Search results for "Robinson annulation"

showing 3 items of 3 documents

ChemInform Abstract: Enantioselective Synthesis of Herbertane Sesquiterpenes: Synthesis of (-)-α-Formylherbertenol.

2010

Abstract The synthesis of 4-hydroxy-3-[(1 S )-1,2,2-trimethylcyclopentyl]benzaldehyde [(−)-α-formylherbertenol 1 ], a herbertane-type sesquiterpene isolated from the leafy liverwort Herberta adunca , from β-cyclogeraniol is described. The synthesis is based on the previously described preparation of an enantiopure 1,2,2-trimethylcyclopentane synthon from which the characteristic aromatic moiety of 1 is elaborated, using a Robinson annulation and a palladium-catalysed methoxycarbonylation of an aryl triflate as key synthetic steps. The synthesis of the natural sesquiterpene (−)-α-herbertenol, also a natural sequiterpene, using the same methodology is also described.

Benzaldehydechemistry.chemical_compoundEnantiopure drugChemistryStereochemistryArylSynthonRobinson annulationEnantioselective synthesisGeneral MedicineSesquiterpeneTrifluoromethanesulfonateChemInform
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Silicon guided rearrangement of epoxydecalines to spirocyclic compounds. Synthesis of gleenol and axenol from carvone

2005

Abstract The synthesis of the spirocyclic sesquiterpenes (−)-gleenol and (−)-axenol in enantiomerically pure form has been achieved starting from R-(−)-carvone. The key step is the silicon guided acid-promoted rearrangement of a 9-trimethylsilyl-5,6-epoxy-noreudesmane prepared from 3-trimethylsilyldihydrocarvone in several steps involving Robinson annulation, enone deconjugation and epoxidation. Acid treatment of the epoxy-noreudesmane gave a norspiroaxane as the main product, which was used as intermediate for the synthesis of two naturally occurring sesquiterpenes gleenol and axenol.

CarvoneSiliconStereochemistryOrganic Chemistrychemistry.chemical_elementCarbocationBiochemistrychemistry.chemical_compoundchemistryDrug DiscoveryRobinson annulationOrganic chemistryAcid treatmentEnoneTetrahedron
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Enantioselective synthesis of herbertane sesquiterpenes: synthesis of (−)-α-formylherbertenol

2000

Abstract The synthesis of 4-hydroxy-3-[(1 S )-1,2,2-trimethylcyclopentyl]benzaldehyde [(−)-α-formylherbertenol 1 ], a herbertane-type sesquiterpene isolated from the leafy liverwort Herberta adunca , from β-cyclogeraniol is described. The synthesis is based on the previously described preparation of an enantiopure 1,2,2-trimethylcyclopentane synthon from which the characteristic aromatic moiety of 1 is elaborated, using a Robinson annulation and a palladium-catalysed methoxycarbonylation of an aryl triflate as key synthetic steps. The synthesis of the natural sesquiterpene (−)-α-herbertenol, also a natural sequiterpene, using the same methodology is also described.

StereochemistryChemistryArylOrganic ChemistrySynthonEnantioselective synthesisSesquiterpeneCatalysisInorganic ChemistryBenzaldehydechemistry.chemical_compoundEnantiopure drugRobinson annulationOrganic chemistryPhysical and Theoretical ChemistryTrifluoromethanesulfonateTetrahedron: Asymmetry
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