<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-13T01:52:50Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:10256/11337" metadataPrefix="qdc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:10256/11337</identifier><datestamp>2024-06-18T13:49:19Z</datestamp><setSpec>com_2072_452955</setSpec><setSpec>com_2072_2054</setSpec><setSpec>col_2072_453073</setSpec></header><metadata><qdc:qualifieddc xmlns:qdc="http://dspace.org/qualifieddc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://purl.org/dc/elements/1.1/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dc.xsd http://purl.org/dc/terms/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dcterms.xsd http://dspace.org/qualifieddc/ http://www.ukoln.ac.uk/metadata/dcmi/xmlschema/qualifieddc.xsd">
   <dc:title>A new mild synthetic route to N-arylated pyridazinones from aryldiazonium salts</dc:title>
   <dc:creator>El Bakouri, Ouissam</dc:creator>
   <dc:creator>Cassú Ponsatí, Daniel</dc:creator>
   <dc:creator>Solà i Puig, Miquel</dc:creator>
   <dc:creator>Parella Coll, Teodor</dc:creator>
   <dc:creator>Pla i Quintana, Anna</dc:creator>
   <dc:creator>Roglans i Ribas, Anna</dc:creator>
   <dc:subject>Funcional de densitat, Teoria del</dc:subject>
   <dc:subject>Density functionals</dc:subject>
   <dc:subject>Compost de diazoni</dc:subject>
   <dc:subject>Diazonium compounds</dc:subject>
   <dcterms:abstract>An efficient method for the synthesis of N-arylated pyridazinones from potassium 2-furantrifluoroborate and aryldiazonium salts is described. The reaction was run in water at 0-5 °C in short reaction times and without any catalyst or additive. A mechanistic proposal is made based on the experimental data and DFT calculations</dcterms:abstract>
   <dcterms:abstract>We thank MINECO (Projects CTQ2011-23121, 23156, and CTQ2012-32436) and the Generalitat de Catalunya (Project 2009SGR637, ICREA Academia for M.S.) for financial support</dcterms:abstract>
   <dcterms:dateAccepted>2024-06-18T13:49:19Z</dcterms:dateAccepted>
   <dcterms:available>2024-06-18T13:49:19Z</dcterms:available>
   <dcterms:created>2024-06-18T13:49:19Z</dcterms:created>
   <dcterms:issued>info:eu-repo/date/embargoEnd/2026-01-01</dcterms:issued>
   <dcterms:issued>info:eu-repo/date/embargoEnd/2026-01-01</dcterms:issued>
   <dcterms:issued>2014</dcterms:issued>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:identifier>http://hdl.handle.net/10256/11337</dc:identifier>
   <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1039/c4cc03190c</dc:relation>
   <dc:relation>info:eu-repo/semantics/altIdentifier/issn/1359-7345</dc:relation>
   <dc:relation>info:eu-repo/semantics/altIdentifier/eissn/1364-548X</dc:relation>
   <dc:relation>info:eu-repo/grantAgreement/MICINN//CTQ2011-23121/ES/APLICACIONES CATALITICAS DE COMPUESTOS DE RODIO, PALADIO Y NIQUEL EN SINTESIS ORGANICA. METODOLOGIA Y ESTUDIOS MECANISTICOS./</dc:relation>
   <dc:relation>info:eu-repo/grantAgreement/MICINN//CTQ2011-23156/ES/AVANCES EN CATALISIS Y AROMATICIDAD/</dc:relation>
   <dc:relation>AGAUR/2009-2014/2009 SGR-637</dc:relation>
   <dc:rights>Tots els drets reservats</dc:rights>
   <dc:rights>info:eu-repo/semantics/embargoedAccess</dc:rights>
   <dc:publisher>Elsevier</dc:publisher>
   <dc:source>© Chemical Communications, 2014, vol. 50, núm. 59, p. 8073-8076</dc:source>
   <dc:source>Articles publicats (D-Q)</dc:source>
</qdc:qualifieddc></metadata></record></GetRecord></OAI-PMH>