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Synlett 2000; 2000(7): 0971-0974
DOI: 10.1055/s-2000-6646
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Synthesis of 6a-Carba-α- and 6a-Carba-β-d-Fructopyranose from an Enzymatically Resolved Cyclohexanetriol Building Block

Idzi Hubrecht* , Erik Van der Eycken, Johan Van der Eycken
  • *Laboratory of Organic and Bio-organic Synthesis, University of Gent, Krijgslaan 281 (S.4), B-9000 Gent, Belgium; Fax + 32(0)9 264 49 98; E-mail: Johan.Vandereycken@rug.ac.be
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Publikationsdatum:
31. Dezember 2000 (online)

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6a-Carba-α-d-fructopyranose (1) and 6a-Carba-β-d-fructopyranose 2 have been synthesized from the enzymatically resolved homochiral building block 1(R)-6 in six steps.

stereoselective synthesis - carbocycles - carbohydrates - carba-sugars - pseudo-sugars