Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Hiroyoshi Iwai"'
Autor:
Shoji Kawatsu, Hiroyoshi Iwai, Takeo Ishigaki, Kojiro Suzuki, Kunihiro Maruyama, Tsuneo Ishiguchi
Publikováno v:
CardioVascular and Interventional Radiology. 24:94-98
To evaluate the effect on dilatation of three types of covering materials used for endovascular stent-grafts.Stent-grafts with three types of covering material [0.1-mm polytetrafluoroethylene (PTFE), 0.2-mm PTFE, and 0.15-mm woven polyester] were pla
Autor:
Shigeo Yanagawa, Hiroyoshi Iwai, Akihiro Nawa, Takeo Ishigaki, Fumitaka Kikkawa, Tetsuya Yamada
Publikováno v:
Gynecologic Oncology. 77:193-196
Objective. To preserve the organs and function of the anus and ureter, radiotherapy was chosen for an advanced vulvar tumor originating from Bartholin's gland. Methods. The patient was a 74-year-old female with stage III (FIGO) vulvar cancer derived
Publikováno v:
Organic Letters. 3:2101-2103
[reaction: see text] O-(2-Naphthoyl)-N-tosyl-L-allo-threonine-derived B-phenyloxazaborolidinone catalyzes the asymmetric Mukaiyama-Michael addition of simple acyclic enones to give adducts of 54-85% ee. 2,6-Diisopropylphenol as an additive is demonst
Publikováno v:
ChemInform. 32
O-(2-Naphthoyl)-N-tosyl-l-allo-threonine-derived B-phenyloxazaborolidinone catalyzes the asymmetric Mukaiyama−Michael addition of simple acyclic enones to give adducts of 54−85% ee. 2,6-Diisopropylphenol as an additive is demonstrated to effectiv
Autor:
Hiroyoshi Iwai, Mikako Kubo, Akira Oku, Shinya Adachi, Katsuhiro Fujita, Toshiro Harada, Hiroshi Takatsuki, Xiaowei Wang
Publikováno v:
ChemInform. 35
allo-Threonine-derived O-aroyl-B-phenyl-N-tosyl-1,3,2-oxazaborolidin-5-ones 1g,n catalyze the asymmetric Mukaiyama−Michael reaction of acyclic enones with a trimethylsilyl ketene S,O-acetal in high enantioselectivity. A range of alkenyl methyl keto
Autor:
Hiroshi Takatsuki, Shinya Adachi, Akira Oku, Xiaowei Wang, Mikako Kubo, Hiroyoshi Iwai, Toshiro Harada, Katsuhiro Fujita
Publikováno v:
The Journal of organic chemistry. 68(26)
allo-Threonine-derived O-aroyl-B-phenyl-N-tosyl-1,3,2-oxazaborolidin-5-ones 1g,n catalyze the asymmetric Mukaiyama-Michael reaction of acyclic enones with a trimethylsilyl ketene S,O-acetal in high enantioselectivity. A range of alkenyl methyl ketone
Publikováno v:
Chirality. 15(1)
In the presence of 2,6-diisopropylphenol and t-BuOMe (1 equiv. each), asymmetric Mukaiyama-Michael reaction of a variety of benzalacetone derivatives 2 with silyl ketene acetal 3 is efficiently catalyzed by O-(2-naphthoyl)-N-tosyl-(L)-allo-threonine-
Autor:
Suzuki, Kojiro, Ishiguchi, Tsuneo, Kawatsu, Shoji, Iwai, Hiroyoshi, Maruyama, Kunihiro, Ishigaki, Takeo
Publikováno v:
CardioVascular & Interventional Radiology; Mar2001, Vol. 24 Issue 2, p94-98, 5p
Publikováno v:
Chirality; 2003, Vol. 15 Issue 1, p28-30, 3p
Autor:
Giovanni Fiandaca
Where is a woman's place in the mob? Does she even have one? Is the rise in women's involvement in organized crime the darker side of their increased presence in the legitimate workplace, or simply a reworking of the mafia's traditional male attitude