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Synlett 1992; 1992(4): 311-312
DOI: 10.1055/s-1992-21351
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Stereoselective Synthesis of 4-Acetylamino-2,4,6-trideoxy-L-ribo-hexose from Ethyl (S)-ß-Hydroxybutyrate

Giuseppe Guanti* , Luca Banfi, Enrica Narisano, Sergio Thea
  • *Istituto di Chimica Organica e C.N.R., Centro di Studio sui Diariloidi, corso Europa 26, I-16132 Genova, Italy
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Publication Date:
08 March 2002 (online)

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The title protected aminosugar 11 was stereoselectively prepared in 14 steps and 8% overall yield from L-allo-threonine synthetic equivalent 2, which is in turn obtained in one step from ethyl (S)-ß-hydroxvbutyrate.

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