An expeditious approach to tri-substituted chiral thiazolines

Raid J. Abdel-Jalil, Muhammad Saeed, Wolfgang Voelter

Research output: Contribution to journalArticle

16 Citations (Scopus)

Abstract

A regio- and stereoselective route from the cis-oriented epoxytriflate pentoses 1 and 4 via 4-amino-4-deoxy sugars 2 and 5 to chiral thiazoline derivatives 3a-e and 6a-e in high yields is described.

Original languageEnglish
Pages (from-to)2435-2437
Number of pages3
JournalTetrahedron Letters
Volume42
Issue number13
DOIs
Publication statusPublished - Mar 26 2001

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Deoxy Sugars
Pentoses
Derivatives

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

An expeditious approach to tri-substituted chiral thiazolines. / Abdel-Jalil, Raid J.; Saeed, Muhammad; Voelter, Wolfgang.

In: Tetrahedron Letters, Vol. 42, No. 13, 26.03.2001, p. 2435-2437.

Research output: Contribution to journalArticle

Abdel-Jalil, Raid J. ; Saeed, Muhammad ; Voelter, Wolfgang. / An expeditious approach to tri-substituted chiral thiazolines. In: Tetrahedron Letters. 2001 ; Vol. 42, No. 13. pp. 2435-2437.
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