<?xml version="1.0" encoding="UTF-8"?>
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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/catal8080305</dc:identifier><dc:language>eng</dc:language><dc:creator>Giménez Sonsona, I.</dc:creator><dc:creator>Marqués-López, E.</dc:creator><dc:creator>Häring, M.</dc:creator><dc:creator>Díaz, D.</dc:creator><dc:creator>Pérez Herrera, R.</dc:creator><dc:title>Urea activation by an external brønsted acid: Breaking self-association and tuning catalytic performance</dc:title><dc:identifier>ART-2018-107612</dc:identifier><dc:description>In this work, we hypothesize that Brønsted acids can activate urea-based catalysts by diminishing its self-assembly tendency. As a proof of concept, we used the asymmetric Friedel–Crafts alkylation of indoles with nitroalkenes as a benchmark reaction. The resulting 3-substituted indole derivatives were obtained with better results due to cooperative effects of the chiral urea and a Brønsted acid additive. Such synergy has been rationalized in terms of disassembly of the supramolecular catalyst aggregates, affording a more acidic and rigid catalytic complex.</dc:description><dc:date>2018</dc:date><dc:source>http://zaguan.unizar.es/record/74967</dc:source><dc:doi>10.3390/catal8080305</dc:doi><dc:identifier>http://zaguan.unizar.es/record/74967</dc:identifier><dc:identifier>oai:zaguan.unizar.es:74967</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/DGA/E07-17R</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MINECO/CTQ2017-88091-P</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/UZ/JIUZ-2017-CIE-05</dc:relation><dc:identifier.citation>CATALYSTS 8, 8 (2018), 305 [21 pp]</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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