Stereoselective bromination of β-ribofuranosyl amide. Enantioselective synthesis of (+)-hydantocidin
1994
Abstract The synthesis of hydantocidin, a potent herbicidal natural product, is highlighted by a stereoselective bromination of β- D -ribofuranosyl amide to give only the α-bromo β-amide and subsequent spirocyclization about the anomeric position with silver cyanate to form the hydantoin moiety.
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