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Brominative cyclisation of nerolidol and geranyl-linalool
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1980
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3-Bromocaparrapi OxideHeterocyclicBrominative Cyclisation ProductsOrganic ChemistryBrominative CyclisationChemistryStereoselective SynthesisPharmacologySynthetic ChemistryEnantioselective SynthesisAnalogous Tricyclic Ethers
(+)-Nerolidol was treated with 2,4,4,6-tetrabromocyclohexa-2,5-dienone to afford the brominative cyclisation products α- and β-snyderols and 3-bromocaparrapi oxide and its 8-epimer; (±)-geranyl-linalool gave the analogous tricyclic ethers.