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<dc:title>Mo‐Catalyzed Synthesis of N‐Polyheterocycles From Functionalized Nitroarenes and Aldehydes</dc:title>
<dc:creator>Martínez González, Raúl</dc:creator>
<dc:creator>Rubio Presa, Rubén</dc:creator>
<dc:creator>Pedrosa Sáez, María de los Remedios</dc:creator>
<dc:creator>Suárez Pantiga, Samuel</dc:creator>
<dc:creator>Sanz Díez, Roberto</dc:creator>
<dc:subject>Catalysis</dc:subject>
<dc:subject>Molybdenum</dc:subject>
<dc:subject>Nitroarenes</dc:subject>
<dc:subject>N-polyheterocycles</dc:subject>
<dc:subject>Tandem processes</dc:subject>
<dc:subject>Química orgánica</dc:subject>
<dc:subject>Chemistry, Organic</dc:subject>
<dc:description>The direct preparation of nitrogen-containing polyaromatic heterocycles in a single operational step from readily availablenitroarenes represents an attractive and sustainable alternative to traditional multistep approaches. In this context, this workdescribes an efficient and versatile methodology for the synthesis of fused N-polyheterocyclic scaffolds from functionalizednitroarenes and aldehydes catalyzed by dioxomolybdenum(VI) complexes and employing pinacol as a readily available andenvironmentally benign reductant. The protocol integrates nitro reduction, imine formation, and intramolecular cyclization ina single operational sequence. Careful fine-tuning of the reaction conditions proved crucial to minimizing competing pathways.This molybdenum-catalyzed strategy exhibits broad substrate scope, accommodating aromatic, aliphatic, and α,β-unsaturatedaldehydes, and enabling access to a variety of pharmaceutically relevant frameworks, such as pyrrolo[1,2-a]quinoxalines,indoloquinoxalines, γ-carbolines, imidazoquinolines, and phenanthridines.</dc:description>
<dc:description>We gratefully acknowledge Ministerio de Ciencia, Innovación y Universidades (PID2023-148198NB-C21) and Junta de Castilla y León and FEDER (BU028P23) for financial support. Raúl Martínez-González thanks Junta de Castilla y León for a predoctoral contract. Samuel Suárez-Pantiga thanks a Ramón y Cajal (RYC2021-031533-I) contract funded by MICIN/AEI/10.13039/501100011033 and European Union “NextGenerationEU”/PRTR.</dc:description>
<dc:description>Open access funding provided by FEDER European Funds and the Junta De Castilla y León under the Research and Innovation Strategy for Smart Specialization (RIS3) of Castilla y León 2021-2027</dc:description>
<dc:date>2026-05-14T11:21:46Z</dc:date>
<dc:date>2026-05-14T11:21:46Z</dc:date>
<dc:date>2026-05</dc:date>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
<dc:identifier>2193-5807</dc:identifier>
<dc:identifier>https://hdl.handle.net/10259/11626</dc:identifier>
<dc:identifier>10.1002/ajoc.70439</dc:identifier>
<dc:identifier>2193-5815</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>Asian Journal of Organic Chemistry. 2026, V. 15, n.5, e70439</dc:relation>
<dc:relation>https://doi.org/10.1002/ajoc.70439</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>
<europeana:object>https://riubu.ubu.es/bitstream/10259/11626/4/Mart%c3%adnez%e2%80%90ajoc_2026.pdf.jpg</europeana:object>
<europeana:provider>Hispana</europeana:provider>
<europeana:type>TEXT</europeana:type>
<europeana:rights>http://creativecommons.org/licenses/by-nc/4.0/</europeana:rights>
<europeana:dataProvider>RIUBU. Repositorio Institucional de la Universidad de Burgos</europeana:dataProvider>
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