<?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>2026-05-30T20:16:35Z</responseDate><request verb="GetRecord" identifier="oai:riubu.ubu.es:10259/3909" metadataPrefix="rdf">https://riubu.ubu.es/oai/request</request><GetRecord><record><header><identifier>oai:riubu.ubu.es:10259/3909</identifier><datestamp>2021-11-10T09:38:19Z</datestamp><setSpec>com_10259_3593</setSpec><setSpec>com_10259_5086</setSpec><setSpec>com_10259_2604</setSpec><setSpec>com_10259_3924</setSpec><setSpec>col_10259_3594</setSpec><setSpec>col_10259_3925</setSpec></header><metadata><rdf:RDF xmlns:rdf="http://www.openarchives.org/OAI/2.0/rdf/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ds="http://dspace.org/ds/elements/1.1/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:ow="http://www.ontoweb.org/ontology/1#" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/rdf/ http://www.openarchives.org/OAI/2.0/rdf.xsd">
<ow:Publication rdf:about="oai:riubu.ubu.es:10259/3909">
<dc:title>A Practical, One-Pot Synthesis of Highly Substituted Thiophenes and Benzo[b]thiophenes from Bromoenynes and o-Alkynylbromobenzenes</dc:title>
<dc:creator>Guilarte Moreno, Verónica</dc:creator>
<dc:creator>Fernández Rodríguez, Manuel A.</dc:creator>
<dc:creator>García García, Patricia</dc:creator>
<dc:creator>Hernando Santa Cruz, Elsa</dc:creator>
<dc:creator>Sanz Díez, Roberto</dc:creator>
<dc:description>An efficient synthesis of thiophenes and benzo[b]thiophenes has been developed from easily available bromoenynes and o-alkynylbromobenzene derivatives. This novel one-pot procedure involves a Pd-catalyzed C–S bond formation using a hydrogen sulfide surrogate followed by a heterocyclization reaction. Moreover, in situ functionalization with selected electrophiles further expands the potential of this methodology to the preparation of the corresponding highly substituted sulfur heterocycles.</dc:description>
<dc:date>2016-01-21T09:51:47Z</dc:date>
<dc:date>2016-01-21T09:51:47Z</dc:date>
<dc:date>2011-09</dc:date>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:identifier>1523-7060</dc:identifier>
<dc:identifier>http://hdl.handle.net/10259/3909</dc:identifier>
<dc:identifier>10.1021/ol201970m</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>Organic Letters. 2011. V. 13, n. 19, p. 5100-5103</dc:relation>
<dc:relation>http://dx.doi.org/10.1021/ol201970m</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/MICINN/CTQ2010-15358</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/MICINN/CTQ2009-09949/BQU</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>info:eu-repo/semantics/openAccess</dc:rights>
<dc:publisher>American Chemical Society</dc:publisher>
</ow:Publication>
</rdf:RDF></metadata></record></GetRecord></OAI-PMH>