<?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>2026-04-18T06:55:01Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:2445/164139" metadataPrefix="oai_dc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:2445/164139</identifier><datestamp>2025-11-19T10:49:19Z</datestamp><setSpec>com_2072_1057</setSpec><setSpec>col_2072_478816</setSpec><setSpec>col_2072_478903</setSpec><setSpec>col_2072_478917</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>A practical synthetic route to enantiopure 6-substituted cis-decahydroquinolines</dc:title>
   <dc:creator>Amat Tusón, Mercedes</dc:creator>
   <dc:creator>Navío, Laura</dc:creator>
   <dc:creator>Llor Brunés, Núria</dc:creator>
   <dc:creator>Molins, Elies</dc:creator>
   <dc:creator>Bosch Cartes, Joan</dc:creator>
   <dc:subject>Síntesi orgànica</dc:subject>
   <dc:subject>Lactames</dc:subject>
   <dc:subject>Enantiòmers</dc:subject>
   <dc:subject>Compostos heterocíclics</dc:subject>
   <dc:subject>Organic synthesis</dc:subject>
   <dc:subject>Lactams</dc:subject>
   <dc:subject>Enantiomers</dc:subject>
   <dc:subject>Heterocyclic compounds</dc:subject>
   <dc:description>Starting from 4-substituted cyclohexanones, a practical synthetic route to enantiopure 6-substituted cis-decahydroquinolines has been developed, the key steps being a stereoselective cyclocondensation of an unsaturated δ-keto ester derivative with (R)-phenylglycinol and the stereoselective hydrogenation of the resulting tricyclic oxazoloquinolone lactams.</dc:description>
   <dc:date>2020-06-03T09:40:22Z</dc:date>
   <dc:date>2020-06-03T09:40:22Z</dc:date>
   <dc:date>2012-01-06</dc:date>
   <dc:date>2020-06-03T09:40:22Z</dc:date>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/acceptedVersion</dc:type>
   <dc:identifier>1523-7060</dc:identifier>
   <dc:identifier>https://hdl.handle.net/2445/164139</dc:identifier>
   <dc:identifier>603300</dc:identifier>
   <dc:identifier>22133083</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>Versió postprint del document publicat a: https://doi.org/10.1021/ol2030058</dc:relation>
   <dc:relation>Organic Letters, 2012, vol. 14, num. 1, p. 210-213</dc:relation>
   <dc:relation>https://doi.org/10.1021/ol2030058</dc:relation>
   <dc:rights>(c) American Chemical Society , 2012</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:format>4 p.</dc:format>
   <dc:format>application/pdf</dc:format>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>American Chemical Society</dc:publisher>
   <dc:source>Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)</dc:source>
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