<?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>2026-05-11T20:25:59Z</responseDate><request verb="GetRecord" identifier="oai:riubu.ubu.es:10259/9336" metadataPrefix="oai_dc">https://riubu.ubu.es/oai/request</request><GetRecord><record><header><identifier>oai:riubu.ubu.es:10259/9336</identifier><datestamp>2024-07-03T00:05:19Z</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>Synthesis of 4‐Furan‐ and 4‐Pyrrol‐3‐yl‐2H‐chromenes from Naturally‐occurring Compounds by Gold(I)‐Catalyed Domino Reactions</dc:title>
<dc:creator>Solas Luera, Marta</dc:creator>
<dc:creator>Renedo Peña, Lorena</dc:creator>
<dc:creator>Suárez Pantiga, Samuel</dc:creator>
<dc:creator>Sanz Díez, Roberto</dc:creator>
<dc:subject>Annulation</dc:subject>
<dc:subject>Chromenes</dc:subject>
<dc:subject>Furans</dc:subject>
<dc:subject>Gold</dc:subject>
<dc:subject>Hydroarylation</dc:subject>
<dc:subject>Pyrroles</dc:subject>
<dc:subject>Química orgánica</dc:subject>
<dc:subject>Chemistry, Organic</dc:subject>
<dc:description>A gold-catalyzed cascade double cyclization reaction has been designed to synthesize heterobiaryl compounds such as furanyl and pyrrolyl 2H-chromenes from bis(alkynyl)-1,2-diols and 1,2-amino alcohols. The starting materials are readily available from biomass platform molecules such as α-hydroxy acids and α-amino acids. The process involves an initial heterocyclodehydration step enabling the formation of the furan or pyrrole ring, followed by an alkyne hydroarylation to form the chromene core.</dc:description>
<dc:description>We gratefully acknowledge Ministerio de Ciencia e Innovación MCIN/AEI/10.13039/501100011033 (PID2020–115789GB-C21), and Junta de Castilla y León and FEDER (BU049P20) for financial support. M.S. and L.R. thank Junta de Castilla y León (Consejería de Educación) and Fondo Social Europeo for predoctoral contracts. S.S.-P. thanks a Ramón y Cajal (RYC2021-031533-I) contract funded by MCIN/AEI/10.13039/501100011033 and European Union “NextGenerationEU”/PRTR.</dc:description>
<dc:date>2024-07-02T07:48:26Z</dc:date>
<dc:date>2024-07-02T07:48:26Z</dc:date>
<dc:date>2023-05-24</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/10259/9336</dc:identifier>
<dc:identifier>10.1002/adsc.202300300</dc:identifier>
<dc:identifier>1615-4169</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>Advanced Synthesis &amp; Catalysis. 2023, V. 365, n. 12, p. 2049-2056</dc:relation>
<dc:relation>https://doi.org/10.1002/adsc.202300300</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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