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dc.contributor.authorRibés Vidal, Celia
dc.contributor.authorFalomir, Eva
dc.contributor.authorCarda, Miguel
dc.contributor.authorMarco, J. Alberto
dc.date.accessioned2013-10-07T10:53:39Z
dc.date.available2013-10-07T10:53:39Z
dc.date.issued2008
dc.identifier.citationJournal of Organic Chemistry, 73, 19, p. 7779–7782ca_CA
dc.identifier.issn0022-3263
dc.identifier.urihttp://hdl.handle.net/10234/73886
dc.description.abstractA short, stereoselective synthesis of the naturally occurring pyrrolidine radicamine B is reported. Garner′s (R)-aldehyde, prepared from d-serine, was the chiral starting material. The pyrrolidine ring was stereoselectively created in a very efficient way through a five-step, one-pot transformation. In addition, an intermediate of this synthesis was transformed into an intermediate of a previously published synthesis of the potent α-glucosidase inhibitor nectrisine.ca_CA
dc.format.extent4 p.ca_CA
dc.language.isoengca_CA
dc.publisherAmerican Chemical Societyca_CA
dc.rightsCopyright © 2008 American Chemical Societyca_CA
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/*
dc.subjectAldehydesca_CA
dc.subjectStereochemistryca_CA
dc.subjectChemical reactionsca_CA
dc.subjectOrganic compoundsca_CA
dc.titleShort, Stereoselective Synthesis of the Naturally Occurring Pyrrolidine Radicamine B and a Formal Synthesis of Nectrisineca_CA
dc.typeinfo:eu-repo/semantics/articleca_CA
dc.identifier.doihttp://dx.doi.org/10.1021/jo8012989
dc.rights.accessRightsinfo:eu-repo/semantics/restrictedAccessca_CA
dc.relation.publisherVersionhttp://pubs.acs.org/doi/abs/10.1021/jo8012989ca_CA


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