<?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>2026-06-29T18:47:13Z</responseDate><request verb="GetRecord" identifier="oai:riubu.ubu.es:10259/6806" metadataPrefix="rdf">https://riubu.ubu.es/oai/request</request><GetRecord><record><header><identifier>oai:riubu.ubu.es:10259/6806</identifier><datestamp>2022-11-16T23:42:07Z</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.openarchives.org/OAI/2.0/rdf/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ds="http://dspace.org/ds/elements/1.1/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:ow="http://www.ontoweb.org/ontology/1#" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/rdf/ http://www.openarchives.org/OAI/2.0/rdf.xsd">
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<dc:title>Deoxygenation reactions in organic synthesis catalyzed by dioxomolybdenum(vi) complexes</dc:title>
<dc:creator>Suarez Pantiga, Samuel</dc:creator>
<dc:creator>Sanz Díez, Roberto</dc:creator>
<dc:description>Dioxomolybdenum(VI) complexes have been applied as efficient, inexpensive and benign catalysts to deoxygenation reactions of a diverse number of compounds in the last two decades. Dioxomolybdenum complexes have demonstrated wide applicability to the deoxygenation of sulfoxides into sulfides and reduction of N–O bonds. Even the challenging nitro functional group was efficiently deoxygenated, affording amines or diverse heterocycles after reductive cyclization reactions. More recently, carbon-based substrates like epoxides, alcohols and ketones have been successfully deoxygenated. Also, dioxomolybdenum complexes accomplished deoxydehydration (DODH) reactions of biomass-derived vicinal 1,2-diols, affording valuable alkenes. The choice of the catalytic systems and reductant is decisive to achieve the desired transformation. Commonly found reducing agents involved phosphorous-based compounds, silanes, molecular hydrogen, or even glycols and other alcohols.</dc:description>
<dc:date>2022-07-29T11:24:53Z</dc:date>
<dc:date>2022-07-29T11:24:53Z</dc:date>
<dc:date>2021-12</dc:date>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:identifier>1477-0520</dc:identifier>
<dc:identifier>http://hdl.handle.net/10259/6806</dc:identifier>
<dc:identifier>10.1039/D1OB01939B</dc:identifier>
<dc:identifier>1477-0539</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>Organic &amp; Biomolecular Chemistry. 2021, V. 19, n. 48, p. 10463-10670</dc:relation>
<dc:relation>https://doi.org/10.1039/D1OB01939B</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2020-115789GB-C21/ES/ESTRATEGIAS SINTETICAS SOSTENIBLES PARA LA TRANSFORMACION DIRECTA DE NITROCOMPUESTOS Y DESARROLLO DE NUEVAS REACCIONES CATALIZADAS POR ORO</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/CTQ2016-75023-C2-1-P/ES/DESARROLLO DE NUEVAS METODOLOGIAS SINTETICAS. APLICACION A LA PREPARACION DE MOLECULAS DE INTERES Y A LA VALORIZACION DE LA LIGNINA</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/Junta de Castilla y León//BU291P18</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/Junta de Castilla y León//BU049P20</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/Fundación Bancaria Caixa d'Estalvis i Pensions de Barcelona//LCF%2FPR%2FPR18%2F51130007 (CAIXA-UBU001)</dc:relation>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:publisher>Royal Society of Chemistry</dc:publisher>
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