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An efficient procedure for the preparation of (1S,3R)- and (1S,3S)-1-amino-3-(hydroxymethyl)cyclopentanes
Authors:Rapoport Henry  Chen Yuewu  Mohareb Rafat M  Ahn Jin Hee  Sim Tae Bo  Ho Jonathan Z
Affiliation:Department of Chemistry, University of California, Berkeley 94720, USA.
Abstract:Enantiomerically pure (1S,3S)- and (1S,3R)-1-amino-3-(hydroxymethyl)cyclopentanes have been efficiently synthesized from L-aspartic acid. The title compounds are isosteres of ribose and may be used to construct nucleoside analogs with important antiviral and antineoplastic activities as demonstrated by a concise total synthesis of (+)-4'-deoxycarbapentostatin nucleoside.
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