Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Kazunori Sugai"'
Autor:
Emiko Sasai, Miyako Negishi, Sanae Miyagawa, Shotaro Hagiwara, Kazunori Sugai, Satoru Suzuki, Miyuki Chiba
Publikováno v:
Journal of Infection and Chemotherapy. 26:1288-1293
Objective Terminally ill patients with hematological malignancy tend to be treated aggressively. We aimed to clarify the status and costs of antimicrobial treatment of patients dying with hematological malignancies. Methods This retrospective study w
Publikováno v:
Macromolecules. 39:6924-6927
Novel polymerized ionic liquids having an organoboron unit were prepared for the purpose of selective lithium cation transport. Hydroboration polymerization of 1,3-diallylimidazolium bromide and subsequent anion exchange reaction with LiTFSI [lithium
Publikováno v:
Macromolecules. 38:4951-4954
Publikováno v:
Macromolecules. 36:2321-2326
Alkylborane type and boric ester type polymer electrolytes bearing mesitylboron units were prepared by hydroboration polymerization or dehydrocoupling polymerization using mesitylborane. The obtained well-defined organoboron polymer electrolytes show
Autor:
Nobuyoshi Ishii, Yoshikazu Inoue, Hiroshi Takeda, Kiriko Miyamoto, Zen'ichiro Kawabata, Chitose Ishii, Shoichi Fuma, Kazunori Sugai, Kei Yanagisawa
Publikováno v:
Bulletin of Environmental Contamination and Toxicology. 66:231-238
ガドリニウムは産業や医療分野でその利用量が増大しつつあるにもかかわらず、生態系に対するガドリニウムの毒性評価が十分に行われるとは言えない。そこで水系マイクロコズムを用
Publikováno v:
Macromolecules. 35:5731-5733
Autor:
Tomoko Teranaka, Masayuki Shimagaki, Tadashi Nakata, Manabu Shiokawa, Takeshi Oishi, Kazunori Sugai
Publikováno v:
Tetrahedron Letters. 29:659-662
A new route for (Z)-α,β-disubstituted acrylate is described which is made up of 1) stereoselective reduction of ketones 3 and 2) conversion of the resulting syn- 2 into (Z)- 1 .
Autor:
Tomoko Teranaka, Tadashi Nakata, Kazunori Sugai, Manabu Shiokawa, Takeshi Oishi, Masayuki Shimagaki
Publikováno v:
ChemInform. 19
A new route for (Z)-α,β-disubstituted acrylate is described which is made up of 1) stereoselective reduction of ketones 3 and 2) conversion of the resulting syn- 2 into (Z)- 1 .