<?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>2026-06-28T15:33:19Z</responseDate><request verb="GetRecord" identifier="oai:docta.ucm.es:20.500.14352/108997" metadataPrefix="qdc">https://docta.ucm.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:docta.ucm.es:20.500.14352/108997</identifier><datestamp>2025-07-17T16:45:03Z</datestamp><setSpec>com_20.500.14352_14</setSpec><setSpec>col_20.500.14352_15</setSpec></header><metadata><qdc:qualifieddc xmlns:qdc="http://dspace.org/qualifieddc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://purl.org/dc/elements/1.1/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dc.xsd http://purl.org/dc/terms/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dcterms.xsd http://dspace.org/qualifieddc/ http://www.ukoln.ac.uk/metadata/dcmi/xmlschema/qualifieddc.xsd">
   <dc:title>Enantioselective synthesis of a-aryl a-hydrazino phosphonates</dc:title>
   <dc:creator>Alberca, Saúl</dc:creator>
   <dc:creator>Romero Parra, Javier</dc:creator>
   <dc:creator>Fernández López, Israel</dc:creator>
   <dc:creator>Fernández, Rosario</dc:creator>
   <dc:creator>Lassaletta, José M.</dc:creator>
   <dc:creator>Monge, David</dc:creator>
   <dcterms:abstract>Catalysts generated in situ by the combination of pyridine–hydrazone N,N-ligands and Pd(TFA)2 have been applied to the addition of arylboronic acids to formylphosphonate-derived hydrazones, yielding α-aryl α-hydrazino phosphonates in excellent enantioselectivities (96 → 99% ee). Subsequent removal of the benzyloxycarbonyl (Cbz) N-protecting group afforded key building blocks en route to appealing artificial peptides, herbicides and antitumoral derivatives. Experimental and computational data support a stereochemical model based on aryl-palladium intermediates in which the phosphono hydrazone coordinates in its Z-configuration, maximizing the interactions between the substrate and the pyridine–hydrazone ligand.</dcterms:abstract>
   <dcterms:dateAccepted>2024-10-16T07:44:16Z</dcterms:dateAccepted>
   <dcterms:available>2024-10-16T07:44:16Z</dcterms:available>
   <dcterms:created>2024-10-16T07:44:16Z</dcterms:created>
   <dcterms:issued>2024</dcterms:issued>
   <dc:type>journal article</dc:type>
   <dc:identifier>https://hdl.handle.net/20.500.14352/108997</dc:identifier>
   <dc:identifier>XXXX-XXXX</dc:identifier>
   <dc:identifier>10.1039/d4sc00822g</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2019-106358GB-C21/ES/CATALIZADORES, LIGANDOS, METODOS Y REACTIVOS PARA SINTESIS ORGANICA SELECTIVA/</dc:relation>
   <dc:relation>info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2019-106358GB-C22/ES/CATALIZADORES, LIGANDOS, METODOS Y REACTIVOS PARA SINTESIS ORGANICA SELECTIVA/</dc:relation>
   <dc:relation>info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2019-106184GB-I00/ES/UNA APROXIMACION DIFERENTE PARA ENTENDER Y CONTROLAR LA CATALISIS/</dc:relation>
   <dc:relation>PID2022-137888NB-I00</dc:relation>
   <dc:relation>PID2022-143230NB-I00</dc:relation>
   <dc:relation>PID2022-139318NB-I00</dc:relation>
   <dc:relation>RED2022-134287-T</dc:relation>
   <dc:relation>P18-FR-3531</dc:relation>
   <dc:relation>P18-FR-644</dc:relation>
   <dc:relation>US-1262867</dc:relation>
   <dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
   <dc:rights>open access</dc:rights>
   <dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 International</dc:rights>
   <dc:publisher>RSC</dc:publisher>
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