<?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>2026-06-21T19:03:34Z</responseDate><request verb="GetRecord" identifier="oai:riubu.ubu.es:10259/5546" metadataPrefix="etdms">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><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>Selective synthesis of phenanthrenes and dihydrophenanthrenes via gold-catalyzed cycloisomerization of biphenyl embedded trienynes</title>
<creator>Milián, Ana</creator>
<creator>García García, Patricia</creator>
<creator>Pérez Redondo, Adrián</creator>
<creator>Sanz Díez, Roberto</creator>
<creator>Vaquero, Juan J.</creator>
<creator>Fernández Rodríguez, Manuel A.</creator>
<subject>Hydrocarbons</subject>
<subject>Catalysts</subject>
<subject>Isomerization</subject>
<subject>Aromatic compounds</subject>
<subject>Solvents</subject>
<description>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.</description>
<date>2020-11-10</date>
<date>2020-11-10</date>
<date>2020-11</date>
<type>info:eu-repo/semantics/article</type>
<identifier>1523-7060</identifier>
<identifier>http://hdl.handle.net/10259/5546</identifier>
<identifier>10.1021/acs.orglett.0c03067</identifier>
<identifier>1523-7052</identifier>
<language>eng</language>
<relation>Organic Letters. 2020, V. 22, n. 21, p. 8464–8469</relation>
<relation>https://doi.org/10.1021/acs.orglett.0c03067</relation>
<relation>info:eu-repo/grantAgreement/MINECO/CTQ2017- 85263-R</relation>
<relation>info:eu-repo/grantAgreement/MINECO/CTQ2016-75023-C2-1-P</relation>
<relation>info:eu-repo/grantAgreement/JCyL/BU291P18</relation>
<relation>info:eu-repo/grantAgreement/Instituto de Salud Carlos III/RD16/ 0009/0015</relation>
<relation>info:eu-repo/grantAgreement/UAH/CCGP2017- EXP/016</relation>
<relation>info:eu-repo/grantAgreement/UAH/CCG2018/EXP-008</relation>
<rights>info:eu-repo/semantics/openAccess</rights>
<publisher>American Chemical Society</publisher>
</thesis></metadata></record></GetRecord></OAI-PMH>