摘要
Sugar-protected 6-halouridine derivatives underwent Suzuki-Miyaura cross-coupling reactions with arylboronic acids in the presence of palladium(II) acetate as a catalyst, triphenylphosphine as a ligand, and sodium carbonate as a base. This methodology is applicable to both the C5- and C6-position of uridine and provides a direct access for versatile uridine derivatives.
原文 | 英語 |
---|---|
頁(從 - 到) | 3915-3923 |
頁數 | 9 |
期刊 | Tetrahedron |
卷 | 67 |
發行號 | 21 |
DOIs | |
出版狀態 | 已發佈 - 2011 五月 27 |
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry