Publication | Closed Access
Absolute Konfiguration des Mevalolactons
56
Citations
14
References
1960
Year
Integral GeometryFrenchBioorganic ChemistryQuinic AcidEngineeringNatural SciencesOrganic ChemistryAbsolute KonfigurationDirect CorrelationStereoselective SynthesisChemistryComparative AnalysisPharmacologyEnantioselective SynthesisNatural Product Synthesis
Abstract The naturally occurring enantiomer of mevalolactone is shown to possess the (R) ‐(−)‐configuration XVIII by a direct correlation of its antipode with quinic acid.
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