Helvetica Chimica Acta · 2011 · 14 citations · 13 references
Bioorganic ChemistryEuonymus FortuneiBiochemistryMedicineNatural SciencesCompound 6First IsolationSecondary MetabolitePhytopharmacologyPhytochemicalPhytochemistryPharmacologyDrug DiscoveryNatural Product Synthesis
Abstract Three new macrocyclic β ‐dihydroagarofuran‐type sesquiterpene pyridine alkaloids, fortuneines A ( 1 ), B ( 2 ), and C ( 3 ), together with the four known alkaloids wilfornine E ( 4 ), aquifoliunine E‐I ( 5 ), euoverrine B ( 6 ), and euojaponine I ( 7 ), were isolated from the aerial parts of Euonymus fortunei. Their structures were elucidated by spectroscopic methods, including HR‐ESI‐MS, 1 H‐ and 13 C‐NMR, DEPT, 1 H, 1 H‐COSY, HSQC, HMBC, and ROESY. This is the first isolation of the above sesquiterpene pyridine alkaloids from this plant, except for compound 6 .
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Insecticidal sesquiterpene pyridine alkaloids from Euonymus species
Zhu Jinbo, Mingan Wang, Wenjun Wu et al. · Phytochemistry · 2002 · 49 citations
Sesquiterpene alkaloids from Euonymus japonica
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