Conformational analysis and absolute stereochemistry of 'spongian'-related metabolites

dc.creatorDíaz Marrero, Ana
dc.creatorDorta, Enrique
dc.creatorCueto, Mercedes
dc.creatorSan Martín Barrientos, Aurelio
dc.creatorDarias, José
dc.date.accessioned2018-12-20T14:10:44Z
dc.date.available2018-12-20T14:10:44Z
dc.date.created2018-12-20T14:10:44Z
dc.date.issued2004
dc.identifierTetrahedron, Volumen 60, Issue 5, 2018, Pages 1073-1078
dc.identifier00404020
dc.identifier10.1016/j.tet.2003.11.077
dc.identifierhttps://repositorio.uchile.cl/handle/2250/154405
dc.description.abstractNew degraded and rearranged diterpenoids, 5-8, have been isolated from the Antarctic sponge Dendrilla membranosa. The structure and relative stereochemistry of these compounds were determined by spectroscopic data. The absolute stereochemistry of 5 was determined by spectroscopic data using a chiral reagent. Conformational studies allowed us to assign also the absolute stereochemistry of 6-8, as well as those previously isolated spongian-derived metabolites with known relative stereochemistries. © 2003 Elsevier Ltd. All rights reserved.
dc.languageen
dc.publisherElsevier Ltd
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
dc.sourceTetrahedron
dc.subjectDendroceratida
dc.subjectDiterpenes
dc.subjectSponges
dc.subjectStereochemistries
dc.titleConformational analysis and absolute stereochemistry of 'spongian'-related metabolites
dc.typeArtículo de revista


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