Unexpected orthogonality of S-benzoxazolyl and S-thiazolinyl glycosides: application to expeditious oligosaccharide assembly.

Org Lett

Department of Chemistry and Biochemistry, University of Missouri, St. Louis, One University Boulevard, St. Louis, Missouri 63121, USA.

Published: February 2009

Thorough mechanistic studies of the alkylation pathway for the activation of glycosyl thioimidates have led to the development of the "thioimidate-only orthogonal strategy". Discrimination among S-thiazolinyl (STaz) and S-benzoxazolyl (SBox) anomeric leaving groups was achieved by fine-tuning of the activation conditions. Preferential glycosidation of a certain thioimidate is not simply determined by the strength of activating reagents; instead, the type of activation--direct vs indirect--comes to the fore and plays the key role.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2642804PMC
http://dx.doi.org/10.1021/ol802740bDOI Listing

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