Facile, highly stereoselective synthesis of 2',3'-dideoxy- and 2',3'-didehydro-2',3'-dideoxy nucleosides via a furanoid glycal intermediate
Regiospecific and highly stereoselective electrophilic addition reactions to the furanoid glycal 10 have been used as key steps in the synthesis of ddA and d4T antiviral nucleosides.
Kim,Misco
p. 5733 - 5736
(2007/10/02)
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