<?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>2026-04-30T03:19:47Z</responseDate><request verb="GetRecord" identifier="oai:riubu.ubu.es:10259/4242" metadataPrefix="oai_dc">https://riubu.ubu.es/oai/request</request><GetRecord><record><header><identifier>oai:riubu.ubu.es:10259/4242</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><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>Combined directed ortho-zincation and palladiumcatalyzed strategies: Synthesis of 4,n-dimethoxysubstituted benzo[b]furans</dc:title>
<dc:creator>Guilarte Moreno, Verónica</dc:creator>
<dc:creator>Castroviejo Fernández, Mª Pilar</dc:creator>
<dc:creator>Álvarez Manuel, Estela</dc:creator>
<dc:creator>Sanz Díez, Roberto</dc:creator>
<dc:subject>benzo[b]furans</dc:subject>
<dc:subject>o-zincation</dc:subject>
<dc:subject>palladium</dc:subject>
<dc:subject>selectivity</dc:subject>
<dc:subject>Química orgánica</dc:subject>
<dc:subject>Chemistry, Organic</dc:subject>
<dc:description>A new route to regioselectively dialkoxy-functionalized benzo[b]furan derivatives has been developed from 3-halo-2-iodoanisoles&#xd;
bearing an additional methoxy group, which have been accessed through an ortho-zincation/iodination reaction. Two palladiumcatalyzed&#xd;
processes, namely a Sonogashira coupling followed by a tandem hydroxylation/cyclization sequence, give rise to new and&#xd;
interesting dimethoxy-substituted benzo[b]furans.</dc:description>
<dc:description>MICINN (CTQ2010-15358) and Junta de&#xd;
Castilla y León (BU021A09 and GR-172)</dc:description>
<dc:date>2016-09-27T07:56:11Z</dc:date>
<dc:date>2016-09-27T07:56:11Z</dc:date>
<dc:date>2011-09</dc:date>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
<dc:identifier>1860-5397</dc:identifier>
<dc:identifier>http://hdl.handle.net/10259/4242</dc:identifier>
<dc:identifier>10.3762/bjoc.7.146</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>Beilstein Journal of Organic Chemistry, 2011. V. 7, p. 1255–1260</dc:relation>
<dc:relation>Directed aromatic functionalization</dc:relation>
<dc:relation>http://dx.doi.org/10.3762/bjoc.7.146</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/MICINN/CTQ2010-15358</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>http://creativecommons.org/licenses/by/2.0/</dc:rights>
<dc:rights>Este documento está sujeto a una licencia de uso Creative Commons, por la cual está permitido hacer copia, distribuir, comunicar públicamente, remezclar, transformar y crear a partir del material para cualquier finalidad, incluso comercial, siempre que se cite al autor original, se proporcione un enlace a la licencia y se indique si se han realizado cambios</dc:rights>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:format>application/pdf</dc:format>
<dc:publisher>Beilstein-Institut</dc:publisher>
</oai_dc:dc></metadata></record></GetRecord></OAI-PMH>