REGIO AND STEREOSELECTIVE HYDROXYLATION OF 5a-HYDROXY-14-EUDESM-11-EN-3-ONE EUDESMANE BY BIOTRANSFORMATION OF RHIZOPUS NIGRICANS

dc.creatorÁGUILA,SERGIO
dc.creatorALARCÓN,JULIO
dc.creatorCONEJEROS,CAROLINA
dc.creatorALDERETE,JOEL B
dc.date2006-06-01
dc.date.accessioned2017-03-07T15:38:23Z
dc.date.available2017-03-07T15:38:23Z
dc.identifierhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072006000200004
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/388547
dc.descriptionThis paper describes a combined synthesis of b-hydroxy-sesquiterpen eudesmane derivative using a microbiological hydroxylation sesquiterpen eudesmane derivative as the key reaction. The stereochemistry of the biohydroxylation was identified using mono and bi-dimensional ¹H-NMR experiments
dc.formattext/html
dc.languageen
dc.publisherSociedad Chilena de Química
dc.sourceJournal of the Chilean Chemical Society v.51 n.2 2006
dc.subjectBiotransformation
dc.subjectSesquiterpenes
dc.subjectStereoselective Hydroxylation
dc.subjectAgarofurans
dc.titleREGIO AND STEREOSELECTIVE HYDROXYLATION OF 5a-HYDROXY-14-EUDESM-11-EN-3-ONE EUDESMANE BY BIOTRANSFORMATION OF RHIZOPUS NIGRICANS
dc.typeArtículos de revistas


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