作者: Michael R. Dyson , Paul L. Coe , Richard T. Walker
DOI: 10.1021/JM00113A016
关键词: Thionucleosides 、 Thio- 、 Chemistry 、 Stereochemistry 、 In vitro 、 Nucleoside 、 Biological activity
摘要: Starting from benzyl 3,5-di-O-benzyl-2-deoxy-1,4-dithio-D-erythro- pentofuranoside (4), the following 2'-deoxy nucleoside analogues have been synthesized: 4'-thiothymidine (8), 3'-azido-4'-thio- deoxythymidine (10), and (E)-5-(2-bromovinyl)-4'-thio-2'-deoxyuridine (22). The first compound is toxic, second not toxic nor has detectable biological activity, third significant activity against some herpesviruses.