A Facile One-Pot Synthesis of 2,3'-Anhydro-2'-Deoxyuridines via 3'-O-Imidazolylsulfonates

Abstract
Continued interests in the novel synthetic methods of the pivotal compound, 2,3′-anhydro-2′-deoxyribonucleosides (7) uncovered a facile one-pot conversion of 5 with 1,1′-sulfonyldiimidazole in basic conditions to 7 with almost quantitative yields (91–99%).

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