Stereoselective Synthesis of 2'-C-Methyl-cyclopropyl-Fused Carbanucleosides as Potential Anti-HCV Agents
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Stereoselective synthesis of 2'-C-methyl-cyclopropyl-fused carbanucleosides was accomplished via stereoselective cyclopropanation,regioselective cleavage of the isopropylidene group, stereoselective Grignard reaction, and cyclic sulfate chemistry.

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