Journal of Natural Products · 1997 · 25 citations · 3 references
PharmacyBotanyMedicinal ChemistryDrug DiscoveryPlant BiochemistrySynthetic Medicinal ChemistryMolecular SimilaritySpectroscopic Analysis Of PharmaceuticalsConfiguration Determination By Nuclear Magnetic Resonance SpectroscopyDiterpene BiosynthesisMedicinal Plant ClassificationMedicinal Plant ResourcesNuclear Magnetic Resonance Structural AnalysisSpectroscopic IdentificationStereochemical Analysis By Nuclear Magnetic Resonance Spectroscopy
In order to confirm the previously proposed stereochemistry for bacrispine ( 1 ), several high-field 2D NMR (500 MHz) experiments were carried out. Complete NMR assignments, as well as the validation of the relative stereochemistry of 1-deoxybacrispine ( 2 ), were established. In an investigation of the aerial parts of Baccharis crispa, a medicinal plant from Argentina, two new neoclerodanes ( 4, and 5 ) have been isolated and their structures determined by spectroscopic means.
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Z. Valenta, Hitomi Yoshimura, Eleni Rogers et al. · Tetrahedron Letters · 1960 · 32 citations
Clerodane diterpenoids from Baccharis articulata
Jin‐Rui Dai, Rutt Suttisri, Eugenia Bordas et al. · Phytochemistry · 1993 · 24 citations
Terpenoids from Pulicaria glutinosa
Ilias Muhammad, Farouk S. El‐Feraly, Jaber S. Mossa et al. · Phytochemistry · 1992 · 22 citations