<?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>2026-06-29T07:44:13Z</responseDate><request verb="GetRecord" identifier="oai:docta.ucm.es:20.500.14352/95778" metadataPrefix="oai_dc">https://docta.ucm.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:docta.ucm.es:20.500.14352/95778</identifier><datestamp>2025-05-10T00:09:06Z</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>Assembly of glycoamino acid building blocks: a new strategy for the straightforward synthesis of heparan sulfate mimics</dc:title>
   <dc:title>Inglés</dc:title>
   <dc:creator>Revuelta, Julia</dc:creator>
   <dc:creator>Fuentes, Roberto </dc:creator>
   <dc:creator>Lagartera, Laura</dc:creator>
   <dc:creator>Hernáiz Gómez-Degano, María Josefa</dc:creator>
   <dc:creator>Bastida, Agatha</dc:creator>
   <dc:creator>García-Junceda, Eduardo</dc:creator>
   <dc:creator>Fernández-Mayoralas, Alfonso</dc:creator>
   <dc:contributor>Fernández-Mayoralas, Alfonso</dc:contributor>
   <dc:subject>Chemical Synthesis, Design, Glycosaminoglycans</dc:subject>
   <dc:subject>Ciencias</dc:subject>
   <dc:subject>23 Química</dc:subject>
   <dc:description>A new strategy that enables a modular straightforward synthesis of heparan sulfate oligosaccharide mimics by the assembly of simple glycoamino acid building blocks is described. The coupling between units is readily carried out by an amidation reaction. Several glycoamino acid oligomers were prepared and their interaction with the FGF2 protein was analyzed.</dc:description>
   <dc:description>Ministerio de Economía y Competitividad (España)</dc:description>
   <dc:description>Depto. de Química en Ciencias Farmacéuticas</dc:description>
   <dc:description>Fac. de Farmacia</dc:description>
   <dc:description>TRUE</dc:description>
   <dc:description>pub</dc:description>
   <dc:date>2024-01-29T09:23:01Z</dc:date>
   <dc:date>2024-01-29T09:23:01Z</dc:date>
   <dc:date>2018</dc:date>
   <dc:type>journal article</dc:type>
   <dc:type>VoR</dc:type>
   <dc:identifier>https://hdl.handle.net/20.500.14352/95778</dc:identifier>
   <dc:identifier>1359-7345</dc:identifier>
   <dc:identifier>10.1039/c8cc08067d</dc:identifier>
   <dc:identifier>1364-548X</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>info:eu-repo/grantAgreement/MAT2015-65184-C2-2-R</dc:relation>
   <dc:relation>info:eu-repo/grantAgreement/CTQ2015-66206-C2-1-R</dc:relation>
   <dc:relation>Revuelta J, Fuentes R, Lagartera L, Hernáiz MJ, Bastida A, García-Junceda E, et al. Assembly of glycoamino acid building blocks: a new strategy for the straightforward synthesis of heparan sulfate mimics. Chem Commun 2018;54:13455–8. https://doi.org/10.1039/C8CC08067D.</dc:relation>
   <dc:rights>restricted access</dc:rights>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>Royal Society of Chemistry</dc:publisher>
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