Y
Yuki Saito
Researcher at Utsunomiya University
Publications - 5
Citations - 109
Yuki Saito is an academic researcher from Utsunomiya University. The author has contributed to research in topics: Porphyrin & Phosphorescence. The author has an hindex of 3, co-authored 5 publications receiving 96 citations.
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Journal ArticleDOI
Inhibition of quorum sensing in gram-negative bacteria by alkylamine-modified cyclodextrins.
Tomohiro Morohoshi,Kazuho Tokita,Satoshi Ito,Yuki Saito,Saki Maeda,Norihiro Kato,Tsukasa Ikeda +6 more
TL;DR: In this study, a series of CD derivatives were designed and synthesized to improve the QS inhibitory activity over that of native CDs, and the synthetic alkylamine-modified CD derivatives had higher equilibrium binding constants for binding with AHL than the native CDs did, consistent with the improved QS inhibition.
Journal ArticleDOI
Phenazine antibiotic production and antifungal activity are regulated by multiple quorum-sensing systems in Pseudomonas chlororaphis subsp. aurantiaca StFRB508.
Tomohiro Morohoshi,Wen-Zhao Wang,Tomonori Suto,Yuki Saito,Satoshi Ito,Nobutaka Someya,Tsukasa Ikeda +6 more
TL;DR: Results demonstrated that the multiple quorum-sensing system play an important role in PCA production and antifungal activity in StFRB508.
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Synthesis of π-extended platinum porphyrins
TL;DR: In this article, the authors reported the efficient synthesis of tetrabicycloporphyrin platinum under mild conditions (60°C), and the platinum complexes were heated under vacuum to give π-extended platinum porphyrins in 100% yield.
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Synthesis of [2,3]naphthoporphyrins using 4,9-dihydro-4,9-ethano-2H-benz[f]isoindole as a benz[f]isoindole equivalent
TL;DR: In this paper, a new synthesis of 1,4dihydro-1,4-ethanonaphthalene using 4,9-dihdro-4, 9-ethano-2H-benz[f]isoindole as the equivalent of benz[f]-isoindoles from p-benzoquinone as a starting material via the Diels-Alder reaction, Luche reduction, and dehydroxylation.
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Titanylation and vanadylation of highly π-conjugated porphyrins
TL;DR: In this paper, the authors reported the efficient synthesis of tetrabicycloporphyrin titanyl and vanadyl without decomposition of the bicyclo[2.2] octadiene unit.