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dc.contributor.authorRosales Martínez, Antonio
dc.contributor.authorRodríguez García, Ignacio Manuel 
dc.contributor.authorLópez Martínez, Josefa Leticia 
dc.date.accessioned2021-07-20T10:45:26Z
dc.date.available2021-07-20T10:45:26Z
dc.date.issued13-05-20
dc.identifier.issn1660-3397
dc.identifier.urihttp://hdl.handle.net/10835/11927
dc.description.abstractThe divergent total synthesis strategy can be successfully applied to the preparation of families of natural products using a common late-stage pluripotent intermediate. This approach is a powerful tool in organic synthesis as it offers opportunities for the efficient preparation of structurally related compounds. This article reviews the synthesis of the marine natural product aureol, as well as its use as a common intermediate in the divergent synthesis of other marine natural and non-natural tetracyclic meroterpenoidses_ES
dc.language.isoenes_ES
dc.publisherMDPIes_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectdivergent total synthesises_ES
dc.subjectmarine natural productses_ES
dc.subjecttetracyclic meroterpenoidses_ES
dc.subjectaureoles_ES
dc.titleDivergent Strategy in Marine Tetracyclic Meroterpenoids Synthesises_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherversionhttps://www.mdpi.com/1660-3397/19/5/273es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.doihttps://doi.org/10.3390/md19050273


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
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