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Potential of (2E,7E)-Nonadienedioates in Asymmetric Synthesis: Construction of Homopipecolic Acid and an Aminoester Building Block for Peptide Nucleic Acids
dc.contributor.authorMartín Garrido, Narciso 
dc.contributor.authorRubia, Alfonso G.
dc.contributor.authorNieto García, Carlos Tomás
dc.contributor.authorDíez Martín, David 
dc.date.accessioned2014-11-04T11:57:08Z
dc.date.available2014-11-04T11:57:08Z
dc.date.issued2010
dc.identifier.citationGarrido, N.M., Rubia, A., Nieto, C., and Díez, D. (2010). Potential of (2E,7E)-Nonadienedioates in Asymmetric Synthesis: Construction of Homopipecolic Acid and an Aminoester Building Block for Peptide Nucleic Acids. SYNLETT 2010, 4, 0587–0590.es_ES
dc.identifier.urihttp://hdl.handle.net/10366/124098
dc.description.abstract[ES]Se describe la adición asimétrica de Michael de (R)-N-bencil-N-alfa- metilbencilamiduro de litio al diester ortogonalmente sustituido (2E,7E)-nonadienedioato de hidrogeno y metilo para obtener un aducto de monoadición que por posterior manipulación del doble enlace remanente conduce a una síntesis eficaz de ácido (R)-homopipecolico y monomeros utiles en la sintesis de ácidos péptido nucleicos.es_ES
dc.description.sponsorshipMICINN (EUI2008-00173), MEC (CTQ2009-11172/BQU), FSE and Junta de Castilla y León (Spain): (SA001A09) y Grupo de Excelencia GR-178es_ES
dc.format.mimetypeapplication/pdf
dc.language.isoenges_ES
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Unported
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/3.0/
dc.subjectInvestigaciónes_ES
dc.subjectBeta-amino acidses_ES
dc.subjectAsymmetric synthesises_ES
dc.subjectMichael additionses_ES
dc.subjectPNAes_ES
dc.subjectHomopipecolic acides_ES
dc.subjectOrthogonally substituted dienedioatees_ES
dc.titlePotential of (2E,7E)-Nonadienedioates in Asymmetric Synthesis: Construction of Homopipecolic Acid and an Aminoester Building Block for Peptide Nucleic Acidses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.identifier.doi10.1055/s-0029-1219375
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess


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