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dc.contributor.authorMerino, Pedro-
dc.contributor.authorTejero, Tomás-
dc.contributor.authorDelso, J. Ignacio-
dc.contributor.authorMatute, Rosa-
dc.date.accessioned2017-09-28T07:45:39Z-
dc.date.available2017-09-28T07:45:39Z-
dc.date.issued2016-
dc.identifierdoi: 10.1055/s-0035-1561505-
dc.identifiere-issn: 1437-210X-
dc.identifierissn: 0039-7881-
dc.identifier.citationSynthesis 48(05): 653-676 (2016)-
dc.identifier.urihttp://hdl.handle.net/10261/155774-
dc.description.abstractThe reaction of aromatic nitroso derivatives with enolizable carbonyl compounds (nitroso aldol reaction) to give either α-hydroxyamino or α-aminoxy carbonyl compounds is an important synthetic method. This review illustrates the recent advances in rendering the process regio- and enantioselective as well as catalytic. By employing metal and organic catalysts a range of α-amino (α-oxyamination) and α-hydroxy (α-aminoxylation) carbonyl derivatives can be generated with total regioselectivity and high levels of enantiomeric excess.-
dc.description.sponsorshipWe thank for their support of our programs: MINECO (Madrid, Spain) and FEDER Program (Project CTQ2013-44367-C2-1-P) and the Government of Aragon, Spain (Bioorganic Chemistry Group E-10).-
dc.publisherThieme-
dc.relationMINECO/ICTI2013-2016/CTQ2013-44367-C2-1-P-
dc.relation.isversionofPostprint-
dc.rightsopenAccess-
dc.subjectAminoxylation-
dc.subjectAsymmetric nitroso aldol-
dc.subjectα-amino carbonyls-
dc.subjectHydroxyamination-
dc.subjectOrganocatalysts-
dc.subjectα-hydroxy carbonyls-
dc.titleRecent advances on asymmetric nitroso aldol reaction-
dc.typeArtículo-
dc.identifier.doi10.1055/s-0035-1561505-
dc.relation.publisherversionhttps://doi.org/10.1055/s-0035-1561505-
dc.date.updated2017-09-28T07:45:39Z-
dc.description.versionPeer Reviewed-
dc.language.rfc3066eng-
dc.contributor.funderMinisterio de Economía y Competitividad (España)-
dc.contributor.funderGobierno de Aragón-
dc.contributor.funderEuropean Commission-
dc.relation.csic-
dc.identifier.funderhttp://dx.doi.org/10.13039/501100000780es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100003329es_ES
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