Abstract
Abstract Pyrrolo[2,3-b]pyridine 2′-deoxynucleosides were synthesized stereoselectively by solid-liquid phase-transfer glycosylation. Also 4-chloropyrrolo[2,3-d]pyrimidine 2′-deoxyribofuranosides were deoxygenated yielding a series of new base-modified 2′,3′-dideoxynucleosides.
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