抄録
The first total synthesis of vineomycin B2 (1) has been accomplished. The aglycon segment, a vineomycinone B2 derivative, and the glycon segment, an α-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.
| 本文言語 | English |
|---|---|
| ページ(範囲) | 15909-15912 |
| ページ数 | 4 |
| ジャーナル | Journal of the American Chemical Society |
| 巻 | 135 |
| 号 | 42 |
| DOI | |
| 出版ステータス | Published - 2013 10月 23 |
ASJC Scopus subject areas
- 触媒
- 化学一般
- 生化学
- コロイド化学および表面化学
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