<?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>2026-04-22T16:43:04Z</responseDate><request verb="GetRecord" identifier="oai:riubu.ubu.es:10259/10505" metadataPrefix="oai_dc">https://riubu.ubu.es/oai/request</request><GetRecord><record><header><identifier>oai:riubu.ubu.es:10259/10505</identifier><datestamp>2025-05-29T00:05:14Z</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>Molybdenum‐Catalyzed Direct Synthesis of Pyrroles from Nitroarenes with Glycols as Reductants</dc:title>
<dc:creator>Gómez Gil, Sara</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>Nitroarenes</dc:subject>
<dc:subject>Pyrroles</dc:subject>
<dc:subject>Reduction</dc:subject>
<dc:subject>Molybdenum</dc:subject>
<dc:subject>Glycols</dc:subject>
<dc:subject>Química</dc:subject>
<dc:subject>Química orgánica</dc:subject>
<dc:subject>Chemistry</dc:subject>
<dc:subject>Chemistry, Organic</dc:subject>
<dc:description>A molybdenum-catalyzed synthesis of N-(hetero)aryl pyrroles directly from inexpensive and commonly available (hetero)nitroarenes via reduction with pinacol and annulation with 1,4-dicarbonyls or cyclobutane-1,2-diols has been described. The process does not require an inert atmosphere and tolerates the presence of air and water. This non-noble catalytic system shows high chemoselectivity, allowing a diverse range of potentially reducible functional groups such as alkynes, alkenes, halogens, cyano, and carbonyls. Moreover, this strategy enables the reuse of a waste byproduct as reactant, facilitating the formation of challenging 1,4-dicarbonyls from accessible cyclobutane-1,2-diols used as reducing agents.</dc:description>
<dc:description>We acknowledge the financial support from Ministerio de Ciencia, Innovación y Universidades (PID2020-115789GB-C21/AEI/10.1039/501100011033 and PDC2021-115789GB-C21), and Junta de Castilla y León and FEDER (BU028P23). S.G.-G. thanks Ministerio de Ciencia, Innovación y Universidades for a FPU predoctoral 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>2025-05-28T07:16:54Z</dc:date>
<dc:date>2025-05-28T07:16:54Z</dc:date>
<dc:date>2024-10</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/10259/10505</dc:identifier>
<dc:identifier>10.1002/adsc.202401170</dc:identifier>
<dc:identifier>1615-4169</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>Advanced Synthesis &amp; Catalysis. 2024, V. 367, n. 4, p. e202401170</dc:relation>
<dc:relation>https://doi.org/10.1002/adsc.202401170</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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