China 29 2.7k 0.9× 1.5k 1.0× 1.8k 2.3× 521 0.7× 664 1.5× 122 4.1k
Pi Wang China 24 1.3k 0.4× 1.9k 1.3× 1.8k 2.4× 643 0.9× 446 1.0× 64 3.2k
Kang Cai China 31 1.2k 0.4× 1.5k 1.0× 488 0.6× 417 0.6× 277 0.6× 84 2.7k
Víctor Blanco Spain 30 2.6k 0.9× 1.4k 0.9× 879 1.2× 458 0.7× 549 1.3× 89 3.3k

Countries citing papers authored by Yuuya Nagata

Since Specialization
Citations

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

Fields of papers citing papers by Yuuya Nagata

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yuuya Nagata

This figure shows the co-authorship network connecting the top 25 collaborators of Yuuya Nagata. A scholar is included among the top collaborators of Yuuya Nagata 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 Yuuya Nagata. Yuuya Nagata 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.
Nagata, Yuuya, et al.. (2025). iso -TEtraQuinoline ( i -TEQ): an inherently chiral N4 macrocyclic quinoline tetramer. Chemical Science. 16(24). 10714–10721. 2 indexed citations
2.
Mizuno, Yuta, et al.. (2025). Enumeration Approach to Atom-to-Atom Mapping Accelerated by Ising Computing. Journal of Chemical Information and Modeling. 65(4). 1901–1910.
3.
Kawano, Kenichi, Katsumi Matsuzaki, Yuuya Nagata, et al.. (2025). Helicene–Fluorescein Hybrids: A Reversible Base‐Triggered (Chir)optical Switch with Sign Inversion of Circularly Polarized Luminescence. Chemistry - A European Journal. 31(17). e202500335–e202500335. 3 indexed citations
4.
5.
Šámal, Michal, Marzena Banasiewicz, Irena Deperasińska, et al.. (2024). Carbonyl mediated fluorescence in aceno[ n ]helicenones and fluoreno[ n ]helicenes. Chemical Science. 15(25). 9842–9850. 3 indexed citations
6.
Inoue, Rintaro, Yuuya Nagata, Taiki Tominaga, et al.. (2024). Dynamics of side chains in poly(quinoxaline-2,3-diyl)s studied via quasielastic neutron scattering. The Journal of Chemical Physics. 161(5). 1 indexed citations
7.
Yu, Longhui, et al.. (2024). Modular, Scalable Total Synthesis of Lapparbin with a Noncanonical Biaryl Linkage. Angewandte Chemie International Edition. 63(42). e202409987–e202409987. 1 indexed citations
8.
Yu, Longhui, et al.. (2024). Modular, Scalable Total Synthesis of Lapparbin with a Noncanonical Biaryl Linkage. Angewandte Chemie. 136(42). 1 indexed citations
9.
Akiyama, Seiji, et al.. (2024). A framework for reviewing the results of automated conversion of structured organic synthesis procedures from the literature. Digital Discovery. 4(1). 172–180. 1 indexed citations
10.
Matsuoka, Wataru, Yu Harabuchi, Yuuya Nagata, & Satoshi Maeda. (2023). Highly chemoselective ligands for Suzuki–Miyaura cross-coupling reaction based on virtual ligand-assisted screening. Organic & Biomolecular Chemistry. 21(15). 3132–3142. 8 indexed citations
11.
Nguyen, Thanh‐Vinh, Asier Marzo, Yuuya Nagata, et al.. (2023). Microfluidic platform using focused ultrasound passing through hydrophobic meshes with jump availability. PNAS Nexus. 2(7). pgad207–pgad207. 13 indexed citations
12.
Tsuji, Nobuya, Pavel Sidorov, Chendan Zhu, et al.. (2023). Predicting Highly Enantioselective Catalysts Using Tunable Fragment Descriptors**. Angewandte Chemie. 135(11).
13.
Tsuji, Nobuya, Pavel Sidorov, Chendan Zhu, et al.. (2023). Predicting Highly Enantioselective Catalysts Using Tunable Fragment Descriptors**. Angewandte Chemie International Edition. 62(11). e202218659–e202218659. 36 indexed citations
14.
Akiyama, Seiji, et al.. (2023). OSPAR: A Corpus for Extraction of Organic Synthesis Procedures with Argument Roles. Journal of Chemical Information and Modeling. 63(21). 6619–6628. 2 indexed citations
15.
Fa, Shixin, Keisuke Wada, Kenichi Kato, et al.. (2023). Adaptive Planar Chirality of Pillar[5]arenes Invertible by n-Alkane Lengths. Journal of the American Chemical Society. 145(14). 8114–8121. 26 indexed citations
16.
Fa, Shixin, Tan‐Hao Shi, Keisuke Wada, et al.. (2022). Real-time chirality transfer monitoring from statistically random to discrete homochiral nanotubes. Nature Communications. 13(1). 7378–7378. 21 indexed citations
17.
Shigemitsu, Hajime, et al.. (2021). Cyclodextrins with Multiple Pyrenyl Groups: An Approach to Organic Molecules Exhibiting Bright Excimer Circularly Polarized Luminescence. Angewandte Chemie International Edition. 61(8). e202114700–e202114700. 82 indexed citations
18.
Fa, Shixin, et al.. (2021). Pre-regulation of the planar chirality of pillar[5]arenes for preparing discrete chiral nanotubes. Chemical Science. 12(10). 3483–3488. 34 indexed citations
19.
20.
Nagata, Yuuya, et al.. (1981). Acheilognathus tabira subsp collected in Tanega-ike, Tottori Prefecture, Japan. 36112. 48–53. 2 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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