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Synthesis of <i>N</i>‐Bz‐Protected <scp>D</scp>‐Daunosamine and <scp>D</scp>‐Ristosamine by Silica Gel Promoted Intramolecular Conjugate Addition of Trichloroacetimidates obtained from Osmundalactone and Its Epimer
28
Citations
35
References
2010
Year
Silica Gel ChromatographyDiversity Oriented SynthesisEngineeringExcellent YieldsOrganic ChemistryChemistryHeterocycle ChemistrySimple SynthesisPharmacologyPharmaceutical ChemistrySynthetic ChemistryBiomolecular EngineeringNatural Product Synthesis
Abstract Trichloroacetimidates prepared from osmundalactone and its epimer unexpectedly undergo intramolecular conjugate addition during silica gel chromatography to produce oxazolines in excellent yields. The novel, simple synthesis of N ‐Bz‐protected D ‐daunosamine and D ‐ristosamine from these oxazolines is described in this paper.
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