Organic Letters · 2003 · 18 citations · 2 references
Natural SciencesChemistryOrganometallic ChemistryCross-coupling ReactionsRetrosynthetic AnalysisAldol ReactionHydride FormationHydride MigrationStereoselective Aldol ReactionsSteric Constraints
[structure: see text] Non-aldol aldol rearrangement of the epoxy silyl ether 13b afforded the expected anti methyl ketone 14, while the diastereomeric epoxy silyl ether 13a afforded the syn methyl ketone 8b via an unprecedented syn hydride migration. Calculations suggest that this unusual reaction proceeds via the carbocation, which cannot easily rotate due to steric hindrance.
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