<?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>2026-06-17T21:31:06Z</responseDate><request verb="GetRecord" identifier="oai:riubu.ubu.es:10259/5546" metadataPrefix="qdc">https://riubu.ubu.es/oai/request</request><GetRecord><record><header><identifier>oai:riubu.ubu.es:10259/5546</identifier><datestamp>2021-11-06T23:42:16Z</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>Selective synthesis of phenanthrenes and dihydrophenanthrenes via gold-catalyzed cycloisomerization of biphenyl embedded trienynes</dc:title>
<dc:creator>Milián, Ana</dc:creator>
<dc:creator>García García, Patricia</dc:creator>
<dc:creator>Pérez Redondo, Adrián</dc:creator>
<dc:creator>Sanz Díez, Roberto</dc:creator>
<dc:creator>Vaquero, Juan J.</dc:creator>
<dc:creator>Fernández Rodríguez, Manuel A.</dc:creator>
<dc:subject>Hydrocarbons</dc:subject>
<dc:subject>Catalysts</dc:subject>
<dc:subject>Isomerization</dc:subject>
<dc:subject>Aromatic compounds</dc:subject>
<dc:subject>Solvents</dc:subject>
<dcterms:abstract>Readily available o′-alkenyl-o-alkynylbiaryls, a particular&#xd;
type of 1,7-enynes, undergo a selective cycloisomerization reaction in&#xd;
the presence of a gold(I) catalyst to give interesting phenanthrene and&#xd;
dihydrophenanthrene derivatives in high yields. The solvent used&#xd;
provokes a switch in the evolution of the gold intermediate and plays a&#xd;
key role in the reaction outcome.</dcterms:abstract>
<dcterms:dateAccepted>2020-11-10T08:58:49Z</dcterms:dateAccepted>
<dcterms:available>2020-11-10T08:58:49Z</dcterms:available>
<dcterms:created>2020-11-10T08:58:49Z</dcterms:created>
<dcterms:issued>2020-11</dcterms:issued>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:identifier>1523-7060</dc:identifier>
<dc:identifier>http://hdl.handle.net/10259/5546</dc:identifier>
<dc:identifier>10.1021/acs.orglett.0c03067</dc:identifier>
<dc:identifier>1523-7052</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>Organic Letters. 2020, V. 22, n. 21, p. 8464–8469</dc:relation>
<dc:relation>https://doi.org/10.1021/acs.orglett.0c03067</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/MINECO/CTQ2017- 85263-R</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/MINECO/CTQ2016-75023-C2-1-P</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/JCyL/BU291P18</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/Instituto de Salud Carlos III/RD16/ 0009/0015</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/UAH/CCGP2017- EXP/016</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/UAH/CCG2018/EXP-008</dc:relation>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:publisher>American Chemical Society</dc:publisher>
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