<?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>2026-04-27T11:46:30Z</responseDate><request verb="GetRecord" identifier="oai:riubu.ubu.es:10259/3908" metadataPrefix="qdc">https://riubu.ubu.es/oai/request</request><GetRecord><record><header><identifier>oai:riubu.ubu.es:10259/3908</identifier><datestamp>2021-11-10T09:38:24Z</datestamp><setSpec>com_10259_3593</setSpec><setSpec>com_10259_5086</setSpec><setSpec>com_10259_2604</setSpec><setSpec>col_10259_3594</setSpec></header><metadata><qdc:qualifieddc xmlns:qdc="http://dspace.org/qualifieddc/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:dc="http://purl.org/dc/elements/1.1/" 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>Gold(I)-Catalyzed Tandem Cyclization–Selective Migration Reaction of 1,3-Dien-5-ynes: Regioselective Synthesis of Highly Substituted Benzenes</dc:title>
<dc:title>info:eu-repo/semantics/acceptedVersion</dc:title>
<dc:creator>García García, Patricia</dc:creator>
<dc:creator>Martínez Cuezva, Alberto</dc:creator>
<dc:creator>Sanjuán Cortázar, Ana María</dc:creator>
<dc:creator>Fernández Rodríguez, Manuel A.</dc:creator>
<dc:creator>Sanz Díez, Roberto</dc:creator>
<dcterms:abstract>Highly substituted benzene derivatives have been easily prepared in a regioselective way from readily available 1,3-hexadien-5-ynes through a gold(I)-catalyzed tandem reaction. The process involves an initial cyclization followed by a selective Wagner-Meerwein shift in which the migration preference seems to be determined by the ability to stabilize a positive charge</dcterms:abstract>
<dcterms:dateAccepted>2016-01-20T12:31:52Z</dcterms:dateAccepted>
<dcterms:available>2016-01-20T12:31:52Z</dcterms:available>
<dcterms:created>2016-01-20T12:31:52Z</dcterms:created>
<dcterms:issued>2011-08</dcterms:issued>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:identifier>1523-7060</dc:identifier>
<dc:identifier>http://hdl.handle.net/10259/3908</dc:identifier>
<dc:identifier>10.1021/ol202129n</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>Organic Letters. 2011, V. 13, n. 18, p. 4970-4973</dc:relation>
<dc:relation>http://dx.doi.org/10.1021/ol202129n</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/MICINN/CTQ2010-15358</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/MICINN/CTQ2009-09949/BQU</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/JCyL/BU021A09</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/JCyL/GR-172</dc:relation>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:publisher>American Chemical Society</dc:publisher>
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