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

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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.