<?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>2026-04-21T08:57:45Z</responseDate><request verb="GetRecord" identifier="oai:riubu.ubu.es:10259/10506" metadataPrefix="oai_dc">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><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
<dc:title>γ‐Terpinene: Biorenewable Reductant for the Molybdenum‐Catalyzed Reduction of Sulfoxides, N‐Oxides and Nitroarenes</dc:title>
<dc:creator>Hernández Ruiz, Raquel</dc:creator>
<dc:creator>Solas Luera, Marta</dc:creator>
<dc:creator>Suárez Pantiga, Samuel</dc:creator>
<dc:creator>Pedrosa Sáez, María de los Remedios</dc:creator>
<dc:creator>Sanz Díez, Roberto</dc:creator>
<dc:subject>γ‐Terpinene</dc:subject>
<dc:subject>Molybdenum</dc:subject>
<dc:subject>Reduction</dc:subject>
<dc:subject>Sulfoxides</dc:subject>
<dc:subject>Nitroarenes</dc:subject>
<dc:subject>Química</dc:subject>
<dc:subject>Chemistry</dc:subject>
<dc:description>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.</dc:description>
<dc:description>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).</dc:description>
<dc:date>2025-05-28T07:31:13Z</dc:date>
<dc:date>2025-05-28T07:31:13Z</dc:date>
<dc:date>2025-05</dc:date>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
<dc:identifier>1615-4150</dc:identifier>
<dc:identifier>http://hdl.handle.net/10259/10506</dc:identifier>
<dc:identifier>10.1002/adsc.202401387</dc:identifier>
<dc:identifier>1615-4169</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>Advanced Synthesis &amp; Catalysis. 2025, V. 367, n. 9, p. e202401387</dc:relation>
<dc:relation>https://doi.org/10.1002/adsc.202401387</dc:relation>
<dc:rights>Atribución-NoComercial 4.0 Internacional</dc:rights>
<dc:rights>http://creativecommons.org/licenses/by-nc/4.0/</dc:rights>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:format>application/pdf</dc:format>
<dc:publisher>Wiley</dc:publisher>
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