Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Shizuki Ide"'
Autor:
Chieko Motokawa, Shizuki Ide, Yoshiro Matsuda, Yasushige Chiyomaru, Kazuki Furuno, Takahiro Itou
Publikováno v:
Tetrahedron. 49:9947-9954
The heteropolycycles, indolizinoquinolizines (7, 8, 20) were obtained by the reaction of either pyridylketene dithioacetal (2) with two molar equivalents of pyridinium salts (4a–c) or pyridiniumketene dithioacetal (19) with two molar equivalents of
Autor:
Makoto Yamashita, K. Torisu, Kazuki Furuno, Kimitoshi Takahashi, Yoshiro Matsuda, Shizuki Ide
Publikováno v:
ChemInform. 23
The reaction of benzimidazolium salt (3) and polarized olefins (1a,b,d and 2c) with K 2 CO 3 in CHCl 3 gave the corresponding benzimidazolium N-allylides (4a-d). Thermolyses of N-allylides (4a,b) in refluxing xylene afforded the 1,5-dipolar cyclizati
Autor:
K. Takahashi, Makoto Yamashita, Kazuki Furuno, Keisuke Katou, Hiromi Gotou, Y. Matsuda, H. Matsumoto, Shizuki Ide, K. Torisu
Publikováno v:
ChemInform. 23
Autor:
Yoshiro Matsuda, Makoto Yamashita, Chieko Motokawa, Kazuki Furuno, Takahiro Itou, K. Torisu, Kimitoshi Takahashi, Shizuki Ide
Publikováno v:
ChemInform. 23
The heteropolycyles, indolizinoquinolines were obtained by the reaction of pyridylketene dithioacetal with two molar equivalents of pyridinium salts
Autor:
Kojiro Takahashi, Kazuki Furuno, Makoto Yamashita, Takahiro Itou, Chieko Motokawa, Hiromi Gotou, Y. Matsuda, Shizuki Ide, K. Torisu
Publikováno v:
ChemInform. 24
Autor:
Yoshiro Matsuda, Chieko Motokawa, Kazuki Furuno, Takahiro Itou, Yasushige Chiyomaru, Shizuki Ide
Publikováno v:
ChemInform. 25
The heteropolycycles, indolizinoquinolizines (7, 8, 20) were obtained by the reaction of either pyridylketene dithioacetal (2) with two molar equivalents of pyridinium salts (4a–c) or pyridiniumketene dithioacetal (19) with two molar equivalents of
Autor:
Kimitoshi Takahashi, Makoto Yamashita, Shizuki Ide, Yoshiro Matsuda, Takahiro Itou, Chieko Motokawa, Yasushige Chiyomaru
Publikováno v:
ChemInform. 25
The reaction of N-aminoimidazolium salts (4, 5) with polarized olefins (2a-d, 3a, b) in the presence of K2CO3 in EtOH gave the corresponding imidazolium N-vinylimino ylides (6, 7). Thermolyses of the N-vinylimino ylides (6c-f, 7a-c) afforded mesomeri
Autor:
Katsura Torisu, Hiroshi Matsumoto, Kimitoshi Takahashi, Syuichi Maeda, Yoshiro Matsuda, Shizuki Ide, Keisuke Katou, Makoto Yamashita, Kazuki Furuno
Publikováno v:
YAKUGAKU ZASSHI. 112:42-49
Autor:
Yoshiro MATSUDA, Hiroshi MATSUMOTO, Shizuki IDE, Kazuki FURUNO, Katsura TORISU, Takahiro ITOU, Chieko MOTOKAWA
Publikováno v:
Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan. 113(1)
By the reaction of 2-benzoylmethylimidazoles (1a, b) with polarized olefins (2, 3) in the presence of K2CO3, the corresponding imidazo[1,2-a]pyridine derivatives (4, 5) were obtained. Methylsulfinylimidazopyridine derivative (7) obtained by the react
Autor:
K. Takahashi, H. Matsumoto, Keisuke Katou, Makoto Yamashita, Y. Matsuda, Shizuki Ide, Hiromi Gotou
Publikováno v:
ChemInform. 21