| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5220125 | Tetrahedron | 2011 | 9 Pages |
Abstract
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.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Yu-Chiao Shih, Tun-Cheng Chien,