<?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>2026-06-01T02:36:16Z</responseDate><request verb="GetRecord" identifier="oai:docta.ucm.es:20.500.14352/109134" metadataPrefix="oai_dc">https://docta.ucm.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:docta.ucm.es:20.500.14352/109134</identifier><datestamp>2025-03-18T13:41:45Z</datestamp><setSpec>com_20.500.14352_14</setSpec><setSpec>col_20.500.14352_15</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
   <dc:title>Regioselective 1,6-Conjugate Addition of Boronic Acids and Grignard Reagents to Dienylpyridines</dc:title>
   <dc:creator>Roscales García, Silvia</dc:creator>
   <dc:creator>García Salado, Irene</dc:creator>
   <dc:creator>García Csaky, Aurelio</dc:creator>
   <dc:subject>547</dc:subject>
   <dc:subject>Addition</dc:subject>
   <dc:subject>Catalysis</dc:subject>
   <dc:subject>Pyridines</dc:subject>
   <dc:subject>Rhodium</dc:subject>
   <dc:subject>Iron</dc:subject>
   <dc:subject>Ciencias</dc:subject>
   <dc:subject>23 Química</dc:subject>
   <dc:description>Functionalization of the lateral chain of dienylpyridines was achieved by the regioselective 1,6-addition of boronic acids catalyzed by rhodium(I) or Grignard reagents under iron(II) catalysis.</dc:description>
   <dc:description>Ministerio de Ciencia e Innovación (España)</dc:description>
   <dc:description>Universidad Complutense de Madrid</dc:description>
   <dc:description>Depto. de Química Orgánica</dc:description>
   <dc:description>Fac. de Ciencias Químicas</dc:description>
   <dc:description>TRUE</dc:description>
   <dc:description>pub</dc:description>
   <dc:date>2024-10-21T09:48:05Z</dc:date>
   <dc:date>2024-10-21T09:48:05Z</dc:date>
   <dc:date>2011</dc:date>
   <dc:type>journal article</dc:type>
   <dc:type>AM</dc:type>
   <dc:identifier>https://hdl.handle.net/20.500.14352/109134</dc:identifier>
   <dc:identifier>XXXX-XXXX</dc:identifier>
   <dc:identifier>10.1055/s-0030-1261183</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>info:eu-repo/grantAgreement/MICINN//CTQ2010-16170/ES/NUEVOS METODOS CATALITICOS DE SINTESIS ESTEREOSELECTIVA BASADOS EN EL EMPLEO DE ACIDOS BORONICOS. EVALUACION DE LA ACTIVIDAD NEUROPROTECTORA DE LOS PRODUCTOS RESULTANTES/</dc:relation>
   <dc:relation>Csákÿ, A., Roscales, S., &amp; Salado, I. G. (2011). Regioselective 1,6-Conjugate Addition of Boronic Acids and Grignard Reagents to Dienylpyridines. Synlett, 2011(15), 2234–2236.</dc:relation>
   <dc:rights>restricted access</dc:rights>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>Thieme Verlag Stuttgart</dc:publisher>
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