Download PDF
Synlett 2000; 2000(7): 0971-0974
DOI: 10.1055/s-2000-6646
letter
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

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
Further Information

Publication History

Publication Date:
31 December 2000 (online)

  PDF Download  Permissions and Reprints All articles of this category

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

      >