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Artículo
Sulfinamide Phosphinates as Chiral Catalysts for the Enantioselective Organocatalytic Reduction of Imines
dc.creator | Chelouan, Ahmed | es |
dc.creator | Recio Jiménez, Rocío | es |
dc.creator | Borrego Sánchez de la Cuesta, Lorenzo Gabriel | es |
dc.creator | Álvarez, Eleuterio | es |
dc.creator | Khiar, Noureddine | es |
dc.creator | Fernández Fernández, Inmaculada | es |
dc.date.accessioned | 2024-01-31T11:28:16Z | |
dc.date.available | 2024-01-31T11:28:16Z | |
dc.date.issued | 2016-07 | |
dc.identifier.citation | Chelouan, A., Recio Jiménez, R., Borrego Sánchez de la Cuesta, L.G., Álvarez, E., Khiar, N. y Fernández Fernández, I. (2016). Sulfinamide Phosphinates as Chiral Catalysts for the Enantioselective Organocatalytic Reduction of Imines. Organic Letters, 18 (13), 3258-3261. https://doi.org/10.1021/acs.orglett.6b01509. | |
dc.identifier.issn | 1523-7060 | es |
dc.identifier.uri | https://hdl.handle.net/11441/154329 | |
dc.description.abstract | A new type of chiral sulfinamide phosphinate catalysts with up to three stereogenic centers, readily accessible from commercially available starting materials, is reported. The naphthyl derivative SulPhos proved to be highly efficient in the organocatalytic asymmetric imine reduction, leading to a wide range of arylmethylamines in high yields with up to 99% ee under 10% catalyst loading. The synthetic utility of this method was demonstrated by the expeditious enantioselective synthesis of the calcimimetic NPS-R568. | es |
dc.format | application/pdf | es |
dc.format.extent | 4 p. | es |
dc.language.iso | eng | es |
dc.publisher | American Chemical Society | es |
dc.relation.ispartof | Organic Letters, 18 (13), 3258-3261. | |
dc.title | Sulfinamide Phosphinates as Chiral Catalysts for the Enantioselective Organocatalytic Reduction of Imines | es |
dc.type | info:eu-repo/semantics/article | es |
dc.type.version | info:eu-repo/semantics/acceptedVersion | es |
dc.rights.accessRights | info:eu-repo/semantics/openAccess | es |
dc.contributor.affiliation | Universidad de Sevilla. Departamento de Química Orgánica y Farmacéutica | es |
dc.relation.projectID | CTQ2013-49066-C2-2-R | es |
dc.relation.projectID | P11-FQM-08046 | es |
dc.relation.publisherversion | https://pubs.acs.org/doi/10.1021/acs.orglett.6b01509 | es |
dc.identifier.doi | 10.1021/acs.orglett.6b01509 | es |
dc.journaltitle | Organic Letters | es |
dc.publication.volumen | 18 | es |
dc.publication.issue | 13 | es |
dc.publication.initialPage | 3258 | es |
dc.publication.endPage | 3261 | es |
dc.contributor.funder | Ministerio de Economía y Competitividad (MINECO). España | es |
dc.contributor.funder | Junta de Andalucía | es |
Ficheros | Tamaño | Formato | Ver | Descripción |
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10.1021_acs.orglett.6b01509.pdf | 1.303Mb | [PDF] | Ver/ | Versión aceptada |
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