Synthetic studies of halichondrin B, an antitumor polyether macrolide isolated from a marine sponge .5. A highly concise and efficient synthesis of the C-37 approximate to C-54 tricyclic JKL-ring part
被引:21
作者:
Horita, K
论文数: 0引用数: 0
h-index: 0
机构:Faculty of Pharmaceutical Sciences, Hokkaido University
Horita, K
Hachiya, S
论文数: 0引用数: 0
h-index: 0
机构:Faculty of Pharmaceutical Sciences, Hokkaido University
Hachiya, S
Ogihara, K
论文数: 0引用数: 0
h-index: 0
机构:Faculty of Pharmaceutical Sciences, Hokkaido University
Ogihara, K
机构:
[1] Faculty of Pharmaceutical Sciences, Hokkaido University
A concise and efficient synthesis of C(37)similar to C-54 tricyclic JKL-ring unit (2) of halichondrin B (1) utilizing C-2-symmetric spiroketal derivative (5) as a synthetic key intermediate, easily provided from dimethyl L-(+)-tartrate, is reported.