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

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

doi:10.1016/S0040-4039(02)02529-7

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

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

^*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

18 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 language	English
Pages (from-to)	315-317
Number of pages	3
Journal	Tetrahedron Letters
Volume	44
Issue number	2
DOIs	https://doi.org/10.1016/S0040-4039(02)02529-7
Publication status	Published - Jan 6 2003
Externally published	Yes

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(02)02529-7

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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.",

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AU - Abbas, Muhammad

AU - Abdel-Jalil, Raid J.

AU - Zahid, Muhammad

AU - Voelter, Wolfgang

PY - 2003/1/6

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AB - 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.

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JO - Tetrahedron Letters

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

Abstract

ASJC Scopus subject areas

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