Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Kei-ichi Kawagoe"'
Autor:
S. C. Burford, Kenji Hirotani, Tamotsu Miwa, Kei-ichi Kawagoe, Ikuo Mitsui, Eiji Kumazawa, Akio Ejima
Publikováno v:
ChemInform. 29
Autor:
Y. Yokomizo, Yuko Honda, S. Yokohama, Y. Ogihara, T. Hosokami, A. Yokomizo, Kei-ichi Kawagoe, Y. Takeda
Publikováno v:
ChemInform. 29
Autor:
Masunobu Sugimura, Masaki Saito, Takanori Yasukouchi, Shinichi Kawajiri, Masayuki Ito, Kei-ichi Kawagoe, Tetuya Mimura, Fusako Kito, Toshiaki Tatematu, Yoshiyuki Yoneda
Publikováno v:
ChemInform. 33
Autor:
Masaki Saito, Yoshiyuki Yoneda, Shinichi Kawajiri, Kei-ichi Kawagoe, Toshiaki Tatematu, Masayuki Ito, Takanori Yasukouchi, Tetuya Mimura, Masunobu Sugimura, Fusako Kito
Publikováno v:
Bioorganicmedicinal chemistry. 10(5)
We designed and synthesized a series of the polyamine derivatives as potent Ca2+-permeable AMPA receptor antagonists. In the course of this study, we found that the polyamine derivatives exhibited strong hypotensive activity which was undesirable act
Autor:
Kei-ichi Kawagoe, Toru Hosokami, Yasuyuki Takeda, Yoshiyasu Ogihara, Yoshiaki Tabuchi, Yokomizo Aki, Rira Otsubo, Shuichi Yokohama, Yuko Honda, Yoshihiro Yokomizo, Yoshimasa Shimoto
Publikováno v:
Chemicalpharmaceutical bulletin. 46(6)
A novel series of phenoxyacetic acid derivatives was synthesized based on considerations of the three-dimensional structural similarity of YM022 and RP72540. The gastrin/cholecystokinin (CCK)-B and CCK-A receptor antagonist activities of these compou
Autor:
Eiji Kumazawa, Tamotsu Miwa, S. Clifford Burford, Kei-ichi Kawagoe, Kenji Hirotani, Akio Ejima, Ikuo Mitsui
Publikováno v:
Chemicalpharmaceutical bulletin. 45(9)
Novel benzophenone derivatives were synthesized and screened for cytotoxic and antitumor activity. Friedel-Crafts condensation was employed to construct the benzophenone skeleton. Among the compounds synthesized, morpholino and thiomorpholino benzoph
Publikováno v:
Chemical and Pharmaceutical Bulletin. 35:1633-1636
Racemic fluoroalkyl (E) -vinyl carbinols (1a-d) were kinetically resolved by Sharpless epoxidation. The optical purity of the resolved alcohols was excellent (98% ee) in mono-and difluoromethyl derivatives (1b and 1c) and moderate (60% ee) in a trifl
Publikováno v:
Tetrahedron Letters. 26:2877-2880
Publikováno v:
Tetrahedron Letters. 26:219-222
3-Trifluoromethyl-2Z, 4E-dienoate ( 14 ) and the dienamide ( 10 , 11 ) were prepared through the Claisen rearrangement of trifluoromethylated propargylic and allylic alcohols.
Publikováno v:
Tetrahedron Letters. 25:4749-4752
The hydrometallation of trifluoromethylated propargyl alcohol derivatives with metal hydride reagents proceeds smoothly to give cis- and trans-olefins on H2O quenching. The halodemetallation of intermediate formed in the reaction process was also exa