Publication | Open Access
Mild and Highly Efficient Stereoselective Synthesis of 2,3‐Unsaturated Glycopyranosides using La(NO<sub>3</sub>)<sub>3</sub> · 6H<sub>2</sub>O as a Catalyst: Ferrier Rearrangement
16
Citations
25
References
2008
Year
Efficient Stereoselective ReactionEngineeringNatural SciencesDiversity-oriented SynthesisGlycobiologyOrganic ChemistryTrimethyl SilaneCatalysisSolvent‐free ConditionsChemistryFerrier RearrangementStereoselective SynthesisSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
Abstract A mild and highly efficient stereoselective reaction of 3,4,6‐tri‐O‐acetyl‐d‐glucal with a variety of nucleophiles, viz. alcohols, phenols, thiols, thiophenols, and allyl trimethyl silane (TMS), in the presence of 5 mol% of lanthanum(III) nitrate hexahydrate under solvent‐free conditions yielded the corresponding 2,3‐unsaturated glycopyranosides (pseudoglycals) in excellent yields.
| Year | Citations | |
|---|---|---|
Page 1
Page 1