132979-39-6Relevant articles and documents
Synthesis, antiviral activity, cytotoxicity and cellular pharmacology of l-3′-azido-2′,3′-dideoxypurine nucleosides
Zhang, Hong-Wang,Detorio, Mervi,Herman, Brian D.,Solomon, Sarah,Bassit, Leda,Nettles, James H.,Obikhod, Aleksandr,Tao, Si-Jia,Mellors, John W.,Sluis-Cremer, Nicolas,Coats, Steven J.,Schinazi, Raymond F.
, p. 3832 - 3844 (2011)
Microwave-assisted optimized transglycosylation reactions were used to prepare eleven modified l-3′-azido-2′,3′-dideoxypurine nucleosides. These l-nucleoside analogs were evaluated against HIV and hepatitis B virus. The l-3′-azido-2′,3′-dideoxypurines nuc
Coupling reaction of 1-thiopentofuranosides with silylated pyrimidine bases by activation with N-bromosuccinimide: Synthesis of 3'-Azido-3'-deoxythymidine and its related nucleoside analogs
Sugimura,Osumi,Yamazaki,Yamaya
, p. 1813 - 1816 (2007/10/02)
3'-Azido-3'-deoxythymidine, 3'-fluoro-3'-deoxythymidine, and their 2'-C-substituted derivatives and L-enantiomers were synthesized by the coupling reaction of the corresponding phenyl 1-thiopentofuranosides with silylated thymine by activation with N-bromosuccinimide.