<?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>2026-04-21T11:06:03Z</responseDate><request verb="GetRecord" identifier="oai:riubu.ubu.es:10259/10506" metadataPrefix="dim">https://riubu.ubu.es/oai/request</request><GetRecord><record><header><identifier>oai:riubu.ubu.es:10259/10506</identifier><datestamp>2025-05-29T00:05:19Z</datestamp><setSpec>com_10259_3593</setSpec><setSpec>com_10259_5086</setSpec><setSpec>com_10259_2604</setSpec><setSpec>col_10259_3594</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="author" authority="277" confidence="600" orcid_id="0000-0001-5018-0845">Hernández Ruiz, Raquel</dim:field>
<dim:field mdschema="dc" element="contributor" qualifier="author" authority="542" confidence="600" orcid_id="0000-0002-0052-7270">Solas Luera, Marta</dim:field>
<dim:field mdschema="dc" element="contributor" qualifier="author" authority="544" confidence="600" orcid_id="0000-0002-4249-7807">Suárez Pantiga, Samuel</dim:field>
<dim:field mdschema="dc" element="contributor" qualifier="author" authority="422" confidence="600" orcid_id="0000-0001-7083-8093">Pedrosa Sáez, María de los Remedios</dim:field>
<dim:field mdschema="dc" element="contributor" qualifier="author" authority="531" confidence="600" orcid_id="0000-0003-2830-0892">Sanz Díez, Roberto</dim:field>
<dim:field mdschema="dc" element="date" qualifier="accessioned">2025-05-28T07:31:13Z</dim:field>
<dim:field mdschema="dc" element="date" qualifier="available">2025-05-28T07:31:13Z</dim:field>
<dim:field mdschema="dc" element="date" qualifier="issued">2025-05</dim:field>
<dim:field mdschema="dc" element="identifier" qualifier="issn">1615-4150</dim:field>
<dim:field mdschema="dc" element="identifier" qualifier="uri">http://hdl.handle.net/10259/10506</dim:field>
<dim:field mdschema="dc" element="identifier" qualifier="doi">10.1002/adsc.202401387</dim:field>
<dim:field mdschema="dc" element="identifier" qualifier="essn">1615-4169</dim:field>
<dim:field mdschema="dc" element="description" qualifier="abstract" lang="en">A molybdenum-catalyzed deoxygenation of sulfoxides, pyridine and quinoline N-oxides, N-hydroxybenzotriazoles, as well as the reduction of nitroarenes to anilines, has been developed using monocyclic terpenes such as γ-terpinene as an environmentally benign hydrogen surrogate. The only byproducts generated are water and p-cymene, under neat reaction conditions in which the terpene acts as both solvent and reducing agent. These features make this approach a highly attractive and sustainable alternative for the reduction of S-O and N-O containing compounds. Additionally, the reaction exhibited excellent chemoselectivity, tolerating a wide variety of functional groups.</dim:field>
<dim:field mdschema="dc" element="description" qualifier="sponsorship" lang="en">Financial support from Junta de Castilla y León and FEDER (BU028P23) and Ministerio de Ciencia, Innovación y Universidades (PID2020-115789GB−C21, PID2023-148198NB−C21, and PDC2021-115789GB−C21) is gratefully acknowledged. R.H.-R. thanks Ministerio de Ciencia, Innovación y Universidades for a FPU predoctoral contract. M.S. thanks Junta de Castilla y León and FEDER for a postdoctoral contract. S.S.-P. thanks Ministerio de Ciencia, Innovación y Universidades and “NextGenerationEU”/PRTR EU for a Ramón y Cajal contract (RYC2021-031533-I).</dim:field>
<dim:field mdschema="dc" element="format" qualifier="mimetype">application/pdf</dim:field>
<dim:field mdschema="dc" element="language" qualifier="iso" lang="es">eng</dim:field>
<dim:field mdschema="dc" element="publisher" lang="es">Wiley</dim:field>
<dim:field mdschema="dc" element="relation" qualifier="ispartof" lang="es">Advanced Synthesis &amp; Catalysis. 2025, V. 367, n. 9, p. e202401387</dim:field>
<dim:field mdschema="dc" element="relation" qualifier="publisherversion" lang="es">https://doi.org/10.1002/adsc.202401387</dim:field>
<dim:field mdschema="dc" element="rights" lang="*">Atribución-NoComercial 4.0 Internacional</dim:field>
<dim:field mdschema="dc" element="rights" qualifier="uri" lang="*">http://creativecommons.org/licenses/by-nc/4.0/</dim:field>
<dim:field mdschema="dc" element="rights" qualifier="accessRights" lang="es">info:eu-repo/semantics/openAccess</dim:field>
<dim:field mdschema="dc" element="subject" lang="en">γ‐Terpinene</dim:field>
<dim:field mdschema="dc" element="subject" lang="en">Molybdenum</dim:field>
<dim:field mdschema="dc" element="subject" lang="en">Reduction</dim:field>
<dim:field mdschema="dc" element="subject" lang="en">Sulfoxides</dim:field>
<dim:field mdschema="dc" element="subject" lang="en">Nitroarenes</dim:field>
<dim:field mdschema="dc" element="subject" qualifier="other" lang="es">Química</dim:field>
<dim:field mdschema="dc" element="subject" qualifier="other" lang="en">Chemistry</dim:field>
<dim:field mdschema="dc" element="title" lang="en">γ‐Terpinene: Biorenewable Reductant for the Molybdenum‐Catalyzed Reduction of Sulfoxides, N‐Oxides and Nitroarenes</dim:field>
<dim:field mdschema="dc" element="type" lang="es">info:eu-repo/semantics/article</dim:field>
<dim:field mdschema="dc" element="type" qualifier="hasVersion" lang="es">info:eu-repo/semantics/publishedVersion</dim:field>
<dim:field mdschema="dc" element="journal" qualifier="title" lang="es">Advanced Synthesis &amp; Catalysis</dim:field>
<dim:field mdschema="dc" element="volume" qualifier="number" lang="es">367</dim:field>
<dim:field mdschema="dc" element="issue" qualifier="number" lang="es">9</dim:field>
<dim:field mdschema="dc" element="page" qualifier="initial" lang="es">e202401387</dim:field>
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