抜粋
2,3-Unsaturated-4-keto glycosyl acetates were found to exhibit low reactivity under several glycosylation conditions. Chemoselective glycosylations were effectively performed using 2,3-unsaturated glycosyl and 2,3-dideoxy glycosyl acetates as armed glycosyl donors, and 2,3-unsaturated-4-keto glycosyl acetates as disarmed glycosyl donors.
| 元の言語 | English |
|---|---|
| ページ（範囲） | 988-990 |
| ページ数 | 3 |
| ジャーナル | Organic and Biomolecular Chemistry |
| 巻 | 8 |
| 発行部数 | 5 |
| DOI | |
| 出版物ステータス | Published - 2010 2 26 |
ASJC Scopus subject areas
- Biochemistry
- Physical and Theoretical Chemistry
- Organic Chemistry
フィンガープリント Chemoselective glycosylations using 2,3-unsaturated-4-keto glycosyl donors' の研究トピックを掘り下げます。これらはともに一意のフィンガープリントを構成します。
これを引用
Kusumi, S., Wang, S., Watanabe, T., Sasaki, K., Takahashi, D., & Toshima, K. (2010). Chemoselective glycosylations using 2,3-unsaturated-4-keto glycosyl donors. Organic and Biomolecular Chemistry, 8(5), 988-990. https://doi.org/10.1039/b925587g