Tetsuta Oshitari

878 total citations
65 papers, 717 citations indexed

About

Tetsuta Oshitari is a scholar working on Organic Chemistry, Spectroscopy and Molecular Biology. According to data from OpenAlex, Tetsuta Oshitari has authored 65 papers receiving a total of 717 indexed citations (citations by other indexed papers that have themselves been cited), including 54 papers in Organic Chemistry, 32 papers in Spectroscopy and 17 papers in Molecular Biology. Recurrent topics in Tetsuta Oshitari's work include Axial and Atropisomeric Chirality Synthesis (32 papers), Molecular spectroscopy and chirality (27 papers) and Chemical synthesis and alkaloids (10 papers). Tetsuta Oshitari is often cited by papers focused on Axial and Atropisomeric Chirality Synthesis (32 papers), Molecular spectroscopy and chirality (27 papers) and Chemical synthesis and alkaloids (10 papers). Tetsuta Oshitari collaborates with scholars based in Japan. Tetsuta Oshitari's co-authors include Hideaki Natsugari, Hideyo Takahashi, Hidetsugu Tabata, Tadakatsu Mandai, Susumu Kobayashi, Masahiro Tomita, Hiroshi Kosano, Yoshiki Miyata, Kosho Makino and Masakatsu Shibasaki and has published in prestigious journals such as Angewandte Chemie International Edition, Journal of Medicinal Chemistry and The Journal of Organic Chemistry.

In The Last Decade

Tetsuta Oshitari

62 papers receiving 705 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tetsuta Oshitari Japan 16 519 239 236 74 74 65 717
Pavel Bobáľ Czechia 15 337 0.6× 62 0.3× 266 1.1× 61 0.8× 35 0.5× 49 651
Jiang‐Ke Qin China 16 258 0.5× 75 0.3× 251 1.1× 175 2.4× 126 1.7× 48 796
Hernán Pessoa‐Mahana Chile 16 357 0.7× 74 0.3× 231 1.0× 128 1.7× 27 0.4× 56 634
Ya Li China 15 955 1.8× 237 1.0× 241 1.0× 28 0.4× 73 1.0× 42 1.2k
Olga Cruz‐López Spain 21 939 1.8× 50 0.2× 527 2.2× 120 1.6× 36 0.5× 54 1.4k
Eric Goffin Belgium 18 330 0.6× 49 0.2× 383 1.6× 59 0.8× 42 0.6× 40 751
Mohamed N. Aboul‐Enein Egypt 15 370 0.7× 81 0.3× 251 1.1× 110 1.5× 26 0.4× 52 653
Toshiko Watanabe Japan 19 677 1.3× 34 0.1× 338 1.4× 95 1.3× 92 1.2× 69 995
Jacques H. Poupaert Belgium 13 270 0.5× 55 0.2× 267 1.1× 82 1.1× 24 0.3× 52 636
M. MIOCQUE France 16 454 0.9× 99 0.4× 258 1.1× 37 0.5× 16 0.2× 91 675

Countries citing papers authored by Tetsuta Oshitari

Since Specialization
Citations

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

Fields of papers citing papers by Tetsuta Oshitari

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tetsuta Oshitari

This figure shows the co-authorship network connecting the top 25 collaborators of Tetsuta Oshitari. A scholar is included among the top collaborators of Tetsuta Oshitari 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 Tetsuta Oshitari. Tetsuta Oshitari 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.
Kimura, Yuka, Kayo Nakamura, Hidetsugu Tabata, et al.. (2024). Photodegradation of Dacarbazine Catalyzed by Vitamin B2 and Flavin Adenine Dinucleotide Under Visible-Light Irradiation. Pharmaceutical Research. 41(12). 2363–2375. 1 indexed citations
2.
Nakamura, Kayo, et al.. (2024). Stereochemical properties of quazepam and its affinity for the GABAA receptor. Bioorganic & Medicinal Chemistry Letters. 110. 129854–129854. 1 indexed citations
3.
Funada, Masahiko, Kenichi Tomiyama, Masaru Hashimoto, et al.. (2024). Fentanyl-Type Antagonist of the μ-Opioid Receptor: Important Role of Axial Chirality in the Active Conformation. Journal of Medicinal Chemistry. 67(12). 10447–10463. 4 indexed citations
4.
Nakamura, Kayo, Kosho Makino, Hidetsugu Tabata, et al.. (2023). Stereochemistry of N-Acyl-5H-dibenzo[b,d]azepin-7(6H)-ones. Molecules. 28(12). 4734–4734.
5.
Makino, Kosho, et al.. (2022). Axial chirality and affinity at the GABAA receptor of triazolobenzodiazepines. Bioorganic & Medicinal Chemistry. 64. 116758–116758. 5 indexed citations
6.
Makino, Kosho, et al.. (2022). Photoisomerization of Sulindac and Ozagrel Hydrochloride by Vitamin B2 Catalyst Under Visible Light Irradiation. Pharmaceutical Research. 39(3). 577–586. 3 indexed citations
7.
Makino, Kosho, et al.. (2022). Atropisomeric Properties of <i>N</i>-Alkyl/Aryl 5<i>H</i>-Dibenz[<i>b</i>,<i>f</i>]azepines. Chemical and Pharmaceutical Bulletin. 70(8). 573–579. 1 indexed citations
8.
Makino, Kosho, Yuki Tanaka, Akiko Inagaki, et al.. (2021). Rapid Photoracemization of Chiral Alkyl Aryl Sulfoxides. The Journal of Organic Chemistry. 86(23). 17249–17256. 9 indexed citations
9.
Tega, Yuma, Hidetsugu Tabata, Toshiki Kurosawa, et al.. (2020). Structural Requirements for Uptake of Diphenhydramine Analogs into hCMEC/D3 Cells Via the Proton-Coupled Organic Cation Antiporter. Journal of Pharmaceutical Sciences. 110(1). 397–403. 14 indexed citations
10.
Tabata, Hidetsugu, Kosho Makino, Tetsuta Oshitari, et al.. (2018). 4-Substituted carbamazepine derivatives: Conformational analysis and sodium channel-blocking properties. Bioorganic & Medicinal Chemistry. 26(9). 2508–2513. 9 indexed citations
11.
Takahashi, Hideyo, Koji Araki, Kosho Makino, et al.. (2018). Synthesis of 3-Aroylindoles as Intermediates of Cannabimimetics and Elucidation of Their Physicochemical Properties. Heterocycles. 96(5). 910–910. 2 indexed citations
12.
Takahashi, Yuka, Hirotaka Ikeda, Kosho Makino, et al.. (2017). Elucidation of the E-Amide Preference of N-Acyl Azoles. The Journal of Organic Chemistry. 82(21). 11370–11382. 11 indexed citations
13.
14.
Itagaki, Fumio, et al.. (2013). Incompatibility between Meropenem Injection and Amino Acid Infusions caused by L-Cysteine. Iryo Yakugaku (Japanese Journal of Pharmaceutical Health Care and Sciences). 39(9). 521–527. 3 indexed citations
15.
Takahashi, Yuka, Hidetsugu Tabata, Tetsuta Oshitari, et al.. (2013). Conformation and Atropisomeric Properties of Indometacin Derivatives. Chemistry - A European Journal. 19(22). 7056–7063. 11 indexed citations
16.
Miyata, Yoshiki, Tetsuta Oshitari, Arata Shimada, et al.. (2012). Polymethoxyflavones as agents that prevent formation of cataract: Nobiletin congeners show potent growth inhibitory effects in human lens epithelial cells. Bioorganic & Medicinal Chemistry Letters. 23(1). 183–187. 15 indexed citations
17.
Tabata, Hidetsugu, et al.. (2011). Atropisomerism in the Vaptan Class of Vasopressin Receptor Ligands: The Active Conformation Recognized by the Receptor. Angewandte Chemie International Edition. 50(13). 3075–3079. 46 indexed citations
18.
Tabata, Hidetsugu, Naoya Wada, Yuko Takada, et al.. (2011). Active Conformation of Seven‐Membered‐Ring Benzolactams as New ACAT Inhibitors: Latent Chirality at N5 in the 1,5‐Benzodiazepin‐2‐one Nucleus. Chemistry - A European Journal. 18(6). 1572–1576. 28 indexed citations
19.
Oshitari, Tetsuta, et al.. (2011). Nobiletin metabolites: Synthesis and inhibitory activity against matrix metalloproteinase-9 production. Bioorganic & Medicinal Chemistry Letters. 21(15). 4540–4544. 25 indexed citations
20.
Oshitari, Tetsuta, et al.. (2011). B-Ring-modified and/or 5-demethylated nobiletin congeners: Inhibitory activity against pro-MMP-9 production. Bioorganic & Medicinal Chemistry. 19(23). 7085–7092. 15 indexed citations

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