@article{4e265a6873bd4f3d82fd04ff804809e4,
title = "Practical synthesis of 6-aryluridines via palladium(II) acetate catalyzed Suzuki-Miyaura cross-coupling reaction",
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.",
keywords = "Boronic acid, Cross-coupling, Nucleoside, Suzuki-Miyaura, Uridine",
author = "Shih, {Yu Chiao} and Chien, {Tun Cheng}",
note = "Funding Information: This work was supported by Research Grant 97-2113-M-003-001-MY2 from the National Science Council , Taiwan. We are grateful to the National Center for High-performance Computing of Taiwan for the electronic resources and facilities. ",
year = "2011",
month = may,
day = "27",
doi = "10.1016/j.tet.2011.03.051",
language = "English",
volume = "67",
pages = "3915--3923",
journal = "Tetrahedron",
issn = "0040-4020",
publisher = "Elsevier Limited",
number = "21",
}