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dc.contributor.authorRodríguez, Santiago
dc.contributor.authorGonzález, Florenci
dc.contributor.authorIzquierdo Ferrer, Javier
dc.date.accessioned2012-10-31T12:53:53Z
dc.date.available2012-10-31T12:53:53Z
dc.date.issued2011
dc.identifier.issn1523-7060
dc.identifier.urihttp://hdl.handle.net/10234/50659
dc.description.abstractEfficient ring opening of 3,4-epoxyesters with alcohols to produce 4-alkoxy-3-hydroxyesters and their isomerization into 4-ketoesters using boron trifluoride as the catalyst are presented. Both transformations are simple and efficient methods for the synthesis of the above named synthetically useful compounds.ca_CA
dc.format.extent4 p.ca_CA
dc.language.isoengca_CA
dc.publisherAmerican Chemical Societyca_CA
dc.relation.isPartOfOrganic Letters (2011), vol. 13, no. 15, 3856–3859ca_CA
dc.rights© 2011 American Chemical Societyca_CA
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/*
dc.subjectIsomerization reactionsca_CA
dc.subjectRegioselective ring openingca_CA
dc.subjectBoron trifluorideca_CA
dc.titleRegioselective ring opening and isomerization reactions of 3,4-epoxyesters catalyzed by boron trifluorideca_CA
dc.typeinfo:eu-repo/semantics/articleca_CA
dc.identifier.doihttp://dx.doi.org/10.1021/ol201378w
dc.rights.accessRightsinfo:eu-repo/semantics/restrictedAccessca_CA
dc.relation.publisherVersionhttp://pubs.acs.org/doi/full/10.1021/ol201378wca_CA


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