Orthogonal sulfation strategy for synthetic heparan sulfate ligands.

Org Lett

Department of Chemistry, Purdue University, West Lafayette, Indiana 47907-2084, USA.

Published: October 2005

[reaction: see text] An orthogonal sulfation strategy involving six different protecting groups has been developed for generating sulfated carbohydrate libraries based on heparan. Chemoselective cleavage conditions (optimized for a heparan disaccharide) can be performed in the presence of sulfate esters as well as the remaining protecting groups.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1851889PMC
http://dx.doi.org/10.1021/ol052130oDOI Listing

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