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dc.contributor.authorBonache de Marcos, María Ángeles-
dc.contributor.authorCativiela, Carlos-
dc.contributor.authorGarcía-López, M. Teresa-
dc.contributor.authorGonzález-Muñiz, Rosario-
dc.date.accessioned2009-12-18T11:55:17Z-
dc.date.available2009-12-18T11:55:17Z-
dc.date.issued2006-08-
dc.identifier.citationTetrahedron Letters 47(··): 5883-5887 (2006)en_US
dc.identifier.issn0040-4039-
dc.identifier.urihttp://hdl.handle.net/10261/19700-
dc.description5 pages, 1 table, 2 schemes.en_US
dc.description.abstractThe enantioselectivity in the base-promoted cyclization of N-chloroacetyl derivatives of Phe, Phg, and Hph is dependent on the side-chain length, with the best results for Phg analogues (up to 74% ee). In contrast, shortening of the N-substituent, from a (p-methoxy)benzyl group to a (p-methoxy)phenyl moiety, led to a decrease in selectivity.en_US
dc.description.sponsorshipThis work was supported by CICYT (SAF 2003-07207- C02). M.A.B. thanks a post-grade fellowship from the CSIC (I3P).en_US
dc.format.extent259768 bytes-
dc.format.mimetypeapplication/pdf-
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.rightsclosedAccessen_US
dc.titleβ-Lactams derived from phenylalanine and homologues: effects of the distance between the aromatic rings and the α-stereogenic reactive center on the memory of chiralityen_US
dc.typeartículoen_US
dc.identifier.doi10.1016/j.tetlet.2006.06.057-
dc.description.peerreviewedPeer revieweden_US
dc.relation.publisherversionhttp://dx.doi.org/10.1016/j.tetlet.2006.06.057en_US
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairetypeartículo-
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