Epoxy pyranoses, chiral synthons for versatile regio- and stereocontrolled functionalizations

W. Voelter, R. Thürmer, R. A. Al-Qawasmeh, T. H. Al-Tel, R. Abdel-Jalil, Y. Al-Abed

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

From epoxy sugars, neighbouring an O-triflyl residue, efficient short-cut new routes to aminodeoxy, (amino acid)-deoxy, cyclopropanated, β-hydroxyketo or γ-butyrolactone pyranoses are developed.

Original languageEnglish
Pages (from-to)55-69
Number of pages15
JournalPolish Journal of Chemistry
Volume73
Issue number1
Publication statusPublished - 1999

Fingerprint

Sugars
Amino Acids

Keywords

  • β-hydroxyketo sugars
  • (amino acid)-deoxy sugars
  • Aminodeoxy sugars
  • Canadensolide
  • Cyclopropanated sugars
  • Epoxy pyranoses
  • Triflate pyranoses

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

Voelter, W., Thürmer, R., Al-Qawasmeh, R. A., Al-Tel, T. H., Abdel-Jalil, R., & Al-Abed, Y. (1999). Epoxy pyranoses, chiral synthons for versatile regio- and stereocontrolled functionalizations. Polish Journal of Chemistry, 73(1), 55-69.

Epoxy pyranoses, chiral synthons for versatile regio- and stereocontrolled functionalizations. / Voelter, W.; Thürmer, R.; Al-Qawasmeh, R. A.; Al-Tel, T. H.; Abdel-Jalil, R.; Al-Abed, Y.

In: Polish Journal of Chemistry, Vol. 73, No. 1, 1999, p. 55-69.

Research output: Contribution to journalArticle

Voelter, W, Thürmer, R, Al-Qawasmeh, RA, Al-Tel, TH, Abdel-Jalil, R & Al-Abed, Y 1999, 'Epoxy pyranoses, chiral synthons for versatile regio- and stereocontrolled functionalizations', Polish Journal of Chemistry, vol. 73, no. 1, pp. 55-69.
Voelter, W. ; Thürmer, R. ; Al-Qawasmeh, R. A. ; Al-Tel, T. H. ; Abdel-Jalil, R. ; Al-Abed, Y. / Epoxy pyranoses, chiral synthons for versatile regio- and stereocontrolled functionalizations. In: Polish Journal of Chemistry. 1999 ; Vol. 73, No. 1. pp. 55-69.
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