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Large-scale synthesis of all stereoisomers of a 2,3-unsaturated C-glycoside scaffold
Authors:Gerard Baudouin  Marié Jean-Charles  Pandya Bhaumik A  Lee Maurice D  Liu Haibo  Marcaurelle Lisa A
Affiliation:Chemical Biology Platform, The Broad Institute of MIT and Harvard, 7 Cambridge Center, Cambridge, Massachusetts 02142, USA.
Abstract:All stereoisomers of a highly functionalized 2,3-unsaturated C-glycoside can be accessed in 10-100 g quantities from readily available starting materials and reagents in 3-7 steps. These chiral scaffolds contain three stereogenic centers along with orthogonally protected functional groups for downstream reactivity.
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