<?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>2026-04-17T20:07:56Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:2072/522726" metadataPrefix="oai_dc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:2072/522726</identifier><datestamp>2024-12-20T20:40:58Z</datestamp><setSpec>com_2072_300912</setSpec><setSpec>com_2072_4427</setSpec><setSpec>col_2072_301309</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>H-Bonded Counterion-Directed Catalysis: Enantioselective Gold(I)-Catalyzed Addition to 2-Alkynyl Enones as a Case Study</dc:title>
   <dc:creator>Martí, Àlex</dc:creator>
   <dc:creator>Montesinos-Magraner, Marc</dc:creator>
   <dc:creator>Echavarren, Antonio M.</dc:creator>
   <dc:creator>Franchino, Allegra</dc:creator>
   <dc:subject>54</dc:subject>
   <dc:description>H-bonded counterion-directed catalysis (HCDC) is a strategy
wherein a chiral anion that is hydrogen-bonded to the achiral
ligand of a metal complex is responsible for enantioinduction.
In this article we present the application of H-bonded counterion-
directed catalysis to the Au(I)-catalyzed enantioselective
tandem cycloisomerization-addition reaction of 2-alkynyl
enones. Following the addition of C-, N- or O-centered
nucleophiles, bicyclic furans were obtained in moderate to
excellent yield and enantioselectivity (28 examples, 59–96%
yield, 62:38 to 95:5 er). The optimal catalytic system, comprising
a phosphinosquaramide Au(I) chloride complex and a
BINOL-derived phosphoramidate Ag(I) salt, was selected in a
combinatorial fashion from a larger library with the help of
high-throughput screening. An enantioselectivity switch of ca.
120 Δee% was observed upon addition of the achiral Au(I)
component to the Ag(I) salt.</dc:description>
   <dc:date>2022-06-23</dc:date>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:identifier>http://hdl.handle.net/2072/522726</dc:identifier>
   <dc:identifier>https://doi.org/10.1002/ejoc.202200518</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>Horizon 2020 Marie Skłodowska- Curie COFUND fellowship 754510 to A.F.</dc:relation>
   <dc:relation>Advanced Grant 835080</dc:relation>
   <dc:relation>MCIN/AEI/10.13039/ 501100011033 (PID2019-104815GB- I00)</dc:relation>
   <dc:relation>MCIN/AEI/10.13039/ 501100011033 (IJC2019040181-I Juan de la Cierva contract to M.M.-M.)</dc:relation>
   <dc:relation>Severo Ochoa Excellence Accreditation 2020–2023 (CEX2019-000925-S, MIC/AEI)</dc:relation>
   <dc:rights>You have selected the Attribution-NonCommercial-NoDerivatives 4.0 International License.
This license is permanently located at
http://creativecommons.org/licenses/by-nc-nd/4.0/.</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:format>518 p.</dc:format>
   <dc:format>application/pdf</dc:format>
   <dc:source>RECERCAT (Dipòsit de la Recerca de Catalunya)</dc:source>
</oai_dc:dc></metadata></record></GetRecord></OAI-PMH>