Journal of the Chemical Society Perkin Transactions 1 · 1998 · 15 citations · 12 references
Natural SciencesChemistryMedicinal ChemistryNatural Product BiosynthesisOrganic ChemistrySynthetic Medicinal ChemistryOrganic SynthesisSteroid StructureEnantioselective Synthesis
As part of our program aimed at the synthesis of bioactive products, the enantiospecific synthesis of 8-epi-vernolepin derivatives, starting from accessible germacrolides, was attempted. Synthesis of (+)-8-O-acetyl-1,2,11β,13-tetrahydro-8-epi-vernolepin (23) from (+)-salonitenolide (6) was performed in nine steps with an acceptable overall yield. On the other hand, the synthesis from (+)-stenophyllolide (5) presented several intrinsic difficulties and was discarded. (+)-Salonitenolide provides one of the most useful raw materials for the synthesis of (+)-vernolepin related compounds preserving its functionalization at C-8.
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Kazuhiko Ohrai, Kazuhiro Kondo, Mikiko Sodeoka et al. · Journal of the American Chemical Society · 1994 · 111 citations
Sesquiterpene lactones and lignans from Centaurea species
J. Alberto Marco, Juan F. Sanz, Félix Sancenón et al. · Phytochemistry · 1992 · 54 citations