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<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:10.3390/molecules200915807</dc:identifier><dc:language>eng</dc:language><dc:creator>Auria-Luna, Fernando</dc:creator><dc:creator>Marqués-López, Eugenia</dc:creator><dc:creator>Mohammadi, Somayeh</dc:creator><dc:creator>Heiran, Roghayeh</dc:creator><dc:creator>Herrera, P.R.</dc:creator><dc:title>New Organocatalytic Asymmetric Synthesis of Highly Substituted Chiral 2-Oxospiro-[indole-3,4'- (1',4'-dihydropyridine)] Derivatives</dc:title><dc:identifier>ART-2015-98041</dc:identifier><dc:description>Herein, we report our preliminary results concerning the first promising asymmetric synthesis of highly functionalized 2-oxospiro-indole-3, 4'-(1', 4'-dihydropyridine)] via the reaction of an enamine with isatylidene malononitrile derivatives in the presence of a chiral base organocatalyst. The moderate, but promising, enantioselectivity observed (30%–58% ee (enantiomeric excess)) opens the door to a new area of research for the asymmetric construction of these appealing spirooxindole skeletons, whose enantioselective syntheses are still very limited.</dc:description><dc:date>2015</dc:date><dc:source>http://zaguan.unizar.es/record/60661</dc:source><dc:doi>10.3390/molecules200915807</dc:doi><dc:identifier>http://zaguan.unizar.es/record/60661</dc:identifier><dc:identifier>oai:zaguan.unizar.es:60661</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/DGA/E104</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MICINN/CTQ2013-44367-C2-1-P</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/UZ/JIUZ-2014-CIE-07</dc:relation><dc:identifier.citation>Molecules 20, 9 (2015), 15807-15826</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>

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