Synthesis of optically active 2′,3′-dideoxy-3′-oxa-4′-thio-ribonucleoside analogues by transposition of a leaving group on chiral oxathiolanes via a reductive-oxidative process
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T. Mansour | Wei Wang | H. Jin
[1] L. Brasili,et al. A novel class of 1,3-oxathiolane nucleoside analogues having potent anti-HIV activity , 1993 .
[2] R. Schinazi,et al. 1,3-dioxolanylpurine nucleosides (2R,4R) and (2R,4S) with selective anti-HIV-1 activity in human lymphocytes. , 1993, Journal of medicinal chemistry.
[3] T. Mansour,et al. Oxidative degradation of L-ascorbic acid acetals to 2′,3′-dideoxy-3′-oxaribofuranosides. Synthesis of enantiomerically pure 2′,3′-dideoxy-3′-oxacytidine stereoisomers as potential antiviral agents , 1992 .
[4] G. Gray,et al. An efficient synthesis of anhydroalditols and allylic-glycosides , 1987 .
[5] H. Vorbrüggen,et al. Nucleoside syntheses, XXII1) Nucleoside synthesis with trimethylsilyl triflate and perchlorate as catalysts , 1981 .