Efficient synthesis of thioglycosides via a Mitsunobu condensation

Robert A. Falconer, Istvan Jablonkai, Istvan Toth

Research output: Contribution to journalArticle

27 Citations (Scopus)

Abstract

Thioglycosides were synthesised from 1-thiosugars and a series of alcohols under Mitsunobu conditions using 1,1'-(azodicarbonyl)dipiperidine and trimethylphosphine. The conditions were found to be compatible with a wide range of functionalities and protecting groups.

Original languageEnglish
Pages (from-to)8663-8666
Number of pages4
JournalTetrahedron Letters
Volume40
Issue number49
DOIs
Publication statusPublished - Dec 3 1999

Fingerprint

Thiosugars
Thioglycosides
Condensation
Alcohols
1,1-(azodicarbonyl)dipiperidine

Keywords

  • Glycolipids
  • Glycosylation
  • Mitsunobu reactions
  • Thiosugars

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Efficient synthesis of thioglycosides via a Mitsunobu condensation. / Falconer, Robert A.; Jablonkai, Istvan; Toth, Istvan.

In: Tetrahedron Letters, Vol. 40, No. 49, 03.12.1999, p. 8663-8666.

Research output: Contribution to journalArticle

Falconer, Robert A. ; Jablonkai, Istvan ; Toth, Istvan. / Efficient synthesis of thioglycosides via a Mitsunobu condensation. In: Tetrahedron Letters. 1999 ; Vol. 40, No. 49. pp. 8663-8666.
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