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Synthesis of Enantiopure Allylamines by Reductive Alkylation of Amino Epoxides with Organolithium Reagents

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dc.contributor.authorConcellón, José M.
dc.contributor.authorSuárez Álvarez, José Ramón
dc.contributor.authorSolar, Virginia del
dc.date.accessioned2024-01-31T12:44:50Z
dc.date.available2024-01-31T12:44:50Z
dc.date.issued2005
dc.description.abstractTransformation of enantiopure (2R,1‘S)-2-(1-aminoalkyl)epoxides into the corresponding allylamines is described. The opening of the epoxide ring with different organolithium compounds takes place with total selectivity and in high yields.
dc.description.departmentDepto. de Química en Ciencias Farmacéuticas
dc.description.facultyFac. de Farmacia
dc.description.refereedTRUE
dc.description.sponsorshipMinisterio de Ciencia y Tecnología (España)
dc.description.statuspub
dc.identifier.citationConcellón, José M., et al. «Synthesis of Enantiopure Allylamines by Reductive Alkylation of Amino Epoxides with Organolithium Reagents». Organic Letters, vol. 8, n.o 2, enero de 2006, pp. 349-51. DOI.org (Crossref), https://doi.org/10.1021/ol0529602.
dc.identifier.doi10.1021/ol0529602
dc.identifier.essn1523-7052
dc.identifier.issn1523-7060
dc.identifier.officialurlhttps://doi.org/10.1021/ol0529602
dc.identifier.relatedurlhttps://pubs.acs.org/doi/10.1021/ol0529602
dc.identifier.urihttps://hdl.handle.net/20.500.14352/97151
dc.issue.number2
dc.journal.titleOrganic Letters
dc.language.isoeng
dc.page.final351
dc.page.initial349
dc.publisherAmerican Chemical Society
dc.relation.projectIDinfo:eu-repo/grantAgreement/CTQ2004-1191/BQU
dc.rights.accessRightsrestricted access
dc.subject.ucmCiencias
dc.subject.unesco23 Química
dc.titleSynthesis of Enantiopure Allylamines by Reductive Alkylation of Amino Epoxides with Organolithium Reagents
dc.typejournal article
dc.volume.number8
dspace.entity.typePublication
relation.isAuthorOfPublication5b1d65e0-9130-49d1-97b4-dc54586e29e8
relation.isAuthorOfPublication.latestForDiscovery5b1d65e0-9130-49d1-97b4-dc54586e29e8

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