lambertellol-b has been researched along with furan* in 1 studies
1 other study(ies) available for lambertellol-b and furan
Article | Year |
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Diels-Alder cycloaddition of o-quinonedimethides and alkylidene-5H-furan-2-ones: new and rapid access to lambertellol cores and arthrinone derivatives.
An efficient synthesis of deoxy-lambertellols was reported through a highly chemo- and diastereoselective intermolecular Diels-Alder cycloaddition between trans-1,2-disiloxybenzocyclobutenes and 2-methylprotoanemonine. Such transformation with δ-substituted γ-alkylidenebutenolides, to prepare new analogues of these tricyclic spirolactones, which would be very difficult to prepare by other ways, was also studied. Topics: Alkylation; Cyclization; Furans; Models, Molecular; Molecular Structure; Naphthalenes; Quinones; Spiro Compounds; Time Factors | 2010 |