Organic Letters · 2015 · 70 citations · 12 references
PharmacyBotanyChemistryDrug DiscoveryOrganic ChemistryStructure-activity RelationshipsNatural Product Drug DiscoveryStructure-activity Relationship AnalysisCircular DichroismCircular Dichroism AnalysisCircular Dichroism Spectroscopy AnalysisElectronic Circular Dichroism
Two enantiomeric pairs of meroterpenoids, (-)- and (+)-rhodonoids A (1a and 1b) and B (2a and 2b), were isolated unprecedentedly from partially racemic mixtures that naturally occurred in Rhododendron capitatum. Their structures were fully determined by spectroscopic data, X-ray crystallography, and electronic circular dichroism analysis. Compounds 1a and 1b are the first examples of meromonoterpenes featuring a unique 6/6/6/4 ring system. Compounds 2a and 2b showed PTP1B inhibitory activity.
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