A convenient method for the synthesis of cyclic trithiocarbonates on carbohydrate scaffolds

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

Research output: Contribution to journalArticle

16 Citations (Scopus)

Abstract

An efficient regio- and stereoselective method for the synthesis of cyclic trithiocarbonates on carbohydrate skeleton is described. A freshly prepared solution of sodium trithiocarbonate reacts with cis-oriented epoxytriflate pentoses 7-11 to yield the corresponding cyclic trithiocarbonates 12-16. Structures of all new compounds are established through MS, 1H and 13C NMR techniques.

Original languageEnglish
Pages (from-to)315-317
Number of pages3
JournalTetrahedron Letters
Volume44
Issue number2
DOIs
Publication statusPublished - Jan 6 2003

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Scaffolds
Carbohydrates
Pentoses
Skeleton
Sodium
Nuclear magnetic resonance
trithiocarbonic acid
Carbon-13 Magnetic Resonance Spectroscopy
Proton Magnetic Resonance Spectroscopy

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

A convenient method for the synthesis of cyclic trithiocarbonates on carbohydrate scaffolds. / Saeed, Muhammad; Abbas, Muhammad; Abdel-Jalil, Raid J.; Zahid, Muhammad; Voelter, Wolfgang.

In: Tetrahedron Letters, Vol. 44, No. 2, 06.01.2003, p. 315-317.

Research output: Contribution to journalArticle

Saeed, Muhammad ; Abbas, Muhammad ; Abdel-Jalil, Raid J. ; Zahid, Muhammad ; Voelter, Wolfgang. / A convenient method for the synthesis of cyclic trithiocarbonates on carbohydrate scaffolds. In: Tetrahedron Letters. 2003 ; Vol. 44, No. 2. pp. 315-317.
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