58435 20200221144254.0 doi 10.1055/s-0035-1561505 sideral 96170 ART-2016-96170 eng (orcid)0000-0002-2202-3460 Merino, P. Universidad de Zaragoza Recent Advances on Asymmetric Nitroso Aldol Reaction 2016 Access copy available to the general public Unrestricted The reaction of aromatic nitroso derivatives with enolizable carbonyl compounds (nitroso aldol reaction) to give either a-hydroxyamino or a-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 a-amino (a-oxyamination) and a-hydroxy (a-aminoxylation) carbonyl derivatives can be generated with total regioselectivity and high levels of enantiomeric excess. info:eu-repo/grantAgreement/ES/DGA/E10 info:eu-repo/grantAgreement/ES/MICINN/CTQ2013-44367-C2-1-P info:eu-repo/semantics/openAccess by http://creativecommons.org/licenses/by/3.0/es/ 2.65 2016 CHEMISTRY, ORGANIC 22 / 59 = 0.373 2016 Q2 T2 1.066 2016 Organic Chemistry 2016 Q1 Catalysis 2016 Q2 info:eu-repo/semantics/article info:eu-repo/semantics/acceptedVersion (orcid)0000-0003-3433-6701 Tejero, T. Universidad de Zaragoza (orcid)0000-0001-8355-2289 Delso, I. Universidad de Zaragoza (orcid)0000-0001-7773-9418 Matute, R. Universidad de Zaragoza 2013 765 Universidad de Zaragoza Dpto. Química Orgánica Área Química Orgánica 5005 790 Universidad de Zaragoza Dpto. Ing.Quím.Tecnol.Med.Amb. Área Tecnologi. Medio Ambiente 48, 5 (2016), 653-676 Synthesis (Stuttgart) SYNTHESIS-STUTTGART 0039-7881 874545 http://zaguan.unizar.es/record/58435/files/texto_completo.pdf Postprint 51318 http://zaguan.unizar.es/record/58435/files/texto_completo.jpg?subformat=icon icon Postprint oai:zaguan.unizar.es:58435 articulos driver 2020-02-21-13:29:12 ARTICLE