Download PDF
Synthesis 1994; 1994(12): 1413-1414
DOI: 10.1055/s-1994-25704
short paper
© 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.

Facile Synthesis of 1,2-trans-Nitrophenyl-1-Thioglycopyranosides

Hugues Driguez* , Wieslaw Szeja
  • *Centre de Recherches sur les Macromolécules Végétales, CNRS, BP 53 X, F-38041 Grenoble Cedex 9, France
Further Information

Publication History

Publication Date:
25 April 2002 (online)

  PDF Download  Permissions and Reprints All articles of this category

1,2-trans-2-Nitro-, 4-nitro- and 2,4-dinitrophenyl-1-thioglycopyranosides were synthesized in high yield by condensation of per-O-acetyl-1-thioglucose with the appropriate nitro- or dinitrofluorobenzene in the presence of potassium carbonate. The pseudothiourea precursor was also used under these coupling conditions. 1,2-trans-4-Nitrophenyl-1-thioglycosides derived from β-D-galactose, β-D-xylose, α-L-arabinose and maltose were also obtained in good yield.