<?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>2026-04-18T00:27:09Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:2445/108386" metadataPrefix="oai_dc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:2445/108386</identifier><datestamp>2025-12-04T21:40:23Z</datestamp><setSpec>com_2072_1057</setSpec><setSpec>col_2072_478917</setSpec><setSpec>col_2072_478933</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>Borane as an efficient directing group. Stereoselective 1,2-addition of organometallic reagents to borane P-stereogenic N-phosphanylimines</dc:title>
   <dc:creator>Flores-Gaspar, Areli</dc:creator>
   <dc:creator>Orgué Gassol, Sílvia</dc:creator>
   <dc:creator>Grabulosa, Arnald</dc:creator>
   <dc:creator>Riera i Escalé, Antoni</dc:creator>
   <dc:creator>Verdaguer i Espaulella, Xavier</dc:creator>
   <dc:subject>Compostos organometàl·lics</dc:subject>
   <dc:subject>Lligands (Bioquímica)</dc:subject>
   <dc:subject>Catàlisi asimètrica</dc:subject>
   <dc:subject>Organometallic compounds</dc:subject>
   <dc:subject>Ligands (Biochemistry)</dc:subject>
   <dc:subject>Enantioselective catalysis</dc:subject>
   <dc:description>In non-coordinating solvents, borane was shown to be an efficient directing group for the stereoselective 1,2-addition of organolithium reagents to P-stereogenic N-phosphanylimines. Selectivity was reversed in coordinating solvents. This process can lead to novel ligand scaffolds for asymmetric catalysis.</dc:description>
   <dc:date>2017-03-14T08:59:50Z</dc:date>
   <dc:date>2017-03-14T08:59:50Z</dc:date>
   <dc:date>2014-12-22</dc:date>
   <dc:date>2017-03-14T08:59:50Z</dc:date>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/acceptedVersion</dc:type>
   <dc:identifier>1359-7345</dc:identifier>
   <dc:identifier>https://hdl.handle.net/2445/108386</dc:identifier>
   <dc:identifier>646126</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>Versió postprint del document publicat a: https://doi.org/10.1039/c4cc09106j</dc:relation>
   <dc:relation>Chemical Communications, 2014, vol. 51, p. 1941-1944</dc:relation>
   <dc:relation>https://doi.org/10.1039/c4cc09106j</dc:relation>
   <dc:rights>(c) Flores-Gaspar, Areli et al., 2014</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:format>4 p.</dc:format>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>Royal Society of Chemistry</dc:publisher>
   <dc:source>Articles publicats en revistes (Química Inorgànica i Orgànica)</dc:source>
</oai_dc:dc></metadata></record></GetRecord></OAI-PMH>