摘要
5-Fluorocytidine was synthesized by condensation of N,O-di-silylated 5-fluorocytosine with 1,2,3,5-tetra-O-acetyl-β-D-ribofuranose and subsequent aminolysis in an overall yield of 46%.
5-Fluorocytidine was synthesized by condensation of N,O-di-silylated 5-fluorocytosine with 1,2,3,5-tetra-O-acetyl-β-D-ribofuranose and subsequent aminolysis in an overall yield of 46%.
出处
《中国医药工业杂志》
CAS
CSCD
北大核心
2005年第11期669-669,696,共2页
Chinese Journal of Pharmaceuticals
基金
山东省卫生厅基金课题(03210206)
