<?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>2026-04-29T04:13:14Z</responseDate><request verb="GetRecord" identifier="oai:riubu.ubu.es:10259/4920" metadataPrefix="oai_dc">https://riubu.ubu.es/oai/request</request><GetRecord><record><header><identifier>oai:riubu.ubu.es:10259/4920</identifier><datestamp>2021-11-10T09:38:25Z</datestamp><setSpec>com_10259_3593</setSpec><setSpec>com_10259_5086</setSpec><setSpec>com_10259_2604</setSpec><setSpec>col_10259_3594</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
<dc:title>Gold(I)-catalyzed diastereoselective synthesis of 1-α-oxybenzyl-1H-indenes</dc:title>
<dc:creator>Virumbrales, Cintia</dc:creator>
<dc:creator>Suarez Pantiga, Samuel</dc:creator>
<dc:creator>Solas Luera, Marta</dc:creator>
<dc:creator>Fernández Rodríguez, Manuel A.</dc:creator>
<dc:creator>Sanz Díez, Roberto</dc:creator>
<dc:subject>Química orgánica</dc:subject>
<dc:subject>Chemistry, Organic</dc:subject>
<dc:description>The gold(I)-catalyzed oxycyclization of β-aryl monosubstituted&#xd;
o-(alkynyl)styrenes gives rise to 1-α-methoxy or 1-α-hydroxybenzyl-&#xd;
1H-indenes in a diastereospecific way. In contrast to&#xd;
β,β-disubstituted o-(alkynyl)styrenes, the stereochemical outcome&#xd;
of this process, diastereospecific reaction supports the higher contribution&#xd;
of a gold intermediate with a cyclopropylcarbene-like&#xd;
character.</dc:description>
<dc:description>Ministerio de Economía y&#xd;
Competitividad (MINECO) and FEDER (CTQ2016-75023-C2-1-&#xd;
P), and Junta de Castilla y León and FEDER (BU076U16)</dc:description>
<dc:date>2018-09-07T08:21:18Z</dc:date>
<dc:date>2019-04-21T02:45:07Z</dc:date>
<dc:date>2018-04</dc:date>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:type>info:eu-repo/semantics/acceptedVersion</dc:type>
<dc:identifier>1477-0520</dc:identifier>
<dc:identifier>http://hdl.handle.net/10259/4920</dc:identifier>
<dc:identifier>10.1039/c8ob00406d</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>Organic &amp; Biomolecular Chemistry. 2018, V. 16, n. 15, p. 2623-2628</dc:relation>
<dc:relation>https://doi.org/10.1039/c8ob00406d</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/MINECO/CTQ2016-75023-C2-1-P</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/JCyL/BU076U16</dc:relation>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:format>application/pdf</dc:format>
<dc:publisher>Royal Society of Chemistry</dc:publisher>
</oai_dc:dc></metadata></record></GetRecord></OAI-PMH>