Australian Journal of Chemistry · 1995 · 16 citations · 0 references
PharmacyChemistryMedicinal ChemistryDrug DiscoveryOrganic ChemistrySynthetic Medicinal ChemistryCrystal ChemistryHeterocycle SynthesisHeterocyclic ChemistryMacrocycle SynthesisChiral Product SynthesisGrignard Reagent SynthesisStereocontrolled Library SynthesisX-ray Diffraction AnalysisX-ray Structure Determination
In a synthetic approach to (+)-dioncophylline C (1), a coupling between the chiral oxazoline (3) and the Grignard reagent obtained from bromide (4) gave the major biaryl (5) and the minor biaryl (12) in good yield and high diastereoselectivity (yield 70%; ratio 91:9). The stereochemistry of the major biaryl (5) was confirmed by X-ray structure analysis of the derived crystalline iodide salt (13).