Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Yushi Yamamoto"'
Autor:
Motoki Ogiso, Chihiro Hashimoto, Eisuke Toriumi, Kanako Nishimura, Seiichiro Iizuka, Kazuhiro Sakamoto, Yushi Yamamoto, Yukiko Yamada
Publikováno v:
Food Hygiene and Safety Science (Shokuhin Eiseigaku Zasshi). 64:29-33
Autor:
Hisako Kanada, Yushi Yamamoto, Hideo Sato, Kohei Chinju, Yuichi Ariyasu, Maria Kawaji, Yoichiro Iwashita, Makiko Hashiguchi, Youichi Yamasaki
Publikováno v:
Journal of Oral Rehabilitation. 50:76-86
Evaluating mouth rinsing skills is useful for assessing oral function, however current evaluation methods are subjective.This study compared mouth rinsing between adults and children using a contactless camera to capture lip motion.The subjects compr
Autor:
Youichi Yamasaki, Hisako Kanada, Yushi Yamamoto, Hideo Sato, Makiko Hashiguchi, Yoichiro Iwashita
Publikováno v:
Journal of oral rehabilitationREFERENCES. 47(4)
Clinical application of a swallowing function evaluation system that is minimally invasive and enables an objective evaluation is necessary. We constructed a system that can synchronise and analyse lip motion with a three-dimensional (3D) camera and
Publikováno v:
Zoomorphology. 132:317-324
Expansion of the ‘pharynx’ during breathing or capturing prey in fishes generally involves posteroventral retraction of the hyoid arch. However, the hyoid arch structure of batoid fishes (skates, rays, guitarfishes, and sawfishes) is unique, and
Autor:
Masami Ishibashi, Takayoshi Arai, Yushi Yamamoto, Kentaro Kamiya, Atsuko Awata, Midori A. Arai
Publikováno v:
Angewandte Chemie International Edition. 52:2486-2490
TOP class: The first efficient catalytic asymmetric coupling reaction of indoles with isatin-derived nitroalkenes was accomplished by using a complex consisting of a chiral imidazoline aminophenol ligand (1; see scheme) and Cu(OTf)(2). Biological act
Autor:
Takayoshi Arai, Yushi Yamamoto
Publikováno v:
Organic letters. 16(6)
The (S,S)-diphenylethylenediamine-derived imidazoline–aminophenol–Ni complex catalyzed tandem asymmetric Michael/Henry reaction of 2-mercaptobenzaldehydes with β-nitrostyrenes to give the corresponding (2S,3R,4R)-2-aryl-3-nitrothiochroman-4-ols
Autor:
Kentaro Kamiya, Masami Ishibashi, Takayoshi Arai, Yushi Yamamoto, Atsuko Awata, Midori A. Arai
Publikováno v:
ChemInform. 44
Friedel—Crafts reaction of isatin-derived nitroalkenes with indoles in the presence of either Cu(O-Tf)2 [conditions A)] or CuOTf [conditions B)] yields 3,3′-bisindoles which represent the skeleton of various indole alkaloids.
Publikováno v:
The Proceedings of the Dynamics & Design Conference. 2003:209-1