<?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>2026-04-18T00:06:55Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:10256/12303" metadataPrefix="qdc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:10256/12303</identifier><datestamp>2024-06-18T13:51:21Z</datestamp><setSpec>com_2072_452955</setSpec><setSpec>com_2072_2054</setSpec><setSpec>col_2072_453073</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>Ein biomimetischer Eisenkatalysator für die Epoxidation von Olefinen mit molekularem Sauerstoff bei Raumtemperatur</dc:title>
   <dc:creator>Schröder, Kristin</dc:creator>
   <dc:creator>Join, Benoët</dc:creator>
   <dc:creator>Amali, Arlin Jose</dc:creator>
   <dc:creator>Junge, Kathrin</dc:creator>
   <dc:creator>Ribas Salamaña, Xavi</dc:creator>
   <dc:creator>Costas Salgueiro, Miquel</dc:creator>
   <dc:creator>Beller, Matthias</dc:creator>
   <dc:subject>Epòxids</dc:subject>
   <dc:subject>Epoxy compounds</dc:subject>
   <dc:subject>Imidazoles</dc:subject>
   <dc:subject>Ferro</dc:subject>
   <dc:subject>Iron</dc:subject>
   <dc:subject>Alquens</dc:subject>
   <dc:subject>Alkenes</dc:subject>
   <dcterms:abstract>Für Synthesen nutzbar ist ein Eisenkatalysator nach biologischem Vorbild, der Olefine unter milden Bedingungen mit Luft zu Epoxiden oxidieren kann (siehe Schema). Aromatische Olefine werden in hohen Ausbeuten mit exzellenten Chemoselektivitäten oxidiert. Mechanistische Untersuchungen zeigen deutliche Unterschiede zu bekannten radikalischen Autoxidationen</dcterms:abstract>
   <dcterms:abstract>M.C. dankt MICINN f r das Projekt CTQ2009-8464/BQU, der Generalitat de Catalunya f r den ICREA Academia Award und der UdG STR’s f r experimentelle Unterst tzung</dcterms:abstract>
   <dcterms:dateAccepted>2024-06-18T13:51:21Z</dcterms:dateAccepted>
   <dcterms:available>2024-06-18T13:51:21Z</dcterms:available>
   <dcterms:created>2024-06-18T13:51:21Z</dcterms:created>
   <dcterms:issued>info:eu-repo/date/embargoEnd/2026-01-01</dcterms:issued>
   <dcterms:issued>info:eu-repo/date/embargoEnd/2026-01-01</dcterms:issued>
   <dcterms:issued>2011</dcterms:issued>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:identifier>http://hdl.handle.net/10256/12303</dc:identifier>
   <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1002/ange.201004623</dc:relation>
   <dc:relation>info:eu-repo/semantics/altIdentifier/issn/0044-8249</dc:relation>
   <dc:relation>info:eu-repo/semantics/altIdentifier/eissn/1521-3757</dc:relation>
   <dc:relation>MICINN/PN 2009/CTQ2009-8464/BQU</dc:relation>
   <dc:rights>Tots els drets reservats</dc:rights>
   <dc:rights>info:eu-repo/semantics/embargoedAccess</dc:rights>
   <dc:publisher>Wiley-VCH Verlag</dc:publisher>
   <dc:source>© Angewandte Chemie, 2011, vol. 123, núm. 6, p. 1461-1465</dc:source>
   <dc:source>Articles publicats (D-Q)</dc:source>
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