np010631m_si_001.pdf (96.98 kB)
Chemical-Microbiological Synthesis of Cryptomeridiol Derivatives by Gliocladium roseum: Semisynthesis of 11-Hydroxyeudesmanolides
journal contribution
posted on 2002-07-03, 00:00 authored by Andrés García-Granados, María C. Gutiérrez, Andrés Parra, Francisco RivasBiotransformations of 4α- and 4β-hydroxyeudesmane derivatives by the filamentous fungus Gliocladium
roseum were achieved. Hydroxylation at C-11 was the main action of this microorganism, producing new
cryptomeridiol (12 and 14) and 4-epi-cryptomeridiol derivatives (6 and 7), respectively, in good yields.
The biotransformation activity of G. roseum toward 4β-hydroxyeudesmane was focused on the isopropyl
moiety, but more scattered on the 4α-hydroxylated derivative, acting in both the “A” and “B” rings and
the isopropyl group of the molecule. Semisyntheses of 11-hydroxyeudesmanolides from the isolated 11,12-dihydroxylated metabolites were also accomplished and used in assigning the stereochemistry of
hydroxylation.
History
Usage metrics
Categories
Keywords
isopropyl groupHydroxyeudesmanolidemicroorganismHydroxylationcryptomeridiol derivativesmetabolitedihydroxylatedhydroxyeudesmaneSemisynthesihydroxylatedfilamentous fungus Gliocladium roseumSynthesibiotransformation activityhydroxyeudesmanolidemoleculeyieldhydroxylationBiotransformationstereochemistrySemisyntheseCryptomeridiol Derivativesisopropyl moietyepi
Licence
Exports
RefWorks
BibTeX
Ref. manager
Endnote
DataCite
NLM
DC