Synthesis of carbohydrates with an anomeric thiol moiety for elaboration into metabolically stable thioglycosides

Article abstract of DOI:10.1080/07328309908544045

The synthesis of thioglycosides for use as metabolically stable biological probes is an area of continued interest. This paper describes the synthesis of functionalised carbohydrates which contain an anomeric thio group. During the course of this work we have examined the most viable route into compounds such as the specifically functionalised carbohydrates 36 and 37, and have also investigated the usefulness of disulfides as protecting groups for anomeric thiols.

Full text of DOI:10.1080/07328309908544045

Journal of Carbohydrate Chemistry
ISSN: 0732-8303 (Print) 1532-2327 (Online) Journal homepage: http://www.tandfonline.com/loi/lcar20
Synthesis of Carbohydrates with an Anomeric
Thiol Moiety for Elaboration into Metabolically
Stable Thioglycosides
Milton J. Kiefel , Robin J. Thomson , Milica Radovanovic & Mark von Itzstein
To cite this article: Milton J. Kiefel , Robin J. Thomson , Milica Radovanovic & Mark von
Itzstein (1999) Synthesis of Carbohydrates with an Anomeric Thiol Moiety for Elaboration into
Metabolically Stable Thioglycosides, Journal of Carbohydrate Chemistry, 18:8, 937-959, DOI:
10.1080/07328309908544045
To link to this article: http://dx.doi.org/10.1080/07328309908544045
Published online: 27 Feb 2008.
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Date: 13 January 2016, At: 07:49