<?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>2026-04-17T01:19:34Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:2072/357528" metadataPrefix="qdc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:2072/357528</identifier><datestamp>2024-12-20T22:33:41Z</datestamp><setSpec>com_2072_300912</setSpec><setSpec>com_2072_4427</setSpec><setSpec>col_2072_301309</setSpec></header><metadata><qdc:qualifieddc xmlns:qdc="http://dspace.org/qualifieddc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" 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>A visible-light mediated three-component radical process using dithiocarbamate anion catalysis</dc:title>
   <dc:creator>Cuadros, Sara</dc:creator>
   <dc:creator>Horwitz, Matthew A.</dc:creator>
   <dc:creator>Schweitzer-Chaput, Bertrand</dc:creator>
   <dc:creator>Melchiorre, Paolo</dc:creator>
   <dcterms:abstract>We report a photoinduced three-component radical process, which couples readily available alkyl chlorides, maleimides, and heteroaromatic fragments to rapidly generate complex chiral products with high diastereocontrol. This method generates radicals via an SN2-based photochemical catalytic mechanism, which is not reliant on the redox properties of the precursors. It therefore grants access to open-shell intermediates from substrates that would be incompatible with or inert to classical radical- generating strategies. The redox-neutral conditions of this process make it tolerant of redox-sensitive substrates and allow the installation of multiple biologically relevant heterocycles within the cascade products.</dcterms:abstract>
   <dcterms:dateAccepted>2019-06-17T12:20:20Z</dcterms:dateAccepted>
   <dcterms:dateAccepted>2024-04-23T10:19:15Z</dcterms:dateAccepted>
   <dcterms:available>2019-06-17T12:20:20Z</dcterms:available>
   <dcterms:available>2024-04-23T10:19:15Z</dcterms:available>
   <dcterms:created>2019-06-17T12:20:20Z</dcterms:created>
   <dcterms:created>2024-04-23T10:19:15Z</dcterms:created>
   <dcterms:issued>2019-02-18</dcterms:issued>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/acceptedVersion</dc:type>
   <dc:identifier>http://hdl.handle.net/2072/357528</dc:identifier>
   <dc:identifier>https://doi.org/10.1039/c9sc00833k</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>info:eu-repo/grantAgreement/EC/FP7/681840</dc:relation>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:rights>L'accés als continguts d'aquest document queda condicionat a l'acceptació de les condicions d'ús establertes per la següent llicència Creative Commons:http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
   <dc:source>RECERCAT (Dipòsit de la Recerca de Catalunya)</dc:source>
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