<?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>2026-06-28T10:26:27Z</responseDate><request verb="GetRecord" identifier="oai:docta.ucm.es:20.500.14352/131542" metadataPrefix="mods">https://docta.ucm.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:docta.ucm.es:20.500.14352/131542</identifier><datestamp>2026-02-06T01:07:05Z</datestamp><setSpec>com_20.500.14352_14</setSpec><setSpec>col_20.500.14352_15</setSpec></header><metadata><mods:mods xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-1.xsd">
   <mods:name>
      <mods:namePart>Lozano, Blanca</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Teresa, Javier</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Fernández López, Israel</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Tortosa, Mariola</mods:namePart>
   </mods:name>
   <mods:extension>
      <mods:dateAvailable encoding="iso8601">2026-02-05T08:11:20Z</mods:dateAvailable>
   </mods:extension>
   <mods:extension>
      <mods:dateAccessioned encoding="iso8601">2026-02-05T08:11:20Z</mods:dateAccessioned>
   </mods:extension>
   <mods:originInfo>
      <mods:dateIssued encoding="iso8601">2025-10-31</mods:dateIssued>
   </mods:originInfo>
   <mods:identifier type="citation">Lozano, Blanca, et al. «Cyclopropylmethyl Boronic Esters as General Reagents in Transition-Metal Catalyzed Homoallylation Reactions». Journal of the American Chemical Society, vol. 147, n.o 45, noviembre de 2025, pp. 41221-28. DOI.org (Crossref), https://doi.org/10.1021/jacs.5c15781.</mods:identifier>
   <mods:identifier type="doi">10.1021/jacs.5c15781</mods:identifier>
   <mods:identifier type="uri">https://hdl.handle.net/20.500.14352/131542</mods:identifier>
   <mods:identifier type="officialurl">https://doi.org/10.1021/jacs.5c15781</mods:identifier>
   <mods:identifier type="relatedurl">https://pubs.acs.org/doi/10.1021/jacs.5c15781</mods:identifier>
   <mods:abstract>Herein we disclose the use of cyclopropylmethyl boronates as general reagents in Negishi-type homoallylation reactions. This strategy provides a novel approach to generate enantioenriched homoallyl-Zn species through boron-to-zinc transmetalation. Subsequent sp2–sp3 cross-coupling offers a platform for the preparation of arenes, ketones, and 1,5-dienes containing a chiral homoallylic scaffold. The method has been applied to the late-stage functionalization of known drugs and the preparation of precursors of biologically relevant compounds. Mechanistic experiments and DFT calculations provide insight into the transmetalation/ring-opening sequence.</mods:abstract>
   <mods:language>
      <mods:languageTerm>eng</mods:languageTerm>
   </mods:language>
   <mods:accessCondition type="useAndReproduction">http://creativecommons.org/licenses/by-nc-nd/4.0/</mods:accessCondition>
   <mods:accessCondition type="useAndReproduction">open access</mods:accessCondition>
   <mods:accessCondition type="useAndReproduction">Attribution-NonCommercial-NoDerivatives 4.0 International</mods:accessCondition>
   <mods:titleInfo>
      <mods:title>Cyclopropylmethyl Boronic Esters as General Reagents in Transition-Metal Catalyzed Homoallylation Reactions</mods:title>
   </mods:titleInfo>
   <mods:genre>journal article</mods:genre>
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