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<dc:title>Gold(I)-catalyzed diastereoselective synthesis of 1-α-oxybenzyl-1H-indenes</dc:title>
<dc:creator>Virumbrales, Cintia</dc:creator>
<dc:creator>Suarez Pantiga, Samuel</dc:creator>
<dc:creator>Solas Luera, Marta</dc:creator>
<dc:creator>Fernández Rodríguez, Manuel A.</dc:creator>
<dc:creator>Sanz Díez, Roberto</dc:creator>
<dc:description>The gold(I)-catalyzed oxycyclization of β-aryl monosubstituted&#xd;
o-(alkynyl)styrenes gives rise to 1-α-methoxy or 1-α-hydroxybenzyl-&#xd;
1H-indenes in a diastereospecific way. In contrast to&#xd;
β,β-disubstituted o-(alkynyl)styrenes, the stereochemical outcome&#xd;
of this process, diastereospecific reaction supports the higher contribution&#xd;
of a gold intermediate with a cyclopropylcarbene-like&#xd;
character.</dc:description>
<dc:date>2018-09-07T08:21:18Z</dc:date>
<dc:date>2019-04-21T02:45:07Z</dc:date>
<dc:date>2018-04</dc:date>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:identifier>1477-0520</dc:identifier>
<dc:identifier>http://hdl.handle.net/10259/4920</dc:identifier>
<dc:identifier>10.1039/c8ob00406d</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>Organic &amp; Biomolecular Chemistry. 2018, V. 16, n. 15, p. 2623-2628</dc:relation>
<dc:relation>https://doi.org/10.1039/c8ob00406d</dc:relation>
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<dc:relation>info:eu-repo/grantAgreement/JCyL/BU076U16</dc:relation>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:publisher>Royal Society of Chemistry</dc:publisher>
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