A new oxa-michael reaction and a gold-catalysed cyclisation en route to C-glycosides

Redon, S., Wierzbicki,, M. and Prunet, J. (2013) A new oxa-michael reaction and a gold-catalysed cyclisation en route to C-glycosides. Tetrahedron Letters, 54(16), pp. 2089-2092. (doi:10.1016/j.tetlet.2013.02.022)

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Abstract

Two new syntheses of benzyl C-glycosides have been developed. The first one involves an unprecedented oxa-Michael cyclisation and the second one relies on an efficient gold-catalysed ring-closure.

Item Type:Articles
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Redon, Dr Sebastien and Prunet, Dr Joelle
Authors: Redon, S., Wierzbicki,, M., and Prunet, J.
College/School:College of Science and Engineering > School of Chemistry
Journal Name:Tetrahedron Letters
ISSN:0040-4039

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