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<dc:title>Brønsted acid−catalyzed synthesis of tetrasubstituted allenes and polysubstituted 2H-chromenes from tertiary propargylic alcohols</dc:title>
<dc:creator>Cabrera Lobera, Natalia</dc:creator>
<dc:creator>Velasco Pérez, Noelia</dc:creator>
<dc:creator>Sanz Díez, Roberto</dc:creator>
<dc:creator>Fernández Rodríguez, Manuel A.</dc:creator>
<dc:subject>Allenes</dc:subject>
<dc:subject>Brønsted acid catalysis</dc:subject>
<dc:subject>Propargylic alcohols</dc:subject>
<dc:subject>2H-chromenes</dc:subject>
<dc:subject>Nucleophilic substitution</dc:subject>
<dc:description>A practical and environmentally benign Brønsted acid−catalyzed protocol for the preparation of all-carbon tetrasubstituted allenes, consisting in the direct SNˈ addition of tri- or dimethoxy arenes or allyltrimethylsilane to tertiary propargylic alcohols, has been developed. In addition, a straightforward synthesis of densely substituted 2H-chromenes by metal-free tandem allenylation/heterocyclization reaction of methoxyphenols and tertiary alkynols is presented.</dc:description>
<dc:date>2019-11-13T08:45:15Z</dc:date>
<dc:date>2019-11-13T08:45:15Z</dc:date>
<dc:date>2019-08</dc:date>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:identifier>0040-4020</dc:identifier>
<dc:identifier>http://hdl.handle.net/10259/5177</dc:identifier>
<dc:identifier>10.1016/j.tet.2019.05.023</dc:identifier>
<dc:identifier>10.1016/j.tet.2019.05.023</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>Tetrahedron. 2019, V. 75, n. 31, p. 4071-4080</dc:relation>
<dc:relation>https://doi.org/10.1016/j.tet.2019.05.023</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/JCyL/BU291P18</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/MINECO/CTQ2016-75023-C2-1-P</dc:relation>
<dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
<dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 Internacional</dc:rights>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:publisher>Elsevier</dc:publisher>
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