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dc.contributor.authorPinedo Rivilla, Cristina
dc.contributor.authorMoraga Galindo, Javier
dc.contributor.authorHernández Galán, Rosario
dc.contributor.authorDurán Patrón, Rosa
dc.contributor.authorGonzález Collado, Isidro
dc.contributor.otherQuímica Orgánicaen_US
dc.date.accessioned2015-05-18T11:52:10Z
dc.date.available2015-05-18T11:52:10Z
dc.date.issued2010-11-11T00:00:00Z
dc.identifier.issn0040-4020
dc.identifier.otherdoi:10.1016/j.tet.2010.11.022
dc.identifier.urihttp://hdl.handle.net/10498/17363
dc.description.abstractThe absolute configuration of botrylactone, a unique compound with an interesting polyketide lactone skeleton with two oxirane bridges previously isolated from Botrytis cinerea and described as a powerful antibiotic, has been reviewed on the basis of sign of the optical rotation, NOE experiments and NMR method. The isolation of 7-deoxybotrylactone and 5-hydroxy-7-(4-hydroxydec-2(3)-enoyl) botrylactone enables us to characterize an intriguing new family of compounds with this interesting polyketide skeleton. A common biosynthetic origin with botcinin derivatives is proposed.en_US
dc.formatapplication/pdf
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.rightsinfo:eu-repo/semantics/openAccess
dc.sourceTetrahedron, 2011, vol. 67, pp. 417-420en_US
dc.subjectBotrylactoneen_US
dc.subjectAbsolute configurationen_US
dc.titleBotrylactone: new interest in an old moleculedreview of its absolute configuration and related compoundsen_US
dc.typeinfo:eu-repo/semantics/articleen_US
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.identifier.doi10.1016/j.tet.2010.11.022


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