<?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>2026-07-10T15:09:43Z</responseDate><request verb="GetRecord" identifier="oai:riubu.ubu.es:10259/4274" metadataPrefix="edm">https://riubu.ubu.es/oai/request</request><GetRecord><record><header><identifier>oai:riubu.ubu.es:10259/4274</identifier><datestamp>2022-12-19T11:11:11Z</datestamp><setSpec>com_10259_3593</setSpec><setSpec>com_10259_5086</setSpec><setSpec>com_10259_2604</setSpec><setSpec>col_10259_3594</setSpec></header><metadata><rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ore="http://www.openarchives.org/ore/terms/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:ds="http://dspace.org/ds/elements/1.1/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:edm="http://www.europeana.eu/schemas/edm/" xsi:schemaLocation="http://www.w3.org/1999/02/22-rdf-syntax-ns# http://www.europeana.eu/schemas/edm/EDM.xsd">
<edm:ProvidedCHO rdf:about="http://hdl.handle.net/10259/4274">
<dc:creator>Aguilar, Enrique</dc:creator>
<dc:creator>Sanz Díez, Roberto</dc:creator>
<dc:creator>Fernández Rodríguez, Manuel A.</dc:creator>
<dc:creator>García García, Patricia</dc:creator>
<dc:date>2016-07</dc:date>
<dc:description>1,3-Dien-5-ynes have been extensively used as starting materials for the&#xd;
synthesis of a wide number of different carbo- and heterocycles. The aim of this review is&#xd;
to give an overview of their utility in organic synthesis, highlighting the variety of&#xd;
compounds that can be directly accessed from single reactions over these systems. Thus,&#xd;
cycloaromatization processes are initially commented, followed by reactions directed&#xd;
toward the syntheses of five-membered rings, other carbocycles and, finally, heterocycles.&#xd;
The diverse methodologies that have been developed for the synthesis of each of these&#xd;
types of compounds from 1,3-dien-5-ynes are presented, emphasizing the influence of&#xd;
the reaction conditions and the use of additional reagents in the outcome of the&#xd;
transformations.</dc:description>
<dc:format>application/pdf</dc:format>
<dc:identifier>http://hdl.handle.net/10259/4274</dc:identifier>
<dc:language>eng</dc:language>
<dc:publisher>American Chemical Society</dc:publisher>
<dc:title>1,3-Dien-5-ynes: Versatile Building Blocks for the Synthesis of Carbo- and Heterocycles</dc:title>
<dc:type>info:eu-repo/semantics/article</dc:type>
<edm:type>TEXT</edm:type>
</edm:ProvidedCHO>
<ore:Aggregation rdf:about="http://hdl.handle.net/10259/4274#aggregation">
<edm:aggregatedCHO rdf:resource="http://hdl.handle.net/10259/4274"/>
<edm:dataProvider>RIUBU. Repositorio Institucional de la Universidad de Burgos</edm:dataProvider>
<edm:isShownAt rdf:resource="http://hdl.handle.net/10259/4274"/>
<edm:isShownBy rdf:resource="https://riubu.ubu.es/bitstream/10259/4274/1/Aguilar-CR_2016.pdf"/>
<edm:object rdf:resource="https://riubu.ubu.es/bitstream/10259/4274/4/Aguilar-CR_2016.pdf.jpg"/>
<edm:provider>Hispana</edm:provider>
<edm:rights rdf:resource="http://rightsstatements.org/vocab/CNE/1.0/"/>
</ore:Aggregation>
<edm:WebResource rdf:about="https://riubu.ubu.es/bitstream/10259/4274/1/Aguilar-CR_2016.pdf">
<edm:rights rdf:resource="http://rightsstatements.org/vocab/CNE/1.0/"/>
</edm:WebResource>
</rdf:RDF></metadata></record></GetRecord></OAI-PMH>