<?xml version="1.0" encoding="UTF-8"?>
<collection>
<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.1055/s-0035-1561505</dc:identifier><dc:language>eng</dc:language><dc:creator>Merino, P.</dc:creator><dc:creator>Tejero, T.</dc:creator><dc:creator>Delso, I.</dc:creator><dc:creator>Matute, R.</dc:creator><dc:title>Recent Advances on Asymmetric Nitroso Aldol Reaction</dc:title><dc:identifier>ART-2016-96170</dc:identifier><dc:description>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.</dc:description><dc:date>2016</dc:date><dc:source>http://zaguan.unizar.es/record/58435</dc:source><dc:doi>10.1055/s-0035-1561505</dc:doi><dc:identifier>http://zaguan.unizar.es/record/58435</dc:identifier><dc:identifier>oai:zaguan.unizar.es:58435</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/DGA/E10</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MICINN/CTQ2013-44367-C2-1-P</dc:relation><dc:identifier.citation>SYNTHESIS-STUTTGART 48, 5 (2016), 653-676</dc:identifier.citation><dc:rights>by</dc:rights><dc:rights>http://creativecommons.org/licenses/by/3.0/es/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

</collection>