Anhydro sugars to enantiomerically pure building blocks

Efficient syntheses of γ-lactones and furanoids

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

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

Efficient and economic syntheses of multifunctional dihydrofurans, tetrahydrofurans and γ-lactones are described. The regiochemistry of the ring junctions of the annulated oxa ring systems are controlled using temporary or permanent protection of the C-4 hydroxyl group.

Original languageEnglish
Pages (from-to)71-75
Number of pages5
JournalPolish Journal of Chemistry
Volume73
Issue number1
Publication statusPublished - 1999

Fingerprint

Furans
Lactones
Sugars
Hydroxyl Radical
Economics

Keywords

  • γ-lactones
  • Anhydro sugars
  • Long-chain sugars
  • Optically pure tetrahydro- and dihydrofurans
  • Tricyclic furanoids

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

Anhydro sugars to enantiomerically pure building blocks : Efficient syntheses of γ-lactones and furanoids. / Al-Qawasmeh, R. A.; Al-Tel, T. H.; Abdel-Jalil, R. J.; Thürmer, R.; Voelter, W.

In: Polish Journal of Chemistry, Vol. 73, No. 1, 1999, p. 71-75.

Research output: Contribution to journalArticle

Al-Qawasmeh, R. A. ; Al-Tel, T. H. ; Abdel-Jalil, R. J. ; Thürmer, R. ; Voelter, W. / Anhydro sugars to enantiomerically pure building blocks : Efficient syntheses of γ-lactones and furanoids. In: Polish Journal of Chemistry. 1999 ; Vol. 73, No. 1. pp. 71-75.
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