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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.1002/chir.23475</dc:identifier><dc:language>eng</dc:language><dc:creator>Lopez-Ram-de-Viu, Pilar</dc:creator><dc:creator>Galvez, Jose A.</dc:creator><dc:creator>Diaz-de-Villegas, Maria D.</dc:creator><dc:title>Synthesis, resolution, and absolute configuration determination of a vicinal amino alcohol with axial chirality. Application to the synthesis of new box and pybox ligands</dc:title><dc:identifier>ART-2022-129231</dc:identifier><dc:description>New racemic vicinal amino alcohol derivatives with 4-benzylidenecyclohexane skeleton and axial chirality have been prepared. A preparatively easy and efficient protocol for resolution of the N-benzoylamino alcohol is described. Using a 250 x 20 mm (L x ID) Chiralpak (R) IA column, and the appropriate mixture of n-hexane/ethanol/chloroform as eluent, both enantiomers of N-benzoylamino alcohol 3 are obtained with &gt;99% enantiomeric excess (ee) by successive injections of a solution of the racemic sample in chloroform. The obtained axially chiral vicinal amino alcohol is used to synthesize structurally novel bisoxazoline ligands in high yields.</dc:description><dc:date>2022</dc:date><dc:source>http://zaguan.unizar.es/record/117634</dc:source><dc:doi>10.1002/chir.23475</dc:doi><dc:identifier>http://zaguan.unizar.es/record/117634</dc:identifier><dc:identifier>oai:zaguan.unizar.es:117634</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/DGA/E45-20R</dc:relation><dc:identifier.citation>Chirality 34, 8 (2022), 1140-1150</dc:identifier.citation><dc:rights>by-nc-nd</dc:rights><dc:rights>http://creativecommons.org/licenses/by-nc-nd/3.0/es/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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