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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:10.1039/c6cc09133d</dc:identifier><dc:language>eng</dc:language><dc:creator>Iturmendi, Amaia</dc:creator><dc:creator>Iglesias, Manuel</dc:creator><dc:creator>Munárriz, Julen</dc:creator><dc:creator>Polo, Víctor</dc:creator><dc:creator>Pérez-Torrente, Jesús J.</dc:creator><dc:creator>Oro, Luis A.</dc:creator><dc:title>Efficient preparation of carbamates by Rh-catalysed oxidative carbonylation: Unveiling the role of the oxidant</dc:title><dc:identifier>ART-2017-97871</dc:identifier><dc:description>The synthesis of a wide variety of carbamates from amines, alcohols and carbon monoxide has been achieved by means of a Rh-catalysed oxidative carbonylation reaction that uses Oxone as a stoichiometric oxidant. In-depth studies on the reaction mechanism shed light on the intimate role of Oxone in the catalytic cycle.</dc:description><dc:date>2017</dc:date><dc:source>http://zaguan.unizar.es/record/70773</dc:source><dc:doi>10.1039/c6cc09133d</dc:doi><dc:identifier>http://zaguan.unizar.es/record/70773</dc:identifier><dc:identifier>oai:zaguan.unizar.es:70773</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/DGA/E07</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MINECO/Consolider-Ingenio/CSD2009-0050</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MINECO/CTQ2013-42532-P</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MINECO/CTQ2015-67366-P</dc:relation><dc:identifier.citation>Chemical Communications 53, 2 (2017), 404-407</dc:identifier.citation><dc:rights>All rights reserved</dc:rights><dc:rights>http://www.europeana.eu/rights/rr-f/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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