Synthesis, conformation and antiviral activity of nucleoside analogues with the (2-hydroxy-1-phenylethoxy)methyl glycone—a family of nucleoside analogues related to d4T and aciclovir
作者:David F. Ewing、Virginie Glaçon、Christophe Len、Grahame Mackenzie
DOI:10.1039/b510056a
日期:——
A complete family of acyclic nucleoside analogues has been obtained by combining the (2-hydroxy-1-phenylethoxy)methyl glycone with the nucleoside bases adenine, guanine, cytosine, thymine and uracil. In each case both optical antipodes have been prepared in enantiomerically pure form from styrene via asymmetric dihydroxylation. The conformation of the uracil and adenine derivatives has been compared
完整的无环核苷类似物家族是通过将(2-羟基-1-苯基乙氧基)甲基甘氨酸与 核苷 基地 腺嘌呤, 鸟嘌呤, 胞嘧啶, 胸腺嘧啶 和 尿嘧啶。在每种情况下,两种光学对映体均以对映体纯形式由苯乙烯 通过不对称的二羟基化。尿嘧啶和腺嘌呤衍生物的构象已通过使用PM3方法的综合计算与以下构象进行了比较:2',3'-二脱氢-2',3'-二脱氧尿苷(d4U)和类似的3-羟甲基-1,3-二氢苯并[ c ]呋喃核苷(bfU)。已经观察到一些抗病毒活性。