Hiroyuki Nakamura
Tokyo Institute of Technology
543 Papers
3.6K Citations
Hiroyuki Nakamura is an academic researcher from Tokyo Institute of Technology. The author has contributed to research in topics: Chemistry & Catalysis. The author has an hindex of 52, co-authored 491 publications. Previous affiliations of Hiroyuki Nakamura include Japanese Foundation for Cancer Research & University of Tokyo.
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Papers
Towards new boron carriers for boron neutron capture therapy: Metallacarboranes bearing cobalt, iron and chromium and their cholesterol conjugates
Magdalena Białek-Pietras,Agnieszka B. Olejniczak,Shoji Tachikawa,Hiroyuki Nakamura,Zbigniew J. Leśnikowski +4 more
TL;DR: Using the metallacarborane-encrusted liposomes as boron delivery system in vivo biodistribution experiments in tumor-bearing mice, high accumulation and selective delivery of borons into tumor tissues was observed.
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Effect of Polyelectrolyte Dispersants on the Preparation of Silica‐Coated Zinc Oxide Particles in Aqueous Media
Hongzhi Wang,Hiroyuki Nakamura,Ken Yao,Masato Uehara,Satoshi Nishimura,Hideaki Maeda,Eiichi Abe +6 more
TL;DR: In this article, two kinds of polyelectrolyte dispersants were used to control the surface charge of the ZnO particles in aqueous media, and the results showed that poly(ethylenimine) (PEI) shifted the isoelectric point from pH 9 to pH 10, and poly(ammonium acrylate) (PAA) made the surface charges of ZnOs negative between pH 6 and pH 11.
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Ortho-carboranyl glycosides for the treatment of cancer by boron neutron capture therapy.
Lutz F. Tietze,Ulrich Bothe,Ulrich Griesbach,Munekazu Nakaichi,Toshinari Hasegawa,Hiroyuki Nakamura,Yoshinori Yamamoto +6 more
TL;DR: Carboranyl maltoside 3 was more effective than boron-10 enriched 5 in killing C-6 rat glioma cells by incubating the cells with the compound and subsequent treatment with thermal neutrons.
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Generation of an 4‐Isoxazolyl Anion Species: Facile Access to Multifunctionalized Isoxazoles
TL;DR: Total synthesis of triumferol, which was isolated from Triumfetta rhomboidea, was achieved from 1 in only three steps, enabling us to synthesize multi-functionalized isoxazoles by introducing each substituent into the desired positions.
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