dc.creatorImamura, P M
dc.creatorCosta, M
dc.date2000-Dec
dc.date2015-11-27T12:22:48Z
dc.date2015-11-27T12:22:48Z
dc.date.accessioned2018-03-29T00:54:36Z
dc.date.available2018-03-29T00:54:36Z
dc.identifierJournal Of Natural Products. v. 63, n. 12, p. 1623-5, 2000-Dec.
dc.identifier0163-3864
dc.identifier
dc.identifierhttp://www.ncbi.nlm.nih.gov/pubmed/11141101
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/194648
dc.identifier11141101
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1294881
dc.descriptionSyntheses of three enantiomers of natural hydroxybutenolide diterpenes, 16,18-dihydroxycleroda-3,13Z-dien-16,15-olide (4), (+)-16-hydroxycleroda-3,13Z-dien-16,15-olide (5), and (-)-16-hydroxyhalima-5(10),13Z-dien-16,15-olide (6), via a furan photosensitized oxygenation reaction of (+)-hardwickiic acid (2), are described.
dc.description63
dc.description1623-5
dc.languageeng
dc.relationJournal Of Natural Products
dc.relationJ. Nat. Prod.
dc.rightsfechado
dc.rights
dc.sourcePubMed
dc.subjectDiterpenes
dc.subjectMolecular Structure
dc.subjectPlants, Medicinal
dc.subjectSpectrum Analysis
dc.titleSynthesis Of 16,18-dihydroxycleroda-3,13z-dien-16,15-olide, (+)-16-hydroxycleroda-3,13z-dien-16,15-olide, And (-)-hydroxyhalima-5(10),13-dien-16,15-olide From (+)-hardwickiic Acid.
dc.typeArtículos de revistas


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