Bulletin of the Chemical Society of Japan · 1976 · 55 citations · 8 references
Life SciencesBiochemistryChemistryDrug DiscoveryEnzymologyStructure-activity RelationshipsEnzyme InhibitionTerpenoid BiosynthesisAutoxidation ChemistryPhotosensitized ReactionsSesquiterpene Biosynthesis
Abstract Two new sesquiterpene lactones of eremophilane-type were isolated from Ligularia Fauriei (Fr.) Koidz., and their structures including absolute stereochemistry were shown to be 8β-hydroxyeremophil-7(11)-ene-12,8α;14β,6α-diolide (1) and eremophil-7(11)-ene-12,8α;14β,6α-diolide (2), respectively. The isolation of the two known lactones, 6β,8β-dihydroxyeremophil-7(11)-en-12,8α-olide (3) and 6β-hydroxyeremophil-7(11)-en-12,8α-olide (4), is also described. The photosensitized autoxidation of the known furanoeremophilan-14β,6α-olide (5) gave 1 and 8β-methoxyeremophil-7(11)-ene-12,8α;14β,6α-diolide (18).
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Components of the root of Lindera strychnifolia Vill.—IX
K. Takeda, Hideo Minato, M. Ishikawa et al. · Tetrahedron · 1964 · 45 citations
Ladislav Novotný, V. Herout, F. Šorm · Collection of Czechoslovak Chemical Communications · 1964 · 22 citations