Abstract
The stereospecific synthesis is described of the first member of a new class of C-nucleoside analogues in which the sugar ring is replaced with a 1, 3-thiazolidine ring. The 1, 3-thiazolidin-2-yl analogues (1) and (2) of pseudouridine were prepared stereospecifically via condensation of L or D-cysteine with a formylated nucleobase.
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