134485-39-5Relevant articles and documents
Stereocontrolled synthesis of β-2'-deoxypyrimidine nucleosides via intramolecular glycosylations
Xia, Xiaoyang,Wang, Jianying,Hager, Michael W.,Sisti, Nicholas,Liotta, Dennis C.
, p. 1111 - 1114 (2007/10/03)
A pyrimidine moiety was tethered at the 3'-β-position of D-threo-furanosides. By carefully controlling the reaction conditions, pyrimidine bases can be delivered to the anomeric center to give of β-pyrimidine nucleosides in good yield and with complete stereocontrol.
Cyclization protocols for controlling the glycosidic stereochemistry of nucleosides. Application to the synthesis of the antiviral agent 3'-azido-3'-deoxythymidine (AZT)
Hager,Liotta
, p. 5117 - 5119 (2007/10/02)
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