Total Synthesis of Vineomycin B2

被引:27
作者
Kusumi, Shunichi [1 ]
Tomono, Satoshi [1 ]
Okuzawa, Shunsuke [1 ]
Kaneko, Erika [1 ]
Ueda, Takashi [1 ]
Sasaki, Kaname [1 ]
Takahashi, Daisuke [1 ]
Toshima, Kazunobu [1 ]
机构
[1] Keio Univ, Fac Sci & Technol, Dept Appl Chem, Kohoku Ku, Yokohama, Kanagawa 2238522, Japan
关键词
C-ARYLGLYCOSYLATION; METHYL-ESTER; GLYCOSYLATION; ARYL; LACTONAMYCIN; GLYCOSIDES; STRATEGY;
D O I
10.1021/ja407827n
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The first total synthesis of vineomycin B-2 (1) has been accomplished. The aglycon segment, a vineomycinone B-2 derivative, and the glycon segment, an alpha-L-acurosyl-L-rhodinose derivative, were prepared via C-glycosylation using an unprotected sugar and powerful chemoselective O-glycosylation using a 2,3-unsaturated sugar, respectively, as the key steps. Furthermore, effective and simultaneous introduction of the two glycon moieties to the aglycon part by concentration-controlled glycosylation led to the total synthesis of 1.
引用
收藏
页码:15909 / 15912
页数:4
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