<?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>2026-08-31T14:38:09Z</responseDate><request verb="GetRecord" identifier="oai:riubu.ubu.es:10259/3908" metadataPrefix="etdms">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><thesis xmlns="http://www.ndltd.org/standards/metadata/etdms/1.0/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.ndltd.org/standards/metadata/etdms/1.0/ http://www.ndltd.org/standards/metadata/etdms/1.0/etdms.xsd">
<title>Gold(I)-Catalyzed Tandem Cyclization–Selective Migration Reaction of 1,3-Dien-5-ynes: Regioselective Synthesis of Highly Substituted Benzenes</title>
<title>info:eu-repo/semantics/acceptedVersion</title>
<creator>García García, Patricia</creator>
<creator>Martínez Cuezva, Alberto</creator>
<creator>Sanjuán Cortázar, Ana María</creator>
<creator>Fernández Rodríguez, Manuel A.</creator>
<creator>Sanz Díez, Roberto</creator>
<description>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</description>
<date>2016-01-20</date>
<date>2016-01-20</date>
<date>2011-08</date>
<type>info:eu-repo/semantics/article</type>
<identifier>1523-7060</identifier>
<identifier>http://hdl.handle.net/10259/3908</identifier>
<identifier>10.1021/ol202129n</identifier>
<language>eng</language>
<relation>Organic Letters. 2011, V. 13, n. 18, p. 4970-4973</relation>
<relation>http://dx.doi.org/10.1021/ol202129n</relation>
<relation>info:eu-repo/grantAgreement/MICINN/CTQ2010-15358</relation>
<relation>info:eu-repo/grantAgreement/MICINN/CTQ2009-09949/BQU</relation>
<relation>info:eu-repo/grantAgreement/JCyL/BU021A09</relation>
<relation>info:eu-repo/grantAgreement/JCyL/GR-172</relation>
<rights>info:eu-repo/semantics/openAccess</rights>
<publisher>American Chemical Society</publisher>
</thesis></metadata></record></GetRecord></OAI-PMH>