Daisuke Sawada

420 total citations
21 papers, 374 citations indexed

About

Daisuke Sawada is a scholar working on Organic Chemistry, Materials Chemistry and Molecular Biology. According to data from OpenAlex, Daisuke Sawada has authored 21 papers receiving a total of 374 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Organic Chemistry, 9 papers in Materials Chemistry and 6 papers in Molecular Biology. Recurrent topics in Daisuke Sawada's work include Luminescence and Fluorescent Materials (9 papers), Photochromic and Fluorescence Chemistry (6 papers) and Molecular Sensors and Ion Detection (5 papers). Daisuke Sawada is often cited by papers focused on Luminescence and Fluorescent Materials (9 papers), Photochromic and Fluorescence Chemistry (6 papers) and Molecular Sensors and Ion Detection (5 papers). Daisuke Sawada collaborates with scholars based in Japan, Czechia and United States. Daisuke Sawada's co-authors include Shinichiro Kamino, Masaru Tanioka, Masanobu Uchiyama, Atsuya Muranaka, Shuichi Enomoto, Masashi Ueda, Yousuke Ooyama, Hiromi Ota, Takumi Abe and Tetsuya Aoyama and has published in prestigious journals such as Journal of the American Chemical Society, Chemical Communications and Physical Chemistry Chemical Physics.

In The Last Decade

Daisuke Sawada

18 papers receiving 372 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Daisuke Sawada Japan 9 270 155 144 73 36 21 374
Masaru Tanioka Japan 9 300 1.1× 158 1.0× 167 1.2× 74 1.0× 41 1.1× 19 400
Chi Cheng United Kingdom 7 350 1.3× 105 0.7× 168 1.2× 118 1.6× 87 2.4× 11 425
Takuma Okura Japan 4 252 0.9× 241 1.6× 95 0.7× 99 1.4× 19 0.5× 4 411
Aya Sakon Japan 7 324 1.2× 127 0.8× 129 0.9× 112 1.5× 24 0.7× 14 370
Anamaria Terec Romania 13 216 0.8× 223 1.4× 90 0.6× 79 1.1× 34 0.9× 49 471
Debabrata Jana India 12 258 1.0× 83 0.5× 129 0.9× 99 1.4× 53 1.5× 29 369
Abdellah Felouat France 12 290 1.1× 323 2.1× 99 0.7× 104 1.4× 58 1.6× 14 594
Anna A. Baranova Russia 10 226 0.8× 117 0.8× 200 1.4× 88 1.2× 28 0.8× 32 352
Taichi Abe Japan 11 230 0.9× 223 1.4× 59 0.4× 160 2.2× 27 0.8× 15 436
Faizal Khan India 11 359 1.3× 127 0.8× 151 1.0× 155 2.1× 35 1.0× 13 435

Countries citing papers authored by Daisuke Sawada

Since Specialization
Citations

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

Fields of papers citing papers by Daisuke Sawada

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Daisuke Sawada

This figure shows the co-authorship network connecting the top 25 collaborators of Daisuke Sawada. A scholar is included among the top collaborators of Daisuke Sawada 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 Daisuke Sawada. Daisuke Sawada 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.
Peluso‐Iltis, Carole, Daniela Rovito, Judit Ősz, et al.. (2024). 4-Hydroxy-1α,25-Dihydroxyvitamin D3: Synthesis and Structure–Function Study. Biomolecules. 14(5). 551–551. 1 indexed citations
2.
Kurogi, H., Nobumasa Takasugi, Sho Kubota, et al.. (2024). Discovery of a Compound That Inhibits IRE1α S-Nitrosylation and Preserves the Endoplasmic Reticulum Stress Response under Nitrosative Stress. ACS Chemical Biology. 19(12). 2429–2437.
3.
Obata, Tohru, et al.. (2023). Nucleophile‐Triggered π‐Topological Transformation: A New Synthetic Approach to Near‐Infrared‐Emissive Rhodamines. Chemistry - A European Journal. 29(59). e202301969–e202301969.
4.
Abe, Takumi, et al.. (2022). Synthesis of 2-monosubstituted indolin-3-ones by cine-substitution of 3-azido-2-methoxyindolines. Organic Chemistry Frontiers. 9(7). 1897–1903. 13 indexed citations
5.
Abe, Takumi, et al.. (2022). Chemo- and Site-Selective Replacement of N-Terminal Carbamates in Peptides. Organic Letters. 24(11). 2131–2136. 3 indexed citations
6.
Abe, Takumi, et al.. (2022). First Total Synthesis of Reassigned Echinosulfonic Acid D. Journal of Natural Products. 85(8). 2122–2125. 7 indexed citations
7.
Abe, Takumi, et al.. (2022). Indole Editing Enabled by HFIP‐Mediated Ring‐Switch Reactions of 3‐Amino‐2‐Hydroxyindolines. Chemistry - A European Journal. 28(37). e202201113–e202201113. 10 indexed citations
8.
Abe, Takumi, et al.. (2021). cis-3-Azido-2-methoxyindolines as safe and stable precursors to overcome the instability of fleeting 3-azidoindoles. Chemical Communications. 57(98). 13381–13384. 9 indexed citations
9.
Abe, Takumi, et al.. (2021). Synthesis of α-substituted indolylacetamide using acetonitriles as acetamide enolate equivalents through O-transfer reactions. Chemical Communications. 57(61). 7493–7496. 12 indexed citations
10.
Tanioka, Masaru, et al.. (2020). Morpholine‐Substituted Rhodamine Analogue with Multi‐Configurational Switches for Optical Sensing of pH Gradient under Extreme Acidic Environments. Chemistry - A European Journal. 27(11). 3761–3765. 8 indexed citations
11.
Tanioka, Masaru, et al.. (2019). Stepwise structural and fluorescent colour conversion in rhodamine analogues based on light and acid stimulations. Journal of Materials Chemistry C. 8(2). 543–549. 9 indexed citations
12.
Sawada, Daisuke, et al.. (2019). Efficient and practical synthesis of N-acetyl enamides from ketoximes by unique iron catalytic system. Tetrahedron Letters. 60(24). 1562–1565.
13.
Tanioka, Masaru, Atsuya Muranaka, Kazunori Miyamoto, et al.. (2018). Stable Thiele’s Hydrocarbon Derivatives Exhibiting Near-Infrared Absorption/Emission and Two-Step Electrochromism. Journal of the American Chemical Society. 140(51). 17857–17861. 43 indexed citations
14.
Kamino, Shinichiro, Masaru Tanioka, & Daisuke Sawada. (2018). Development of Chromic Molecule that Can Change Color and Absorption/Fluorescence Wavelengths Largely in Response to External Stimuli. Journal of Synthetic Organic Chemistry Japan. 76(10). 1066–1075. 1 indexed citations
15.
Kamino, Shinichiro, et al.. (2018). Syntheses and Acid-Stimulus Responsiveness of Aminobenzopyranoxanthene Spiroethers. Heterocycles. 99(2). 820–820. 2 indexed citations
16.
Kamino, Shinichiro, et al.. (2017). Synthesis of Aminobenzopyranoxanthenes with Nitrogen-Containing Fused Rings. The Journal of Organic Chemistry. 82(24). 13626–13631. 6 indexed citations
17.
Kamino, Shinichiro, Shuichi Enomoto, Masaru Tanioka, & Daisuke Sawada. (2017). Syntheses and Photophysical Properties of Aminobenzopyranoxanthene Dyes Containing Various Alkyl Chains at Amine Moieties. Heterocycles. 95(2). 1167–1167. 3 indexed citations
18.
Kamino, Shinichiro, et al.. (2017). Direct C-H substitution reaction of anilides using hypervalent iodine and their regioselective issues. Tetrahedron Letters. 58(41). 3936–3938. 4 indexed citations
19.
Muranaka, Atsuya, et al.. (2016). Fused-Fluoran Leuco Dyes with Large Color-Change Derived from Two-Step Equilibrium: iso-Aminobenzopyranoxanthenes. The Journal of Organic Chemistry. 81(23). 12046–12051. 29 indexed citations
20.
Tanioka, Masaru, Shinichiro Kamino, Atsuya Muranaka, et al.. (2016). Water-tunable solvatochromic and nanoaggregate fluorescence: dual colour visualisation and quantification of trace water in tetrahydrofuran. Physical Chemistry Chemical Physics. 19(2). 1209–1216. 43 indexed citations

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