<?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>2026-06-16T07:49:32Z</responseDate><request verb="GetRecord" identifier="oai:riubu.ubu.es:10259/4278" metadataPrefix="qdc">https://riubu.ubu.es/oai/request</request><GetRecord><record><header><identifier>oai:riubu.ubu.es:10259/4278</identifier><datestamp>2022-04-29T12:02:48Z</datestamp><setSpec>com_10259_3593</setSpec><setSpec>com_10259_5086</setSpec><setSpec>com_10259_2604</setSpec><setSpec>col_10259_3594</setSpec></header><metadata><qdc:qualifieddc xmlns:qdc="http://dspace.org/qualifieddc/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://purl.org/dc/elements/1.1/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dc.xsd http://purl.org/dc/terms/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dcterms.xsd http://dspace.org/qualifieddc/ http://www.ukoln.ac.uk/metadata/dcmi/xmlschema/qualifieddc.xsd">
<dc:title>Brønsted Acid-Catalyzed Cascade Reactions Involving 1,2-Indole Migration</dc:title>
<dc:creator>Álvarez Manuel, Estela</dc:creator>
<dc:creator>Nieto Faza, Olalla .</dc:creator>
<dc:creator>Silva López, Carlos</dc:creator>
<dc:creator>Fernández Rodríguez, Manuel A.</dc:creator>
<dc:creator>Sanz Díez, Roberto</dc:creator>
<dc:subject>benzofulvenes</dc:subject>
<dc:subject>Brønsted acid</dc:subject>
<dc:subject>catalysis</dc:subject>
<dc:subject>indolemigration</dc:subject>
<dc:subject>Nazarov cyclization</dc:subject>
<dcterms:abstract>A cascade reaction of indoles with propargylic diols&#xd;
involving an unprecedented metal-free 1,2-indole migration onto an&#xd;
alkyne is here described. DFT calculations support a mechanism&#xd;
consisting in a concerted nucleophilic attack of the indole nucleus&#xd;
with loss of water followed by the 1,2-migration and subsequent&#xd;
Nazarov cyclization. This Brønsted acid-catalyzed protocol affords&#xd;
indole-functionalized benzofulvene derivatives in high yields.</dcterms:abstract>
<dcterms:dateAccepted>2016-11-22T09:15:54Z</dcterms:dateAccepted>
<dcterms:available>2016-11-22T09:15:54Z</dcterms:available>
<dcterms:created>2016-11-22T09:15:54Z</dcterms:created>
<dcterms:issued>2015-09</dcterms:issued>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:identifier>0947-6539</dc:identifier>
<dc:identifier>http://hdl.handle.net/10259/4278</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>Chemistry-a european journal. 2015, V. 21, n. 37, p. 12889–12893</dc:relation>
<dc:relation>http://dx.doi.org/10.1002/chem.201502174</dc:relation>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:publisher>Wiley-VCH Verlag</dc:publisher>
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