Journal of Natural Products · 2003 · 23 citations · 15 references
AgricultureBotanyPlant SciencesFood ChemistryNatural Product BiosynthesisPlant BiochemistryBiotransformation PathwaysSecondary Metabolite ProductionSpecies Differences In MetabolismTerpenoid BiosynthesisDiterpene BiosynthesisMonoterpene BiosynthesisTerpene Biotransformation
The microbiological transformation of the diterpene epicandicandiol (1) with Mucor plumbeus gave foliol (3), sideritriol (5), and 7beta,16alpha,17,18-tetrahydroxy-ent-kaurane (7), while the incubation of candicandiol (2) gave 7alpha,9beta,18-trihydroxy-ent-kaur-16-ene (10), canditriol (11), and 7alpha,16alpha,17,18-tetrahydroxy-ent-kaurane (12). Thus, the main difference observed in both feedings, resulting from the spatial change in the orientation of the 7-hydroxyl, from axial in the substrate 1 to equatorial in 2, was the formation of a 3alpha- and a 9beta-hydroxylated derivative, respectively.
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The 13C NMR spectra of some ent-18-hydroxykaur-16-enes
Antonio González, Braulio M. Fraga, Melchor G. Hernández et al. · Phytochemistry · 1981 · 48 citations
Microbial hydroxylation of sclareol by mucor plumbeus
Gérard Aranda, Jean‐Yves Lallemand, Abderrahmane Hammoumi et al. · Tetrahedron Letters · 1991 · 35 citations