<?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>2026-04-28T21:22:51Z</responseDate><request verb="GetRecord" identifier="oai:uvadoc.uva.es:10324/79054" metadataPrefix="dim">https://uvadoc.uva.es/oai/request</request><GetRecord><record><header><identifier>oai:uvadoc.uva.es:10324/79054</identifier><datestamp>2025-10-27T20:05:45Z</datestamp><setSpec>com_10324_38</setSpec><setSpec>col_10324_787</setSpec></header><metadata><dim:dim xmlns:dim="http://www.dspace.org/xmlns/dspace/dim" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.dspace.org/xmlns/dspace/dim http://www.dspace.org/schema/dim.xsd">
<dim:field mdschema="dc" element="contributor" qualifier="advisor" lang="es" authority="5016add2ae8bf6cb" confidence="600" orcid_id="0000-0001-7290-3979">Manzano San José, Rubén</dim:field>
<dim:field mdschema="dc" element="contributor" qualifier="advisor" lang="es" authority="dfbcb1d8-0e86-4ce4-a394-d1a8ad5eb872" confidence="600" orcid_id="">Medrano González, Nerea</dim:field>
<dim:field mdschema="dc" element="contributor" qualifier="author" authority="c908129c-1d9c-4951-9c18-fe07c5bb1519" confidence="600" orcid_id="">Marcel Postai, Kevin Benjamín</dim:field>
<dim:field mdschema="dc" element="contributor" qualifier="editor" lang="es" authority="EDUVA45" confidence="600" orcid_id="">Universidad de Valladolid. Facultad de Ciencias</dim:field>
<dim:field mdschema="dc" element="date" qualifier="accessioned">2025-10-27T09:08:25Z</dim:field>
<dim:field mdschema="dc" element="date" qualifier="available">2025-10-27T09:08:25Z</dim:field>
<dim:field mdschema="dc" element="date" qualifier="issued">2025</dim:field>
<dim:field mdschema="dc" element="date" qualifier="embargoEndDate">2027-12-31</dim:field>
<dim:field mdschema="dc" element="identifier" qualifier="uri">https://uvadoc.uva.es/handle/10324/79054</dim:field>
<dim:field mdschema="dc" element="description" qualifier="abstract" lang="es">Enantioselective organocatalysis has become a prominent area of interest in synthetic&#xd;
chemistry, offering new tools for the development of more efficient synthetic methodologies.&#xd;
Although sulfide-catalyzed reactions have been reported for the formation of 3-membered&#xd;
rings their use in higher-order cycloadditions remains unexplored. In this work, several&#xd;
enantioselective sulfide-catalyzed higher-order cycloadditions between (aza)heptafulvenes&#xd;
and different bromides were studied. Three chiral sulfide catalysts were specifically&#xd;
synthesized for this study. While the reaction with methyl bromocrotonate as a substrate&#xd;
afforded different cycloadducts under catalytic conditions, bromoacetophenones were found&#xd;
to undergo a non-catalyzed pathway.</dim:field>
<dim:field mdschema="dc" element="description" qualifier="abstract" lang="es">La organocatálisis enantioselectiva se ha vuelto una importante área de interés en química&#xd;
sintética, ofreciendo nuevas herramientas para el desarrollo de metodologías sintéticas más&#xd;
eficientes. Aunque las reacciones catalizadas por sulfuros se han reportado extensamente&#xd;
en cicloadiciones para dar anillos de tres miembros, su uso en cicloadiciones de alto orden&#xd;
no se ha explorado. En este trabajo, se estudiaron cicloadiciones de alto orden catalizadas&#xd;
por sulfuros entre (aza)heptafulvenos y diferentes sustratos. Tres catalizadores basados en&#xd;
sulfuro se han sintetizado específicamente para este estudio. A pesar de que las reacciones&#xd;
con bromocrotonato de metilo como sustrato formaron diferentes cicloaductos en&#xd;
condiciones catalíticas, se ha observado que las bromoacetofenonas reaccionaron mediante&#xd;
una vía no catalizada.</dim:field>
<dim:field mdschema="dc" element="description" qualifier="sponsorship" lang="es">Departamento de Química Orgánica</dim:field>
<dim:field mdschema="dc" element="description" qualifier="degree" lang="es">Máster en Química Sintética e Industrial</dim:field>
<dim:field mdschema="dc" element="format" qualifier="mimetype" lang="es">application/pdf</dim:field>
<dim:field mdschema="dc" element="language" qualifier="iso" lang="es">eng</dim:field>
<dim:field mdschema="dc" element="rights" qualifier="accessRights" lang="es">info:eu-repo/semantics/embargoedAccess</dim:field>
<dim:field mdschema="dc" element="rights" qualifier="uri" lang="*">http://creativecommons.org/licenses/by-nc-nd/4.0/</dim:field>
<dim:field mdschema="dc" element="rights" lang="*">Attribution-NonCommercial-NoDerivatives 4.0 Internacional</dim:field>
<dim:field mdschema="dc" element="subject" qualifier="classification" lang="es">Enantioselective organocatalysis</dim:field>
<dim:field mdschema="dc" element="subject" qualifier="classification" lang="es">Higher-order cycloadditions</dim:field>
<dim:field mdschema="dc" element="title" lang="es">Enantioselective Higher-Order Cycloadditions between Catalytically Generated Sulfur Ylides and Troponoid Systems</dim:field>
<dim:field mdschema="dc" element="type" lang="es">info:eu-repo/semantics/masterThesis</dim:field>
</dim:dim></metadata></record></GetRecord></OAI-PMH>