Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Noriko Ohsawa"'
Autor:
Yuji Matsuya, Noriko Ohsawa, Keiichi Kamoshita, Jacques Eustache, Solange Adam, Hideo Nemoto, Yoshikazu Sukenaga, T. Tschamber, Seiji Masuda
Publikováno v:
European Journal of Organic Chemistry. 2005:803-808
The estrane analogue of OSW-1, a potent antitumor natural saponin, was efficiently synthesized from estrone in 12 steps. The cytostatic activity of the compound against several human malignant tumor cells was examined and compared to those of the nat
Autor:
Kazunori Konno, Shinsuke Yoshimura, Hajime Yamaguchi, Akiko Chisaka, Satoshi Noguchi, Noriko Ohsawa
Publikováno v:
Journal of Toxicologic Pathology. 18:141-157
Autor:
Shinsuke Yoshimura, Noriko Ohsawa, Kazunori Konno, Akiko Chisaka, Satoshi Noguchi, Hajime Yamaguchi
Publikováno v:
Journal of Toxicologic Pathology. 17:113-118
Hypospadias was induced in male Sprague-Dawley rats by prenatal exposure to 30 mg/kg/day of flutamide from gestational days 14 to 17, or from 18 to 21. Their external genitalia were examined histopathologically and compared to untreated controls. On
Autor:
Théophile Tschamber, Seiji Masuda, Solange Adam, Noriko Ohsawa, Sakiko Maruyama, Yuji Matsuya, Keiichi Kamoshita, Hideo Nemoto, Jacques Eustache
Publikováno v:
Bioorganicmedicinal chemistry letters. 17(18)
4 OSW-1 analogues featuring modified carbohydrate moieties were prepared. The purpose of these modifications was to assess the importance of certain chemical functions with respect to biological activity. The synthesis and biological activity of the
Publikováno v:
ChemInform. 38
Efficient transformations of benzocyclobutenones into 2,3-benzodiazepines by a formal insertion of diazomethylene compounds are described. This sequential process includes nucleophilic addition of diazomethylene anion, oxy-anion accelerated o-quinodi
Publikováno v:
Journal of the American Chemical Society. 128(2)
A significant acceleration effect of a beta-silicon atom was observed on the electrocyclic ring-opening reaction of benzocyclobutene derivatives to form o-quinodimethanes. This acceleration effect could be attributed to an electronic sigma-donating n
Publikováno v:
Journal of the American Chemical Society. 128:412-413
A significant acceleration effect of a β-silicon atom was observed on the electrocyclic ring-opening reaction of benzocyclobutene derivatives to form o-quinodimethanes. This acceleration effect could be attributed to an electronic σ-donating nature
Accelerated Electrocyclic Ring-Opening of Benzocyclobutenes under the Influence of a β-Silicon Atom.
Publikováno v:
Journal of the American Chemical Society. 1/18/2006, Vol. 128 Issue 2, p412-413. 2p.